2022
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Journal Articles
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| Harvie P. Portugaliza, H. Magloire Natama, Pieter Guetens, Eduard Rovira-Vallbona, Athanase M. Somé, Aida Millogo, D. Florence Ouédraogo, Innocent Valéa, Hermann Sorgho, Halidou Tinto, Nguyen Hong, Antonio Sitoe, Rosauro Varo, Quique Bassat, Alfred Cortés, Anna Rosanas-Urgell Plasmodium falciparum sexual conversion rates can be affected by artemisinin-based treatment in naturally infected malaria patients Journal Article In: eBioMedicine, vol. 83, pp. 104198, 2022, ISSN: 23523964. @article{Portugaliza2022,
title = {Plasmodium falciparum sexual conversion rates can be affected by artemisinin-based treatment in naturally infected malaria patients},
author = {Harvie P. Portugaliza and H. Magloire Natama and Pieter Guetens and Eduard Rovira-Vallbona and Athanase M. Som\'{e} and Aida Millogo and D. Florence Ou\'{e}draogo and Innocent Val\'{e}a and Hermann Sorgho and Halidou Tinto and Nguyen Hong and Antonio Sitoe and Rosauro Varo and Quique Bassat and Alfred Cort\'{e}s and Anna Rosanas-Urgell},
url = {https://linkinghub.elsevier.com/retrieve/pii/S2352396422003802},
doi = {10.1016/j.ebiom.2022.104198},
issn = {23523964},
year = {2022},
date = {2022-01-01},
journal = {eBioMedicine},
volume = {83},
pages = {104198},
abstract = {BACKGROUND Artemisinins (ART) are the key component of the frontline antimalarial treatment, but their impact on Plasmodium falciparum sexual conversion rates in natural malaria infections remains unknown. This is an important knowledge gap because sexual conversion rates determine the relative parasite investment between maintaining infection in the same human host and transmission to mosquitoes. METHODS The primary outcome of this study was to assess the impact of ART-based treatment on sexual conversion rates by comparing the relative transcript levels of pfap2-g and other sexual ring biomarkers (SRBs) before and after treatment. We analysed samples from previously existing cohorts in Vietnam, Burkina Faso and Mozambique (in total},
keywords = {Artemisinin, Malaria transmission, pfap2-g, Plasmodium falciparum, Sexual conversion},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND Artemisinins (ART) are the key component of the frontline antimalarial treatment, but their impact on Plasmodium falciparum sexual conversion rates in natural malaria infections remains unknown. This is an important knowledge gap because sexual conversion rates determine the relative parasite investment between maintaining infection in the same human host and transmission to mosquitoes. METHODS The primary outcome of this study was to assess the impact of ART-based treatment on sexual conversion rates by comparing the relative transcript levels of pfap2-g and other sexual ring biomarkers (SRBs) before and after treatment. We analysed samples from previously existing cohorts in Vietnam, Burkina Faso and Mozambique (in total |
| Salla Sariola, Andrea Butcher, Jose A. Cañada, Mariette Aïkpé, Adélaïde Compaore Closing the GAP in Antimicrobial Resistance Policy in Benin and Burkina Faso Journal Article In: mSystems, vol. 7, iss. 4, 2022, ISSN: 2379-5077. @article{Sariola2022,
title = {Closing the GAP in Antimicrobial Resistance Policy in Benin and Burkina Faso},
author = {Salla Sariola and Andrea Butcher and Jose A. Ca\~{n}ada and Mariette A\"{i}kp\'{e} and Ad\'{e}la\"{i}de Compaore},
editor = {Li Cui},
url = {https://journals.asm.org/doi/10.1128/msystems.00150-22},
doi = {10.1128/msystems.00150-22},
issn = {2379-5077},
year = {2022},
date = {2022-01-01},
journal = {mSystems},
volume = {7},
issue = {4},
abstract = {\<p\>The burden of antimicrobial resistance (AMR) is unequally distributed across the globe. Low-income countries face a more severe AMR situation and have fewer means to solve the problem.\</p\>},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
<p>The burden of antimicrobial resistance (AMR) is unequally distributed across the globe. Low-income countries face a more severe AMR situation and have fewer means to solve the problem.</p> |
| Laetitia Duval, Elisa Sicuri, Susana Scott, Maminata Traoré, Bunja Daabo, Halidou Tinto, Koen Peeters Grietens, Umberto d’Alessando, Henk Schallig, Petra Mens, Lesong Conteh Household costs associated with seeking malaria treatment during pregnancy: evidence from Burkina Faso and The Gambia Journal Article In: Cost Effectiveness and Resource Allocation, vol. 20, iss. 1, pp. 42, 2022, ISSN: 1478-7547. @article{Duval2022,
title = {Household costs associated with seeking malaria treatment during pregnancy: evidence from Burkina Faso and The Gambia},
author = {Laetitia Duval and Elisa Sicuri and Susana Scott and Maminata Traor\'{e} and Bunja Daabo and Halidou Tinto and Koen Peeters Grietens and Umberto d’Alessando and Henk Schallig and Petra Mens and Lesong Conteh},
url = {https://resource-allocation.biomedcentral.com/articles/10.1186/s12962-022-00376-x},
doi = {10.1186/s12962-022-00376-x},
issn = {1478-7547},
year = {2022},
date = {2022-01-01},
journal = {Cost Effectiveness and Resource Allocation},
volume = {20},
issue = {1},
pages = {42},
abstract = {BACKGROUND Malaria in pregnancy remains a major health threat in sub-Saharan Africa to both expectant mothers and their unborn children. To date, there have been very few studies focused on the out of pocket costs associated with seeking treatment for malaria during pregnancy. METHODS A cross-sectional survey was undertaken in Burkina Faso and The Gambia to estimate the direct and indirect costs associated with outpatient consultations (OP) and inpatient admissions (IP). Direct costs were broken down into medical (admission fees, drug charges, and laboratory fees), and non-medical (transportation and food). Indirect costs reflected time lost due to illness. In total, 220 pregnant women in Burkina Faso and 263 in The Gambia were interviewed about their treatment seeking decisions, expenditure, time use and financial support associated with each malaria episode. RESULTS In Burkina Faso 6.7% sought treatment elsewhere before their OP visits, and 27.1% before their IP visits. This compares to 1.3% for OP and 25.92% for IP in The Gambia. Once at the facility, the average direct costs (out of pocket) were 3.91US$ for an OP visit and 15.38US$ of an IP visit in Burkina Faso, and 0.80US$ for an OP visit and 9.19US$ for an IP visit in The Gambia. Inpatient direct costs were driven by drug costs (9.27US$) and transportation costs (2.72US$) in Burkina Faso and drug costs (3.44 US$) and food costs (3.44 US$) in The Gambia. Indirect costs of IP visits, valued as the opportunity cost of time lost due to the illness, were estimated at 11.85US$ in Burkina Faso and 4.07US$ in The Gambia. The difference across the two countries was mainly due to the longer time of hospitalization in Burkina Faso compared to The Gambia. In The Gambia, the vast majority of pregnant women reported receiving financial support from family members living abroad, most commonly siblings (65%). CONCLUSIONS High malaria treatment costs are incurred by pregnant women in Burkina Faso and The Gambia. Beyond the medical costs of fees and drugs, costs in terms of transport, food and time are significant drivers. The role of remittances, particularly their effect on accessing health care, needs further investigation.},
keywords = {Burkina Faso, Cost, Gambia, Malaria, Pregnancy, Remittances, sub-Saharan Africa},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND Malaria in pregnancy remains a major health threat in sub-Saharan Africa to both expectant mothers and their unborn children. To date, there have been very few studies focused on the out of pocket costs associated with seeking treatment for malaria during pregnancy. METHODS A cross-sectional survey was undertaken in Burkina Faso and The Gambia to estimate the direct and indirect costs associated with outpatient consultations (OP) and inpatient admissions (IP). Direct costs were broken down into medical (admission fees, drug charges, and laboratory fees), and non-medical (transportation and food). Indirect costs reflected time lost due to illness. In total, 220 pregnant women in Burkina Faso and 263 in The Gambia were interviewed about their treatment seeking decisions, expenditure, time use and financial support associated with each malaria episode. RESULTS In Burkina Faso 6.7% sought treatment elsewhere before their OP visits, and 27.1% before their IP visits. This compares to 1.3% for OP and 25.92% for IP in The Gambia. Once at the facility, the average direct costs (out of pocket) were 3.91US$ for an OP visit and 15.38US$ of an IP visit in Burkina Faso, and 0.80US$ for an OP visit and 9.19US$ for an IP visit in The Gambia. Inpatient direct costs were driven by drug costs (9.27US$) and transportation costs (2.72US$) in Burkina Faso and drug costs (3.44 US$) and food costs (3.44 US$) in The Gambia. Indirect costs of IP visits, valued as the opportunity cost of time lost due to the illness, were estimated at 11.85US$ in Burkina Faso and 4.07US$ in The Gambia. The difference across the two countries was mainly due to the longer time of hospitalization in Burkina Faso compared to The Gambia. In The Gambia, the vast majority of pregnant women reported receiving financial support from family members living abroad, most commonly siblings (65%). CONCLUSIONS High malaria treatment costs are incurred by pregnant women in Burkina Faso and The Gambia. Beyond the medical costs of fees and drugs, costs in terms of transport, food and time are significant drivers. The role of remittances, particularly their effect on accessing health care, needs further investigation. |
| Jean-Tristan Brandenburg, Melanie A. Govender, Cheryl A. Winkler, Palwende Romuald Boua, Godfred Agongo, June Fabian, Michèle Ramsay Apolipoprotein L1 High-Risk Genotypes and Albuminuria in Sub-Saharan African Populations Journal Article In: Clinical Journal of the American Society of Nephrology, vol. 17, iss. 6, pp. 798-808, 2022, ISSN: 1555-9041. @article{Brandenburg2022,
title = {Apolipoprotein L1 High-Risk Genotypes and Albuminuria in Sub-Saharan African Populations},
author = {Jean-Tristan Brandenburg and Melanie A. Govender and Cheryl A. Winkler and Palwende Romuald Boua and Godfred Agongo and June Fabian and Mich\`{e}le Ramsay},
url = {https://journals.lww.com/10.2215/CJN.14321121},
doi = {10.2215/CJN.14321121},
issn = {1555-9041},
year = {2022},
date = {2022-01-01},
journal = {Clinical Journal of the American Society of Nephrology},
volume = {17},
issue = {6},
pages = {798-808},
abstract = {BACKGROUND AND OBJECTIVES Recessive inheritance of African-specific APOL1 kidney risk variants is associated with higher risk of nondiabetic kidney disease, progression to kidney failure, and early-onset albuminuria that precedes eGFR decline. The effect of APOL1 risk variants on kidney disease in continental Africans is understudied. Objectives of this study were to determine APOL1 risk allele prevalence and associations between APOL1 genotypes and kidney disease in West, East, and South Africa. DESIGN, SETTING, PARTICIPANTS, \& MEASUREMENTS This cross-sectional population-based study in four African countries included 10,769 participants largely aged 40-60 years with sociodemographic and health information, anthropometry data, and blood and urine tests for biomarkers of kidney disease. APOL1 risk alleles were imputed from the H3Africa genotyping array, APOL1 risk allele and genotype frequencies were determined, and genetic associations were assessed for kidney disease. Kidney disease was defined as the presence of eGFR \<60 ml/min per 1.73 m2, albuminuria, or a composite end point including eGFR \<60 ml/min per 1.73 m2 and/or albuminuria. RESULTS High G1 allele frequencies occurred in South and West Africa (approximately 7%-13%). G2 allele frequencies were highest in South Africa (15%-24%), followed by West Africa (9%-12%). Associations between APOL1 risk variants and albuminuria were significant for recessive (odds ratio, 1.63; 95% confidence interval, 1.25 to 2.12) and additive (odds ratio, 1.39; 95% confidence interval, 1.09 to 1.76) models. Associations were stronger for APOL1 G1/G1 genotypes versus G0/G0 (odds ratio, 3.87; 95% confidence interval, 2.16 to 6.93) compared with either G2/G2 (odds ratio, 1.65; 95% confidence interval, 1.09 to 2.51) or G1/G2 (odds ratio, 1.24; 95% confidence interval, 0.83 to 1.87). No association between APOL1 risk variants and eGFR \<60 ml/min per 1.73 m2 was observed. CONCLUSIONS APOL1 G1 and G2 alleles and high-risk genotype frequencies differed between and within West and South Africa and were almost absent from East Africa. APOL1 risk variants were associated with albuminuria but not eGFR \<60 ml/min per 1.73 m2. There may be differential effects of homozygous G1 and G2 genotypes on albuminuria that require further investigation. PODCAST This article contains a podcast at https://www.asn-online.org/media/podcast/CJASN/2022_05_16_CJN14321121.mp3.},
keywords = {albuminuria, apolipoprotein L1, chronic kidney disease, glomerular filtration rate, molecular genetics},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND AND OBJECTIVES Recessive inheritance of African-specific APOL1 kidney risk variants is associated with higher risk of nondiabetic kidney disease, progression to kidney failure, and early-onset albuminuria that precedes eGFR decline. The effect of APOL1 risk variants on kidney disease in continental Africans is understudied. Objectives of this study were to determine APOL1 risk allele prevalence and associations between APOL1 genotypes and kidney disease in West, East, and South Africa. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS This cross-sectional population-based study in four African countries included 10,769 participants largely aged 40-60 years with sociodemographic and health information, anthropometry data, and blood and urine tests for biomarkers of kidney disease. APOL1 risk alleles were imputed from the H3Africa genotyping array, APOL1 risk allele and genotype frequencies were determined, and genetic associations were assessed for kidney disease. Kidney disease was defined as the presence of eGFR <60 ml/min per 1.73 m2, albuminuria, or a composite end point including eGFR <60 ml/min per 1.73 m2 and/or albuminuria. RESULTS High G1 allele frequencies occurred in South and West Africa (approximately 7%-13%). G2 allele frequencies were highest in South Africa (15%-24%), followed by West Africa (9%-12%). Associations between APOL1 risk variants and albuminuria were significant for recessive (odds ratio, 1.63; 95% confidence interval, 1.25 to 2.12) and additive (odds ratio, 1.39; 95% confidence interval, 1.09 to 1.76) models. Associations were stronger for APOL1 G1/G1 genotypes versus G0/G0 (odds ratio, 3.87; 95% confidence interval, 2.16 to 6.93) compared with either G2/G2 (odds ratio, 1.65; 95% confidence interval, 1.09 to 2.51) or G1/G2 (odds ratio, 1.24; 95% confidence interval, 0.83 to 1.87). No association between APOL1 risk variants and eGFR <60 ml/min per 1.73 m2 was observed. CONCLUSIONS APOL1 G1 and G2 alleles and high-risk genotype frequencies differed between and within West and South Africa and were almost absent from East Africa. APOL1 risk variants were associated with albuminuria but not eGFR <60 ml/min per 1.73 m2. There may be differential effects of homozygous G1 and G2 genotypes on albuminuria that require further investigation. PODCAST This article contains a podcast at https://www.asn-online.org/media/podcast/CJASN/2022_05_16_CJN14321121.mp3. |
| Philip J. Rosenthal, Anders Björkman, Mehul Dhorda, Abdoulaye Djimde, Arjen M. Dondorp, Oumar Gaye, Philippe J. Guerin, Elizabeth Juma, Dominic P. Kwiatkowski, Laura Merson, Francine Ntoumi, Ric N. Price, Jaishree Raman, David S. Roos, Feiko Kuile, Halidou Tinto, Sheena S. Tomko, Nicholas J. White, Karen I. Barnes Cooperation in Countering Artemisinin Resistance in Africa: Learning from COVID-19 Journal Article In: The American Journal of Tropical Medicine and Hygiene, vol. 106, iss. 6, pp. 1568-1570, 2022, ISSN: 0002-9637. @article{Rosenthal2022,
title = {Cooperation in Countering Artemisinin Resistance in Africa: Learning from COVID-19},
author = {Philip J. Rosenthal and Anders Bj\"{o}rkman and Mehul Dhorda and Abdoulaye Djimde and Arjen M. Dondorp and Oumar Gaye and Philippe J. Guerin and Elizabeth Juma and Dominic P. Kwiatkowski and Laura Merson and Francine Ntoumi and Ric N. Price and Jaishree Raman and David S. Roos and Feiko Kuile and Halidou Tinto and Sheena S. Tomko and Nicholas J. White and Karen I. Barnes},
url = {https://www.ajtmh.org/view/journals/tpmd/106/6/article-p1568.xml},
doi = {10.4269/ajtmh.22-0148},
issn = {0002-9637},
year = {2022},
date = {2022-01-01},
journal = {The American Journal of Tropical Medicine and Hygiene},
volume = {106},
issue = {6},
pages = {1568-1570},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
|
| KOAMA Benjamin Kouliga, YERBANGA Rakiswendé Serge, DA Ollo, YOUGBARE Sibidou, NATAMA Hamtandi Magloire, OUEDRAOGO Georges Anicet, OUEDRAOGO Jean Bosco, TRAORE/COULIBALY Maminata In vivo antimalarial activity, safety and phytochemical screening of Canthium multiflorum (Schumach. &Thonn.) Hiern (Rubiaceae) Journal Article In: Journal of Medicinal Plants Research, vol. 16, iss. 6, pp. 196-204, 2022. @article{nokey,
title = {In vivo antimalarial activity, safety and phytochemical screening of Canthium multiflorum (Schumach. \&Thonn.) Hiern (Rubiaceae)},
author = {KOAMA Benjamin Kouliga and YERBANGA Rakiswend\'{e} Serge and DA Ollo and YOUGBARE Sibidou and NATAMA Hamtandi Magloire and OUEDRAOGO Georges Anicet and OUEDRAOGO Jean Bosco and TRAORE/COULIBALY Maminata},
url = {https://academicjournals.org/journal/JMPR/article-abstract/48516B269295},
doi = {10.5897/JMPR2022.7226},
year = {2022},
date = {2022-01-01},
journal = {Journal of Medicinal Plants Research},
volume = {16},
issue = {6},
pages = {196-204},
abstract = {Canthium multiflorum (Thonn.) Hiern (Rubiaceae) is a popular herb used by traditional healers in western Burkina Faso. C. multiflorum leaves are widely used in decoction to treat malaria. The present study aims to evaluate its in vivo potential against malaria parasites in mice. The antimalarial activity of the organic and aqueous extracts of C. multiflorum leaves was evaluated on Plasmodium berghei Anka in NMRI mice using the Peters 4-day suppressive test. The fractions of the extracts were also tested. The acute toxicity study was performed according to Lorke method and sub-acute toxicity by Seewaboon method. Phytochemical analysis of extracts was carried out according to Ciulei method. The results showed that ethanolic and decoctions were the best inhibitors of parasites’ growth. The ethanolic extract exhibited an inhibition of 22.5, 30.8 and 81.9% at 100, 250 and 500 mg/kg body weight, respectively. While the decoction with water, an inhibition of 10.1, 25.9 and 74.2% at the same doses. Fractions’ extracts showed moderate activities at dose of 250 mg/kg bw. In addition, no mortality was recorded with the ethanolic extract. No signs of toxicity were observed in animals in the sub-acute toxicity study. The phytochemical constituents of the extracts were mainly steroids and/or triterpenes, flavonoids, emodols, carotenoids, coumarins, tannins, saponins, anthocyanosides and reducing compounds. Ethanol and decoctions of C. multiflorum leaves have been shown to have significant antimalarial activity in infected mice, with no toxicity. Phytochemical analysis confirmed the previously chemical groups found in the roots of the plant.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Canthium multiflorum (Thonn.) Hiern (Rubiaceae) is a popular herb used by traditional healers in western Burkina Faso. C. multiflorum leaves are widely used in decoction to treat malaria. The present study aims to evaluate its in vivo potential against malaria parasites in mice. The antimalarial activity of the organic and aqueous extracts of C. multiflorum leaves was evaluated on Plasmodium berghei Anka in NMRI mice using the Peters 4-day suppressive test. The fractions of the extracts were also tested. The acute toxicity study was performed according to Lorke method and sub-acute toxicity by Seewaboon method. Phytochemical analysis of extracts was carried out according to Ciulei method. The results showed that ethanolic and decoctions were the best inhibitors of parasites’ growth. The ethanolic extract exhibited an inhibition of 22.5, 30.8 and 81.9% at 100, 250 and 500 mg/kg body weight, respectively. While the decoction with water, an inhibition of 10.1, 25.9 and 74.2% at the same doses. Fractions’ extracts showed moderate activities at dose of 250 mg/kg bw. In addition, no mortality was recorded with the ethanolic extract. No signs of toxicity were observed in animals in the sub-acute toxicity study. The phytochemical constituents of the extracts were mainly steroids and/or triterpenes, flavonoids, emodols, carotenoids, coumarins, tannins, saponins, anthocyanosides and reducing compounds. Ethanol and decoctions of C. multiflorum leaves have been shown to have significant antimalarial activity in infected mice, with no toxicity. Phytochemical analysis confirmed the previously chemical groups found in the roots of the plant. |
| Ananyo Choudhury, Jean-Tristan Brandenburg, Tinashe Chikowore, Dhriti Sengupta, Palwende Romuald Boua, Nigel J. Crowther, Godfred Agongo, Gershim Asiki, F. Xavier Gómez-Olivé, Isaac Kisiangani, Eric Maimela, Matshane Masemola-Maphutha, Lisa K. Micklesfield, Engelbert A. Nonterah, Shane A. Norris, Hermann Sorgho, Halidou Tinto, Stephen Tollman, Sarah E. Graham, Cristen J. Willer, Scott Hazelhurst, Michèle Ramsay Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits Journal Article In: Nature Communications, vol. 13, iss. 1, pp. 2578, 2022, ISSN: 2041-1723. @article{Choudhury2022,
title = {Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits},
author = {Ananyo Choudhury and Jean-Tristan Brandenburg and Tinashe Chikowore and Dhriti Sengupta and Palwende Romuald Boua and Nigel J. Crowther and Godfred Agongo and Gershim Asiki and F. Xavier G\'{o}mez-Oliv\'{e} and Isaac Kisiangani and Eric Maimela and Matshane Masemola-Maphutha and Lisa K. Micklesfield and Engelbert A. Nonterah and Shane A. Norris and Hermann Sorgho and Halidou Tinto and Stephen Tollman and Sarah E. Graham and Cristen J. Willer and Scott Hazelhurst and Mich\`{e}le Ramsay},
url = {https://www.nature.com/articles/s41467-022-30098-w},
doi = {10.1038/s41467-022-30098-w},
issn = {2041-1723},
year = {2022},
date = {2022-01-01},
journal = {Nature Communications},
volume = {13},
issue = {1},
pages = {2578},
abstract = {\<p\> Genetic associations for lipid traits have identified hundreds of variants with clear differences across European, Asian and African studies. Based on a sub-Saharan-African GWAS for lipid traits in the population cross-sectional AWI-Gen cohort ( \<italic\>N\</italic\> = 10,603) we report a novel LDL-C association in the \<italic\>GATB\</italic\> region ( \<italic\>P\</italic\> -value=1.56 × 10 ^{−8} ). Meta-analysis with four other African cohorts ( \<italic\>N\</italic\> = 23,718) provides supporting evidence for the LDL-C association with the \<italic\>GATB/FHIP1A\</italic\> region and identifies a novel triglyceride association signal close to the \<italic\>FHIT\</italic\> gene ( \<italic\>P\</italic\> -value =2.66 × 10 ^{−8} ). Our data enable fine-mapping of several well-known lipid-trait loci including \<italic\>LDLR, PMFBP1\</italic\> and \<italic\>LPA\</italic\> . The transferability of signals detected in two large global studies (GLGC and PAGE) consistently improves with an increase in the size of the African replication cohort. Polygenic risk score analysis shows increased predictive accuracy for LDL-C levels with the narrowing of genetic distance between the discovery dataset and our cohort. Novel discovery is enhanced with the inclusion of African data. \</p\>},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
<p> Genetic associations for lipid traits have identified hundreds of variants with clear differences across European, Asian and African studies. Based on a sub-Saharan-African GWAS for lipid traits in the population cross-sectional AWI-Gen cohort ( <italic>N</italic> = 10,603) we report a novel LDL-C association in the <italic>GATB</italic> region ( <italic>P</italic> -value=1.56 × 10 −8 ). Meta-analysis with four other African cohorts ( <italic>N</italic> = 23,718) provides supporting evidence for the LDL-C association with the <italic>GATB/FHIP1A</italic> region and identifies a novel triglyceride association signal close to the <italic>FHIT</italic> gene ( <italic>P</italic> -value =2.66 × 10 −8 ). Our data enable fine-mapping of several well-known lipid-trait loci including <italic>LDLR, PMFBP1</italic> and <italic>LPA</italic> . The transferability of signals detected in two large global studies (GLGC and PAGE) consistently improves with an increase in the size of the African replication cohort. Polygenic risk score analysis shows increased predictive accuracy for LDL-C levels with the narrowing of genetic distance between the discovery dataset and our cohort. Novel discovery is enhanced with the inclusion of African data. </p> |
| Charlie Franck Alfred Compaoré, Jacques Kaboré, Hamidou Ilboudo, Lian Francesca Thomas, Laura Cristina Falzon, Mohamed Bamba, Hassane Sakande, Minayégninrin Koné, Dramane Kaba, Clarisse Bougouma, Ilboudo Adama, Ouedraogo Amathe, Adrien Marie Gaston Belem, Eric Maurice Fèvre, Philippe Büscher, Veerle Lejon, Vincent Jamonneau Monitoring the elimination of gambiense human African trypanosomiasis in the historical focus of Batié, South–West Burkina Faso Journal Article In: Parasite, vol. 29, pp. 25, 2022, ISSN: 1776-1042. @article{nokey,
title = {Monitoring the elimination of \textit{gambiense} human African trypanosomiasis in the historical focus of Bati\'{e}, South\textendashWest Burkina Faso},
author = {Charlie Franck Alfred Compaor\'{e} and Jacques Kabor\'{e} and Hamidou Ilboudo and Lian Francesca Thomas and Laura Cristina Falzon and Mohamed Bamba and Hassane Sakande and Minay\'{e}gninrin Kon\'{e} and Dramane Kaba and Clarisse Bougouma and Ilboudo Adama and Ouedraogo Amathe and Adrien Marie Gaston Belem and Eric Maurice F\`{e}vre and Philippe B\"{u}scher and Veerle Lejon and Vincent Jamonneau},
url = {https://www.parasite-journal.org/10.1051/parasite/2022024},
doi = {10.1051/parasite/2022024},
issn = {1776-1042},
year = {2022},
date = {2022-01-01},
journal = {Parasite},
volume = {29},
pages = {25},
abstract = {\<p\> The World Health Organisation has targeted the elimination of human African trypanosomiasis (HAT) as zero transmission by 2030. Continued surveillance needs to be in place for early detection of re-emergent cases. In this context, the performance of diagnostic tests and testing algorithms for detection of the re-emergence of \<italic\>Trypanosoma brucei gambiense\</italic\> HAT remains to be assessed. We carried out a door-to-door active medical survey for HAT in the historical focus of Bati\'{e}, South\textendashWest Burkina Faso. Screening was done using three rapid diagnostic tests (RDTs). Two laboratory tests (ELISA/ \<italic\>T. b. gambiense\</italic\> and immune trypanolysis) and parasitological examination were performed on RDT positives only. In total, 5883 participants were screened, among which 842 (14%) tested positive in at least one RDT. Blood from 519 RDT positives was examined microscopically but no trypanosomes were observed. The HAT Sero- \<italic\>K\</italic\> -Set test showed the lowest specificity of 89%, while the specificities of SD Bioline HAT and rHAT Sero-Strip were 92% and 99%, respectively. The specificity of ELISA/ \<italic\>T. b. gambiense\</italic\> and trypanolysis was 99% (98\textendash99%) and 100% (99\textendash100%), respectively. Our results suggest that \<italic\>T. b. gambiense\</italic\> is no longer circulating in the study area and that zero transmission has probably been attained. While a least cost analysis is still required, our study showed that RDT preselection followed by trypanolysis may be a useful strategy for post-elimination surveillance in Burkina Faso. \</p\>},
keywords = {Burkina Faso, Diagnosis, Dried blood spot, Elimination, Human African trypanosomiasis, Rapid diagnostic test, Specificity, Trypanosoma brucei gambiense},
pubstate = {published},
tppubtype = {article}
}
<p> The World Health Organisation has targeted the elimination of human African trypanosomiasis (HAT) as zero transmission by 2030. Continued surveillance needs to be in place for early detection of re-emergent cases. In this context, the performance of diagnostic tests and testing algorithms for detection of the re-emergence of <italic>Trypanosoma brucei gambiense</italic> HAT remains to be assessed. We carried out a door-to-door active medical survey for HAT in the historical focus of Batié, South–West Burkina Faso. Screening was done using three rapid diagnostic tests (RDTs). Two laboratory tests (ELISA/ <italic>T. b. gambiense</italic> and immune trypanolysis) and parasitological examination were performed on RDT positives only. In total, 5883 participants were screened, among which 842 (14%) tested positive in at least one RDT. Blood from 519 RDT positives was examined microscopically but no trypanosomes were observed. The HAT Sero- <italic>K</italic> -Set test showed the lowest specificity of 89%, while the specificities of SD Bioline HAT and rHAT Sero-Strip were 92% and 99%, respectively. The specificity of ELISA/ <italic>T. b. gambiense</italic> and trypanolysis was 99% (98–99%) and 100% (99–100%), respectively. Our results suggest that <italic>T. b. gambiense</italic> is no longer circulating in the study area and that zero transmission has probably been attained. While a least cost analysis is still required, our study showed that RDT preselection followed by trypanolysis may be a useful strategy for post-elimination surveillance in Burkina Faso. </p> |
| Engelbert A. Nonterah, Daniel Boateng, Nigel J. Crowther, Kerstin Klipstein-Grobusch, Abraham R. Oduro, Godfred Agongo, Shukri F. Mohamed, Palwendé R. Boua, Solomon S. R. Choma, Shane A. Norris, Stephen M. Tollman, Michiel L. Bots, Michèle Ramsay, Diederick Grobbee Carotid Atherosclerosis, Microalbuminuria, and Estimated 10-Year Atherosclerotic Cardiovascular Disease Risk in Sub-Saharan Africa Journal Article In: JAMA Network Open, vol. 5, iss. 4, pp. e227559, 2022, ISSN: 2574-3805. @article{Nonterah2022,
title = {Carotid Atherosclerosis, Microalbuminuria, and Estimated 10-Year Atherosclerotic Cardiovascular Disease Risk in Sub-Saharan Africa},
author = {Engelbert A. Nonterah and Daniel Boateng and Nigel J. Crowther and Kerstin Klipstein-Grobusch and Abraham R. Oduro and Godfred Agongo and Shukri F. Mohamed and Palwend\'{e} R. Boua and Solomon S. R. Choma and Shane A. Norris and Stephen M. Tollman and Michiel L. Bots and Mich\`{e}le Ramsay and Diederick Grobbee},
url = {https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2791534},
doi = {10.1001/jamanetworkopen.2022.7559},
issn = {2574-3805},
year = {2022},
date = {2022-01-01},
journal = {JAMA Network Open},
volume = {5},
issue = {4},
pages = {e227559},
abstract = {Importance: Carotid atherosclerosis and microalbuminuria are associated with atherosclerotic cardiovascular disease (ASCVD) but are understudied in sub-Saharan Africa. Objective: To evaluate the association of carotid atherosclerosis and microalbuminuria with 10-year ASCVD risk in middle-aged sub-Saharan African individuals. Design, Setting, and Participants: This cross-sectional study conducted analyses of baseline data from the African-Wits-INDEPTH (International Network for the Demographic Evaluation of Populations and Their Health in Low- and Middle-Income Countries) genomic study (AWI-Gen). Women and men aged 40 to 60 years without baseline CVD and drawn from Burkina Faso, Ghana, Kenya, and South Africa were included. Main Outcomes and Measures: Hypotheses for the analyses were formulated after data collection. The main exposures were carotid atherosclerosis, assessed using carotid intima-media thickness (CIMT) using B-mode ultrasonography, and microalbuminuria, measured using spot urine albumin (SUA) and urine albumin-creatinine ratio (uACR). The main outcome was high ASCVD risk, defined as a 2018 Pooled Cohort Equations score of 7.5% or greater. Associations were estimated using adjusted multivariable logistic regression analyses. Findings: A total of 9010 participants with a mean (SD) age of 50 (6) years and 4533 (50.3%) women were included. High CIMT, SUA, and uACR were each associated with older age (eg, mean [SD] age of participants with high vs reference range CIMT: 55 [5] years vs 50 [6] years; P \<.001) and high prevalence of both diabetes and hypertension (eg, hypertension among those with high vs reference range SUA: 213 of 1117 [19.1%] vs 356 of 2549 [14.0%]; P \<.001). Smokers were likely to have higher vs reference range SUA (210 [18.8%] vs 407 [16.0%]) and uACR (138 of 707 [19.5%] vs 456 of 2797 [16.3%]). Carotid atherosclerosis was common in Burkina Faso (82 of 262 [31.3%]) and Ghana (91 [34.7%]), while microalbuminuria, measured by SUA, was common in Kenya (272 [24.4%]) and South Africa (519 [46.5%]). SUA was associated with higher odds of carotid atherosclerosis (odds ratio [OR], 1.77; 95% CI, 1.04-3.01) compared with uACR (OR, 0.51; 95% CI, 0.27-0.95). Common CIMT, SUA, and uACR were associated with 10-year ASCVD risk, with CIMT having a stronger association with 10-year ASCVD risk in both women (OR, 1.95; 95% CI, 1.78-2.14) and men (OR, 1.73; 95% CI, 1.55-1.93) than SUA (women: OR, 1.29; 95% CI, 1.12-1.43; men: OR, 1.46; 95% CI, 1.26-1.55) and uACR (women: OR, 1.32; 95% CI, 1.10-1.54; men: OR, 1.35; 95% CI, 1.15-1.46). Conclusions and Relevance: The presence of microalbuminuria measured by SUA may indicate risk of subclinical carotid atherosclerosis and high 10-year ASCVD risk in middle-aged residents of sub-Saharan Africa. These data should be confirmed in longitudinal studies of cardiovascular events.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Importance: Carotid atherosclerosis and microalbuminuria are associated with atherosclerotic cardiovascular disease (ASCVD) but are understudied in sub-Saharan Africa. Objective: To evaluate the association of carotid atherosclerosis and microalbuminuria with 10-year ASCVD risk in middle-aged sub-Saharan African individuals. Design, Setting, and Participants: This cross-sectional study conducted analyses of baseline data from the African-Wits-INDEPTH (International Network for the Demographic Evaluation of Populations and Their Health in Low- and Middle-Income Countries) genomic study (AWI-Gen). Women and men aged 40 to 60 years without baseline CVD and drawn from Burkina Faso, Ghana, Kenya, and South Africa were included. Main Outcomes and Measures: Hypotheses for the analyses were formulated after data collection. The main exposures were carotid atherosclerosis, assessed using carotid intima-media thickness (CIMT) using B-mode ultrasonography, and microalbuminuria, measured using spot urine albumin (SUA) and urine albumin-creatinine ratio (uACR). The main outcome was high ASCVD risk, defined as a 2018 Pooled Cohort Equations score of 7.5% or greater. Associations were estimated using adjusted multivariable logistic regression analyses. Findings: A total of 9010 participants with a mean (SD) age of 50 (6) years and 4533 (50.3%) women were included. High CIMT, SUA, and uACR were each associated with older age (eg, mean [SD] age of participants with high vs reference range CIMT: 55 [5] years vs 50 [6] years; P <.001) and high prevalence of both diabetes and hypertension (eg, hypertension among those with high vs reference range SUA: 213 of 1117 [19.1%] vs 356 of 2549 [14.0%]; P <.001). Smokers were likely to have higher vs reference range SUA (210 [18.8%] vs 407 [16.0%]) and uACR (138 of 707 [19.5%] vs 456 of 2797 [16.3%]). Carotid atherosclerosis was common in Burkina Faso (82 of 262 [31.3%]) and Ghana (91 [34.7%]), while microalbuminuria, measured by SUA, was common in Kenya (272 [24.4%]) and South Africa (519 [46.5%]). SUA was associated with higher odds of carotid atherosclerosis (odds ratio [OR], 1.77; 95% CI, 1.04-3.01) compared with uACR (OR, 0.51; 95% CI, 0.27-0.95). Common CIMT, SUA, and uACR were associated with 10-year ASCVD risk, with CIMT having a stronger association with 10-year ASCVD risk in both women (OR, 1.95; 95% CI, 1.78-2.14) and men (OR, 1.73; 95% CI, 1.55-1.93) than SUA (women: OR, 1.29; 95% CI, 1.12-1.43; men: OR, 1.46; 95% CI, 1.26-1.55) and uACR (women: OR, 1.32; 95% CI, 1.10-1.54; men: OR, 1.35; 95% CI, 1.15-1.46). Conclusions and Relevance: The presence of microalbuminuria measured by SUA may indicate risk of subclinical carotid atherosclerosis and high 10-year ASCVD risk in middle-aged residents of sub-Saharan Africa. These data should be confirmed in longitudinal studies of cardiovascular events. |
| Daniel Valia, Brecht Ingelbeen, Bérenger Kaboré, Ibrahima Karama, Marjan Peeters, Palpouguini Lompo, Erika Vlieghe, Annelies Post, Janneke Cox, Quirijn Mast, Annie Robert, Marianne A. B. Sande, Hector Rodriguez Villalobos, Andre Ven, Halidou Tinto, Jan Jacobs Use of WATCH antibiotics prior to presentation to the hospital in rural Burkina Faso Journal Article In: Antimicrobial Resistance & Infection Control, vol. 11, iss. 1, pp. 59, 2022, ISSN: 2047-2994. @article{Valia2022,
title = {Use of WATCH antibiotics prior to presentation to the hospital in rural Burkina Faso},
author = {Daniel Valia and Brecht Ingelbeen and B\'{e}renger Kabor\'{e} and Ibrahima Karama and Marjan Peeters and Palpouguini Lompo and Erika Vlieghe and Annelies Post and Janneke Cox and Quirijn Mast and Annie Robert and Marianne A. B. Sande and Hector Rodriguez Villalobos and Andre Ven and Halidou Tinto and Jan Jacobs},
url = {https://aricjournal.biomedcentral.com/articles/10.1186/s13756-022-01098-8},
doi = {10.1186/s13756-022-01098-8},
issn = {2047-2994},
year = {2022},
date = {2022-01-01},
urldate = {2022-01-01},
journal = {Antimicrobial Resistance \& Infection Control},
volume = {11},
issue = {1},
pages = {59},
abstract = {BACKGROUND: In low- and middle-income countries, the prevalence of antimicrobial resistance (AMR) is increasing. To control AMR, WHO recommends monitoring antibiotic use, in particular Watch antibiotics. These are critically important antibiotics, with restricted use because at risk of becoming ineffective due to increasing AMR. We investigated pre-hospital antibiotic use in rural Burkina Faso. METHODS: During 2016-2017, we collected data from patients aged \> 3 months presenting with severe acute fever to the rural hospital of Nanoro Health District, Burkina Faso, including antibiotic use in the two weeks prior to consultation or hospitalization. We analysed reported antibiotic use by applying the WHO Access, Watch, Reserve classification. RESULTS: Of 920 febrile participants (63.0% ≤ 14 years), pre-hospital antibiotic use was reported by 363 (39.5%). Among these 363, microbiological diagnoses were available for 275 (75.8%) patients, of whom 162 (58.9%) were non-bacterial infections. Use of more than one antibiotic was reported by 58/363 (16.0%) participants. Of 491 self-referred patients who did not previously visit a primary health care center, 131 (26.7%) reported antibiotic use. Of 424 antibiotics reported, 265 (62.5%) were Access and 159 (37.5%) Watch antibiotics. Watch antibiotic use was more frequent among patients \> 14 year olds (51.1%) compared to those 0-14 year old (30.7%, p \< 0.001) and among referrals from the primary health care centers (42.2%) compared to self-referred patients (28.1%, p = 0.004). Most frequently reported Watch antibiotics were ceftriaxone (114, 71.7%) and ciprofloxacin (32, 20.1%). CONCLUSION: The reported frequent use of Watch group antibiotics among febrile patients prior to presentation to the hospital in rural Burkina Faso highlights the need to develop targeted interventions to improve antibiotic use in community settings as part of strengthening antibiotic stewardship in low- and middle-income countries. This should include facilitating referral, access to qualified prescribers and diagnostic tools in rural primary health care centers. Trial registration ClinicalTrials.gov identifier: NCT02669823. Registration date was February 1, 2016.},
keywords = {Antimicrobial resistance, AWaRe, Burkina Faso, Community antibiotic use},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: In low- and middle-income countries, the prevalence of antimicrobial resistance (AMR) is increasing. To control AMR, WHO recommends monitoring antibiotic use, in particular Watch antibiotics. These are critically important antibiotics, with restricted use because at risk of becoming ineffective due to increasing AMR. We investigated pre-hospital antibiotic use in rural Burkina Faso. METHODS: During 2016-2017, we collected data from patients aged > 3 months presenting with severe acute fever to the rural hospital of Nanoro Health District, Burkina Faso, including antibiotic use in the two weeks prior to consultation or hospitalization. We analysed reported antibiotic use by applying the WHO Access, Watch, Reserve classification. RESULTS: Of 920 febrile participants (63.0% ≤ 14 years), pre-hospital antibiotic use was reported by 363 (39.5%). Among these 363, microbiological diagnoses were available for 275 (75.8%) patients, of whom 162 (58.9%) were non-bacterial infections. Use of more than one antibiotic was reported by 58/363 (16.0%) participants. Of 491 self-referred patients who did not previously visit a primary health care center, 131 (26.7%) reported antibiotic use. Of 424 antibiotics reported, 265 (62.5%) were Access and 159 (37.5%) Watch antibiotics. Watch antibiotic use was more frequent among patients > 14 year olds (51.1%) compared to those 0-14 year old (30.7%, p < 0.001) and among referrals from the primary health care centers (42.2%) compared to self-referred patients (28.1%, p = 0.004). Most frequently reported Watch antibiotics were ceftriaxone (114, 71.7%) and ciprofloxacin (32, 20.1%). CONCLUSION: The reported frequent use of Watch group antibiotics among febrile patients prior to presentation to the hospital in rural Burkina Faso highlights the need to develop targeted interventions to improve antibiotic use in community settings as part of strengthening antibiotic stewardship in low- and middle-income countries. This should include facilitating referral, access to qualified prescribers and diagnostic tools in rural primary health care centers. Trial registration ClinicalTrials.gov identifier: NCT02669823. Registration date was February 1, 2016. |
| Moussa Lingani, Serge H. Zango, Innocent Valéa, Maïmouna Sanou, Serge Ouoba, Sékou Samadoulougou, Annie Robert, Halidou Tinto, Michèle Dramaix, Philippe Donnen Prevalence and risk factors of malaria among first antenatal care attendees in rural Burkina Faso Journal Article In: Tropical Medicine and Health, vol. 50, iss. 1, pp. 49, 2022, ISSN: 1349-4147. @article{Lingani2022,
title = {Prevalence and risk factors of malaria among first antenatal care attendees in rural Burkina Faso},
author = {Moussa Lingani and Serge H. Zango and Innocent Val\'{e}a and Ma\"{i}mouna Sanou and Serge Ouoba and S\'{e}kou Samadoulougou and Annie Robert and Halidou Tinto and Mich\`{e}le Dramaix and Philippe Donnen},
url = {https://tropmedhealth.biomedcentral.com/articles/10.1186/s41182-022-00442-3},
doi = {10.1186/s41182-022-00442-3},
issn = {1349-4147},
year = {2022},
date = {2022-01-01},
journal = {Tropical Medicine and Health},
volume = {50},
issue = {1},
pages = {49},
abstract = {BACKGROUND The WHO recommends continuous surveillance of malaria in endemic countries to identify areas and populations most in need for targeted interventions. The aim of this study was to assess the prevalence of malaria and its associated factors among first antenatal care (ANC) attendees in rural Burkina Faso. METHODS A cross-sectional survey was conducted between August 2019 and September 2020 at the Yako health district and included 1067 first ANC attendees. Sociodemographic, gyneco-obstetric, and medical characteristics were collected. Malaria was diagnosed by standard microscopy and hemoglobin level was measured by spectrophotometry. A multivariate logistic regression analysis was used to identify factors associated with malaria infection. RESULTS Overall malaria infection prevalence was 16.1% (167/1039). Among malaria-positive women, the geometric mean parasite density was 1204 [95% confidence interval (CI) 934-1552] parasites/µL and the proportion of very low (1-199 parasites/µL), low (200-999 parasites/µL), medium (1000-9999 parasites/µL) and high (≥ 10,000 parasites/µL) parasite densities were 15.0%, 35.3%, 38.3% and 11.4%, respectively. Age \< 20 years (adjusted odds ratio (aOR): 2.2; 95% CI 1.4-3.5), anemia (hemoglobin \< 11 g/deciliter) (aOR: 3.4; 95% CI 2.2-5.5), the non-use of bed net (aOR: 1.8; 95% CI 1.1-2.8), and the absence of intermittent preventive treatment with sulfadoxine-pyrimethamine (aOR: 5.8; 95% CI 2.1-24.5) were positively associated with malaria infection. CONCLUSIONS The study showed that one out of six pregnant women had a microscopy-detected P. falciparum malaria infection at their first ANC visit. Strengthening malaria prevention strategies during the first ANC visit is needed to prevent unfavorable birth outcomes.},
keywords = {Burkina Faso, First antenatal care visit, Malaria, Pregnancy},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND The WHO recommends continuous surveillance of malaria in endemic countries to identify areas and populations most in need for targeted interventions. The aim of this study was to assess the prevalence of malaria and its associated factors among first antenatal care (ANC) attendees in rural Burkina Faso. METHODS A cross-sectional survey was conducted between August 2019 and September 2020 at the Yako health district and included 1067 first ANC attendees. Sociodemographic, gyneco-obstetric, and medical characteristics were collected. Malaria was diagnosed by standard microscopy and hemoglobin level was measured by spectrophotometry. A multivariate logistic regression analysis was used to identify factors associated with malaria infection. RESULTS Overall malaria infection prevalence was 16.1% (167/1039). Among malaria-positive women, the geometric mean parasite density was 1204 [95% confidence interval (CI) 934-1552] parasites/µL and the proportion of very low (1-199 parasites/µL), low (200-999 parasites/µL), medium (1000-9999 parasites/µL) and high (≥ 10,000 parasites/µL) parasite densities were 15.0%, 35.3%, 38.3% and 11.4%, respectively. Age < 20 years (adjusted odds ratio (aOR): 2.2; 95% CI 1.4-3.5), anemia (hemoglobin < 11 g/deciliter) (aOR: 3.4; 95% CI 2.2-5.5), the non-use of bed net (aOR: 1.8; 95% CI 1.1-2.8), and the absence of intermittent preventive treatment with sulfadoxine-pyrimethamine (aOR: 5.8; 95% CI 2.1-24.5) were positively associated with malaria infection. CONCLUSIONS The study showed that one out of six pregnant women had a microscopy-detected P. falciparum malaria infection at their first ANC visit. Strengthening malaria prevention strategies during the first ANC visit is needed to prevent unfavorable birth outcomes. |
| Rashid Mansoor, Robert J. Commons, Nicholas M. Douglas, Benjamin Abuaku, Jane Achan, Ishag Adam, George O. Adjei, Martin Adjuik, Bereket H. Alemayehu, Richard Allan, Elizabeth N. Allen, Anupkumar R. Anvikar, Emmanuel Arinaitwe, Elizabeth A. Ashley, Hazel Ashurst, Puji B. S. Asih, Nathan Bakyaita, Hubert Barennes, Karen I. Barnes, Leonardo Basco, Quique Bassat, Elisabeth Baudin, David J Bell, Delia Bethell, Anders Bjorkman, Caroline Boulton, Teun Bousema, Philippe Brasseur, Hasifa Bukirwa, Rebekah Burrow, Verena I. Carrara, Michel Cot, Umberto D’Alessandro, Debashish Das, Sabyasachi Das, Timothy M. E. Davis, Meghna Desai, Abdoulaye A. Djimde, Arjen M. Dondorp, Grant Dorsey, Chris J. Drakeley, Stephan Duparc, Emmanuelle Espié, Jean-Francois Etard, Catherine Falade, Jean Francois Faucher, Scott Filler, Carole Fogg, Mark Fukuda, Oumar Gaye, Blaise Genton, Awab Ghulam Rahim, Julius Gilayeneh, Raquel Gonzalez, Rebecca F. Grais, Francesco Grandesso, Brian Greenwood, Anastasia Grivoyannis, Christoph Hatz, Eva Maria Hodel, Georgina S. Humphreys, Jimee Hwang, Deus Ishengoma, Elizabeth Juma, S. Patrick Kachur, Piet A. Kager, Erasmus Kamugisha, Moses R. Kamya, Corine Karema, Kassoum Kayentao, Adama Kazienga, Jean-René Kiechel, Poul-Erik Kofoed, Kwadwo Koram, Peter G. Kremsner, David G. Lalloo, Moses Laman, Sue J. Lee, Bertrand Lell, Amelia W. Maiga, Andreas Mårtensson, Mayfong Mayxay, Wilfred Mbacham, Rose McGready, Hervé Menan, Didier Ménard, Frank Mockenhaupt, Brioni R. Moore, Olaf Müller, Alain Nahum, Jean-Louis Ndiaye, Paul N. Newton, Billy E. Ngasala, Frederic Nikiema, Akindeh M. Nji, Harald Noedl, Francois Nosten, Bernhards R. Ogutu, Olusola Ojurongbe, Lyda Osorio, Jean-Bosco Ouédraogo, Seth Owusu-Agyei, Anil Pareek, Louis K. Penali, Patrice Piola, Mateusz Plucinski, Zul Premji, Michael Ramharter, Caitlin L. Richmond, Lars Rombo, Cally Roper, Philip J. Rosenthal, Sam Salman, Albert Same-Ekobo, Carol Sibley, Sodiomon B. Sirima, Frank M. Smithuis, Fabrice A. Somé, Sarah G. Staedke, Peter Starzengruber, Nathalie Strub-Wourgaft, Inge Sutanto, Todd D. Swarthout, Din Syafruddin, Ambrose O. Talisuna, Walter R. Taylor, Emmanuel A. Temu, Julie I. Thwing, Halidou Tinto, Emiliana Tjitra, Offianan A. Touré, T. Hien Tran, Johan Ursing, Innocent Valea, Giovanni Valentini, Michele Vugt, Lorenz Seidlein, Stephen A. Ward, Vincent Were, Nicholas J. White, Charles J. Woodrow, William Yavo, Adoke Yeka, Issaka Zongo, Julie A. Simpson, Philippe J. Guerin, Kasia Stepniewska, Ric N. Price Haematological consequences of acute uncomplicated falciparum malaria: a WorldWide Antimalarial Resistance Network pooled analysis of individual patient data Journal Article In: BMC Medicine, vol. 20, iss. 1, pp. 85, 2022, ISSN: 1741-7015. @article{Mansoor2022,
title = {Haematological consequences of acute uncomplicated falciparum malaria: a WorldWide Antimalarial Resistance Network pooled analysis of individual patient data},
author = {Rashid Mansoor and Robert J. Commons and Nicholas M. Douglas and Benjamin Abuaku and Jane Achan and Ishag Adam and George O. Adjei and Martin Adjuik and Bereket H. Alemayehu and Richard Allan and Elizabeth N. Allen and Anupkumar R. Anvikar and Emmanuel Arinaitwe and Elizabeth A. Ashley and Hazel Ashurst and Puji B. S. Asih and Nathan Bakyaita and Hubert Barennes and Karen I. Barnes and Leonardo Basco and Quique Bassat and Elisabeth Baudin and David J Bell and Delia Bethell and Anders Bjorkman and Caroline Boulton and Teun Bousema and Philippe Brasseur and Hasifa Bukirwa and Rebekah Burrow and Verena I. Carrara and Michel Cot and Umberto D’Alessandro and Debashish Das and Sabyasachi Das and Timothy M. E. Davis and Meghna Desai and Abdoulaye A. Djimde and Arjen M. Dondorp and Grant Dorsey and Chris J. Drakeley and Stephan Duparc and Emmanuelle Espi\'{e} and Jean-Francois Etard and Catherine Falade and Jean Francois Faucher and Scott Filler and Carole Fogg and Mark Fukuda and Oumar Gaye and Blaise Genton and Awab Ghulam Rahim and Julius Gilayeneh and Raquel Gonzalez and Rebecca F. Grais and Francesco Grandesso and Brian Greenwood and Anastasia Grivoyannis and Christoph Hatz and Eva Maria Hodel and Georgina S. Humphreys and Jimee Hwang and Deus Ishengoma and Elizabeth Juma and S. Patrick Kachur and Piet A. Kager and Erasmus Kamugisha and Moses R. Kamya and Corine Karema and Kassoum Kayentao and Adama Kazienga and Jean-Ren\'{e} Kiechel and Poul-Erik Kofoed and Kwadwo Koram and Peter G. Kremsner and David G. Lalloo and Moses Laman and Sue J. Lee and Bertrand Lell and Amelia W. Maiga and Andreas Mr{a}rtensson and Mayfong Mayxay and Wilfred Mbacham and Rose McGready and Herv\'{e} Menan and Didier M\'{e}nard and Frank Mockenhaupt and Brioni R. Moore and Olaf M\"{u}ller and Alain Nahum and Jean-Louis Ndiaye and Paul N. Newton and Billy E. Ngasala and Frederic Nikiema and Akindeh M. Nji and Harald Noedl and Francois Nosten and Bernhards R. Ogutu and Olusola Ojurongbe and Lyda Osorio and Jean-Bosco Ou\'{e}draogo and Seth Owusu-Agyei and Anil Pareek and Louis K. Penali and Patrice Piola and Mateusz Plucinski and Zul Premji and Michael Ramharter and Caitlin L. Richmond and Lars Rombo and Cally Roper and Philip J. Rosenthal and Sam Salman and Albert Same-Ekobo and Carol Sibley and Sodiomon B. Sirima and Frank M. Smithuis and Fabrice A. Som\'{e} and Sarah G. Staedke and Peter Starzengruber and Nathalie Strub-Wourgaft and Inge Sutanto and Todd D. Swarthout and Din Syafruddin and Ambrose O. Talisuna and Walter R. Taylor and Emmanuel A. Temu and Julie I. Thwing and Halidou Tinto and Emiliana Tjitra and Offianan A. Tour\'{e} and T. Hien Tran and Johan Ursing and Innocent Valea and Giovanni Valentini and Michele Vugt and Lorenz Seidlein and Stephen A. Ward and Vincent Were and Nicholas J. White and Charles J. Woodrow and William Yavo and Adoke Yeka and Issaka Zongo and Julie A. Simpson and Philippe J. Guerin and Kasia Stepniewska and Ric N. Price},
url = {https://bmcmedicine.biomedcentral.com/articles/10.1186/s12916-022-02265-9},
doi = {10.1186/s12916-022-02265-9},
issn = {1741-7015},
year = {2022},
date = {2022-01-01},
urldate = {2022-01-01},
journal = {BMC Medicine},
volume = {20},
issue = {1},
pages = {85},
abstract = {BACKGROUND Plasmodium falciparum malaria is associated with anaemia-related morbidity, attributable to host, parasite and drug factors. We quantified the haematological response following treatment of uncomplicated P. falciparum malaria to identify the factors associated with malarial anaemia. METHODS Individual patient data from eligible antimalarial efficacy studies of uncomplicated P. falciparum malaria, available through the WorldWide Antimalarial Resistance Network data repository prior to August 2015, were pooled using standardised methodology. The haematological response over time was quantified using a multivariable linear mixed effects model with nonlinear terms for time, and the model was then used to estimate the mean haemoglobin at day of nadir and day 7. Multivariable logistic regression quantified risk factors for moderately severe anaemia (haemoglobin \< 7 g/dL) at day 0, day 3 and day 7 as well as a fractional fall ≥ 25% at day 3 and day 7. RESULTS A total of 70,226 patients, recruited into 200 studies between 1991 and 2013, were included in the analysis: 50,859 (72.4%) enrolled in Africa, 18,451 (26.3%) in Asia and 916 (1.3%) in South America. The median haemoglobin concentration at presentation was 9.9 g/dL (range 5.0-19.7 g/dL) in Africa, 11.6 g/dL (range 5.0-20.0 g/dL) in Asia and 12.3 g/dL (range 6.9-17.9 g/dL) in South America. Moderately severe anaemia (Hb \< 7g/dl) was present in 8.4% (4284/50,859) of patients from Africa, 3.3% (606/18,451) from Asia and 0.1% (1/916) from South America. The nadir haemoglobin occurred on day 2 post treatment with a mean fall from baseline of 0.57 g/dL in Africa and 1.13 g/dL in Asia. Independent risk factors for moderately severe anaemia on day 7, in both Africa and Asia, included moderately severe anaemia at baseline (adjusted odds ratio (AOR) = 16.10 and AOR = 23.00, respectively), young age (age \< 1 compared to ≥ 12 years AOR = 12.81 and AOR = 6.79, respectively), high parasitaemia (AOR = 1.78 and AOR = 1.58, respectively) and delayed parasite clearance (AOR = 2.44 and AOR = 2.59, respectively). In Asia, patients treated with an artemisinin-based regimen were at significantly greater risk of moderately severe anaemia on day 7 compared to those treated with a non-artemisinin-based regimen (AOR = 2.06 [95%CI 1.39-3.05], p \< 0.001). CONCLUSIONS In patients with uncomplicated P. falciparum malaria, the nadir haemoglobin occurs 2 days after starting treatment. Although artemisinin-based treatments increase the rate of parasite clearance, in Asia they are associated with a greater risk of anaemia during recovery.},
keywords = {Antimalarials, Artemisinin-based therapy, Haemoglobin, Non-artemisinin-based therapy, Plasmodium falciparum, Pooled analysis of individual patient data, Severe anaemia},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND Plasmodium falciparum malaria is associated with anaemia-related morbidity, attributable to host, parasite and drug factors. We quantified the haematological response following treatment of uncomplicated P. falciparum malaria to identify the factors associated with malarial anaemia. METHODS Individual patient data from eligible antimalarial efficacy studies of uncomplicated P. falciparum malaria, available through the WorldWide Antimalarial Resistance Network data repository prior to August 2015, were pooled using standardised methodology. The haematological response over time was quantified using a multivariable linear mixed effects model with nonlinear terms for time, and the model was then used to estimate the mean haemoglobin at day of nadir and day 7. Multivariable logistic regression quantified risk factors for moderately severe anaemia (haemoglobin < 7 g/dL) at day 0, day 3 and day 7 as well as a fractional fall ≥ 25% at day 3 and day 7. RESULTS A total of 70,226 patients, recruited into 200 studies between 1991 and 2013, were included in the analysis: 50,859 (72.4%) enrolled in Africa, 18,451 (26.3%) in Asia and 916 (1.3%) in South America. The median haemoglobin concentration at presentation was 9.9 g/dL (range 5.0-19.7 g/dL) in Africa, 11.6 g/dL (range 5.0-20.0 g/dL) in Asia and 12.3 g/dL (range 6.9-17.9 g/dL) in South America. Moderately severe anaemia (Hb < 7g/dl) was present in 8.4% (4284/50,859) of patients from Africa, 3.3% (606/18,451) from Asia and 0.1% (1/916) from South America. The nadir haemoglobin occurred on day 2 post treatment with a mean fall from baseline of 0.57 g/dL in Africa and 1.13 g/dL in Asia. Independent risk factors for moderately severe anaemia on day 7, in both Africa and Asia, included moderately severe anaemia at baseline (adjusted odds ratio (AOR) = 16.10 and AOR = 23.00, respectively), young age (age < 1 compared to ≥ 12 years AOR = 12.81 and AOR = 6.79, respectively), high parasitaemia (AOR = 1.78 and AOR = 1.58, respectively) and delayed parasite clearance (AOR = 2.44 and AOR = 2.59, respectively). In Asia, patients treated with an artemisinin-based regimen were at significantly greater risk of moderately severe anaemia on day 7 compared to those treated with a non-artemisinin-based regimen (AOR = 2.06 [95%CI 1.39-3.05], p < 0.001). CONCLUSIONS In patients with uncomplicated P. falciparum malaria, the nadir haemoglobin occurs 2 days after starting treatment. Although artemisinin-based treatments increase the rate of parasite clearance, in Asia they are associated with a greater risk of anaemia during recovery. |
| Joel Dofinissery Bognini, Sekou Samadoulougou, Mady Ouedraogo, Francis Smart, David Tiga Kankoye, Osman Sankoh, Fati Kirakoya-Samadoulougou What are the trends in seeking health care for fever in children under-five in Sierra Leone? evidence from four population-based studies before and after the free health care initiative Journal Article In: PLOS ONE, vol. 17, iss. 2, pp. e0263364, 2022, ISSN: 1932-6203. @article{Bognini2022,
title = {What are the trends in seeking health care for fever in children under-five in Sierra Leone? evidence from four population-based studies before and after the free health care initiative},
author = {Joel Dofinissery Bognini and Sekou Samadoulougou and Mady Ouedraogo and Francis Smart and David Tiga Kankoye and Osman Sankoh and Fati Kirakoya-Samadoulougou},
editor = {Mary Hamer Hodges},
url = {https://dx.plos.org/10.1371/journal.pone.0263364},
doi = {10.1371/journal.pone.0263364},
issn = {1932-6203},
year = {2022},
date = {2022-01-01},
journal = {PLOS ONE},
volume = {17},
issue = {2},
pages = {e0263364},
abstract = {Background In 2010, the government of Sierra Leone implemented the Free Health Care Initiative (FHCI) in the country with the objective of reducing the high maternal, infant, and child mortality rates and improving general health indicators. The objective of this study was to assess the trends in the prevalence of health care-seeking and to identify the determinants of healthcare service utilization by caregivers of children younger than five years. Methods The analysis of health-care-seeking behavior was done using data from four populationbased surveys in Sierra Leone before (2008) and after (2013, 2016, 2019) the FHCI was implemented. Care-seeking behavior was assessed with regard to caregivers seeking care for children under-five in the two weeks prior to each survey. We compared the percentages of healthcare-seeking behavior change and identify factors associated with healthcareseeking using a modified Poisson regression model with generalized estimating equations. Results In 2008, a total of 1208 children with fever were recorded, compared with 2823 children in 2013, 1633 in 2016, and 1464 in 2019. Care-seeking for children with fever was lowest in 2008 (51%; 95% CI (46.4-55.5)) than in 2013 (71.5%; 95% CI (68.4-74.5)), 2016 (70.3%; 95% CI (66.6-73.8)), and 2019 (74.6%; 95% CI (71.6-77.3)) (p \< 0.001). Care-seeking in 2013, 2016 and 2019 was at least 1.4 time higher than in 2008 (p \< 0.001) after adjusting for mother's age, wealth, religion, education level, household head and the child's age. Careseeking was lowest for children older than 12 months, mothers older than 35 years, children living in the poorest households, and in the northern region. A trend was observed for the sex of the household head. The level of care-seeking was lowest when the household head was a man. Conclusions The increase in healthcare-seeking for children under-five with fever followed the introduction of the FHCI in Sierra Leone. Care-seeking for fever varied by the child's age, caregiver's age, household wealth, the sex of the household head and region. Maintaining the FHCI with adequate strategies to address other barriers beyond financial ones is essential to reduce disparities between age groups, regions and, households.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Background In 2010, the government of Sierra Leone implemented the Free Health Care Initiative (FHCI) in the country with the objective of reducing the high maternal, infant, and child mortality rates and improving general health indicators. The objective of this study was to assess the trends in the prevalence of health care-seeking and to identify the determinants of healthcare service utilization by caregivers of children younger than five years. Methods The analysis of health-care-seeking behavior was done using data from four populationbased surveys in Sierra Leone before (2008) and after (2013, 2016, 2019) the FHCI was implemented. Care-seeking behavior was assessed with regard to caregivers seeking care for children under-five in the two weeks prior to each survey. We compared the percentages of healthcare-seeking behavior change and identify factors associated with healthcareseeking using a modified Poisson regression model with generalized estimating equations. Results In 2008, a total of 1208 children with fever were recorded, compared with 2823 children in 2013, 1633 in 2016, and 1464 in 2019. Care-seeking for children with fever was lowest in 2008 (51%; 95% CI (46.4-55.5)) than in 2013 (71.5%; 95% CI (68.4-74.5)), 2016 (70.3%; 95% CI (66.6-73.8)), and 2019 (74.6%; 95% CI (71.6-77.3)) (p < 0.001). Care-seeking in 2013, 2016 and 2019 was at least 1.4 time higher than in 2008 (p < 0.001) after adjusting for mother's age, wealth, religion, education level, household head and the child's age. Careseeking was lowest for children older than 12 months, mothers older than 35 years, children living in the poorest households, and in the northern region. A trend was observed for the sex of the household head. The level of care-seeking was lowest when the household head was a man. Conclusions The increase in healthcare-seeking for children under-five with fever followed the introduction of the FHCI in Sierra Leone. Care-seeking for fever varied by the child's age, caregiver's age, household wealth, the sex of the household head and region. Maintaining the FHCI with adequate strategies to address other barriers beyond financial ones is essential to reduce disparities between age groups, regions and, households. |
| Martin Somda, Médina Karambiri, Jacques Kaboré, Emilie Dama, Compaoré Alfred, Ernest Salou, Hamidou Ilboudo, Idriss Gali-Gali, Sèsséya Soha, Zakaria Bengaly, Adrien Belem, Der Dabire PERCEPTIONS ET PRATIQUES DE GESTION DE LA MALADIE DU SOMMEIL DES COMMUNAUTES VIVANT A PROXIMITE DES SITES AURIFERES AU SUD-OUEST DU BURKINA FASO Journal Article In: International Journal of Development Research, vol. 12, pp. 53422-53427, 2022. @article{Somda2022a,
title = {PERCEPTIONS ET PRATIQUES DE GESTION DE LA MALADIE DU SOMMEIL DES COMMUNAUTES VIVANT A PROXIMITE DES SITES AURIFERES AU SUD-OUEST DU BURKINA FASO},
author = {Martin Somda and M\'{e}dina Karambiri and Jacques Kabor\'{e} and Emilie Dama and Compaor\'{e} Alfred and Ernest Salou and Hamidou Ilboudo and Idriss Gali-Gali and S\`{e}ss\'{e}ya Soha and Zakaria Bengaly and Adrien Belem and Der Dabire},
doi = {10.37118/ijdr.23859.01.2022},
year = {2022},
date = {2022-01-01},
journal = {International Journal of Development Research},
volume = {12},
pages = {53422-53427},
abstract = {Une prospection m\'{e}dicale r\'{e}cente sur la trypanosomose humaine africaine (THA) dans des sites d'orpaillage au Sud-Ouest du Burkina Faso, a mis en \'{e}vidence la pr\'{e}sence de mouches ts\'{e}-ts\'{e} infect\'{e}es et des populations venant de la C\^{o}te d'Ivoire et de la Guin\'{e}e, les deux pays d'Afrique de l'Ouest les plus affect\'{e}s par cette maladie. Cet \'{e}tat de fait, montre un risque de r\'{e}\'{e}mergence de cette maladie. L'objectif de cette \'{e}tude \'{e}tait de recueillir les perceptions des populations vivant \`{a} proximit\'{e} de ces sites d'orpaillage du Sud-Ouest du Burkina Faso afin de proposer des strat\'{e}gies pour minimiser ce risque de r\'{e}\'{e}mergence de la THA. Pour ce faire une enqu\^{e}te sur les connaissances, attitudes et pratiques (CAP) a \'{e}t\'{e} r\'{e}alis\'{e}e en entretien semi-structur\'{e} aupr\`{e}s des personnes ressources, suivie des enqu\^{e}tes CAP individuelles ciblant les orpailleurs dans la zone d'\'{e}tude. Les r\'{e}sultats ont montr\'{e} que les 29 personnes ressources sont peu inform\'{e}es sur la THA. Ce r\'{e}sultat a \'{e}t\'{e} confirm\'{e} par les CAP individuelles aupr\`{e}s des 130 orpailleurs enqu\^{e}t\'{e}s qui sont peu inform\'{e}s sur la THA : 87,69% sur ses modes de transmission, 78,46% sur ses sympt\^{o}mes et 100% sur les strat\'{e}gies appropri\'{e}es de gestion. A l'issue de cette \'{e}tude, des recommandations ont \'{e}t\'{e} faites.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Une prospection médicale récente sur la trypanosomose humaine africaine (THA) dans des sites d'orpaillage au Sud-Ouest du Burkina Faso, a mis en évidence la présence de mouches tsé-tsé infectées et des populations venant de la Côte d'Ivoire et de la Guinée, les deux pays d'Afrique de l'Ouest les plus affectés par cette maladie. Cet état de fait, montre un risque de réémergence de cette maladie. L'objectif de cette étude était de recueillir les perceptions des populations vivant à proximité de ces sites d'orpaillage du Sud-Ouest du Burkina Faso afin de proposer des stratégies pour minimiser ce risque de réémergence de la THA. Pour ce faire une enquête sur les connaissances, attitudes et pratiques (CAP) a été réalisée en entretien semi-structuré auprès des personnes ressources, suivie des enquêtes CAP individuelles ciblant les orpailleurs dans la zone d'étude. Les résultats ont montré que les 29 personnes ressources sont peu informées sur la THA. Ce résultat a été confirmé par les CAP individuelles auprès des 130 orpailleurs enquêtés qui sont peu informés sur la THA : 87,69% sur ses modes de transmission, 78,46% sur ses symptômes et 100% sur les stratégies appropriées de gestion. A l'issue de cette étude, des recommandations ont été faites. |
| Jane Grant, Issaka Sagara, Issaka Zongo, Matthew Cairns, Rakiswendé Serge Yerbanga, Modibo Diarra, Charles Zoungrana, Djibrilla Issiaka, Frédéric Nikièma, Frédéric Sompougdou, Amadou Tapily, Mahamadou Kaya, Alassane Haro, Koualy Sanogo, Abdoul Aziz Sienou, Seydou Traore, Ismaila Thera, Hama Yalcouye, Irene Kuepfer, Paul Snell, Paul Milligan, Christian Ockenhouse, Opokua Ofori-Anyinam, Halidou Tinto, Abdoulaye Djimde, Daniel Chandramohan, Brian Greenwood, Alassane Dicko, Jean-Bosco Ouédraogo Impact of seasonal RTS,S/AS01E vaccination plus seasonal malaria chemoprevention on the nutritional status of children in Burkina Faso and Mali Journal Article In: Malaria Journal, vol. 21, iss. 1, pp. 59, 2022, ISSN: 1475-2875. @article{Grant2022,
title = {Impact of seasonal RTS,S/AS01E vaccination plus seasonal malaria chemoprevention on the nutritional status of children in Burkina Faso and Mali},
author = {Jane Grant and Issaka Sagara and Issaka Zongo and Matthew Cairns and Rakiswend\'{e} Serge Yerbanga and Modibo Diarra and Charles Zoungrana and Djibrilla Issiaka and Fr\'{e}d\'{e}ric Niki\`{e}ma and Fr\'{e}d\'{e}ric Sompougdou and Amadou Tapily and Mahamadou Kaya and Alassane Haro and Koualy Sanogo and Abdoul Aziz Sienou and Seydou Traore and Ismaila Thera and Hama Yalcouye and Irene Kuepfer and Paul Snell and Paul Milligan and Christian Ockenhouse and Opokua Ofori-Anyinam and Halidou Tinto and Abdoulaye Djimde and Daniel Chandramohan and Brian Greenwood and Alassane Dicko and Jean-Bosco Ou\'{e}draogo},
url = {https://malariajournal.biomedcentral.com/articles/10.1186/s12936-022-04077-x},
doi = {10.1186/s12936-022-04077-x},
issn = {1475-2875},
year = {2022},
date = {2022-01-01},
urldate = {2022-02-01},
journal = {Malaria Journal},
volume = {21},
issue = {1},
pages = {59},
abstract = {Background: A recent trial in Burkina Faso and Mali showed that combining seasonal RTS,S/AS01E malaria vaccination with seasonal malaria chemoprevention (SMC) substantially reduced the incidence of uncomplicated and severe malaria in young children compared to either intervention alone. Given the possible negative effect of malaria on nutrition, the study investigated whether these children also experienced lower prevalence of acute and chronic malnutrition. Methods: In Burkina Faso and Mali 5920 children were randomized to receive either SMC alone, RTS,S/AS01E alone, or SMC combined with RTS,S/AS01E for three malaria transmission seasons (2017\textendash2019). After each transmission season, anthropometric measurements were collected from all study children at a cross-sectional survey and used to derive nutritional status indicators, including the binary variables wasted and stunted (weight-for-height and height-for-age z-scores below − 2, respectively). Binary and continuous outcomes between treatment groups were compared by Poisson and linear regression. Results: In 2017, compared to SMC alone, the combined intervention reduced the prevalence of wasting by approximately 12% [prevalence ratio (PR) = 0.88 (95% CI 0.75, 1.03)], and approximately 21% in 2018 [PR = 0.79 (95% CI 0.62, 1.01)]. Point estimates were similar for comparisons with RTS,S/AS01E, but there was stronger evidence of a difference. There was at least a 30% reduction in the point estimates for the prevalence of severe wasting in the combined group compared to the other two groups in 2017 and 2018. There was no difference in the prevalence of moderate or severe wasting between the groups in 2019. The prevalence of stunting, low-MUAC-for-age or being underweight did not differ between groups for any of the three years. The prevalence of severe stunting was higher in the combined group compared to both other groups in 2018, and compared to RTS,S/AS01E alone in 2017; this observation does not have an obvious explanation and may be a chance finding. Overall, malnutrition was very common in this cohort, but declined over the study as the children became older. Conclusions: Despite a high burden of malnutrition and malaria in the study populations, and a major reduction in the incidence of malaria in children receiving both interventions, this had only a modest impact on nutritional status. Therefore, other interventions are needed to reduce the high burden of malnutrition in these areas. Trial registration: https://www.clinicaltrials.gov/ct2/show/NCT03143218, registered 8th May 2017.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Background: A recent trial in Burkina Faso and Mali showed that combining seasonal RTS,S/AS01E malaria vaccination with seasonal malaria chemoprevention (SMC) substantially reduced the incidence of uncomplicated and severe malaria in young children compared to either intervention alone. Given the possible negative effect of malaria on nutrition, the study investigated whether these children also experienced lower prevalence of acute and chronic malnutrition. Methods: In Burkina Faso and Mali 5920 children were randomized to receive either SMC alone, RTS,S/AS01E alone, or SMC combined with RTS,S/AS01E for three malaria transmission seasons (2017–2019). After each transmission season, anthropometric measurements were collected from all study children at a cross-sectional survey and used to derive nutritional status indicators, including the binary variables wasted and stunted (weight-for-height and height-for-age z-scores below − 2, respectively). Binary and continuous outcomes between treatment groups were compared by Poisson and linear regression. Results: In 2017, compared to SMC alone, the combined intervention reduced the prevalence of wasting by approximately 12% [prevalence ratio (PR) = 0.88 (95% CI 0.75, 1.03)], and approximately 21% in 2018 [PR = 0.79 (95% CI 0.62, 1.01)]. Point estimates were similar for comparisons with RTS,S/AS01E, but there was stronger evidence of a difference. There was at least a 30% reduction in the point estimates for the prevalence of severe wasting in the combined group compared to the other two groups in 2017 and 2018. There was no difference in the prevalence of moderate or severe wasting between the groups in 2019. The prevalence of stunting, low-MUAC-for-age or being underweight did not differ between groups for any of the three years. The prevalence of severe stunting was higher in the combined group compared to both other groups in 2018, and compared to RTS,S/AS01E alone in 2017; this observation does not have an obvious explanation and may be a chance finding. Overall, malnutrition was very common in this cohort, but declined over the study as the children became older. Conclusions: Despite a high burden of malnutrition and malaria in the study populations, and a major reduction in the incidence of malaria in children receiving both interventions, this had only a modest impact on nutritional status. Therefore, other interventions are needed to reduce the high burden of malnutrition in these areas. Trial registration: https://www.clinicaltrials.gov/ct2/show/NCT03143218, registered 8th May 2017. |
| Liesbeth Martens, Bérenger Kaboré, Annelies Post, Christa E. Gaast-de Jongh, Jeroen D. Langereis, Halidou Tinto, Jan Jacobs, André J. Ven, Quirijn Mast, Marien I. Jonge Nasopharyngeal colonisation dynamics of bacterial pathogens in patients with fever in rural Burkina Faso: an observational study Journal Article In: BMC Infectious Diseases, vol. 22, iss. 1, pp. 15, 2022, ISSN: 14712334. @article{Martens2022,
title = {Nasopharyngeal colonisation dynamics of bacterial pathogens in patients with fever in rural Burkina Faso: an observational study},
author = {Liesbeth Martens and B\'{e}renger Kabor\'{e} and Annelies Post and Christa E. Gaast-de Jongh and Jeroen D. Langereis and Halidou Tinto and Jan Jacobs and Andr\'{e} J. Ven and Quirijn Mast and Marien I. Jonge},
doi = {10.1186/s12879-021-06996-7},
issn = {14712334},
year = {2022},
date = {2022-01-01},
urldate = {2022-01-01},
journal = {BMC Infectious Diseases},
volume = {22},
issue = {1},
pages = {15},
abstract = {Background: Nasopharyngeal colonisation with clinically relevant bacterial pathogens is a risk factor for severe infections, such as pneumonia and bacteraemia. In this study, we investigated the determinants of nasopharyngeal carriage in febrile patients in rural Burkina Faso. Methods: From March 2016 to June 2017, we recruited 924 paediatric and adult patients presenting with fever, hypothermia or suspicion of severe infection to the Centre Medical avec Antenne Chirurgicale Saint Camille de Nanoro, Burkina Faso. We recorded a broad range of clinical data, collected nasopharyngeal swabs and tested them for the presence of Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, Staphylococcus aureus and Klebsiella pneumoniae by quantitative polymerase chain reaction. Using logistic regression, we investigated the determinants of carriage and aimed to find correlations with clinical outcome. Results: Nasopharyngeal colonisation with S. pneumoniae, H. influenzae and M. catarrhalis was highly prevalent and strongly dependent on age and season. Females were less likely to be colonised with S. pneumoniae (OR 0.71},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Background: Nasopharyngeal colonisation with clinically relevant bacterial pathogens is a risk factor for severe infections, such as pneumonia and bacteraemia. In this study, we investigated the determinants of nasopharyngeal carriage in febrile patients in rural Burkina Faso. Methods: From March 2016 to June 2017, we recruited 924 paediatric and adult patients presenting with fever, hypothermia or suspicion of severe infection to the Centre Medical avec Antenne Chirurgicale Saint Camille de Nanoro, Burkina Faso. We recorded a broad range of clinical data, collected nasopharyngeal swabs and tested them for the presence of Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, Staphylococcus aureus and Klebsiella pneumoniae by quantitative polymerase chain reaction. Using logistic regression, we investigated the determinants of carriage and aimed to find correlations with clinical outcome. Results: Nasopharyngeal colonisation with S. pneumoniae, H. influenzae and M. catarrhalis was highly prevalent and strongly dependent on age and season. Females were less likely to be colonised with S. pneumoniae (OR 0.71 |
| Estomih Mduma, Tinto Halidou, Berenger Kaboré, Thomas Walongo, Palpouguini Lompo, Justine Museveni, Joshua Gidabayda, Jean Gratz, Godfrey Guga, Caroline Kimathi, Jie Liu, Paschal Mdoe, Robert Moshiro, Max Petzold, Jan Singlovic, Martine Guillerm, Melba F. Gomes, Eric R. Houpt, Christine M. Halleux Etiology of severe invasive infections in young infants in rural settings in sub-Saharan Africa Journal Article In: PLOS ONE, vol. 17, iss. 2, pp. e0264322, 2022, ISSN: 1932-6203. @article{Mduma2022,
title = {Etiology of severe invasive infections in young infants in rural settings in sub-Saharan Africa},
author = {Estomih Mduma and Tinto Halidou and Berenger Kabor\'{e} and Thomas Walongo and Palpouguini Lompo and Justine Museveni and Joshua Gidabayda and Jean Gratz and Godfrey Guga and Caroline Kimathi and Jie Liu and Paschal Mdoe and Robert Moshiro and Max Petzold and Jan Singlovic and Martine Guillerm and Melba F. Gomes and Eric R. Houpt and Christine M. Halleux},
editor = {Eleni Magira},
url = {https://dx.plos.org/10.1371/journal.pone.0264322},
doi = {10.1371/journal.pone.0264322},
issn = {1932-6203},
year = {2022},
date = {2022-01-01},
urldate = {2022-01-01},
journal = {PLOS ONE},
volume = {17},
issue = {2},
pages = {e0264322},
abstract = {BACKGROUND Serious invasive infections in newborns are a major cause of death. Lack of data on etiological causes hampers progress towards reduction of mortality. This study aimed to identify pathogens responsible for such infections in young infants in sub-Saharan Africa and to describe their antibiotics resistance profile. METHODS Between September 2016 and April 2018 we implemented an observational study in two rural sites in Burkina Faso and Tanzania enrolling young infants aged 0-59 days old with serious invasive infection. Blood samples underwent blood culture and molecular biology. RESULTS In total 634 infants with clinical diagnosis of serious invasive infection were enrolled and 4.2% of the infants had a positive blood culture. The most frequent pathogens identified by blood culture were Klebsiella pneumonia and Staphylococcus aureus, followed by Escherichia coli. Gram-negative isolates were only partially susceptible to first line WHO recommended treatment for neonatal sepsis at community level. A total of 18.6% of the infants were PCR positive for at least one pathogen and Escherichia coli and Staphylococcus aureus were the most common bacteria detected. Among infants enrolled, 60/634 (9.5%) died. Positive blood culture but not positive PCR was associated with risk of death. For most deaths, no pathogen was identified either by blood culture or molecular testing, and hence a causal agent remained unclear. Mortality was associated with low body temperature, tachycardia, respiratory symptoms, convulsions, history of difficult feeding, movement only when stimulated or reduced level of consciousness, diarrhea and/or vomiting. CONCLUSION While Klebsiella pneumonia and Staphylococcus aureus, as well as Escherichia coli were pathogens most frequently identified in infants with clinical suspicion of serious invasive infections, most cases remain without definite diagnosis, making more accurate diagnostic tools urgently needed. Antibiotics resistance to first line antibiotics is an increasing challenge even in rural Africa.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND Serious invasive infections in newborns are a major cause of death. Lack of data on etiological causes hampers progress towards reduction of mortality. This study aimed to identify pathogens responsible for such infections in young infants in sub-Saharan Africa and to describe their antibiotics resistance profile. METHODS Between September 2016 and April 2018 we implemented an observational study in two rural sites in Burkina Faso and Tanzania enrolling young infants aged 0-59 days old with serious invasive infection. Blood samples underwent blood culture and molecular biology. RESULTS In total 634 infants with clinical diagnosis of serious invasive infection were enrolled and 4.2% of the infants had a positive blood culture. The most frequent pathogens identified by blood culture were Klebsiella pneumonia and Staphylococcus aureus, followed by Escherichia coli. Gram-negative isolates were only partially susceptible to first line WHO recommended treatment for neonatal sepsis at community level. A total of 18.6% of the infants were PCR positive for at least one pathogen and Escherichia coli and Staphylococcus aureus were the most common bacteria detected. Among infants enrolled, 60/634 (9.5%) died. Positive blood culture but not positive PCR was associated with risk of death. For most deaths, no pathogen was identified either by blood culture or molecular testing, and hence a causal agent remained unclear. Mortality was associated with low body temperature, tachycardia, respiratory symptoms, convulsions, history of difficult feeding, movement only when stimulated or reduced level of consciousness, diarrhea and/or vomiting. CONCLUSION While Klebsiella pneumonia and Staphylococcus aureus, as well as Escherichia coli were pathogens most frequently identified in infants with clinical suspicion of serious invasive infections, most cases remain without definite diagnosis, making more accurate diagnostic tools urgently needed. Antibiotics resistance to first line antibiotics is an increasing challenge even in rural Africa. |
| Paul Sondo, Marc Christian Tahita, Hamidou Ilboudo, Toussaint Rouamba, Karim Derra, Gauthier Tougri, Florence Ouédraogo, Béatrice Marie Adélaïde Konseibo, Eli Roamba, Sabina Dahlström Otienoburu, Bérenger Kaboré, Kalynn Kennon, Kadija Ouédraogo, Wend-Timbe-Noma Arlette Raïssa Zongo, Fadima Yaya Bocoum, Kasia Stepniewska, Mehul Dhorda, Philippe J. Guérin, Halidou Tinto Boosting the impact of seasonal malaria chemoprevention (SMC) through simultaneous screening and treatment of household members of children receiving SMC in Burkina Faso: a protocol for a randomized open label trial Journal Article In: Archives of Public Health, vol. 80, iss. 1, pp. 41, 2022, ISSN: 2049-3258. @article{Sondo2022,
title = {Boosting the impact of seasonal malaria chemoprevention (SMC) through simultaneous screening and treatment of household members of children receiving SMC in Burkina Faso: a protocol for a randomized open label trial},
author = {Paul Sondo and Marc Christian Tahita and Hamidou Ilboudo and Toussaint Rouamba and Karim Derra and Gauthier Tougri and Florence Ou\'{e}draogo and B\'{e}atrice Marie Ad\'{e}la\"{i}de Konseibo and Eli Roamba and Sabina Dahlstr\"{o}m Otienoburu and B\'{e}renger Kabor\'{e} and Kalynn Kennon and Kadija Ou\'{e}draogo and Wend-Timbe-Noma Arlette Ra\"{i}ssa Zongo and Fadima Yaya Bocoum and Kasia Stepniewska and Mehul Dhorda and Philippe J. Gu\'{e}rin and Halidou Tinto},
url = {https://archpublichealth.biomedcentral.com/articles/10.1186/s13690-022-00800-x},
doi = {10.1186/s13690-022-00800-x},
issn = {2049-3258},
year = {2022},
date = {2022-01-01},
urldate = {2022-01-01},
journal = {Archives of Public Health},
volume = {80},
issue = {1},
pages = {41},
abstract = {BACKGROUND Plasmodium falciparum malaria remains a major public health concern in sub-Sahara Africa. Seasonal malaria chemoprevention (SMC) with amodiaquine + sulfadoxine-pyrimethamine is one of the most important preventive interventions. Despite its implementation, the burden of malaria is still very high in children under five years old in Burkina Faso, suggesting that the expected impact of this promising strategy might not be attained. Development of innovative strategies to improve the efficacy of these existing malaria control measures is essential. In such context, we postulate that screening and treatment of malaria in household members of children receiving SMC could greatly improve the impact of SMC intervention and reduce malaria transmission in endemic settings. METHODS This randomized superiority trial will be carried out in the Nanoro health district, Burkina Faso. The unit of randomisation will be the household and all eligible children from a household will be allocated to the same study group. Households with 3-59 months old children will be assigned to either (i) control group (SMC alone) or (ii) intervention (SMC+ screening of household members with standard Histidin Rich Protein Rapid Diagnostic Test (HRP2-RDT) and treatment if positive). The sample size will be 526 isolated households per arm, i.e., around 1052 children under SMC coverage and an expected 1315 household members. Included children will be followed-up for 24 months to fully cover two consecutive malaria transmission seasons and two SMC cycles. Children will be actively followed-up during the malaria transmission seasons while in the dry seasons the follow-up will be passive. CONCLUSION The study will respond to a major public health concern by providing evidence of the efficacy of an innovative strategy to boost the impact of SMC intervention.},
keywords = {Africa, Amodiaquine, Burkina Faso, Chemoprevention, Dihydro artemisinin Piperaquine, Malaria, Plasmodium falciparum, Sulfadoxine-pyrimethamine},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND Plasmodium falciparum malaria remains a major public health concern in sub-Sahara Africa. Seasonal malaria chemoprevention (SMC) with amodiaquine + sulfadoxine-pyrimethamine is one of the most important preventive interventions. Despite its implementation, the burden of malaria is still very high in children under five years old in Burkina Faso, suggesting that the expected impact of this promising strategy might not be attained. Development of innovative strategies to improve the efficacy of these existing malaria control measures is essential. In such context, we postulate that screening and treatment of malaria in household members of children receiving SMC could greatly improve the impact of SMC intervention and reduce malaria transmission in endemic settings. METHODS This randomized superiority trial will be carried out in the Nanoro health district, Burkina Faso. The unit of randomisation will be the household and all eligible children from a household will be allocated to the same study group. Households with 3-59 months old children will be assigned to either (i) control group (SMC alone) or (ii) intervention (SMC+ screening of household members with standard Histidin Rich Protein Rapid Diagnostic Test (HRP2-RDT) and treatment if positive). The sample size will be 526 isolated households per arm, i.e., around 1052 children under SMC coverage and an expected 1315 household members. Included children will be followed-up for 24 months to fully cover two consecutive malaria transmission seasons and two SMC cycles. Children will be actively followed-up during the malaria transmission seasons while in the dry seasons the follow-up will be passive. CONCLUSION The study will respond to a major public health concern by providing evidence of the efficacy of an innovative strategy to boost the impact of SMC intervention. |
| Palwende Romuald Boua, Jean-Tristan Brandenburg, Ananyo Choudhury, Hermann Sorgho, Engelbert A. Nonterah, Godfred Agongo, Gershim Asiki, Lisa Micklesfield, Solomon Choma, Francesc Xavier Gómez-Olivé, Scott Hazelhurst, Halidou Tinto, Nigel J. Crowther, Christopher G. Mathew, Michèle Ramsay Genetic associations with carotid intima-media thickness link to atherosclerosis with sex-specific effects in sub-Saharan Africans Journal Article In: Nature Communications, vol. 13, iss. 1, pp. 855, 2022, ISSN: 2041-1723. @article{Boua2022,
title = {Genetic associations with carotid intima-media thickness link to atherosclerosis with sex-specific effects in sub-Saharan Africans},
author = {Palwende Romuald Boua and Jean-Tristan Brandenburg and Ananyo Choudhury and Hermann Sorgho and Engelbert A. Nonterah and Godfred Agongo and Gershim Asiki and Lisa Micklesfield and Solomon Choma and Francesc Xavier G\'{o}mez-Oliv\'{e} and Scott Hazelhurst and Halidou Tinto and Nigel J. Crowther and Christopher G. Mathew and Mich\`{e}le Ramsay},
url = {https://www.nature.com/articles/s41467-022-28276-x},
doi = {10.1038/s41467-022-28276-x},
issn = {2041-1723},
year = {2022},
date = {2022-01-01},
urldate = {2022-02-01},
journal = {Nature Communications},
volume = {13},
issue = {1},
pages = {855},
abstract = {\<p\> Atherosclerosis precedes the onset of clinical manifestations of cardiovascular diseases (CVDs). We used carotid intima-media thickness (cIMT) to investigate genetic susceptibility to atherosclerosis in 7894 unrelated adults (3963 women, 3931 men; 40 to 60 years) resident in four sub-Saharan African countries. cIMT was measured by ultrasound and genotyping was performed on the H3Africa SNP Array. Two new African-specific genome-wide significant loci for mean-max cIMT, \<italic\>SIRPA\</italic\> (p = 4.7E-08), and \<italic\>FBXL17\</italic\> (p = 2.5E-08), were identified. Sex-stratified analysis revealed associations with one male-specific locus, \<italic\>SNX29\</italic\> (p = 6.3E-09), and two female-specific loci, \<italic\>LARP6\</italic\> (p = 2.4E-09) and \<italic\>PROK1\</italic\> (p = 1.0E-08). We replicate previous cIMT associations with different lead SNPs in linkage disequilibrium with SNPs primarily identified in European populations. Our study find significant enrichment for genes involved in oestrogen response from female-specific signals. The genes identified show biological relevance to atherosclerosis and/or CVDs, sex-differences and transferability of signals from non-African studies. \</p\>},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
<p> Atherosclerosis precedes the onset of clinical manifestations of cardiovascular diseases (CVDs). We used carotid intima-media thickness (cIMT) to investigate genetic susceptibility to atherosclerosis in 7894 unrelated adults (3963 women, 3931 men; 40 to 60 years) resident in four sub-Saharan African countries. cIMT was measured by ultrasound and genotyping was performed on the H3Africa SNP Array. Two new African-specific genome-wide significant loci for mean-max cIMT, <italic>SIRPA</italic> (p = 4.7E-08), and <italic>FBXL17</italic> (p = 2.5E-08), were identified. Sex-stratified analysis revealed associations with one male-specific locus, <italic>SNX29</italic> (p = 6.3E-09), and two female-specific loci, <italic>LARP6</italic> (p = 2.4E-09) and <italic>PROK1</italic> (p = 1.0E-08). We replicate previous cIMT associations with different lead SNPs in linkage disequilibrium with SNPs primarily identified in European populations. Our study find significant enrichment for genes involved in oestrogen response from female-specific signals. The genes identified show biological relevance to atherosclerosis and/or CVDs, sex-differences and transferability of signals from non-African studies. </p> |
| Toussaint Rouamba, Paul Sondo, Isidore W. Yerbanga, Adelaide Compaore, Maminata Traore‐Coulibaly, Franck S. Hien, Nassirou A. Diande, Innocent Valea, Marc Christian Tahita, Rita Baiden, Fred Binka, Halidou Tinto Prospective observational study to evaluate the clinical and biological safety profile of pyronaridine–artesunate in a rural health district in Burkina Faso Journal Article In: Pharmacology Research & Perspectives, vol. 10, iss. 4, pp. 224-229, 2022, ISSN: 2052-1707. @article{Rouamba2022,
title = {Prospective observational study to evaluate the clinical and biological safety profile of pyronaridine\textendashartesunate in a rural health district in Burkina Faso},
author = {Toussaint Rouamba and Paul Sondo and Isidore W. Yerbanga and Adelaide Compaore and Maminata Traore‐Coulibaly and Franck S. Hien and Nassirou A. Diande and Innocent Valea and Marc Christian Tahita and Rita Baiden and Fred Binka and Halidou Tinto},
url = {https://bpspubs.onlinelibrary.wiley.com/doi/10.1002/prp2.987},
doi = {10.1002/prp2.987},
issn = {2052-1707},
year = {2022},
date = {2022-01-01},
urldate = {2022-02-01},
journal = {Pharmacology Research \& Perspectives},
volume = {10},
issue = {4},
pages = {224-229},
abstract = {\<p\>The assessment in real‐life conditions of the safety and efficacy of new antimalarial drugs is of greatest interest. This study aimed to monitor and evaluate both clinical and biological safety of pyronaridine‐artesunate (PA) in real‐life conditions in Burkina Faso's health system. This was a single‐arm, open‐label study, where patients attending Nanoro health facilities with uncomplicated malaria were consented to be part of a cohort event monitoring (CEM). At inclusion (day‐0), PA was administered orally once a day for 3 days. Patients spontaneous reported any clinical adverse events (AEs) occurring within 28 days following the treatment. Additionally, the study focused on AEs of special interest (AESI), namely clinical signs related to hepatotoxicity and increased alanine aminotransferase (ALT) and aspartate aminotransferase (AST). A nested subset of patients with blood sample collection at day‐0 and day‐7 were monitored to investigate the effect of PA on biochemistry parameters. From September 2017 to October 2018, 2786 patients were treated with PA. About 97.8% (2720/2786) of patients did not report any AE. The most commonly reported events were respiratory, thoracic, and mediastinal disorders (8.3 per 1000), infections and infestations (7.9 per 1000), and gastrointestinal disorders (7.2 per 1000). No clinical or biological hepatotoxicity event related to PA was reported during the follow‐up. Changes in biochemistry parameters remained within laboratory reference ranges. The study showed that PA is a well‐tolerated drug and should be considered as a good option by malaria control programs in countries where existing first‐line antimalarial drugs are continuously threatened by the emergence of drug resistance.\</p\>},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
<p>The assessment in real‐life conditions of the safety and efficacy of new antimalarial drugs is of greatest interest. This study aimed to monitor and evaluate both clinical and biological safety of pyronaridine‐artesunate (PA) in real‐life conditions in Burkina Faso's health system. This was a single‐arm, open‐label study, where patients attending Nanoro health facilities with uncomplicated malaria were consented to be part of a cohort event monitoring (CEM). At inclusion (day‐0), PA was administered orally once a day for 3 days. Patients spontaneous reported any clinical adverse events (AEs) occurring within 28 days following the treatment. Additionally, the study focused on AEs of special interest (AESI), namely clinical signs related to hepatotoxicity and increased alanine aminotransferase (ALT) and aspartate aminotransferase (AST). A nested subset of patients with blood sample collection at day‐0 and day‐7 were monitored to investigate the effect of PA on biochemistry parameters. From September 2017 to October 2018, 2786 patients were treated with PA. About 97.8% (2720/2786) of patients did not report any AE. The most commonly reported events were respiratory, thoracic, and mediastinal disorders (8.3 per 1000), infections and infestations (7.9 per 1000), and gastrointestinal disorders (7.2 per 1000). No clinical or biological hepatotoxicity event related to PA was reported during the follow‐up. Changes in biochemistry parameters remained within laboratory reference ranges. The study showed that PA is a well‐tolerated drug and should be considered as a good option by malaria control programs in countries where existing first‐line antimalarial drugs are continuously threatened by the emergence of drug resistance.</p> |
| Martin Bienvenu Somda, Martial Kassi N'Djetchi, Jacques Kaboré, Hamidou Ilboudo, Emilie Dama, Soudah Boma, Fabrice Courtin, Anne Poinsignon, Zakaria Bengaly, Franck Remoué, Adrien Marie Gaston Belem, Bruno Bucheton, Vincent Jamonneau, Mathurin Koffi Evaluation of antibody responses to tsetse fly saliva in domestic animals in the sleeping sickness endemic foci of Bonon and Sinfra, Côte d'Ivoire Journal Article In: Veterinary Parasitology: Regional Studies and Reports, vol. 34, iss. 2, pp. 100773, 2022, ISSN: 24059390. @article{Somda2022,
title = {Evaluation of antibody responses to tsetse fly saliva in domestic animals in the sleeping sickness endemic foci of Bonon and Sinfra, C\^{o}te d'Ivoire},
author = {Martin Bienvenu Somda and Martial Kassi N'Djetchi and Jacques Kabor\'{e} and Hamidou Ilboudo and Emilie Dama and Soudah Boma and Fabrice Courtin and Anne Poinsignon and Zakaria Bengaly and Franck Remou\'{e} and Adrien Marie Gaston Belem and Bruno Bucheton and Vincent Jamonneau and Mathurin Koffi},
url = {https://linkinghub.elsevier.com/retrieve/pii/S2405939022000892},
doi = {10.1016/j.vprsr.2022.100773},
issn = {24059390},
year = {2022},
date = {2022-01-01},
urldate = {2022-01-01},
journal = {Veterinary Parasitology: Regional Studies and Reports},
volume = {34},
issue = {2},
pages = {100773},
address = {Switzerland},
abstract = {After intensive control efforts, human African trypanosomiasis (HAT) was declared eliminated in C\^{o}te d'Ivoire as a public health problem in December 2020 and the current objective is to achieve the interruption of the transmission (zero cases). Reaching this objective could be hindered by the existence of an animal reservoir of Trypanosoma (T.) brucei (b.) gambiense. In the framework of a study led in 2013 to assess the role of domestic animals in the epidemiology of HAT in the two last active foci from C\^{o}te d'Ivoire (Bonon and Sinfra), plasmas were sampled from four species of domestic animals for parasitological (microscopic examination by the buffy coat technique (BCT)), serological (immune trypanolysis (TL)) and molecular (specific PCR: TBR for T. brucei s.l., TCF for T. congolense forest type, TVW for T. vivax and PCR for T. b. gambiense) testing. In order to improve the understanding of the involvement/role of these animals in the transmission of T. b. gambiense, we have quantified in this study the IgG response to whole saliva extracts of Glossina palpalis gambiensis in order to perform an association analysis between anti-saliva responses and the positivity of diagnostic tests. Cattle and pigs had significantly higher rates of anti-tsetse saliva responses compared to goats and sheep (p \< 0.01). In addition, the anti-tsetse saliva responses were strongly associated with the parasitology (BCT+), serology (TL+) and PCR (TBR+ and TCF+) results (p \< 0.001). These associations indicate a high level of contacts between the positive/infected animals and tsetse flies. Our findings suggest that protecting cattle and pigs against tsetse bites could have a significant impact in reducing transmission of both animal and human trypanosome species, and advocates for a "One health" approach to better control African trypanosomosis in C\^{o}te d'Ivoire.},
keywords = {Animal reservoirs, Biomarker of exposure, C\^{o}te d'Ivoire, Trypanosoma brucei gambiense, Tsetse fly},
pubstate = {published},
tppubtype = {article}
}
After intensive control efforts, human African trypanosomiasis (HAT) was declared eliminated in Côte d'Ivoire as a public health problem in December 2020 and the current objective is to achieve the interruption of the transmission (zero cases). Reaching this objective could be hindered by the existence of an animal reservoir of Trypanosoma (T.) brucei (b.) gambiense. In the framework of a study led in 2013 to assess the role of domestic animals in the epidemiology of HAT in the two last active foci from Côte d'Ivoire (Bonon and Sinfra), plasmas were sampled from four species of domestic animals for parasitological (microscopic examination by the buffy coat technique (BCT)), serological (immune trypanolysis (TL)) and molecular (specific PCR: TBR for T. brucei s.l., TCF for T. congolense forest type, TVW for T. vivax and PCR for T. b. gambiense) testing. In order to improve the understanding of the involvement/role of these animals in the transmission of T. b. gambiense, we have quantified in this study the IgG response to whole saliva extracts of Glossina palpalis gambiensis in order to perform an association analysis between anti-saliva responses and the positivity of diagnostic tests. Cattle and pigs had significantly higher rates of anti-tsetse saliva responses compared to goats and sheep (p < 0.01). In addition, the anti-tsetse saliva responses were strongly associated with the parasitology (BCT+), serology (TL+) and PCR (TBR+ and TCF+) results (p < 0.001). These associations indicate a high level of contacts between the positive/infected animals and tsetse flies. Our findings suggest that protecting cattle and pigs against tsetse bites could have a significant impact in reducing transmission of both animal and human trypanosome species, and advocates for a "One health" approach to better control African trypanosomosis in Côte d'Ivoire. |
| Jui-Chi Kuo, Shih-Hua Tan, Yu-Cheng Hsiao, Chinmaya Mutalik, Hui-Min Chen, Sibidou Yougbaré, Tsung-Rong Kuo Unveiling the Antibacterial Mechanism of Gold Nanoclusters via In Situ Transmission Electron Microscopy Journal Article In: ACS Sustainable Chem Eng, vol. 10, no. 1, pp. 464–471, 2022. @article{Kuo2022-bm,
title = {Unveiling the Antibacterial Mechanism of Gold Nanoclusters via In Situ Transmission Electron Microscopy},
author = {Jui-Chi Kuo and Shih-Hua Tan and Yu-Cheng Hsiao and Chinmaya Mutalik and Hui-Min Chen and Sibidou Yougbar\'{e} and Tsung-Rong Kuo},
doi = {https://doi.org/10.1021/acssuschemeng.1c06714},
year = {2022},
date = {2022-01-01},
urldate = {2022-01-01},
journal = {ACS Sustainable Chem Eng},
volume = {10},
number = {1},
pages = {464--471},
publisher = {American Chemical Society},
abstract = {Metal nanoclusters (NCs) with unique chemical and physical properties have been extensively demonstrated to be emerging nanoantibiotics for fighting bacterial infections. Understanding the antibacterial mechanisms of metal nanoclusters is important for evaluating their clinical applications as nanoantibiotics. To understand the antibacterial mechanism, gold nanoclusters (AuNCs) were applied as an antibacterial agent for real-time observations of their interactions with bacteria by in situ transmission electron microscopy (TEM). In this work, a surface ligand of glutathione-conjugated (GSH)-AuNCs was prepared via a simple hydrothermal method. Optical and structural characterizations validated the successful preparation of GSH-AuNCs. Bacterial growth curves of Acetobacter aceti revealed that the antibacterial activity of GSH-AuNCs increased with the weight concentration. The antibacterial activity of GSH-AuNCs was confirmed by the intracellular reactive oxygen species (ROS) generation induced by GSH-AuNCs in A. aceti. Furthermore, real-time observations of interactions between GSH-AuNCs and A. aceti were made using in situ liquid cell TEM. Based on the results of real-time observations, GSH-AuNCs first attached onto the bacterial membranes of A. aceti by physical adsorption and then penetrated into A. aceti by internalization. Eventually, the production of intracellular ROS induced by GSH-AuNCs caused destruction of the bacterial membranes, which led to the death of A. aceti. After the bacterial membranes had been destroyed, A. aceti eventually died.},
keywords = {antibacterial mechanism, in situ TEM, nanocluster, reactive oxygen species, real-time observation},
pubstate = {published},
tppubtype = {article}
}
Metal nanoclusters (NCs) with unique chemical and physical properties have been extensively demonstrated to be emerging nanoantibiotics for fighting bacterial infections. Understanding the antibacterial mechanisms of metal nanoclusters is important for evaluating their clinical applications as nanoantibiotics. To understand the antibacterial mechanism, gold nanoclusters (AuNCs) were applied as an antibacterial agent for real-time observations of their interactions with bacteria by in situ transmission electron microscopy (TEM). In this work, a surface ligand of glutathione-conjugated (GSH)-AuNCs was prepared via a simple hydrothermal method. Optical and structural characterizations validated the successful preparation of GSH-AuNCs. Bacterial growth curves of Acetobacter aceti revealed that the antibacterial activity of GSH-AuNCs increased with the weight concentration. The antibacterial activity of GSH-AuNCs was confirmed by the intracellular reactive oxygen species (ROS) generation induced by GSH-AuNCs in A. aceti. Furthermore, real-time observations of interactions between GSH-AuNCs and A. aceti were made using in situ liquid cell TEM. Based on the results of real-time observations, GSH-AuNCs first attached onto the bacterial membranes of A. aceti by physical adsorption and then penetrated into A. aceti by internalization. Eventually, the production of intracellular ROS induced by GSH-AuNCs caused destruction of the bacterial membranes, which led to the death of A. aceti. After the bacterial membranes had been destroyed, A. aceti eventually died. |
Proceedings Articles
|
| Philip J. Rosenthal, Anders Björkman, Mehul Dhorda, Abdoulaye Djimde, Arjen M. Dondorp, Oumar Gaye, Philippe J. Guerin, Elizabeth Juma, Dominic P. Kwiatkowski, Laura Merson, Francine Ntoumi, Ric N. Price, Jaishree Raman, David S. Roos, Feiko Ter Kuile, Halidou Tinto, Sheena S. Tomko, Nicholas J. White, Karen I. Barnes Cooperation in Countering Artemisinin Resistance in Africa: Learning from COVID-19. Proceedings Article In: The American journal of tropical medicine and hygiene, pp. 1568-70, 2022, ISSN: 1476-1645 0002-9637. @inproceedings{nokey,
title = {Cooperation in Countering Artemisinin Resistance in Africa: Learning from COVID-19.},
author = {Philip J. Rosenthal and Anders Bj\"{o}rkman and Mehul Dhorda and Abdoulaye Djimde and Arjen M. Dondorp and Oumar Gaye and Philippe J. Guerin and Elizabeth Juma and Dominic P. Kwiatkowski and Laura Merson and Francine Ntoumi and Ric N. Price and Jaishree Raman and David S. Roos and Feiko Ter Kuile and Halidou Tinto and Sheena S. Tomko and Nicholas J. White and Karen I. Barnes},
doi = {10.4269/ajtmh.22-0148},
issn = {1476-1645 0002-9637},
year = {2022},
date = {2022-04-01},
urldate = {2022-04-01},
booktitle = {The American journal of tropical medicine and hygiene},
volume = {106},
issue = {6},
pages = {1568-70},
keywords = {},
pubstate = {published},
tppubtype = {inproceedings}
}
|
2021
|
Journal Articles
|
| Barkissa Mélika Traoré, Mathurin Koffi, Martial Kassi N'Djetchi, Dramane Kaba, Jacques Kaboré, Hamidou Ilboudo, Bernadin Ahouty Ahouty, Minayégninrin Koné, Bamoro Coulibaly, Thomas Konan, Adeline Segard, Lingué Kouakou, Thierry De Meeûs, Sophie Ravel, Philippe Solano, Jean-Mathieu Bart, Vincent Jamonneau Free-ranging pigs identified as a multi-reservoir of Trypanosoma brucei and Trypanosoma congolense in the Vavoua area, a historical sleeping sickness focus of Côte d'Ivoire. Journal Article In: PLoS neglected tropical diseases, vol. 15, iss. 12, pp. e0010036, 2021, ISSN: 1935-2735 1935-2727. @article{nokey,
title = {Free-ranging pigs identified as a multi-reservoir of Trypanosoma brucei and Trypanosoma congolense in the Vavoua area, a historical sleeping sickness focus of C\^{o}te d'Ivoire.},
author = {Barkissa M\'{e}lika Traor\'{e} and Mathurin Koffi and Martial Kassi N'Djetchi and Dramane Kaba and Jacques Kabor\'{e} and Hamidou Ilboudo and Bernadin Ahouty Ahouty and Minay\'{e}gninrin Kon\'{e} and Bamoro Coulibaly and Thomas Konan and Adeline Segard and Lingu\'{e} Kouakou and Thierry De Mee\^{u}s and Sophie Ravel and Philippe Solano and Jean-Mathieu Bart and Vincent Jamonneau},
doi = {10.1371/journal.pntd.0010036},
issn = {1935-2735 1935-2727},
year = {2021},
date = {2021-12-01},
urldate = {2021-12-01},
journal = {PLoS neglected tropical diseases},
volume = {15},
issue = {12},
pages = {e0010036},
abstract = {BACKGROUND: The existence of an animal reservoir of Trypanosoma brucei gambiense (T. b. gambiense), the agent of human African trypanosomiasis (HAT), may compromise the interruption of transmission targeted by World Health Organization. The aim of this study was to investigate the presence of trypanosomes in pigs and people in the Vavoua HAT historical focus where cases were still diagnosed in the early 2010's. METHODS: For the human survey, we used the CATT, mini-anion exchange centrifugation technique and immune trypanolysis tests. For the animal survey, the buffy coat technique was also used as well as the PCR using Trypanosoma species specific, including the T. b. gambiense TgsGP detection using single round and nested PCRs, performed from animal blood samples and from strains isolated from subjects positive for parasitological investigations. RESULTS: No HAT cases were detected among 345 people tested. A total of 167 pigs were investigated. Free-ranging pigs appeared significantly more infected than pigs in pen. Over 70% of free-ranging pigs were positive for CATT and parasitological investigations and 27-43% were positive to trypanolysis depending on the antigen used. T. brucei was the most prevalent species (57%) followed by T. congolense (24%). Blood sample extracted DNA of T. brucei positive subjects were negative to single round TgsGP PCR. However, 1/22 and 6/22 isolated strains were positive with single round and nested TgsGP PCRs, respectively. DISCUSSION: Free-ranging pigs were identified as a multi-reservoir of T. brucei and/or T. congolense with mixed infections of different strains. This trypanosome diversity hinders the easy and direct detection of T. b. gambiense. We highlight the lack of tools to prove or exclude with certainty the presence of T. b. gambiense. This study once more highlights the need of technical improvements to explore the role of animals in the epidemiology of HAT.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: The existence of an animal reservoir of Trypanosoma brucei gambiense (T. b. gambiense), the agent of human African trypanosomiasis (HAT), may compromise the interruption of transmission targeted by World Health Organization. The aim of this study was to investigate the presence of trypanosomes in pigs and people in the Vavoua HAT historical focus where cases were still diagnosed in the early 2010's. METHODS: For the human survey, we used the CATT, mini-anion exchange centrifugation technique and immune trypanolysis tests. For the animal survey, the buffy coat technique was also used as well as the PCR using Trypanosoma species specific, including the T. b. gambiense TgsGP detection using single round and nested PCRs, performed from animal blood samples and from strains isolated from subjects positive for parasitological investigations. RESULTS: No HAT cases were detected among 345 people tested. A total of 167 pigs were investigated. Free-ranging pigs appeared significantly more infected than pigs in pen. Over 70% of free-ranging pigs were positive for CATT and parasitological investigations and 27-43% were positive to trypanolysis depending on the antigen used. T. brucei was the most prevalent species (57%) followed by T. congolense (24%). Blood sample extracted DNA of T. brucei positive subjects were negative to single round TgsGP PCR. However, 1/22 and 6/22 isolated strains were positive with single round and nested TgsGP PCRs, respectively. DISCUSSION: Free-ranging pigs were identified as a multi-reservoir of T. brucei and/or T. congolense with mixed infections of different strains. This trypanosome diversity hinders the easy and direct detection of T. b. gambiense. We highlight the lack of tools to prove or exclude with certainty the presence of T. b. gambiense. This study once more highlights the need of technical improvements to explore the role of animals in the epidemiology of HAT. |
| Serge Ouoba, Jean Claude Romaric Pingdwinde Ouedraogo, Moussa Lingani, Bunthen E, Md Razeen Ashraf Hussain, Ko Ko, Shintaro Nagashima, Aya Sugiyama, Tomoyuki Akita, Halidou Tinto, Junko Tanaka Epidemiologic profile of hepatitis C virus infection and genotype distribution in Burkina Faso: a systematic review with meta-analysis Journal Article In: BMC Infect. Dis., vol. 21, no. 1, pp. 1126, 2021, ISSN: 1471-2334, (© 2021. The Author(s).
PMID: 34724902
PMCID: PMC8561994). @article{Ouoba2021-ug,
title = {Epidemiologic profile of hepatitis C virus infection and genotype distribution in Burkina Faso: a systematic review with meta-analysis},
author = {Serge Ouoba and Jean Claude Romaric Pingdwinde Ouedraogo and Moussa Lingani and Bunthen E and Md Razeen Ashraf Hussain and Ko Ko and Shintaro Nagashima and Aya Sugiyama and Tomoyuki Akita and Halidou Tinto and Junko Tanaka},
doi = {10.1186/s12879-021-06817-x},
issn = {1471-2334},
year = {2021},
date = {2021-11-01},
urldate = {2021-11-01},
journal = {BMC Infect. Dis.},
volume = {21},
number = {1},
pages = {1126},
publisher = {Springer Science and Business Media LLC},
abstract = {BACKGROUND: Detailed characteristics of Hepatitis C virus (HCV)
infection in Burkina Faso are scarce. The main aim of this study
was to assess HCV seroprevalence in various settings and
populations at risk in Burkina Faso between 1990 and 2020.
Secondary objectives included the prevalence of HCV Ribonucleic
acid (RNA) and the distribution of HCV genotypes. METHODS: A
systematic database search, supplemented by a manual search, was
conducted in PubMed, Web of Science, Scopus, and African Index
Medicus. Studies reporting HCV seroprevalence data in low and
high-risk populations in Burkina Faso were included, and a
random-effects meta-analysis was applied. Risk of bias was
assessed using the Joanna Briggs institute checklist. RESULTS:
Low-risk populations were examined in 31 studies involving a
total of 168,151 subjects, of whom 8330 were positive for HCV
antibodies. Six studies included a total of 1484 high-risk
persons, and 96 had antibodies to HCV. The pooled seroprevalence
in low-risk populations was 3.72% (95% CI: 3.20-4.28) and
4.75% (95% CI: 1.79-8.94) in high-risk groups. A
non-significant decreasing trend was observed over the study
period. Seven studies tested HCV RNA in a total of 4759
individuals at low risk for HCV infection, and 81 were positive.
The meta-analysis of HCV RNA yielded a pooled prevalence of
1.65% (95% CI: 0.74-2.89%) in low-risk populations, which is
assumed to be indicative of HCV prevalence in the general
population of Burkina Faso and suggests that about 301,174
people are active HCV carriers in the country. Genotypes 2 and 1
were the most frequent, with 60.3% and 25.0%, respectively.
CONCLUSIONS: HCV seroprevalence is intermediate in Burkina Faso
and indicates the need to implement effective control
strategies. There is a paucity of data at the national level and
for rural and high-risk populations. General population
screening and linkage to care are recommended, with special
attention to rural and high-risk populations.},
note = {© 2021. The Author(s).
PMID: 34724902
PMCID: PMC8561994},
keywords = {Burkina Faso, Burkina Faso/epidemiology, Genotype, Hepacivirus/genetics, Hepatitis C, Hepatitis C/epidemiology, Humans, Prevalence, Seroepidemiologic Studies, Seroprevalence, Systematic review},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Detailed characteristics of Hepatitis C virus (HCV)
infection in Burkina Faso are scarce. The main aim of this study
was to assess HCV seroprevalence in various settings and
populations at risk in Burkina Faso between 1990 and 2020.
Secondary objectives included the prevalence of HCV Ribonucleic
acid (RNA) and the distribution of HCV genotypes. METHODS: A
systematic database search, supplemented by a manual search, was
conducted in PubMed, Web of Science, Scopus, and African Index
Medicus. Studies reporting HCV seroprevalence data in low and
high-risk populations in Burkina Faso were included, and a
random-effects meta-analysis was applied. Risk of bias was
assessed using the Joanna Briggs institute checklist. RESULTS:
Low-risk populations were examined in 31 studies involving a
total of 168,151 subjects, of whom 8330 were positive for HCV
antibodies. Six studies included a total of 1484 high-risk
persons, and 96 had antibodies to HCV. The pooled seroprevalence
in low-risk populations was 3.72% (95% CI: 3.20-4.28) and
4.75% (95% CI: 1.79-8.94) in high-risk groups. A
non-significant decreasing trend was observed over the study
period. Seven studies tested HCV RNA in a total of 4759
individuals at low risk for HCV infection, and 81 were positive.
The meta-analysis of HCV RNA yielded a pooled prevalence of
1.65% (95% CI: 0.74-2.89%) in low-risk populations, which is
assumed to be indicative of HCV prevalence in the general
population of Burkina Faso and suggests that about 301,174
people are active HCV carriers in the country. Genotypes 2 and 1
were the most frequent, with 60.3% and 25.0%, respectively.
CONCLUSIONS: HCV seroprevalence is intermediate in Burkina Faso
and indicates the need to implement effective control
strategies. There is a paucity of data at the national level and
for rural and high-risk populations. General population
screening and linkage to care are recommended, with special
attention to rural and high-risk populations. |
| Moussa Lingani, Serge H Zango, Innocent Valéa, Massa Dit A Bonko, Sékou O Samadoulougou, Toussaint Rouamba, Marc C Tahita, Ma"imouna Sanou, Annie Robert, Halidou Tinto, Philippe Donnen, Mich`ele Dramaix Malaria and curable sexually transmitted and reproductive tract coinfection among pregnant women in rural Burkina Faso Journal Article In: Trop. Med. Health, vol. 49, no. 1, pp. 90, 2021, ISSN: 1348-8945 1349-4147, (© 2021. The Author(s).
PMID: 34736524
PMCID: PMC8567650). @article{Lingani2021-is,
title = {Malaria and curable sexually transmitted and reproductive tract coinfection among pregnant women in rural Burkina Faso},
author = {Moussa Lingani and Serge H Zango and Innocent Val\'{e}a and Massa Dit A Bonko and S\'{e}kou O Samadoulougou and Toussaint Rouamba and Marc C Tahita and Ma"imouna Sanou and Annie Robert and Halidou Tinto and Philippe Donnen and Mich`ele Dramaix},
doi = {10.1186/s41182-021-00381-5},
issn = {1348-8945 1349-4147},
year = {2021},
date = {2021-11-01},
urldate = {2021-11-01},
journal = {Trop. Med. Health},
volume = {49},
number = {1},
pages = {90},
publisher = {Springer Science and Business Media LLC},
abstract = {BACKGROUND: Malaria and sexually transmitted/reproductive tract
infections (STI/RTI) are leading and preventable causes of low
birthweight in sub-Saharan Africa. Reducing their impact on
pregnancy outcomes requires efficient interventions that can be
easily integrated into the antenatal care package. The paucity
of data on malaria and STI/RTI coinfection, however, limits
efforts to control these infections. This study aimed to
determine the prevalence and associated factors of malaria and
STI/RTI coinfection among pregnant women in rural Burkina Faso.
METHODS: A cross-sectional survey was conducted among 402
pregnant women attending antenatal clinics at the Yako health
district. Sociodemographic and behavioral data were collected,
and pregnant women were tested for peripheral malaria by
microscopy. Hemoglobin levels were also measured by
spectrophotometry and curable bacterial STI/RTI were tested on
cervico-vaginal swabs using rapid diagnostic test for chlamydia
and syphilis, and Gram staining for bacterial vaginosis. A
multivariate logistic regression model was used to assess the
association of malaria and STI/RTI coinfection with the
characteristics of included pregnant women. RESULTS: The
prevalence of malaria and at least one STI/RTI coinfection was
12.9% (95% confidence interval, CI: [9.8-16.7]), malaria and
bacterial vaginosis coinfection was 12.2% (95% CI:
[9.3-15.9]), malaria and chlamydial coinfection was 1.6% (95%
CI: [0.6-3.8]). No coinfection was reported for malaria and
syphilis. The individual prevalence was 17.2%, 7.2%, 0.6%,
67.7% and 73.3%, respectively, for malaria infection,
chlamydia, syphilis, bacterial vaginosis and STI/RTI
combination. Only 10% of coinfections were symptomatic, and
thus, 90% of women with coinfection would have been missed by
the symptoms-based diagnostic approach. In the multivariate analysis, the first pregnancy (aOR = 2.4 [95% CI: 1.2-4.7]) was
the only factor significantly associated with malaria and
STI/RTI coinfection. Clinical symptoms were not associated with
malaria and STI/RTI coinfection. CONCLUSION: The prevalence of
malaria and curable STI/RTI coinfection was high among pregnant
women. The poor performance of the clinical symptoms to predict
coinfection suggests that alternative interventions are needed.},
note = {© 2021. The Author(s).
PMID: 34736524
PMCID: PMC8567650},
keywords = {Bacterial vaginosis, Burkina Faso, Chlamydia, Coinfection, Malaria, Pregnancy, Syphilis},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Malaria and sexually transmitted/reproductive tract
infections (STI/RTI) are leading and preventable causes of low
birthweight in sub-Saharan Africa. Reducing their impact on
pregnancy outcomes requires efficient interventions that can be
easily integrated into the antenatal care package. The paucity
of data on malaria and STI/RTI coinfection, however, limits
efforts to control these infections. This study aimed to
determine the prevalence and associated factors of malaria and
STI/RTI coinfection among pregnant women in rural Burkina Faso.
METHODS: A cross-sectional survey was conducted among 402
pregnant women attending antenatal clinics at the Yako health
district. Sociodemographic and behavioral data were collected,
and pregnant women were tested for peripheral malaria by
microscopy. Hemoglobin levels were also measured by
spectrophotometry and curable bacterial STI/RTI were tested on
cervico-vaginal swabs using rapid diagnostic test for chlamydia
and syphilis, and Gram staining for bacterial vaginosis. A
multivariate logistic regression model was used to assess the
association of malaria and STI/RTI coinfection with the
characteristics of included pregnant women. RESULTS: The
prevalence of malaria and at least one STI/RTI coinfection was
12.9% (95% confidence interval, CI: [9.8-16.7]), malaria and
bacterial vaginosis coinfection was 12.2% (95% CI:
[9.3-15.9]), malaria and chlamydial coinfection was 1.6% (95%
CI: [0.6-3.8]). No coinfection was reported for malaria and
syphilis. The individual prevalence was 17.2%, 7.2%, 0.6%,
67.7% and 73.3%, respectively, for malaria infection,
chlamydia, syphilis, bacterial vaginosis and STI/RTI
combination. Only 10% of coinfections were symptomatic, and
thus, 90% of women with coinfection would have been missed by
the symptoms-based diagnostic approach. In the multivariate analysis, the first pregnancy (aOR = 2.4 [95% CI: 1.2-4.7]) was
the only factor significantly associated with malaria and
STI/RTI coinfection. Clinical symptoms were not associated with
malaria and STI/RTI coinfection. CONCLUSION: The prevalence of
malaria and curable STI/RTI coinfection was high among pregnant
women. The poor performance of the clinical symptoms to predict
coinfection suggests that alternative interventions are needed. |
| Rafael Dal-Ré, Linda-Gail Bekker, Christian Gluud, Søren Holm, Vivekanand Jha, Gregory A Poland, Frits R Rosendaal, Brigitte Schwarzer-Daum, Esperanc ca Sevene, Halidou Tinto, Teck Chuan Voo, Nadarajah Sreeharan Ongoing and future COVID-19 vaccine clinical trials: challenges and opportunities Journal Article In: Lancet Infect. Dis., vol. 21, no. 11, pp. e342–e347, 2021, ISSN: 1474-4457 1473-3099, (Copyright © 2021 Elsevier Ltd. All rights reserved.
PMID: 34019801
PMCID: PMC8131060). @article{Dal-Re2021-mr,
title = {Ongoing and future COVID-19 vaccine clinical trials: challenges and opportunities},
author = {Rafael Dal-R\'{e} and Linda-Gail Bekker and Christian Gluud and S\oren Holm and Vivekanand Jha and Gregory A Poland and Frits R Rosendaal and Brigitte Schwarzer-Daum and Esperanc ca Sevene and Halidou Tinto and Teck Chuan Voo and Nadarajah Sreeharan},
doi = {10.1016/S1473-3099(21)00263-2},
issn = {1474-4457 1473-3099},
year = {2021},
date = {2021-11-01},
urldate = {2021-11-01},
journal = {Lancet Infect. Dis.},
volume = {21},
number = {11},
pages = {e342--e347},
abstract = {Large-scale deployment of COVID-19 vaccines will seriously affect
the ongoing phases 2 and 3 randomised placebo-controlled trials
assessing SARS-CoV-2 vaccine candidates. The effect will be
particularly acute in high-income countries where the entire
adult or older population could be vaccinated by late 2021.
Regrettably, only a small proportion of the population in many
low-income and middle-income countries will have access to
available vaccines. Sponsors of COVID-19 vaccine candidates
currently in phase 2 or initiating phase 3 trials in 2021 should
consider continuing the research in countries with limited
affordability and availability of COVID-19 vaccines. Several
ethical principles must be implemented to ensure the equitable,
non-exploitative, and respectful conduct of trials in
resource-poor settings. Once sufficient knowledge on the
immunogenicity response to COVID-19 vaccines is acquired,
non-inferiority immunogenicity trials-comparing the immune
response of a vaccine candidate to that of an authorised
vaccine-would probably be the most common trial design. Until
then, placebo-controlled, double-blind, crossover trials will
continue to play a role in the development of new vaccine
candidates. WHO or the Council for International Organizations of
Medical Sciences should define an ethical framework for the
requirements and benefits for trial participants and host
communities in resource-poor settings that should require
commitment from all vaccine candidate sponsors from high-income
countries.},
note = {Copyright © 2021 Elsevier Ltd. All rights reserved.
PMID: 34019801
PMCID: PMC8131060},
keywords = {Clinical Trials as Topic, COVID-19 Vaccines/administration \& dosage/immunology, COVID-19/epidemiology/immunology/prevention \& control/virology, Double-Blind Method, Humans, Immunogenicity, Pandemics/prevention \& control, SARS-CoV-2/immunology, Vaccine},
pubstate = {published},
tppubtype = {article}
}
Large-scale deployment of COVID-19 vaccines will seriously affect
the ongoing phases 2 and 3 randomised placebo-controlled trials
assessing SARS-CoV-2 vaccine candidates. The effect will be
particularly acute in high-income countries where the entire
adult or older population could be vaccinated by late 2021.
Regrettably, only a small proportion of the population in many
low-income and middle-income countries will have access to
available vaccines. Sponsors of COVID-19 vaccine candidates
currently in phase 2 or initiating phase 3 trials in 2021 should
consider continuing the research in countries with limited
affordability and availability of COVID-19 vaccines. Several
ethical principles must be implemented to ensure the equitable,
non-exploitative, and respectful conduct of trials in
resource-poor settings. Once sufficient knowledge on the
immunogenicity response to COVID-19 vaccines is acquired,
non-inferiority immunogenicity trials-comparing the immune
response of a vaccine candidate to that of an authorised
vaccine-would probably be the most common trial design. Until
then, placebo-controlled, double-blind, crossover trials will
continue to play a role in the development of new vaccine
candidates. WHO or the Council for International Organizations of
Medical Sciences should define an ethical framework for the
requirements and benefits for trial participants and host
communities in resource-poor settings that should require
commitment from all vaccine candidate sponsors from high-income
countries. |
| Moussa Lingani, Serge H Zango, Innocent Valéa, Daniel Valia, Ma"imouna Sanou, Sékou O Samandoulougou, Annie Robert, Halidou Tinto, Mich`ele Dramaix, Philippe Donnen Magnitude of low birthweight in malaria endemic settings of Nanoro, rural Burkina Faso: a secondary data analysis Journal Article In: Sci. Rep., vol. 11, no. 1, pp. 21332, 2021, ISSN: 2045-2322, (© 2021. The Author(s).
PMID: 34716389
PMCID: PMC8556330). @article{Lingani2021-ae,
title = {Magnitude of low birthweight in malaria endemic settings of Nanoro, rural Burkina Faso: a secondary data analysis},
author = {Moussa Lingani and Serge H Zango and Innocent Val\'{e}a and Daniel Valia and Ma"imouna Sanou and S\'{e}kou O Samandoulougou and Annie Robert and Halidou Tinto and Mich`ele Dramaix and Philippe Donnen},
doi = {10.1038/s41598-021-00881-8},
issn = {2045-2322},
year = {2021},
date = {2021-10-29},
urldate = {2021-10-01},
journal = {Sci. Rep.},
volume = {11},
number = {1},
pages = {21332},
publisher = {Springer Science and Business Media LLC},
abstract = {Low birthweight (LBW) is a worldwide problem that particularly
affects developing countries. However, limited information is
available on its magnitude in rural area of Burkina Faso. This
study aimed to estimate the prevalence of low birthweight and to
identify its associated factors in Nanoro health district. A
secondary analysis of data collected during a cross-sectional
survey was conducted to assess the prevalence of low birthweight
in Nanoro health and demographic surveillance system area
(HDSS). Maternal characteristics extracted from antenatal care
books or by interview, completed by malaria diagnosis were
examined through a multi-level logistic regression to estimate
odd-ratios of association with low birthweight. Significance
level was set at 5%. Of the 291 neonates examined, the
prevalence of low birthweight was 12%. After adjustment for
socio-demographic, obstetric and malaria prevention variables, being primigravid (OR = 8.84, [95% CI: 3.72-21.01]), or multigravid with history of stillbirth (OR = 5.03, [95% CI:
1.54-16.40]), as well as the lack of long-lasting insecticide
treated bed net use by the mother the night preceding the admission for delivery (OR = 2.5, [95% CI: 1.1-5.9]) were
significantly associated with neonate low birthweight. The
number of antenatal visits however did not confer any direct
benefit on birthweight status within this study area. The
prevalence of low birthweight was high in the study area and
represents an important public health problem in Burkina Faso.
In light of these results, a redefinition of the content of the
antenatal care package is needed.},
note = {© 2021. The Author(s).
PMID: 34716389
PMCID: PMC8556330},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Low birthweight (LBW) is a worldwide problem that particularly
affects developing countries. However, limited information is
available on its magnitude in rural area of Burkina Faso. This
study aimed to estimate the prevalence of low birthweight and to
identify its associated factors in Nanoro health district. A
secondary analysis of data collected during a cross-sectional
survey was conducted to assess the prevalence of low birthweight
in Nanoro health and demographic surveillance system area
(HDSS). Maternal characteristics extracted from antenatal care
books or by interview, completed by malaria diagnosis were
examined through a multi-level logistic regression to estimate
odd-ratios of association with low birthweight. Significance
level was set at 5%. Of the 291 neonates examined, the
prevalence of low birthweight was 12%. After adjustment for
socio-demographic, obstetric and malaria prevention variables, being primigravid (OR = 8.84, [95% CI: 3.72-21.01]), or multigravid with history of stillbirth (OR = 5.03, [95% CI:
1.54-16.40]), as well as the lack of long-lasting insecticide
treated bed net use by the mother the night preceding the admission for delivery (OR = 2.5, [95% CI: 1.1-5.9]) were
significantly associated with neonate low birthweight. The
number of antenatal visits however did not confer any direct
benefit on birthweight status within this study area. The
prevalence of low birthweight was high in the study area and
represents an important public health problem in Burkina Faso.
In light of these results, a redefinition of the content of the
antenatal care package is needed. |
| Serge Henri Zango, Moussa Lingani, Innocent Valea, Ouindpanga Sekou Samadoulougou, Biebo Bihoun, Diagniagou Lankoande, Phillipe Donnen, Michele Dramaix, Halidou Tinto, Annie Robert Association of malaria and curable sexually transmitted infections with pregnancy outcomes in rural Burkina Faso Journal Article In: BMC Pregnancy Childbirth, vol. 21, no. 1, pp. 722, 2021, ISSN: 1471-2393, (© 2021. The Author(s).
PMID: 34706705
PMCID: PMC8549350). @article{Zango2021-ti,
title = {Association of malaria and curable sexually transmitted infections with pregnancy outcomes in rural Burkina Faso},
author = {Serge Henri Zango and Moussa Lingani and Innocent Valea and Ouindpanga Sekou Samadoulougou and Biebo Bihoun and Diagniagou Lankoande and Phillipe Donnen and Michele Dramaix and Halidou Tinto and Annie Robert},
doi = {10.1186/s12884-021-04205-6},
issn = {1471-2393},
year = {2021},
date = {2021-10-27},
urldate = {2021-10-27},
journal = {BMC Pregnancy Childbirth},
volume = {21},
number = {1},
pages = {722},
publisher = {Springer Science and Business Media LLC},
abstract = {BACKGROUND: Malaria and curable sexually transmitted infections
(STIs) are severe infections associated with poor pregnancy
outcomes in sub-Saharan countries. These infections are
responsible for low birth weight, preterm birth, and
miscarriage. In Burkina Faso, many interventions recommended by
the World Health Organization were implemented to control the
impact of these infections. After decades of intervention, we
assessed the impact of these infections on pregnancy outcomes in
rural setting of Burkina Faso. METHODS: Antenatal care and
delivery data of pregnant women attending health facilities in
2016 and 2017 were collected in two rural districts namely
Nanoro and Yako, in Burkina Faso. Regression models with
likelihood ratio test were used to assess the association
between infections and pregnancy outcomes. RESULTS: During the
two years, 31639 pregnant women received antenatal care. Malaria
without STI, STI without malaria, and their coinfections were
reported for 7359 (23.3%), 881 (2.8 %), and 388 (1.2%) women,
respectively. Low birth weight, miscarriage, and stillbirth were
observed in 2754 (10.5 %), 547 (2.0 %), and 373 (1.3 %)
women, respectively. Our data did not show an association
between low birth weight and malaria [Adjusted OR: 0.91 (0.78 -
1.07)], STIs [Adjusted OR: 0.74 (0.51 - 1.07)] and coinfection
[Adjusted OR: 1.15 (0.75 - 1.78)]. Low birth weight was strongly
associated with primigravidae [Adjusted OR: 3.53 (3.12 - 4.00)].
Both miscarriage and stillbirth were associated with malaria
[Adjusted OR: 1.31 (1.07 - 1.59)], curable STI [Adjusted OR:
1.65 (1.06 - 2.59)], and coinfection [Adjusted OR: 2.00 (1.13 -
3.52)]. CONCLUSION: Poor pregnancy outcomes remained frequent in
rural Burkina Faso. Malaria, curable STIs, and their
coinfections were associated with both miscarriage and
stillbirth in rural Burkina. More effort should be done to
reduce the proportion of pregnancies lost associated with these
curable infections by targeting interventions in primigravidae
women.},
note = {© 2021. The Author(s).
PMID: 34706705
PMCID: PMC8549350},
keywords = {Coinfection, Impact, Malaria, Outcome, Pregnancy, STI},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Malaria and curable sexually transmitted infections
(STIs) are severe infections associated with poor pregnancy
outcomes in sub-Saharan countries. These infections are
responsible for low birth weight, preterm birth, and
miscarriage. In Burkina Faso, many interventions recommended by
the World Health Organization were implemented to control the
impact of these infections. After decades of intervention, we
assessed the impact of these infections on pregnancy outcomes in
rural setting of Burkina Faso. METHODS: Antenatal care and
delivery data of pregnant women attending health facilities in
2016 and 2017 were collected in two rural districts namely
Nanoro and Yako, in Burkina Faso. Regression models with
likelihood ratio test were used to assess the association
between infections and pregnancy outcomes. RESULTS: During the
two years, 31639 pregnant women received antenatal care. Malaria
without STI, STI without malaria, and their coinfections were
reported for 7359 (23.3%), 881 (2.8 %), and 388 (1.2%) women,
respectively. Low birth weight, miscarriage, and stillbirth were
observed in 2754 (10.5 %), 547 (2.0 %), and 373 (1.3 %)
women, respectively. Our data did not show an association
between low birth weight and malaria [Adjusted OR: 0.91 (0.78 -
1.07)], STIs [Adjusted OR: 0.74 (0.51 - 1.07)] and coinfection
[Adjusted OR: 1.15 (0.75 - 1.78)]. Low birth weight was strongly
associated with primigravidae [Adjusted OR: 3.53 (3.12 - 4.00)].
Both miscarriage and stillbirth were associated with malaria
[Adjusted OR: 1.31 (1.07 - 1.59)], curable STI [Adjusted OR:
1.65 (1.06 - 2.59)], and coinfection [Adjusted OR: 2.00 (1.13 -
3.52)]. CONCLUSION: Poor pregnancy outcomes remained frequent in
rural Burkina Faso. Malaria, curable STIs, and their
coinfections were associated with both miscarriage and
stillbirth in rural Burkina. More effort should be done to
reduce the proportion of pregnancies lost associated with these
curable infections by targeting interventions in primigravidae
women. |
| Tim Starck, Caroline A Bulstra, Halidou Tinto, Toussaint Rouamba, Ali Sie, Thomas Jaenisch, Till Bärnighausen The effect of malaria on haemoglobin concentrations: a nationally representative household fixed-effects study of 17,599 children under 5 years of age in Burkina Faso Journal Article In: Malar. J., vol. 20, no. 1, pp. 416, 2021, ISSN: 1475-2875, (© 2021. The Author(s).
PMID: 34688294
PMCID: PMC8542337). @article{Starck2021-mb,
title = {The effect of malaria on haemoglobin concentrations: a nationally representative household fixed-effects study of 17,599 children under 5 years of age in Burkina Faso},
author = {Tim Starck and Caroline A Bulstra and Halidou Tinto and Toussaint Rouamba and Ali Sie and Thomas Jaenisch and Till B\"{a}rnighausen},
doi = {10.1186/s12936-021-03948-z},
issn = {1475-2875},
year = {2021},
date = {2021-10-23},
urldate = {2021-10-23},
journal = {Malar. J.},
volume = {20},
number = {1},
pages = {416},
publisher = {Springer Science and Business Media LLC},
abstract = {BACKGROUND: Although the association between malaria and anaemia
is widely studied in patient cohorts, the
population-representative causal effects of malaria on anaemia
remain unknown. This study estimated the malaria-induced
decrease in haemoglobin levels among young children in
malaria-endemic Burkina Faso. METHODS: The study was based on
pooled individual-level nationally representative health survey
data (2010-2011, 2014, 2017-2018) from 17 599 children under 5
years of age. This data was used to estimate the effects of
malaria on haemoglobin concentration, controlling for household
fixed-effects, age, and sex in a series of regression analyses.
The fixed-effects controlled for observed and unobserved
confounding on the household level and allowed to determine the
impact of malaria infection status on haemoglobin levels and
anaemia prevalence. Furthermore, the diagnostic results from
microscopy and rapid diagnostic tests were leveraged to provide
a quasi-longitudinal perspective of acute and prolonged effects
after malaria infection. RESULTS: The prevalence of both malaria
(survey prevalence ranging from 17.4% to 65.2%) and anaemia
(survey prevalence ranging from 74% to 88.2%) was very high in
the included surveys. Malaria was estimated to significantly
reduce haemoglobin levels, with an overall effect of - 7.5 g/dL
(95% CI - 8.5, - 6.5). Acute malaria resulted in a - 7.7 g/dL
(95% CI - 8.8, - 6.6) decrease in haemoglobin levels. Recent
malaria without current parasitaemia decreased haemoglobin
concentration by - 7.1 g/dL (95% CI - 8.3, - 5.9). The
in-sample predicted prevalence of severe anaemia was 9.4% among
malaria positives, but only 2.2% among children without
malaria. CONCLUSION: Malaria infection has a strong detrimental
effect on haemoglobin levels among young children in Burkina
Faso. This effect seems to carry over even after acute
infection, indicating prolonged haemoglobin reductions even
after successful parasite-elimination. The quasi-experimental
fixed-effect approach adds a population level perspective to
existing clinical evidence.},
note = {© 2021. The Author(s).
PMID: 34688294
PMCID: PMC8542337},
keywords = {Anaemia, Burkina Faso, Haemoglobin, Household fixed-effects, Malaria, Microscopy, Rapid diagnostic tests},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Although the association between malaria and anaemia
is widely studied in patient cohorts, the
population-representative causal effects of malaria on anaemia
remain unknown. This study estimated the malaria-induced
decrease in haemoglobin levels among young children in
malaria-endemic Burkina Faso. METHODS: The study was based on
pooled individual-level nationally representative health survey
data (2010-2011, 2014, 2017-2018) from 17 599 children under 5
years of age. This data was used to estimate the effects of
malaria on haemoglobin concentration, controlling for household
fixed-effects, age, and sex in a series of regression analyses.
The fixed-effects controlled for observed and unobserved
confounding on the household level and allowed to determine the
impact of malaria infection status on haemoglobin levels and
anaemia prevalence. Furthermore, the diagnostic results from
microscopy and rapid diagnostic tests were leveraged to provide
a quasi-longitudinal perspective of acute and prolonged effects
after malaria infection. RESULTS: The prevalence of both malaria
(survey prevalence ranging from 17.4% to 65.2%) and anaemia
(survey prevalence ranging from 74% to 88.2%) was very high in
the included surveys. Malaria was estimated to significantly
reduce haemoglobin levels, with an overall effect of - 7.5 g/dL
(95% CI - 8.5, - 6.5). Acute malaria resulted in a - 7.7 g/dL
(95% CI - 8.8, - 6.6) decrease in haemoglobin levels. Recent
malaria without current parasitaemia decreased haemoglobin
concentration by - 7.1 g/dL (95% CI - 8.3, - 5.9). The
in-sample predicted prevalence of severe anaemia was 9.4% among
malaria positives, but only 2.2% among children without
malaria. CONCLUSION: Malaria infection has a strong detrimental
effect on haemoglobin levels among young children in Burkina
Faso. This effect seems to carry over even after acute
infection, indicating prolonged haemoglobin reductions even
after successful parasite-elimination. The quasi-experimental
fixed-effect approach adds a population level perspective to
existing clinical evidence. |
| Soumeya Hema-Ouangraoua, Juliette Tranchot-Diallo, Issaka Zongo, Nongodo Firmin Kabore, Frédéric Niki`ema, Rakiswende Serge Yerbanga, Halidou Tinto, Daniel Chandramohan, Georges-Anicet Ouedraogo, Brian Greenwood, Jean-Bosco Ouedraogo Impact of mass administration of azithromycin as a preventive treatment on the prevalence and resistance of nasopharyngeal carriage of Staphylococcus aureus Journal Article In: PLoS One, vol. 16, no. 10, pp. e0257190, 2021, ISSN: 1932-6203, (PMID: 34644317
PMCID: PMC8513893). @article{Hema-Ouangraoua2021-xf,
title = {Impact of mass administration of azithromycin as a preventive treatment on the prevalence and resistance of nasopharyngeal carriage of Staphylococcus aureus},
author = {Soumeya Hema-Ouangraoua and Juliette Tranchot-Diallo and Issaka Zongo and Nongodo Firmin Kabore and Fr\'{e}d\'{e}ric Niki`ema and Rakiswende Serge Yerbanga and Halidou Tinto and Daniel Chandramohan and Georges-Anicet Ouedraogo and Brian Greenwood and Jean-Bosco Ouedraogo},
doi = {10.1371/journal.pone.0257190},
issn = {1932-6203},
year = {2021},
date = {2021-10-13},
urldate = {2021-10-01},
journal = {PLoS One},
volume = {16},
number = {10},
pages = {e0257190},
publisher = {Public Library of Science (PLoS)},
abstract = {Staphylococcus aureus is a major cause of serious illness and
death in children, indicating the need to monitor prevalent
strains, particularly in the vulnerable pediatric population.
Nasal carriage of S. aureus is important as carriers have an
increased risk of serious illness due to systemic invasion by
this pathogen and can transmit the infection. Recent studies
have demonstrated the effectiveness of azithromycin in reducing
the prevalence of nasopharyngeal carrying of pneumococci, which
are often implicated in respiratory infections in children.
However, very few studies of the impact of azithromycin on
staphylococci have been undertaken. During a clinical trial
under taken in 2016, nasal swabs were collected from 778
children aged 3 to 59 months including 385 children who were
swabbed before administration of azithromycin or placebo and 393
after administration of azithromycin or placebo. Azithromycin
was given in a dose of 100 mg for three days, together with the
antimalarials sulfadoxine-pyrimethamine and amodiaquine, on four
occasions at monthly intervals during the malaria transmission
season. These samples were cultured for S. aureus as well as for
the pneumococcus. The S. aureus isolates were tested for their
susceptibility to azithromycin (15 g), penicillin (10 IU), and
cefoxitine (30 g) (Oxoid Ltd). S. aureus was isolated from
13.77% (53/385) swabs before administration of azithromycin and from 20.10% (79/393) six months after administration (PR = 1.46 [1.06; 2.01},
note = {PMID: 34644317
PMCID: PMC8513893},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Staphylococcus aureus is a major cause of serious illness and
death in children, indicating the need to monitor prevalent
strains, particularly in the vulnerable pediatric population.
Nasal carriage of S. aureus is important as carriers have an
increased risk of serious illness due to systemic invasion by
this pathogen and can transmit the infection. Recent studies
have demonstrated the effectiveness of azithromycin in reducing
the prevalence of nasopharyngeal carrying of pneumococci, which
are often implicated in respiratory infections in children.
However, very few studies of the impact of azithromycin on
staphylococci have been undertaken. During a clinical trial
under taken in 2016, nasal swabs were collected from 778
children aged 3 to 59 months including 385 children who were
swabbed before administration of azithromycin or placebo and 393
after administration of azithromycin or placebo. Azithromycin
was given in a dose of 100 mg for three days, together with the
antimalarials sulfadoxine-pyrimethamine and amodiaquine, on four
occasions at monthly intervals during the malaria transmission
season. These samples were cultured for S. aureus as well as for
the pneumococcus. The S. aureus isolates were tested for their
susceptibility to azithromycin (15 g), penicillin (10 IU), and
cefoxitine (30 g) (Oxoid Ltd). S. aureus was isolated from
13.77% (53/385) swabs before administration of azithromycin and from 20.10% (79/393) six months after administration (PR = 1.46 [1.06; 2.01 |
| Jeoffray Diendéré, Augustin Nawidimbasba Zeba, Sibraogo Kiemtoré, Olivier Ouahamin Sombié, Philippe Fayemendy, Pierre Jésus, Athanase Millogo, Aly Savadogo, Halidou Tinto, Jean-Claude Desport Associations between dental problems and underweight status among rural women in Burkina Faso: results from the first WHO Stepwise Approach to Surveillance (STEPS) survey Journal Article In: Public Health Nutr., pp. 1–11, 2021, ISSN: 1475-2727 1368-9800, (Place: England
PMID: 34615560). @article{Diendere2021-lc,
title = {Associations between dental problems and underweight status among rural women in Burkina Faso: results from the first WHO Stepwise Approach to Surveillance (STEPS) survey},
author = {Jeoffray Diend\'{e}r\'{e} and Augustin Nawidimbasba Zeba and Sibraogo Kiemtor\'{e} and Olivier Ouahamin Sombi\'{e} and Philippe Fayemendy and Pierre J\'{e}sus and Athanase Millogo and Aly Savadogo and Halidou Tinto and Jean-Claude Desport},
doi = {10.1017/S1368980021004080},
issn = {1475-2727 1368-9800},
year = {2021},
date = {2021-10-07},
urldate = {2021-10-07},
journal = {Public Health Nutr.},
pages = {1--11},
publisher = {Cambridge University Press (CUP)},
abstract = {OBJECTIVE: To explore the relationships between dental problems
and underweight status among rural women in Burkina Faso by
using nationally representative data. DESIGN: This was a
cross-sectional secondary study of primary data obtained by the
2013 WHO Stepwise Approach to Surveillance survey conducted in
Burkina Faso. Descriptive and analytical analyses were performed
using Student's t test, ANOVA, the $chi$2 test, Fisher's exact
test and logistic regression. SETTING: All thirteen
Burkinab`e regions were categorised using quartiles of
urbanisation rates. PARTICIPANTS: The participants were 1730
rural women aged 25-64 years. RESULTS: The prevalence of
underweight was 16·0 %, and 24·1 % of participants experienced
dental problems during the 12-month period. The women with
dental problems were more frequently underweight (19·9 % and
14·7 %; P 49 years old) and smokeless tobacco users. Age \> 49
years, professions with inconsistent income, a lack of
education, smokeless tobacco use and low BMI were factors that
were significantly associated with dental problems, while
residency in a low-urbanisation area was a protective factor.
CONCLUSION: The prevalence of underweight in rural Burkinab`e
women is among the highest in sub-Saharan Africa, and women with
dental problems are more frequently affected than those without
dental problems. Public health measures for the prevention of
these disorders should specifically target women aged over 49
years and smokeless tobacco users.},
note = {Place: England
PMID: 34615560},
keywords = {Burkina Faso, Dental problems, Prevalence, Risk Factors, Rural women, Underweight},
pubstate = {published},
tppubtype = {article}
}
OBJECTIVE: To explore the relationships between dental problems
and underweight status among rural women in Burkina Faso by
using nationally representative data. DESIGN: This was a
cross-sectional secondary study of primary data obtained by the
2013 WHO Stepwise Approach to Surveillance survey conducted in
Burkina Faso. Descriptive and analytical analyses were performed
using Student's t test, ANOVA, the $chi$2 test, Fisher's exact
test and logistic regression. SETTING: All thirteen
Burkinab`e regions were categorised using quartiles of
urbanisation rates. PARTICIPANTS: The participants were 1730
rural women aged 25-64 years. RESULTS: The prevalence of
underweight was 16·0 %, and 24·1 % of participants experienced
dental problems during the 12-month period. The women with
dental problems were more frequently underweight (19·9 % and
14·7 %; P 49 years old) and smokeless tobacco users. Age > 49
years, professions with inconsistent income, a lack of
education, smokeless tobacco use and low BMI were factors that
were significantly associated with dental problems, while
residency in a low-urbanisation area was a protective factor.
CONCLUSION: The prevalence of underweight in rural Burkinab`e
women is among the highest in sub-Saharan Africa, and women with
dental problems are more frequently affected than those without
dental problems. Public health measures for the prevention of
these disorders should specifically target women aged over 49
years and smokeless tobacco users. |
| Mphatso Dennis Phiri, Matthew Cairns, Issaka Zongo, Frederic Nikiema, Modibo Diarra, Rakiswendé Serge Yerbanga, Amadou Barry, Amadou Tapily, Samba Coumare, Ismaila Thera, Irene Kuepfer, Paul Milligan, Halidou Tinto, Alassane Dicko, Jean Bosco Ouédraogo, Brian Greenwood, Daniel Chandramohan, Issaka Sagara The duration of protection from azithromycin against malaria, acute respiratory, gastrointestinal, and skin infections when given alongside seasonal malaria chemoprevention: Secondary analyses of data from a clinical trial in houndé, Burkina Faso, and bougouni, Mali Journal Article In: Clin. Infect. Dis., vol. 73, no. 7, pp. e2379–e2386, 2021, ISSN: 1537-6591 1058-4838, (© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.
PMID: 33417683
PMCID: PMC8492219). @article{Phiri2021-oy,
title = {The duration of protection from azithromycin against malaria, acute respiratory, gastrointestinal, and skin infections when given alongside seasonal malaria chemoprevention: Secondary analyses of data from a clinical trial in hound\'{e}, Burkina Faso, and bougouni, Mali},
author = {Mphatso Dennis Phiri and Matthew Cairns and Issaka Zongo and Frederic Nikiema and Modibo Diarra and Rakiswend\'{e} Serge Yerbanga and Amadou Barry and Amadou Tapily and Samba Coumare and Ismaila Thera and Irene Kuepfer and Paul Milligan and Halidou Tinto and Alassane Dicko and Jean Bosco Ou\'{e}draogo and Brian Greenwood and Daniel Chandramohan and Issaka Sagara},
doi = {10.1093/cid/ciaa1905},
issn = {1537-6591 1058-4838},
year = {2021},
date = {2021-10-01},
urldate = {2021-10-01},
journal = {Clin. Infect. Dis.},
volume = {73},
number = {7},
pages = {e2379--e2386},
publisher = {Oxford University Press (OUP)},
abstract = {BACKGROUND: Mass drug administration (MDA) with azithromycin
(AZ) is being considered as a strategy to promote child survival
in sub-Saharan Africa, but the mechanism by which AZ reduces
mortality is unclear. To better understand the nature and extent
of protection provided by AZ, we explored the profile of
protection by time since administration, using data from a
household-randomized, placebo-controlled trial in Burkina Faso
and Mali. METHODS: Between 2014 and 2016, 30 977 children aged
3-59 months received seasonal malaria chemoprevention (SMC) with
sulfadoxine-pyrimethamine plus amodiaquine and either AZ or
placebo monthly, on 4 occasions each year. Poisson regression
with gamma-distributed random effects, accounting for the
household randomization and within-individual clustering of
illness episodes, was used to compare incidence of prespecified
outcomes between SMC+AZ versus SMC+placebo groups in fixed time
strata post-treatment. The likelihood ratio test was used to
assess evidence for a time-treatment group interaction. RESULTS:
Relative to SMC+placebo, there was no evidence of protection
from SMC+AZ against hospital admissions and deaths. Additional
protection from SMC+AZ against malaria was confined to the first
2 weeks post-administration (protective efficacy (PE): 24.2%
[95% CI: 17.8%, 30.1%]). Gastroenteritis and pneumonia were
reduced by 29.9% [21.7; 37.3%], and 34.3% [14.9; 49.3%],
respectively, in the first 2 weeks postadministration.
Protection against nonmalaria fevers with a skin condition
persisted up to 28 days: PE: 46.3% [35.1; 55.6%]. CONCLUSIONS:
The benefits of AZ-MDA are broad-ranging but short-lived. To
maximize impact, timing of AZ-MDA must address the challenge of
targeting asynchronous morbidity and mortality peaks from
different causes.},
note = {© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.
PMID: 33417683
PMCID: PMC8492219},
keywords = {Antimalarials/therapeutic use, Azithromycin, Azithromycin/therapeutic use, Burkina Faso/epidemiology, Chemoprevention, Child, child mortality, Drug Combinations, duration of protection, Humans, Infant, Malaria/drug therapy/epidemiology/prevention \& control, Mali/epidemiology, Preschool, Sahel, seasonal malaria chemoprevention, Seasons},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Mass drug administration (MDA) with azithromycin
(AZ) is being considered as a strategy to promote child survival
in sub-Saharan Africa, but the mechanism by which AZ reduces
mortality is unclear. To better understand the nature and extent
of protection provided by AZ, we explored the profile of
protection by time since administration, using data from a
household-randomized, placebo-controlled trial in Burkina Faso
and Mali. METHODS: Between 2014 and 2016, 30 977 children aged
3-59 months received seasonal malaria chemoprevention (SMC) with
sulfadoxine-pyrimethamine plus amodiaquine and either AZ or
placebo monthly, on 4 occasions each year. Poisson regression
with gamma-distributed random effects, accounting for the
household randomization and within-individual clustering of
illness episodes, was used to compare incidence of prespecified
outcomes between SMC+AZ versus SMC+placebo groups in fixed time
strata post-treatment. The likelihood ratio test was used to
assess evidence for a time-treatment group interaction. RESULTS:
Relative to SMC+placebo, there was no evidence of protection
from SMC+AZ against hospital admissions and deaths. Additional
protection from SMC+AZ against malaria was confined to the first
2 weeks post-administration (protective efficacy (PE): 24.2%
[95% CI: 17.8%, 30.1%]). Gastroenteritis and pneumonia were
reduced by 29.9% [21.7; 37.3%], and 34.3% [14.9; 49.3%],
respectively, in the first 2 weeks postadministration.
Protection against nonmalaria fevers with a skin condition
persisted up to 28 days: PE: 46.3% [35.1; 55.6%]. CONCLUSIONS:
The benefits of AZ-MDA are broad-ranging but short-lived. To
maximize impact, timing of AZ-MDA must address the challenge of
targeting asynchronous morbidity and mortality peaks from
different causes. |
| Massa Dit Achille Bonko, Marc Christian Tahita, Francois Kiemde, Palpouguini Lompo, Sibidou Yougbaré, Athanase M Some, Halidou Tinto, Petra F Mens, Sandra Menting, Henk D F H Schallig Antibiotic susceptibility profile of bacterial isolates from febrile children under 5 years of age in Nanoro, Burkina Faso Journal Article In: Trop. Med. Int. Health, vol. 26, no. 10, pp. 1220–1230, 2021, ISSN: 1365-3156 1360-2276, (© 2021 The Authors Tropical Medicine & International Health Published by John Wiley & Sons Ltd.
Place: England
PMID: 34185935). @article{Bonko2021-en,
title = {Antibiotic susceptibility profile of bacterial isolates from febrile children under 5 years of age in Nanoro, Burkina Faso},
author = {Massa Dit Achille Bonko and Marc Christian Tahita and Francois Kiemde and Palpouguini Lompo and Sibidou Yougbar\'{e} and Athanase M Some and Halidou Tinto and Petra F Mens and Sandra Menting and Henk D F H Schallig},
doi = {10.1111/tmi.13644},
issn = {1365-3156 1360-2276},
year = {2021},
date = {2021-10-01},
urldate = {2021-10-01},
journal = {Trop. Med. Int. Health},
volume = {26},
number = {10},
pages = {1220--1230},
publisher = {Wiley},
abstract = {OBJECTIVES: Antibiotics efficacy is severely threatened due to
emerging resistance worldwide, but there is a paucity of
antibiotics efficacy data for the West African region in
general. Therefore, this study aimed to determine the antibiotic
susceptibility profile of bacterial isolated from febrile
children under 5 years of age in Nanoro (Burkina Faso). METHODS:
Blood, stool and urine samples were collected from 1099 febrile
children attending peripheral health facilities and the referral
hospital in Nanoro Health district. Bacterial isolates from
these samples were assessed for their susceptibility against
commonly used antibiotics by Kirby-Bauer method. RESULTS: In
total, 141 bacterial isolates were recovered from 127 febrile
children of which 65 from blood, 65 from stool and 11 from
urine. Salmonella isolates were most frequently isolated and
found to be highly resistant to ampicillin (70%; 56/80) and
trimethoprim-sulphamethoxazole (65%; 52/80). Escherichia coli
isolates showed a high resistance rate to
trimethoprim-sulphamethoxazole (100%), ampicillin (100%),
ciprofloxacin (71.4%; 10/14), amoxicillin-clavulanate (64.3%;
9/14), ceftriaxone (64.3%; 9/14) and gentamycin (50%; 7/14).
Moreover, half of the E. coli isolates produced \ss-lactamase
suggesting multi-drug resistance against $beta$-lactam as well
as non-$beta$-lactam antibiotics. Multi-drug resistance was
observed in 54.6% (59/108) of the isolates, mainly
Gram-negative bacteria. CONCLUSIONS: This study showed high
resistance rates to common antibiotics used to treat bacterial
infections in Nanoro. The work prompts the need to expand
antibiotic resistance surveillance studies in Burkina Faso.},
note = {© 2021 The Authors Tropical Medicine \& International Health Published by John Wiley \& Sons Ltd.
Place: England
PMID: 34185935},
keywords = {antibiotic resistance, bacteria, febrile children},
pubstate = {published},
tppubtype = {article}
}
OBJECTIVES: Antibiotics efficacy is severely threatened due to
emerging resistance worldwide, but there is a paucity of
antibiotics efficacy data for the West African region in
general. Therefore, this study aimed to determine the antibiotic
susceptibility profile of bacterial isolated from febrile
children under 5 years of age in Nanoro (Burkina Faso). METHODS:
Blood, stool and urine samples were collected from 1099 febrile
children attending peripheral health facilities and the referral
hospital in Nanoro Health district. Bacterial isolates from
these samples were assessed for their susceptibility against
commonly used antibiotics by Kirby-Bauer method. RESULTS: In
total, 141 bacterial isolates were recovered from 127 febrile
children of which 65 from blood, 65 from stool and 11 from
urine. Salmonella isolates were most frequently isolated and
found to be highly resistant to ampicillin (70%; 56/80) and
trimethoprim-sulphamethoxazole (65%; 52/80). Escherichia coli
isolates showed a high resistance rate to
trimethoprim-sulphamethoxazole (100%), ampicillin (100%),
ciprofloxacin (71.4%; 10/14), amoxicillin-clavulanate (64.3%;
9/14), ceftriaxone (64.3%; 9/14) and gentamycin (50%; 7/14).
Moreover, half of the E. coli isolates produced ß-lactamase
suggesting multi-drug resistance against $beta$-lactam as well
as non-$beta$-lactam antibiotics. Multi-drug resistance was
observed in 54.6% (59/108) of the isolates, mainly
Gram-negative bacteria. CONCLUSIONS: This study showed high
resistance rates to common antibiotics used to treat bacterial
infections in Nanoro. The work prompts the need to expand
antibiotic resistance surveillance studies in Burkina Faso. |
| Daniel Chandramohan, Issaka Zongo, Issaka Sagara, Matthew Cairns, Rakiswendé-Serge Yerbanga, Modibo Diarra, Frédéric Niki`ema, Amadou Tapily, Frédéric Sompougdou, Djibrilla Issiaka, Charles Zoungrana, Koualy Sanogo, Alassane Haro, Mahamadou Kaya, Abdoul-Aziz Sienou, Seydou Traore, Almahamoudou Mahamar, Ismaila Thera, Kalifa Diarra, Amagana Dolo, Irene Kuepfer, Paul Snell, Paul Milligan, Christian Ockenhouse, Opokua Ofori-Anyinam, Halidou Tinto, Abdoulaye Djimde, Jean-Bosco Ouédraogo, Alassane Dicko, Brian Greenwood Seasonal malaria vaccination with or without seasonal malaria chemoprevention Journal Article In: N. Engl. J. Med., vol. 385, no. 11, pp. 1005–1017, 2021, ISSN: 1533-4406 0028-4793, (Copyright © 2021 Massachusetts Medical Society.
Place: United States
PMID: 34432975). @article{Chandramohan2021-qm,
title = {Seasonal malaria vaccination with or without seasonal malaria chemoprevention},
author = {Daniel Chandramohan and Issaka Zongo and Issaka Sagara and Matthew Cairns and Rakiswend\'{e}-Serge Yerbanga and Modibo Diarra and Fr\'{e}d\'{e}ric Niki`ema and Amadou Tapily and Fr\'{e}d\'{e}ric Sompougdou and Djibrilla Issiaka and Charles Zoungrana and Koualy Sanogo and Alassane Haro and Mahamadou Kaya and Abdoul-Aziz Sienou and Seydou Traore and Almahamoudou Mahamar and Ismaila Thera and Kalifa Diarra and Amagana Dolo and Irene Kuepfer and Paul Snell and Paul Milligan and Christian Ockenhouse and Opokua Ofori-Anyinam and Halidou Tinto and Abdoulaye Djimde and Jean-Bosco Ou\'{e}draogo and Alassane Dicko and Brian Greenwood},
doi = {10.1056/NEJMoa2026330},
issn = {1533-4406 0028-4793},
year = {2021},
date = {2021-09-09},
urldate = {2021-09-09},
journal = {N. Engl. J. Med.},
volume = {385},
number = {11},
pages = {1005--1017},
publisher = {Massachusetts Medical Society},
abstract = {BACKGROUND: Malaria control remains a challenge in many parts of
the Sahel and sub-Sahel regions of Africa. METHODS: We conducted
an individually randomized, controlled trial to assess whether
seasonal vaccination with RTS,S/AS01E was noninferior to
chemoprevention in preventing uncomplicated malaria and whether
the two interventions combined were superior to either one alone
in preventing uncomplicated malaria and severe malaria-related
outcomes. RESULTS: We randomly assigned 6861 children 5 to 17
months of age to receive sulfadoxine-pyrimethamine and
amodiaquine (2287 children [chemoprevention-alone group]),
RTS,S/AS01E (2288 children [vaccine-alone group]), or
chemoprevention and RTS,S/AS01E (2286 children [combination
group]). Of these, 1965, 1988, and 1967 children in the three
groups, respectively, received the first dose of the assigned
intervention and were followed for 3 years. Febrile seizure
developed in 5 children the day after receipt of the vaccine,
but the children recovered and had no sequelae. There were 305
events of uncomplicated clinical malaria per 1000 person-years
at risk in the chemoprevention-alone group, 278 events per 1000
person-years in the vaccine-alone group, and 113 events per 1000
person-years in the combination group. The hazard ratio for the
protective efficacy of RTS,S/AS01E as compared with
chemoprevention was 0.92 (95% confidence interval [CI], 0.84 to
1.01), which excluded the prespecified noninferiority margin of
1.20. The protective efficacy of the combination as compared
with chemoprevention alone was 62.8% (95% CI, 58.4 to 66.8)
against clinical malaria, 70.5% (95% CI, 41.9 to 85.0) against
hospital admission with severe malaria according to the World
Health Organization definition, and 72.9% (95% CI, 2.9 to
92.4) against death from malaria. The protective efficacy of the
combination as compared with the vaccine alone against these
outcomes was 59.6% (95% CI, 54.7 to 64.0), 70.6% (95% CI,
42.3 to 85.0), and 75.3% (95% CI, 12.5 to 93.0), respectively.
CONCLUSIONS: Administration of RTS,S/AS01E was noninferior to
chemoprevention in preventing uncomplicated malaria. The
combination of these interventions resulted in a substantially
lower incidence of uncomplicated malaria, severe malaria, and
death from malaria than either intervention alone. (Funded by
the Joint Global Health Trials and PATH; ClinicalTrials.gov
number, NCT03143218.).},
note = {Copyright © 2021 Massachusetts Medical Society.
Place: United States
PMID: 34432975},
keywords = {Amodiaquine/therapeutic use, Antimalarials/adverse effects/therapeutic use, Burkina Faso/epidemiology, Chemoprevention, Combination, Combined Modality Therapy, Double-Blind Method, Drug Combinations, Drug Therapy, Falciparum/epidemiology/mortality/prevention \& control, Febrile/etiology, Female, Hospitalization/statistics \& numerical data, Humans, Infant, Malaria, Malaria Vaccines/administration \& dosage/adverse effects, Male, Mali/epidemiology, Pyrimethamine/therapeutic use, Seasons, Seizures, Sulfadoxine/therapeutic use},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Malaria control remains a challenge in many parts of
the Sahel and sub-Sahel regions of Africa. METHODS: We conducted
an individually randomized, controlled trial to assess whether
seasonal vaccination with RTS,S/AS01E was noninferior to
chemoprevention in preventing uncomplicated malaria and whether
the two interventions combined were superior to either one alone
in preventing uncomplicated malaria and severe malaria-related
outcomes. RESULTS: We randomly assigned 6861 children 5 to 17
months of age to receive sulfadoxine-pyrimethamine and
amodiaquine (2287 children [chemoprevention-alone group]),
RTS,S/AS01E (2288 children [vaccine-alone group]), or
chemoprevention and RTS,S/AS01E (2286 children [combination
group]). Of these, 1965, 1988, and 1967 children in the three
groups, respectively, received the first dose of the assigned
intervention and were followed for 3 years. Febrile seizure
developed in 5 children the day after receipt of the vaccine,
but the children recovered and had no sequelae. There were 305
events of uncomplicated clinical malaria per 1000 person-years
at risk in the chemoprevention-alone group, 278 events per 1000
person-years in the vaccine-alone group, and 113 events per 1000
person-years in the combination group. The hazard ratio for the
protective efficacy of RTS,S/AS01E as compared with
chemoprevention was 0.92 (95% confidence interval [CI], 0.84 to
1.01), which excluded the prespecified noninferiority margin of
1.20. The protective efficacy of the combination as compared
with chemoprevention alone was 62.8% (95% CI, 58.4 to 66.8)
against clinical malaria, 70.5% (95% CI, 41.9 to 85.0) against
hospital admission with severe malaria according to the World
Health Organization definition, and 72.9% (95% CI, 2.9 to
92.4) against death from malaria. The protective efficacy of the
combination as compared with the vaccine alone against these
outcomes was 59.6% (95% CI, 54.7 to 64.0), 70.6% (95% CI,
42.3 to 85.0), and 75.3% (95% CI, 12.5 to 93.0), respectively.
CONCLUSIONS: Administration of RTS,S/AS01E was noninferior to
chemoprevention in preventing uncomplicated malaria. The
combination of these interventions resulted in a substantially
lower incidence of uncomplicated malaria, severe malaria, and
death from malaria than either intervention alone. (Funded by
the Joint Global Health Trials and PATH; ClinicalTrials.gov
number, NCT03143218.). |
| Isidore Tiandiogo Traoré, Samiratou Ouedraogo, Dramane Kania, Firmin Nongodo Kaboré, Blahima Konaté, Rachel Médah, Hermann Badolo, Nathalie Rekeneire, Ariane Mamguem Kamga, Armel Poda, Arnaud Eric Diendere, Boukary Ouédraogo, Esperance Ouédraogo, Oumar Billa, Halidou Tinto, Tienhan Sandrine Dabakuyo-Yonli COVID-19 epidemiological, sociological and anthropological investigation: study protocol for a multidisciplinary mixed methods research in Burkina Faso Journal Article In: BMC Infect. Dis., vol. 21, no. 1, pp. 896, 2021, ISSN: 1471-2334, (© 2021. The Author(s).
PMID: 34479501
PMCID: PMC8414025). @article{Traore2021-vr,
title = {COVID-19 epidemiological, sociological and anthropological investigation: study protocol for a multidisciplinary mixed methods research in Burkina Faso},
author = {Isidore Tiandiogo Traor\'{e} and Samiratou Ouedraogo and Dramane Kania and Firmin Nongodo Kabor\'{e} and Blahima Konat\'{e} and Rachel M\'{e}dah and Hermann Badolo and Nathalie Rekeneire and Ariane Mamguem Kamga and Armel Poda and Arnaud Eric Diendere and Boukary Ou\'{e}draogo and Esperance Ou\'{e}draogo and Oumar Billa and Halidou Tinto and Tienhan Sandrine Dabakuyo-Yonli},
doi = {10.1186/s12879-021-06543-4},
issn = {1471-2334},
year = {2021},
date = {2021-09-03},
urldate = {2021-09-03},
journal = {BMC Infect. Dis.},
volume = {21},
number = {1},
pages = {896},
abstract = {BACKGROUND: The world has high hopes of vaccination against
COVID-19 to protect the population, boost economies and return to
normal life. Vaccination programmes are being rolled out in high
income countries, but the pandemic continues to progress in many
low-and middle-income countries (LMICs) despite implementation of
strict hygiene measures. We aim to present a comprehensive
research protocol that will generate epidemiological,
sociological and anthropological data about the COVID-19 epidemic
in Burkina Faso, a landlocked country in West Africa with scarce
resources. METHODS: We will perform a multidisciplinary research
using mixed methods in the two main cities in Burkina Faso
(Ouagadougou and Bobo-Dioulasso). Data will be collected in the
general population and in COVID-19 patients, caregivers and
health care professionals in reference care centers: (i) to
determine cumulative incidence of SARS-CoV-2 infection in the
Burkinabe population using blood samples collected from randomly
selected households according to the WHO-recommended protocol;
(ii) develop a score to predict severe complications of COVID-19
in persons infected with SARS-CoV-2 using retrospective and
prospective data; (iii) perform semi-structured interviews and
direct observation on site, to describe and analyze the
healthcare pathways and experiences of patients with COVID-19
attending reference care centers, and to identify the
perceptions, acceptability and application of preventive
strategies among the population. DISCUSSION: This study will
generate comprehensive data that will contribute to improving
COVID-19 response strategies in Burkina Faso. The lessons learned
from the management of this epidemic may serve as examples to the
country authorities to better design preventive strategies in the
case of future epidemics or pandemics. The protocol was approved
by the Ministry for Health (N° 2020-00952/MS/CAB/INSP/CM) and the
Health Research Ethics Committee in Burkina Faso (N° 2020-8-140).},
note = {© 2021. The Author(s).
PMID: 34479501
PMCID: PMC8414025},
keywords = {Burkina Faso/epidemiology, Clinical epidemiology, COVID-19, Humans, Predictive score, Prospective Studies, Retrospective Studies, SARS-Cov-2, Sero-epidemiology, Socio-anthropology},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: The world has high hopes of vaccination against
COVID-19 to protect the population, boost economies and return to
normal life. Vaccination programmes are being rolled out in high
income countries, but the pandemic continues to progress in many
low-and middle-income countries (LMICs) despite implementation of
strict hygiene measures. We aim to present a comprehensive
research protocol that will generate epidemiological,
sociological and anthropological data about the COVID-19 epidemic
in Burkina Faso, a landlocked country in West Africa with scarce
resources. METHODS: We will perform a multidisciplinary research
using mixed methods in the two main cities in Burkina Faso
(Ouagadougou and Bobo-Dioulasso). Data will be collected in the
general population and in COVID-19 patients, caregivers and
health care professionals in reference care centers: (i) to
determine cumulative incidence of SARS-CoV-2 infection in the
Burkinabe population using blood samples collected from randomly
selected households according to the WHO-recommended protocol;
(ii) develop a score to predict severe complications of COVID-19
in persons infected with SARS-CoV-2 using retrospective and
prospective data; (iii) perform semi-structured interviews and
direct observation on site, to describe and analyze the
healthcare pathways and experiences of patients with COVID-19
attending reference care centers, and to identify the
perceptions, acceptability and application of preventive
strategies among the population. DISCUSSION: This study will
generate comprehensive data that will contribute to improving
COVID-19 response strategies in Burkina Faso. The lessons learned
from the management of this epidemic may serve as examples to the
country authorities to better design preventive strategies in the
case of future epidemics or pandemics. The protocol was approved
by the Ministry for Health (N° 2020-00952/MS/CAB/INSP/CM) and the
Health Research Ethics Committee in Burkina Faso (N° 2020-8-140). |
| Stephen A Roberts, Loretta Brabin, Halidou Tinto, Sabine Gies, Salou Diallo, Bernard Brabin Seasonal patterns of malaria, genital infection, nutritional and iron status in non-pregnant and pregnant adolescents in Burkina Faso: a secondary analysis of trial data Journal Article In: BMC Public Health, vol. 21, no. 1, pp. 1764, 2021, ISSN: 1471-2458, (© 2021. The Author(s).
PMID: 34579679
PMCID: PMC8477466). @article{Roberts2021-gg,
title = {Seasonal patterns of malaria, genital infection, nutritional and iron status in non-pregnant and pregnant adolescents in Burkina Faso: a secondary analysis of trial data},
author = {Stephen A Roberts and Loretta Brabin and Halidou Tinto and Sabine Gies and Salou Diallo and Bernard Brabin},
doi = {10.1186/s12889-021-11819-0},
issn = {1471-2458},
year = {2021},
date = {2021-09-01},
urldate = {2021-09-01},
journal = {BMC Public Health},
volume = {21},
number = {1},
pages = {1764},
publisher = {Springer Science and Business Media LLC},
abstract = {BACKGROUND: Adolescents are considered at high risk of developing iron deficiency. Studies in children indicate that the prevalence of iron deficiency increased with malaria transmission, suggesting malaria seasonally may drive iron deficiency. This paper examines monthly seasonal infection patterns of malaria, abnormal vaginal flora, chorioamnionitis, antibiotic and antimalarial prescriptions, in relation to changes in iron biomarkers and nutritional indices in adolescents living in a rural area of Burkina Faso, in order to assess the requirement for seasonal infection control and nutrition interventions. METHODS: Data collected between April 2011 and January 2014 were available for an observational seasonal analysis, comprising scheduled visits for 1949 non-pregnant adolescents (≤19 years), (315 of whom subsequently became pregnant), enrolled in a randomised trial of periconceptional iron supplementation. Data from trial arms were combined. Body Iron Stores (BIS) were calculated using an internal regression for ferritin to allow for inflammation. At recruitment 11% had low BIS (\< 0 mg/kg). Continuous outcomes were fitted to a mixed-effects linear model with month, age and pregnancy status as fixed effect covariates and woman as a random effect. Dichotomous infection outcomes were fitted with analogous logistic regression models. RESULTS: Seasonal variation in malaria parasitaemia prevalence ranged between 18 and 70% in non-pregnant adolescents (P \< 0.001), peaking at 81% in those who became pregnant. Seasonal variation occurred in antibiotic prescription rates (0.7-1.8 prescriptions/100 weekly visits, P \< 0.001) and chorioamnionitis prevalence (range 15-68%, P = 0.026). Mucosal vaginal lactoferrin concentration was lower at the end of the wet season (range 2-22 μg/ml, P \< 0.016), when chorioamnionitis was least frequent. BIS fluctuated annually by up to 53.2% per year around the mean BIS (5.1 mg/kg(2), range 4.1-6.8 mg/kg), with low BIS (\< 0 mg/kg) of 8.7% in the dry and 9.8% in the wet seasons (P = 0.36). Median serum transferrin receptor increased during the wet season (P \< 0.001). Higher hepcidin concentration in the wet season corresponded with rising malaria prevalence and use of prescriptions, but with no change in BIS. Mean Body Mass Index and Mid-Upper-Arm-Circumference values peaked mid-dry season (both P \< 0.001). CONCLUSIONS: Our analysis supports preventive treatment of malaria among adolescents 15-19 years to decrease their disease burden, especially asymptomatic malaria. As BIS were adequate in most adolescents despite seasonal malaria, a requirement for programmatic iron supplementation was not substantiated.},
note = {© 2021. The Author(s).
PMID: 34579679
PMCID: PMC8477466},
keywords = {Abnormal vaginal flora, Adolescents, Bacterial vaginosis, Body Mass Index, Burkina Faso/epidemiology, Child, Female, Humans, Iron, iron biomarkers, Malaria, Malaria/drug therapy/epidemiology, MUAC, Pregnancy, Seasons, Vagina},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Adolescents are considered at high risk of developing iron deficiency. Studies in children indicate that the prevalence of iron deficiency increased with malaria transmission, suggesting malaria seasonally may drive iron deficiency. This paper examines monthly seasonal infection patterns of malaria, abnormal vaginal flora, chorioamnionitis, antibiotic and antimalarial prescriptions, in relation to changes in iron biomarkers and nutritional indices in adolescents living in a rural area of Burkina Faso, in order to assess the requirement for seasonal infection control and nutrition interventions. METHODS: Data collected between April 2011 and January 2014 were available for an observational seasonal analysis, comprising scheduled visits for 1949 non-pregnant adolescents (≤19 years), (315 of whom subsequently became pregnant), enrolled in a randomised trial of periconceptional iron supplementation. Data from trial arms were combined. Body Iron Stores (BIS) were calculated using an internal regression for ferritin to allow for inflammation. At recruitment 11% had low BIS (< 0 mg/kg). Continuous outcomes were fitted to a mixed-effects linear model with month, age and pregnancy status as fixed effect covariates and woman as a random effect. Dichotomous infection outcomes were fitted with analogous logistic regression models. RESULTS: Seasonal variation in malaria parasitaemia prevalence ranged between 18 and 70% in non-pregnant adolescents (P < 0.001), peaking at 81% in those who became pregnant. Seasonal variation occurred in antibiotic prescription rates (0.7-1.8 prescriptions/100 weekly visits, P < 0.001) and chorioamnionitis prevalence (range 15-68%, P = 0.026). Mucosal vaginal lactoferrin concentration was lower at the end of the wet season (range 2-22 μg/ml, P < 0.016), when chorioamnionitis was least frequent. BIS fluctuated annually by up to 53.2% per year around the mean BIS (5.1 mg/kg(2), range 4.1-6.8 mg/kg), with low BIS (< 0 mg/kg) of 8.7% in the dry and 9.8% in the wet seasons (P = 0.36). Median serum transferrin receptor increased during the wet season (P < 0.001). Higher hepcidin concentration in the wet season corresponded with rising malaria prevalence and use of prescriptions, but with no change in BIS. Mean Body Mass Index and Mid-Upper-Arm-Circumference values peaked mid-dry season (both P < 0.001). CONCLUSIONS: Our analysis supports preventive treatment of malaria among adolescents 15-19 years to decrease their disease burden, especially asymptomatic malaria. As BIS were adequate in most adolescents despite seasonal malaria, a requirement for programmatic iron supplementation was not substantiated. |
| Adéla"ide Compaoré, Kadija Ouedraogo, Palwende R Boua, Daniella Watson, Sarah H Kehoe, Marie-Louise Newell, Halidou Tinto, Mary Barker, Hermann Sorgho, INPreP group 'Men are not playing their roles', maternal and child nutrition in Nanoro, Burkina Faso Journal Article In: Public Health Nutr., vol. 24, no. 12, pp. 3780–3790, 2021, ISSN: 1475-2727 1368-9800, (Place: England
PMID: 33000717). @article{Compaore2021-hg,
title = {'Men are not playing their roles', maternal and child nutrition in Nanoro, Burkina Faso},
author = {Ad\'{e}la"ide Compaor\'{e} and Kadija Ouedraogo and Palwende R Boua and Daniella Watson and Sarah H Kehoe and Marie-Louise Newell and Halidou Tinto and Mary Barker and Hermann Sorgho and INPreP group},
doi = {10.1017/S1368980020003365},
issn = {1475-2727 1368-9800},
year = {2021},
date = {2021-08-01},
urldate = {2021-08-01},
journal = {Public Health Nutr.},
volume = {24},
number = {12},
pages = {3780--3790},
publisher = {Cambridge University Press (CUP)},
abstract = {OBJECTIVE: To collect context-specific insights into maternal
and child health and nutrition issues, and to explore potential
solutions in Nanoro, Burkina Faso. DESIGN: Eleven focus groups
with men and women from eleven communities, facilitated by local
researchers. SETTING: The study took place in the Nanoro Health
district, in the West-Central part of Burkina Faso.
PARTICIPANTS: Eighty-six men (18-55 years) and women by age
group: 18-25; 26-34 and 35-55 years, participated in the group
discussions. RESULTS: Participants described barriers to optimal
nutrition of mothers and children related to a range of
community factors, with gender inequality as central. Major
themes in the discussions are related to poverty and challenges
generated by socially and culturally determined gender roles.
Sub-themes are women lacking access to food whilst pregnant and
having limited access to health care and opportunities to
generate income. Although communities believe that food
donations should be implemented to overcome this, they also
pointed out the need for enhancing their own food production,
requiring improved agricultural technologies. Given the
important role that women could play in reducing malnutrition,
these communities felt they needed to be empowered to do so and
supported by men. They also felt that this had to be carried out
in the context of an enhanced health care system. CONCLUSIONS:
Findings reported here highlight the importance of
nutrition-sensitive interventions and women's empowerment in
improving maternal and child nutrition. There is a need to
integrate a sustainable multi-sectorial approach which goes
beyond food support.},
note = {Place: England
PMID: 33000717},
keywords = {Burkina Faso, Child, Child nutrition, Child Nutritional Physiological Phenomena, Community perceptions, Empowerment, Female, Humans, Male, Maternal nutrition, Mothers, Nutritional Status, Pregnancy, Qualitative research},
pubstate = {published},
tppubtype = {article}
}
OBJECTIVE: To collect context-specific insights into maternal
and child health and nutrition issues, and to explore potential
solutions in Nanoro, Burkina Faso. DESIGN: Eleven focus groups
with men and women from eleven communities, facilitated by local
researchers. SETTING: The study took place in the Nanoro Health
district, in the West-Central part of Burkina Faso.
PARTICIPANTS: Eighty-six men (18-55 years) and women by age
group: 18-25; 26-34 and 35-55 years, participated in the group
discussions. RESULTS: Participants described barriers to optimal
nutrition of mothers and children related to a range of
community factors, with gender inequality as central. Major
themes in the discussions are related to poverty and challenges
generated by socially and culturally determined gender roles.
Sub-themes are women lacking access to food whilst pregnant and
having limited access to health care and opportunities to
generate income. Although communities believe that food
donations should be implemented to overcome this, they also
pointed out the need for enhancing their own food production,
requiring improved agricultural technologies. Given the
important role that women could play in reducing malnutrition,
these communities felt they needed to be empowered to do so and
supported by men. They also felt that this had to be carried out
in the context of an enhanced health care system. CONCLUSIONS:
Findings reported here highlight the importance of
nutrition-sensitive interventions and women's empowerment in
improving maternal and child nutrition. There is a need to
integrate a sustainable multi-sectorial approach which goes
beyond food support. |
| Koudraogo Bienvenue Yaméogo, Rakiswendé Serge Yerbanga, Seydou Bienvenu Ouattara, Franck A Yao, Thierry Lef`evre, Issaka Zongo, Frederic Niki`ema, Yves Daniel Compaoré, Halidou Tinto, Daniel Chandramohan, Brian Greenwood, Adrien M G Belem, Anna Cohuet, Jean Bosco Ouédraogo Effect of seasonal malaria chemoprevention plus azithromycin on Plasmodium falciparum transmission: gametocyte infectivity and mosquito fitness Journal Article In: Malar. J., vol. 20, no. 1, pp. 326, 2021, ISSN: 1475-2875, (© 2021. The Author(s).
PMID: 34315475
PMCID: PMC8314489). @article{Yameogo2021-bb,
title = {Effect of seasonal malaria chemoprevention plus azithromycin on Plasmodium falciparum transmission: gametocyte infectivity and mosquito fitness},
author = {Koudraogo Bienvenue Yam\'{e}ogo and Rakiswend\'{e} Serge Yerbanga and Seydou Bienvenu Ouattara and Franck A Yao and Thierry Lef`evre and Issaka Zongo and Frederic Niki`ema and Yves Daniel Compaor\'{e} and Halidou Tinto and Daniel Chandramohan and Brian Greenwood and Adrien M G Belem and Anna Cohuet and Jean Bosco Ou\'{e}draogo},
doi = {10.1186/s12936-021-03855-3},
issn = {1475-2875},
year = {2021},
date = {2021-07-27},
urldate = {2021-07-27},
journal = {Malar. J.},
volume = {20},
number = {1},
pages = {326},
publisher = {Springer Science and Business Media LLC},
abstract = {BACKGROUND: Seasonal malaria chemoprevention (SMC) consists of administration of sulfadoxine-pyrimethamine (SP) + amodiaquine (AQ) at monthly intervals to children during the malaria transmission period. Whether the addition of azithromycin (AZ) to SMC could potentiate the benefit of the intervention was tested through a double-blind, randomized, placebo-controlled trial. The effect of SMC and the addition of AZ, on malaria transmission and on the life history traits of Anopheles gambiae mosquitoes have been investigated. METHODS: The study included 438 children randomly selected from among participants in the SMC + AZ trial and 198 children from the same area who did not receive chemoprevention. For each participant in the SMC + AZ trial, blood was collected 14 to 21 days post treatment, examined for the presence of malaria sexual and asexual stages and provided as a blood meal to An. gambiae females using a direct membrane-feeding assay. RESULTS: The SMC treatment, with or without AZ, significantly reduced the prevalence of asexual Plasmodium falciparum (LRT X(2)(2) = 69, P \< 0.0001) and the gametocyte prevalence (LRT X(2)(2) = 54, P \< 0.0001). In addition, the proportion of infectious feeds (LRT X(2)(2) = 61, P \< 0.0001) and the prevalence of oocysts among exposed mosquitoes (LRT X(2)(2) = 22.8, P \< 0.001) was reduced when mosquitoes were fed on blood from treated children compared to untreated controls. The addition of AZ to SPAQ was associated with an increased proportion of infectious feeds (LRT X(2)(1) = 5.2, P = 0.02), suggesting a significant effect of AZ on gametocyte infectivity. There was a slight negative effect of SPAQ and SPAQ + AZ on mosquito survival compared to mosquitoes fed with blood from control children (LRTX(2)(2) = 330, P \< 0.0001). CONCLUSION: This study demonstrates that SMC may contribute to a reduction in human to mosquito transmission of P. falciparum, and the reduced mosquito longevity observed for females fed on treated blood may increase the benefit of this intervention in control of malaria. The addition of AZ to SPAQ in SMC appeared to enhance the infectivity of gametocytes providing further evidence that this combination is not an appropriate intervention.},
note = {© 2021. The Author(s).
PMID: 34315475
PMCID: PMC8314489},
keywords = {Amodiaquine/administration \& dosage, Animals, Antimalarials/administration \& dosage, Chemoprevention, Child, Culicidae/physiology, Drug Combinations, Falciparum/prevention \& control/transmission, Gametocytes, Genetic Fitness, Humans, Malaria, Plasmodium falciparum/physiology, Preschool, Pyrimethamine/administration \& dosage, seasonal malaria chemoprevention, Seasons, Sulfadoxine/administration \& dosage, Transmission},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Seasonal malaria chemoprevention (SMC) consists of administration of sulfadoxine-pyrimethamine (SP) + amodiaquine (AQ) at monthly intervals to children during the malaria transmission period. Whether the addition of azithromycin (AZ) to SMC could potentiate the benefit of the intervention was tested through a double-blind, randomized, placebo-controlled trial. The effect of SMC and the addition of AZ, on malaria transmission and on the life history traits of Anopheles gambiae mosquitoes have been investigated. METHODS: The study included 438 children randomly selected from among participants in the SMC + AZ trial and 198 children from the same area who did not receive chemoprevention. For each participant in the SMC + AZ trial, blood was collected 14 to 21 days post treatment, examined for the presence of malaria sexual and asexual stages and provided as a blood meal to An. gambiae females using a direct membrane-feeding assay. RESULTS: The SMC treatment, with or without AZ, significantly reduced the prevalence of asexual Plasmodium falciparum (LRT X(2)(2) = 69, P < 0.0001) and the gametocyte prevalence (LRT X(2)(2) = 54, P < 0.0001). In addition, the proportion of infectious feeds (LRT X(2)(2) = 61, P < 0.0001) and the prevalence of oocysts among exposed mosquitoes (LRT X(2)(2) = 22.8, P < 0.001) was reduced when mosquitoes were fed on blood from treated children compared to untreated controls. The addition of AZ to SPAQ was associated with an increased proportion of infectious feeds (LRT X(2)(1) = 5.2, P = 0.02), suggesting a significant effect of AZ on gametocyte infectivity. There was a slight negative effect of SPAQ and SPAQ + AZ on mosquito survival compared to mosquitoes fed with blood from control children (LRTX(2)(2) = 330, P < 0.0001). CONCLUSION: This study demonstrates that SMC may contribute to a reduction in human to mosquito transmission of P. falciparum, and the reduced mosquito longevity observed for females fed on treated blood may increase the benefit of this intervention in control of malaria. The addition of AZ to SPAQ in SMC appeared to enhance the infectivity of gametocytes providing further evidence that this combination is not an appropriate intervention. |
| Navideh Noori, Karim Derra, Innocent Valea, Assaf P Oron, Aminata Welgo, Toussaint Rouamba, Palwende Romuald Boua, Athanase M Somé, Eli Rouamba, Edward Wenger, Hermann Sorgho, Halidou Tinto, Andre Lin Ouédraogo Patterns of child mortality in rural area of Burkina Faso: evidence from the Nanoro health and demographic surveillance system (HDSS) Journal Article In: BMC Public Health, vol. 21, no. 1, pp. 1425, 2021, ISSN: 1471-2458, (© 2021. The Author(s).
PMID: 34281547
PMCID: PMC8287796). @article{Noori2021-te,
title = {Patterns of child mortality in rural area of Burkina Faso: evidence from the Nanoro health and demographic surveillance system (HDSS)},
author = {Navideh Noori and Karim Derra and Innocent Valea and Assaf P Oron and Aminata Welgo and Toussaint Rouamba and Palwende Romuald Boua and Athanase M Som\'{e} and Eli Rouamba and Edward Wenger and Hermann Sorgho and Halidou Tinto and Andre Lin Ou\'{e}draogo},
doi = {10.1186/s12889-021-11483-4},
issn = {1471-2458},
year = {2021},
date = {2021-07-19},
urldate = {2021-07-19},
journal = {BMC Public Health},
volume = {21},
number = {1},
pages = {1425},
publisher = {Springer Science and Business Media LLC},
abstract = {BACKGROUND: Half of global child deaths occur in sub-Saharan
Africa. Understanding child mortality patterns and risk factors
will help inform interventions to reduce this heavy toll. The
Nanoro Health and Demographic Surveillance System (HDSS),
Burkina Faso was described previously, but patterns and
potential drivers of heterogeneity in child mortality in the
district had not been studied. Similar studies in other
districts indicated proximity to health facilities as a risk
factor, usually without distinction between facility types.
METHODS: Using Nanoro HDSS data from 2009 to 2013, we estimated
the association between under-5 mortality and proximity to
inpatient and outpatient health facilities, seasonality of
death, age group, and standard demographic risk factors.
RESULTS: Living in homes 40-60 min and \> 60 min travel time from
an inpatient facility was associated with 1.52 (95% CI:
1.13-2.06) and 1.74 (95% CI: 1.27-2.40) greater hazard of
under-5 mortality, respectively, than living in homes \< 20 min
from an inpatient facility. No such association was found for
outpatient facilities. The wet season (July-November) was
associated with 1.28 (95% CI: 1.07, 1.53) higher under-5
mortality than the dry season (December-June), likely reflecting
the malaria season. CONCLUSIONS: Our results emphasize the
importance of geographical proximity to health care, distinguish
between inpatient and outpatient facilities, and also show a
seasonal effect, probably driven by malaria.},
note = {© 2021. The Author(s).
PMID: 34281547
PMCID: PMC8287796},
keywords = {Burkina Faso, Burkina Faso/epidemiology, child mortality, ChildHealth Facilities, Children under 5, Demographic surveillance, HDSS, Humans, Infant, Malaria, Nanoro, Spatial analysis, Travel},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Half of global child deaths occur in sub-Saharan
Africa. Understanding child mortality patterns and risk factors
will help inform interventions to reduce this heavy toll. The
Nanoro Health and Demographic Surveillance System (HDSS),
Burkina Faso was described previously, but patterns and
potential drivers of heterogeneity in child mortality in the
district had not been studied. Similar studies in other
districts indicated proximity to health facilities as a risk
factor, usually without distinction between facility types.
METHODS: Using Nanoro HDSS data from 2009 to 2013, we estimated
the association between under-5 mortality and proximity to
inpatient and outpatient health facilities, seasonality of
death, age group, and standard demographic risk factors.
RESULTS: Living in homes 40-60 min and > 60 min travel time from
an inpatient facility was associated with 1.52 (95% CI:
1.13-2.06) and 1.74 (95% CI: 1.27-2.40) greater hazard of
under-5 mortality, respectively, than living in homes < 20 min
from an inpatient facility. No such association was found for
outpatient facilities. The wet season (July-November) was
associated with 1.28 (95% CI: 1.07, 1.53) higher under-5
mortality than the dry season (December-June), likely reflecting
the malaria season. CONCLUSIONS: Our results emphasize the
importance of geographical proximity to health care, distinguish
between inpatient and outpatient facilities, and also show a
seasonal effect, probably driven by malaria. |
| Marie Jaspard, Mamadou Saliou Sow, Sylvain Juchet, Eric Dienderé, Beatrice Serra, Richard Kojan, Billy Sivahera, Caroline Martin, Moumouni Kinda, Hans-Joerg Lang, Fodé Bangaly Sako, Fodé Amara Traoré, Eudoxie Koumbem, Halidou Tinto, Adama Sanou, Apoline Sondo, Flavien Kaboré, Joseph Donamou, Jean-Paul-Yassa Guilavogui, Fanny Velardo, Brice Bicaba, Olivier Marcy, Augustin Augier, Sani Sayadi, Armel Poda, Sakoba Keita, Xavier Anglaret, Denis Malvy, COVISTA group Clinical presentation, outcomes and factors associated with mortality: A prospective study from three COVID-19 referral care centres in West Africa Journal Article In: Int. J. Infect. Dis., vol. 108, pp. 45–52, 2021, ISSN: 1878-3511 1201-9712, (Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.
PMID: 34000419
PMCID: PMC8120805). @article{Jaspard2021-bl,
title = {Clinical presentation, outcomes and factors associated with mortality: A prospective study from three COVID-19 referral care centres in West Africa},
author = {Marie Jaspard and Mamadou Saliou Sow and Sylvain Juchet and Eric Diender\'{e} and Beatrice Serra and Richard Kojan and Billy Sivahera and Caroline Martin and Moumouni Kinda and Hans-Joerg Lang and Fod\'{e} Bangaly Sako and Fod\'{e} Amara Traor\'{e} and Eudoxie Koumbem and Halidou Tinto and Adama Sanou and Apoline Sondo and Flavien Kabor\'{e} and Joseph Donamou and Jean-Paul-Yassa Guilavogui and Fanny Velardo and Brice Bicaba and Olivier Marcy and Augustin Augier and Sani Sayadi and Armel Poda and Sakoba Keita and Xavier Anglaret and Denis Malvy and COVISTA group},
doi = {10.1016/j.ijid.2021.05.024},
issn = {1878-3511 1201-9712},
year = {2021},
date = {2021-07-01},
urldate = {2021-07-01},
journal = {Int. J. Infect. Dis.},
volume = {108},
pages = {45--52},
publisher = {Elsevier BV},
abstract = {OBJECTIVES: The overall death toll from COVID-19 in Africa is
reported to be low but there is little individual-level evidence
on the severity of the disease. This study examined the clinical
spectrum and outcome of patients monitored in COVID-19 care
centres (CCCs) in two West-African countries. METHODS: Burkina
Faso and Guinea set up referral CCCs to hospitalise all
symptomatic SARS-CoV-2 carriers, regardless of the severity of
their symptoms. Data collected from hospitalised patients by
November 2020 are presented. RESULT: A total of 1,805 patients
(64% men, median age 41 years) were admitted with COVID-19.
Symptoms lasted for a median of 7 days (IQR 4-11). During
hospitalisation, 443 (25%) had a SpO2 \< 94% at least once, 237
(13%) received oxygen and 266 (15%) took corticosteroids.
Mortality was 5% overall, and 1%, 5% and 14% in patients
aged \<40, 40-59 and $geq$60 years, respectively. In
multivariable analysis, the risk of death was higher in men (aOR
2.0, 95% CI 1.1; 3.6), people aged $geq$60 years (aOR 2.9,
95% CI 1.7; 4.8) and those with chronic hypertension (aOR 2.1,
95% CI 1.2; 3.4). CONCLUSION: COVID-19 is as severe in Africa
as elsewhere, and there must be more vigilance for common risk
factors such as older age and hypertension.},
note = {Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.
PMID: 34000419
PMCID: PMC8120805},
keywords = {Adult, Aged, Burkina Faso/epidemiology, Comorbidities, COVID-19, Female, Hospitalization, Humans, Male, Mortality, Prospective Studies, Referral and Consultation, SARS-Cov-2, sub-Saharan Africa},
pubstate = {published},
tppubtype = {article}
}
OBJECTIVES: The overall death toll from COVID-19 in Africa is
reported to be low but there is little individual-level evidence
on the severity of the disease. This study examined the clinical
spectrum and outcome of patients monitored in COVID-19 care
centres (CCCs) in two West-African countries. METHODS: Burkina
Faso and Guinea set up referral CCCs to hospitalise all
symptomatic SARS-CoV-2 carriers, regardless of the severity of
their symptoms. Data collected from hospitalised patients by
November 2020 are presented. RESULT: A total of 1,805 patients
(64% men, median age 41 years) were admitted with COVID-19.
Symptoms lasted for a median of 7 days (IQR 4-11). During
hospitalisation, 443 (25%) had a SpO2 < 94% at least once, 237
(13%) received oxygen and 266 (15%) took corticosteroids.
Mortality was 5% overall, and 1%, 5% and 14% in patients
aged <40, 40-59 and $geq$60 years, respectively. In
multivariable analysis, the risk of death was higher in men (aOR
2.0, 95% CI 1.1; 3.6), people aged $geq$60 years (aOR 2.9,
95% CI 1.7; 4.8) and those with chronic hypertension (aOR 2.1,
95% CI 1.2; 3.4). CONCLUSION: COVID-19 is as severe in Africa
as elsewhere, and there must be more vigilance for common risk
factors such as older age and hypertension. |
| Mariken Wit, Matthew Cairns, Yves Daniel Compaoré, Issaka Sagara, Irene Kuepfer, Issaka Zongo, Amadou Barry, Modibo Diarra, Amadou Tapily, Samba Coumare, Ismaila Thera, Frederic Nikiema, R Serge Yerbanga, Rosemonde M Guissou, Halidou Tinto, Alassane Dicko, Daniel Chandramohan, Brian Greenwood, Jean Bosco Ouedraogo Nutritional status in young children prior to the malaria transmission season in Burkina Faso and Mali, and its impact on the incidence of clinical malaria Journal Article In: Malar. J., vol. 20, no. 1, pp. 274, 2021, ISSN: 1475-2875, (PMID: 34158054
PMCID: PMC8220741). @article{De_Wit2021-yi,
title = {Nutritional status in young children prior to the malaria transmission season in Burkina Faso and Mali, and its impact on the incidence of clinical malaria},
author = {Mariken Wit and Matthew Cairns and Yves Daniel Compaor\'{e} and Issaka Sagara and Irene Kuepfer and Issaka Zongo and Amadou Barry and Modibo Diarra and Amadou Tapily and Samba Coumare and Ismaila Thera and Frederic Nikiema and R Serge Yerbanga and Rosemonde M Guissou and Halidou Tinto and Alassane Dicko and Daniel Chandramohan and Brian Greenwood and Jean Bosco Ouedraogo},
doi = {10.1186/s12936-021-03802-2},
issn = {1475-2875},
year = {2021},
date = {2021-06-22},
urldate = {2021-06-22},
journal = {Malar. J.},
volume = {20},
number = {1},
pages = {274},
publisher = {Springer Science and Business Media LLC},
abstract = {BACKGROUND: Malaria and malnutrition remain major problems in
Sahel countries, especially in young children. The direct effect
of malnutrition on malaria remains poorly understood, and may
have important implications for malaria control. In this study,
nutritional status and the association between malnutrition and
subsequent incidence of symptomatic malaria were examined in
children in Burkina Faso and Mali who received either
azithromycin or placebo, alongside seasonal malaria
chemoprevention. METHODS: Mid-upper arm circumference (MUAC) was
measured in all 20,185 children who attended a screening visit
prior to the malaria transmission season in 2015. Prior to the
2016 malaria season, weight, height and MUAC were measured among
4149 randomly selected children. Height-for-age, weight-for-age,
weight-for-height, and MUAC-for-age were calculated as
indicators of nutritional status. Malaria incidence was measured
during the following rainy seasons. Multivariable random effects
Poisson models were created for each nutritional indicator to
study the effect of malnutrition on clinical malaria incidence
for each country. RESULTS: In both 2015 and 2016, nutritional
status prior to the malaria season was poor. The most prevalent
form of malnutrition in Burkina Faso was being underweight
(30.5%; 95% CI 28.6-32.6), whereas in Mali stunting was most
prevalent (27.5%; 95% CI 25.6-29.5). In 2016, clinical malaria
incidence was 675 per 1000 person-years (95% CI 613-744) in
Burkina Faso, and 1245 per 1000 person-years (95% CI 1152-1347)
in Mali. There was some evidence that severe stunting was
associated with lower incidence of malaria in Mali (RR 0.81; 95% CI 0.64-1.02; p = 0.08), but this association was not seen
in Burkina Faso. Being moderately underweight tended to be
associated with higher incidence of clinical malaria in Burkina Faso (RR 1.27; 95% CI 0.98-1.64; p = 0.07), while this was the
case in Mali for moderate wasting (RR 1.27; 95% CI 0.98-1.64; p = 0.07). However, these associations were not observed in
severely affected children, nor consistent between countries.
MUAC-for-age was not associated with malaria risk. CONCLUSIONS:
Both malnutrition and malaria were common in the study areas,
high despite high coverage of seasonal malaria chemoprevention
and long-lasting insecticidal nets. However, no strong or
consistent evidence was found for an association between any of
the nutritional indicators and the subsequent incidence of
clinical malaria.},
note = {PMID: 34158054
PMCID: PMC8220741},
keywords = {Acute malnutrition, Antimalarials/administration \& dosage, Azithromycin/administration \& dosage, Burkina Faso, Burkina Faso/epidemiology, Child, Chronic malnutrition, Female, Humans, Incidence, Infant, Malaria, Malaria/epidemiology/transmission, Male, Nutritional Status, Preschool, seasonal malaria chemoprevention, Seasons},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Malaria and malnutrition remain major problems in
Sahel countries, especially in young children. The direct effect
of malnutrition on malaria remains poorly understood, and may
have important implications for malaria control. In this study,
nutritional status and the association between malnutrition and
subsequent incidence of symptomatic malaria were examined in
children in Burkina Faso and Mali who received either
azithromycin or placebo, alongside seasonal malaria
chemoprevention. METHODS: Mid-upper arm circumference (MUAC) was
measured in all 20,185 children who attended a screening visit
prior to the malaria transmission season in 2015. Prior to the
2016 malaria season, weight, height and MUAC were measured among
4149 randomly selected children. Height-for-age, weight-for-age,
weight-for-height, and MUAC-for-age were calculated as
indicators of nutritional status. Malaria incidence was measured
during the following rainy seasons. Multivariable random effects
Poisson models were created for each nutritional indicator to
study the effect of malnutrition on clinical malaria incidence
for each country. RESULTS: In both 2015 and 2016, nutritional
status prior to the malaria season was poor. The most prevalent
form of malnutrition in Burkina Faso was being underweight
(30.5%; 95% CI 28.6-32.6), whereas in Mali stunting was most
prevalent (27.5%; 95% CI 25.6-29.5). In 2016, clinical malaria
incidence was 675 per 1000 person-years (95% CI 613-744) in
Burkina Faso, and 1245 per 1000 person-years (95% CI 1152-1347)
in Mali. There was some evidence that severe stunting was
associated with lower incidence of malaria in Mali (RR 0.81; 95% CI 0.64-1.02; p = 0.08), but this association was not seen
in Burkina Faso. Being moderately underweight tended to be
associated with higher incidence of clinical malaria in Burkina Faso (RR 1.27; 95% CI 0.98-1.64; p = 0.07), while this was the
case in Mali for moderate wasting (RR 1.27; 95% CI 0.98-1.64; p = 0.07). However, these associations were not observed in
severely affected children, nor consistent between countries.
MUAC-for-age was not associated with malaria risk. CONCLUSIONS:
Both malnutrition and malaria were common in the study areas,
high despite high coverage of seasonal malaria chemoprevention
and long-lasting insecticidal nets. However, no strong or
consistent evidence was found for an association between any of
the nutritional indicators and the subsequent incidence of
clinical malaria. |
| Paul Sondo, Biebo Bihoun, Bérenger Kabore, Marc Christian Tahita, Karim Derra, Toussaint Rouamba, Seydou Nakanabo Diallo, Adama Kazienga, Hamidou Ilboudo, Innocent Valea, Zekiba Tarnagda, Hermann Sorgho, Thierry Lefevre, Halidou Tinto Polymorphisms in Plasmodium falciparum parasites and mutations in the resistance genes Pfcrt and Pfmdr1 in Nanoro area, Burkina Faso. Journal Article In: Pan Afr. Med. J., vol. 39, pp. 118, 2021, ISSN: 1937-8688, (Copyright: Paul Sondo et al.
PMID: 34512854
PMCID: PMC8396377). @article{Sondo2021-qe,
title = {Polymorphisms in Plasmodium falciparum parasites and mutations in the resistance genes Pfcrt and Pfmdr1 in Nanoro area, Burkina Faso.},
author = {Paul Sondo and Biebo Bihoun and B\'{e}renger Kabore and Marc Christian Tahita and Karim Derra and Toussaint Rouamba and Seydou Nakanabo Diallo and Adama Kazienga and Hamidou Ilboudo and Innocent Valea and Zekiba Tarnagda and Hermann Sorgho and Thierry Lefevre and Halidou Tinto},
doi = {10.11604/pamj.2021.39.118.26959},
issn = {1937-8688},
year = {2021},
date = {2021-06-10},
urldate = {2021-06-10},
journal = {Pan Afr. Med. J.},
volume = {39},
pages = {118},
publisher = {Pan African Medical Journal},
abstract = {Introduction: from a genetic point of view P. falciparumis
extremely polymorphic. There is a variety of parasite strains
infesting individuals living in malaria endemic areas. The
purpose of this study is to investigate the relationship between
polymorphisms in Plasmodium falciparum parasites and Pfcrt and
Pfmdr1 gene mutations in Nanoro area, Burkina Faso. Methods:
blood samples from plasmodium carriers residing in the Nanoro
Health District were genotyped using nested PCR. Parasite gene
mutations associated with resistance to antimalarial drugs were
detected by PCR-RFLP. Results: samples of 672 patients were
successfully genotyped. No msp1and msp2allelic families
exhibited an increase in developing mutations in resistance
genes. However, mutant strains of these genes were present at
greater levels in monoclonal infections than in multi-clonal
infections. Conclusion: this study provides an overview of the
relationship between polymorphisms in Plasmodium falciparum
parasites and mutations in resistance genes. These data will
undoubtedly contribute to improving knowledge of the parasite´s
biology and its mechanisms of resistance to antimalarial drugs.},
note = {Copyright: Paul Sondo et al.
PMID: 34512854
PMCID: PMC8396377},
keywords = {Antimalarials/pharmacology, Burkina Faso, Drug Resistance, Falciparum/drug therapy/parasitology, GeneticRestriction Fragment Length, Genotype, Humans, Malaria, Membrane Transport Proteins/genetics, msp1, msp2, Multidrug Resistance-Associated Proteins/genetics, Mutation, Pfcrt, Pfmdr1, Plasmodium falciparum, Plasmodium falciparum/drug effects/genetics/isolation \& purification, Polymerase Chain Reaction, Polymorphism, Protozoan Proteins/genetics},
pubstate = {published},
tppubtype = {article}
}
Introduction: from a genetic point of view P. falciparumis
extremely polymorphic. There is a variety of parasite strains
infesting individuals living in malaria endemic areas. The
purpose of this study is to investigate the relationship between
polymorphisms in Plasmodium falciparum parasites and Pfcrt and
Pfmdr1 gene mutations in Nanoro area, Burkina Faso. Methods:
blood samples from plasmodium carriers residing in the Nanoro
Health District were genotyped using nested PCR. Parasite gene
mutations associated with resistance to antimalarial drugs were
detected by PCR-RFLP. Results: samples of 672 patients were
successfully genotyped. No msp1and msp2allelic families
exhibited an increase in developing mutations in resistance
genes. However, mutant strains of these genes were present at
greater levels in monoclonal infections than in multi-clonal
infections. Conclusion: this study provides an overview of the
relationship between polymorphisms in Plasmodium falciparum
parasites and mutations in resistance genes. These data will
undoubtedly contribute to improving knowledge of the parasite´s
biology and its mechanisms of resistance to antimalarial drugs. |
| Annelies Post, Berenger Kaboré, Mike Berendsen, Salou Diallo, Ousmane Traore, Rob J W Arts, Mihai G Netea, Leo A B Joosten, Halidou Tinto, Jan Jacobs, Quirijn Mast, André Ven Altered ex-vivo cytokine responses in children with asymptomatic Plasmodium falciparum infection in Burkina Faso: An additional argument to treat asymptomatic malaria? Journal Article In: Front. Immunol., vol. 12, pp. 614817, 2021, ISSN: 1664-3224, (Copyright © 2021 Post, Kaboré, Berendsen, Diallo, Traore, Arts, Netea, Joosten, Tinto, Jacobs, de Mast and van der Ven.
PMID: 34177883
PMCID: PMC8220162). @article{Post2021-oo,
title = {Altered ex-vivo cytokine responses in children with asymptomatic Plasmodium falciparum infection in Burkina Faso: An additional argument to treat asymptomatic malaria?},
author = {Annelies Post and Berenger Kabor\'{e} and Mike Berendsen and Salou Diallo and Ousmane Traore and Rob J W Arts and Mihai G Netea and Leo A B Joosten and Halidou Tinto and Jan Jacobs and Quirijn Mast and Andr\'{e} Ven},
doi = {10.3389/fimmu.2021.614817},
issn = {1664-3224},
year = {2021},
date = {2021-06-09},
urldate = {2021-06-09},
journal = {Front. Immunol.},
volume = {12},
pages = {614817},
publisher = {Frontiers Media SA},
abstract = {Introduction: Patients with clinical malaria have an increased
risk for bacterial bloodstream infections. We hypothesized that
asymptomatic malaria parasitemia increases susceptibility for
bacterial infections through an effect on the innate immune
system. We measured circulating cytokine levels and ex-vivo
cytokine production capacity in asymptomatic malaria and
compared with controls. Methods: Data were collected from
asymptomatic participants \<5 years old with and without positive
malaria microscopy, as well as from hospitalized patients \<5
years old with clinical malaria, bacteremia, or
malaria/bacteremia co-infections in a malaria endemic region of
Burkina Faso. Circulating cytokines (TNF-$alpha$, IFN-$gamma$,
IL-6, IL-10) were measured using multiplex assays. Whole blood
from asymptomatic participants with and without positive malaria
microscopy were ex-vivo stimulated with S. aureus, E. coli LPS
and Salmonella Typhimurium; cytokine concentrations
(TNF-$alpha$, IFN-$gamma$, IL-1$beta$, IL-6, IL-10) were
measured on supernatants using ELISA. Results: Included were children with clinical malaria (n=118), bacteremia (n=22), malaria and bacteremia co-infection (n=9), asymptomatic malaria (n=125), and asymptomatic controls (n=237). Children with either
clinical or asymptomatic malaria had higher plasma cytokine
concentrations than controls. Cytokine concentrations correlated
positively with malaria parasite density with the strongest correlation for IL-10 in both asymptomatic (r=0.63) and clinical malaria (r=0.53). Patients with bacteremia had lower circulating
IL-10, TNF-$alpha$ and IFN-$gamma$ and higher IL-6
concentrations, compared to clinical malaria. Ex-vivo whole
blood cytokine production to LPS and S. aureus was significantly
lower in asymptomatic malaria compared to controls. Whole blood
IFN-$gamma$ and IL-10 production in response to Salmonella was
also lower in asymptomatic malaria. Interpretation: In children
with asymptomatic malaria, cytokine responses upon ex-vivo
bacterial stimulation are downregulated. Further studies are
needed to explore if the suggested impaired innate immune
response to bacterial pathogens also translates into impaired
control of pathogens such as Salmonella spp.},
note = {Copyright © 2021 Post, Kabor\'{e}, Berendsen, Diallo, Traore, Arts, Netea, Joosten, Tinto, Jacobs, de Mast and van der Ven.
PMID: 34177883
PMCID: PMC8220162},
keywords = {Asymptomatic Diseases, asymptomatic malaria, bacteraemia, Bacteremia, bloodstream infection, Burkina Faso/epidemiology, Cells, Child, Cultured, Cytokines/metabolism, Endemic Diseases, Female, Humans, Infant, iNTS, Lipopolysaccharides/immunology, Malaria/epidemiology/immunology, Male, Parasite Load, Plasmodium falciparum/physiology, Preschool, Salmonella},
pubstate = {published},
tppubtype = {article}
}
Introduction: Patients with clinical malaria have an increased
risk for bacterial bloodstream infections. We hypothesized that
asymptomatic malaria parasitemia increases susceptibility for
bacterial infections through an effect on the innate immune
system. We measured circulating cytokine levels and ex-vivo
cytokine production capacity in asymptomatic malaria and
compared with controls. Methods: Data were collected from
asymptomatic participants <5 years old with and without positive
malaria microscopy, as well as from hospitalized patients <5
years old with clinical malaria, bacteremia, or
malaria/bacteremia co-infections in a malaria endemic region of
Burkina Faso. Circulating cytokines (TNF-$alpha$, IFN-$gamma$,
IL-6, IL-10) were measured using multiplex assays. Whole blood
from asymptomatic participants with and without positive malaria
microscopy were ex-vivo stimulated with S. aureus, E. coli LPS
and Salmonella Typhimurium; cytokine concentrations
(TNF-$alpha$, IFN-$gamma$, IL-1$beta$, IL-6, IL-10) were
measured on supernatants using ELISA. Results: Included were children with clinical malaria (n=118), bacteremia (n=22), malaria and bacteremia co-infection (n=9), asymptomatic malaria (n=125), and asymptomatic controls (n=237). Children with either
clinical or asymptomatic malaria had higher plasma cytokine
concentrations than controls. Cytokine concentrations correlated
positively with malaria parasite density with the strongest correlation for IL-10 in both asymptomatic (r=0.63) and clinical malaria (r=0.53). Patients with bacteremia had lower circulating
IL-10, TNF-$alpha$ and IFN-$gamma$ and higher IL-6
concentrations, compared to clinical malaria. Ex-vivo whole
blood cytokine production to LPS and S. aureus was significantly
lower in asymptomatic malaria compared to controls. Whole blood
IFN-$gamma$ and IL-10 production in response to Salmonella was
also lower in asymptomatic malaria. Interpretation: In children
with asymptomatic malaria, cytokine responses upon ex-vivo
bacterial stimulation are downregulated. Further studies are
needed to explore if the suggested impaired innate immune
response to bacterial pathogens also translates into impaired
control of pathogens such as Salmonella spp. |
| Paul Sondo, Marc Christian Tahita, Toussaint Rouamba, Karim Derra, Bérenger Kaboré, Cheick Sa"id Compaoré, Florence Ouédraogo, Eli Rouamba, Hamidou Ilboudo, Estelle A"issa Bambara, Macaire Nana, Edmond Yabré Sawadogo, Hermann Sorgho, Athanase Mwinessobaonfou Somé, Innocent Valéa, Prabin Dahal, Maminata Traoré/Coulibaly, Halidou Tinto Assessment of a combined strategy of seasonal malaria chemoprevention and supplementation with vitamin A, zinc and Plumpy'Doz™ to prevent malaria and malnutrition in children under 5 years old in Burkina Faso: a randomized open-label trial (SMC-NUT) Journal Article In: Trials, vol. 22, no. 1, pp. 360, 2021, ISSN: 1745-6215, (PMID: 34030705
PMCID: PMC8142067). @article{Sondo2021-kc,
title = {Assessment of a combined strategy of seasonal malaria chemoprevention and supplementation with vitamin A, zinc and Plumpy'Doz™ to prevent malaria and malnutrition in children under 5 years old in Burkina Faso: a randomized open-label trial (SMC-NUT)},
author = {Paul Sondo and Marc Christian Tahita and Toussaint Rouamba and Karim Derra and B\'{e}renger Kabor\'{e} and Cheick Sa"id Compaor\'{e} and Florence Ou\'{e}draogo and Eli Rouamba and Hamidou Ilboudo and Estelle A"issa Bambara and Macaire Nana and Edmond Yabr\'{e} Sawadogo and Hermann Sorgho and Athanase Mwinessobaonfou Som\'{e} and Innocent Val\'{e}a and Prabin Dahal and Maminata Traor\'{e}/Coulibaly and Halidou Tinto},
doi = {10.1186/s13063-021-05320-7},
issn = {1745-6215},
year = {2021},
date = {2021-05-24},
urldate = {2021-05-24},
journal = {Trials},
volume = {22},
number = {1},
pages = {360},
publisher = {Springer Science and Business Media LLC},
abstract = {BACKGROUND: Malaria and malnutrition represent major public
health concerns worldwide especially in Sub-Sahara Africa.
Despite implementation of seasonal malaria chemoprophylaxis
(SMC), an intervention aimed at reducing malaria incidence among
children aged 3-59 months, the burden of malaria and associated
mortality among children below age 5 years remains high in
Burkina Faso. Malnutrition, in particular micronutrient
deficiency, appears to be one of the potential factors that can
negatively affect the effectiveness of SMC. Treating
micronutrient deficiencies is known to reduce the incidence of
malaria in highly prevalent malaria zone such as rural settings.
Therefore, we hypothesized that a combined strategy of SMC
together with a daily oral nutrients supplement will enhance the
immune response and decrease the incidence of malaria and
malnutrition among children under SMC coverage. METHODS:
Children (6-59 months) under SMC coverage receiving vitamin A
supplementation will be randomly assigned to one of the three
study arms (a) SMC + vitamin A alone, (b) SMC + vitamin A +
zinc, or (c) SMC + vitamin A + Plumpy'Doz™ using 1:1:1
allocation ratio. After each SMC monthly distribution, children
will be visited at home to confirm drug administration and
followed-up for 1 year. Anthropometric indicators will be
recorded at each visit and blood samples will be collected for
microscopy slides, haemoglobin measurement, and spotted onto
filter paper for further PCR analyses. The primary outcome
measure is the incidence of malaria in each arm. Secondary
outcome measures will include mid-upper arm circumference and
weight gain from baseline measurements, coverage and compliance
to SMC, occurrence of adverse events (AEs), and prevalence of
molecular markers of antimalarial resistance comprising Pfcrt,
Pfmdr1, Pfdhfr, and Pfdhps. DISCUSSION: This study will
demonstrate an integrated strategy of malaria and malnutrition
programmes in order to mutualize resources for best impact. By
relying on existing strategies, the policy implementation of
this joint intervention will be scalable at country and regional
levels. TRIAL REGISTRATION: ClinicalTrials.gov NCT04238845 .
Registered on 23 January 2020
https://clinicaltrials.gov/ct2/show/NCT04238845.},
note = {PMID: 34030705
PMCID: PMC8142067},
keywords = {Antimalarials/adverse effects, Burkina Faso/epidemiology, Chemoprevention, Child, Child Nutrition Disorders, Dietary Supplements, Humans, Infant, Malaria, Malaria/diagnosis/epidemiology/prevention \& control, Malnutrition, Malnutrition/diagnosis/drug therapy/prevention \& control, Pharmaceutical Preparations, Plumpy’Doz™, Preschool, Randomized controlled trial, Seasonal chemoprevention, Seasons, Vitamin A, Vitamin A/adverse effects, Zinc},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Malaria and malnutrition represent major public
health concerns worldwide especially in Sub-Sahara Africa.
Despite implementation of seasonal malaria chemoprophylaxis
(SMC), an intervention aimed at reducing malaria incidence among
children aged 3-59 months, the burden of malaria and associated
mortality among children below age 5 years remains high in
Burkina Faso. Malnutrition, in particular micronutrient
deficiency, appears to be one of the potential factors that can
negatively affect the effectiveness of SMC. Treating
micronutrient deficiencies is known to reduce the incidence of
malaria in highly prevalent malaria zone such as rural settings.
Therefore, we hypothesized that a combined strategy of SMC
together with a daily oral nutrients supplement will enhance the
immune response and decrease the incidence of malaria and
malnutrition among children under SMC coverage. METHODS:
Children (6-59 months) under SMC coverage receiving vitamin A
supplementation will be randomly assigned to one of the three
study arms (a) SMC + vitamin A alone, (b) SMC + vitamin A +
zinc, or (c) SMC + vitamin A + Plumpy'Doz™ using 1:1:1
allocation ratio. After each SMC monthly distribution, children
will be visited at home to confirm drug administration and
followed-up for 1 year. Anthropometric indicators will be
recorded at each visit and blood samples will be collected for
microscopy slides, haemoglobin measurement, and spotted onto
filter paper for further PCR analyses. The primary outcome
measure is the incidence of malaria in each arm. Secondary
outcome measures will include mid-upper arm circumference and
weight gain from baseline measurements, coverage and compliance
to SMC, occurrence of adverse events (AEs), and prevalence of
molecular markers of antimalarial resistance comprising Pfcrt,
Pfmdr1, Pfdhfr, and Pfdhps. DISCUSSION: This study will
demonstrate an integrated strategy of malaria and malnutrition
programmes in order to mutualize resources for best impact. By
relying on existing strategies, the policy implementation of
this joint intervention will be scalable at country and regional
levels. TRIAL REGISTRATION: ClinicalTrials.gov NCT04238845 .
Registered on 23 January 2020
https://clinicaltrials.gov/ct2/show/NCT04238845. |
| Joel D Bognini, Sekou Samadoulougou, Mady Ouedraogo, Tiga David Kangoye, Carine Van Malderen, Halidou Tinto, Fati Kirakoya-Samadoulougou Socioeconomic inequalities in curative healthcare-seeking for children under five before and after the free healthcare initiative in Sierra Leone: analysis of population-based survey data Journal Article In: Int. J. Equity Health, vol. 20, no. 1, pp. 124, 2021, ISSN: 1475-9276, (PMID: 34020665
PMCID: PMC8140517). @article{Bognini2021-mk,
title = {Socioeconomic inequalities in curative healthcare-seeking for children under five before and after the free healthcare initiative in Sierra Leone: analysis of population-based survey data},
author = {Joel D Bognini and Sekou Samadoulougou and Mady Ouedraogo and Tiga David Kangoye and Carine Van Malderen and Halidou Tinto and Fati Kirakoya-Samadoulougou},
doi = {10.1186/s12939-021-01474-7},
issn = {1475-9276},
year = {2021},
date = {2021-05-21},
urldate = {2021-05-21},
journal = {Int. J. Equity Health},
volume = {20},
number = {1},
pages = {124},
publisher = {Springer Science and Business Media LLC},
abstract = {BACKGROUND: Socioeconomic inequalities between and within countries lead to disparities in the use of health services. These disparities could lead to child mortality in children under 5 years by depriving them of healthcare. Therefore, initiatives to remove healthcare fees such as the Free Healthcare Initiative (FHCI) adopted in Sierra Leone can contribute to reducing these inequities in healthcare-seeking for children. This study aimed to assess the socioeconomic inequalities in healthcare-seeking for children under 5 years of age before and after the implementation of the FHCI. METHODS: Data were included on 1207, 2815, 1633, and 1476 children under 5 years of age with fever from the 2008, 2013, 2016, and 2019 nationwide surveys, respectively. Concentration curves were drawn for the period before (2008) and after (2013-2019) the implementation of the FHCI to assess socioeconomic inequalities in healthcare-seeking. Finally, Erreyger's corrected concentration indices were calculated to understand the magnitude of these inequalities. RESULTS: Before the implementation of the FHCI, there were inequalities in healthcare-seeking for children under five (Erreyger's corrected concentration index (CI) = 0.168, standard error (SE) = 0.049; p \< 0.001) in favor of the wealthy households. These inequalities decreased after the implementation of the FHCI (CI = 0.061, SE = 0.033; p = 0.06 in 2013, CI = 0.039, SE = 0.04; p = 0.32 in 2016, and CI = - 0.0005, SE = 0.362; p = 0.98 in 2019). Furthermore, before the implementation of the FHCI, a significant pro-rich inequality in the districts of Kenema (CI = 0.117, SE = 0.168, p = 0.021), Kono (CI = 0.175, SE = 0.078, p = 0.028) and Western Area Urban (CI = 0.070, SE = 0.032, p = 0.031) has been observed. After the implementation of the FHCI in 2019, these disparities were reduced, 11 of the 14 districts had a CI around the value of equality, and only in 2 districts the pro-rich inequality were significant (Western Area Urban (CI = 0.035, SE = 0.016, p = 0.039) and Western Area Rural (CI = 0.066, SE = 0.030, p = 0.027)). CONCLUSION: The results of this study demonstrated that socio-economic inequalities in healthcare-seeking for children have been considerably reduced after the FHCI in Sierra Leone. To further reduce these inequalities, policy actions can focus on the increase of availability of health services in the districts where the healthcare-seeking remained pro-rich.},
note = {PMID: 34020665
PMCID: PMC8140517},
keywords = {Adolescent, Adult, Child, Children under five, Delivery of Health Care/economics, Female, Health Care Surveys, Healthcare Disparities/economics/statistics \& numerical data, Healthcare utilization, Humans, Infant, Male, Parents/psychology, Patient Acceptance of Health Care/statistics \& numerical data, Preschool, Sierra Leone, Socioeconomic Factors, Young Adult},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Socioeconomic inequalities between and within countries lead to disparities in the use of health services. These disparities could lead to child mortality in children under 5 years by depriving them of healthcare. Therefore, initiatives to remove healthcare fees such as the Free Healthcare Initiative (FHCI) adopted in Sierra Leone can contribute to reducing these inequities in healthcare-seeking for children. This study aimed to assess the socioeconomic inequalities in healthcare-seeking for children under 5 years of age before and after the implementation of the FHCI. METHODS: Data were included on 1207, 2815, 1633, and 1476 children under 5 years of age with fever from the 2008, 2013, 2016, and 2019 nationwide surveys, respectively. Concentration curves were drawn for the period before (2008) and after (2013-2019) the implementation of the FHCI to assess socioeconomic inequalities in healthcare-seeking. Finally, Erreyger's corrected concentration indices were calculated to understand the magnitude of these inequalities. RESULTS: Before the implementation of the FHCI, there were inequalities in healthcare-seeking for children under five (Erreyger's corrected concentration index (CI) = 0.168, standard error (SE) = 0.049; p < 0.001) in favor of the wealthy households. These inequalities decreased after the implementation of the FHCI (CI = 0.061, SE = 0.033; p = 0.06 in 2013, CI = 0.039, SE = 0.04; p = 0.32 in 2016, and CI = - 0.0005, SE = 0.362; p = 0.98 in 2019). Furthermore, before the implementation of the FHCI, a significant pro-rich inequality in the districts of Kenema (CI = 0.117, SE = 0.168, p = 0.021), Kono (CI = 0.175, SE = 0.078, p = 0.028) and Western Area Urban (CI = 0.070, SE = 0.032, p = 0.031) has been observed. After the implementation of the FHCI in 2019, these disparities were reduced, 11 of the 14 districts had a CI around the value of equality, and only in 2 districts the pro-rich inequality were significant (Western Area Urban (CI = 0.035, SE = 0.016, p = 0.039) and Western Area Rural (CI = 0.066, SE = 0.030, p = 0.027)). CONCLUSION: The results of this study demonstrated that socio-economic inequalities in healthcare-seeking for children have been considerably reduced after the FHCI in Sierra Leone. To further reduce these inequalities, policy actions can focus on the increase of availability of health services in the districts where the healthcare-seeking remained pro-rich. |
| Yeka Adoke, Rella Zoleko-Manego, Serge Ouoba, Alfred B Tiono, Grace Kaguthi, Juv^encio Eduardo Bonzela, Tran Thanh Duong, Alain Nahum, Marielle Bouyou-Akotet, Bernhards Ogutu, Alphonse Ouedraogo, Fiona Macintyre, Andreas Jessel, Bart Laurijssens, Mohammed H Cherkaoui-Rbati, Cathy Cantalloube, Anne Claire Marrast, Rapha"el Bejuit, David White, Timothy N C Wells, Florian Wartha, Didier Leroy, Afizi Kibuuka, Ghyslain Mombo-Ngoma, Daouda Ouattara, Ir`ene Mugenya, Bui Quang Phuc, Francis Bohissou, Denise P Mawili-Mboumba, Fredrick Olewe, Issiaka Soulama, Halidou Tinto, FALCI Study Group A randomized, double-blind, phase 2b study to investigate the efficacy, safety, tolerability and pharmacokinetics of a single-dose regimen of ferroquine with artefenomel in adults and children with uncomplicated Plasmodium falciparum malaria Journal Article In: Malar. J., vol. 20, no. 1, pp. 222, 2021, ISSN: 1475-2875, (PMID: 34011358
PMCID: PMC8135182). @article{Adoke2021-el,
title = {A randomized, double-blind, phase 2b study to investigate the efficacy, safety, tolerability and pharmacokinetics of a single-dose regimen of ferroquine with artefenomel in adults and children with uncomplicated Plasmodium falciparum malaria},
author = {Yeka Adoke and Rella Zoleko-Manego and Serge Ouoba and Alfred B Tiono and Grace Kaguthi and Juv^encio Eduardo Bonzela and Tran Thanh Duong and Alain Nahum and Marielle Bouyou-Akotet and Bernhards Ogutu and Alphonse Ouedraogo and Fiona Macintyre and Andreas Jessel and Bart Laurijssens and Mohammed H Cherkaoui-Rbati and Cathy Cantalloube and Anne Claire Marrast and Rapha"el Bejuit and David White and Timothy N C Wells and Florian Wartha and Didier Leroy and Afizi Kibuuka and Ghyslain Mombo-Ngoma and Daouda Ouattara and Ir`ene Mugenya and Bui Quang Phuc and Francis Bohissou and Denise P Mawili-Mboumba and Fredrick Olewe and Issiaka Soulama and Halidou Tinto and FALCI Study Group},
doi = {10.1186/s12936-021-03749-4},
issn = {1475-2875},
year = {2021},
date = {2021-05-19},
urldate = {2021-05-19},
journal = {Malar. J.},
volume = {20},
number = {1},
pages = {222},
publisher = {Springer Science and Business Media LLC},
abstract = {BACKGROUND: For uncomplicated Plasmodium falciparum malaria,
highly efficacious single-dose treatments are expected to
increase compliance and improve treatment outcomes, and thereby
may slow the development of resistance. The efficacy and safety
of a single-dose combination of artefenomel (800 mg) plus
ferroquine (400/600/900/1200 mg doses) for the treatment of
uncomplicated P. falciparum malaria were evaluated in Africa
(focusing on children $\leq$ 5 years) and Asia. METHODS: The
study was a randomized, double-blind, single-dose, multi-arm
clinical trial in patients aged \> 6 months to 5 years and 20
Asian patients. None of the treatment arms met the target
efficacy criterion for PCR-adjusted ACPR at Day 28 (lower limit
of 95% confidence interval [CI] \> 90%). PCR-adjusted ACPR at
Day 28 [95% CI] in the PP Set ranged from 78.4% [64.7; 88.7%]
to 91.7% [81.6; 97.2%] for the 400 mg to 1200 mg ferroquine
dose. Efficacy rates were low in Vietnamese patients, ranging
from 20 to 40%. A clear relationship was found between drug
exposure (artefenomel and ferroquine concentrations at Day 7)
and efficacy (primary endpoint), with higher concentrations of
both drugs resulting in higher efficacy. Six distinct kelch-13
mutations were detected in parasite isolates from 10/272 African
patients (with 2 mutations known to be associated with
artemisinin resistance) and 18/20 Asian patients (all C580Y
mutation). Vomiting within 6 h of initial artefenomel
administration was common (24.6%) and associated with lower
drug exposures. CONCLUSION: The efficacy of
artefenomel/ferroquine combination was suboptimal in African
children aged $\leq$ 5 years, the population of interest, and
vomiting most likely had a negative impact on efficacy. Trial
registration ClinicalTrials.gov, NCT02497612. Registered 14 Jul
2015, https://clinicaltrials.gov/ct2/show/NCT02497612?term=NCT02497612\&draw=2\&rank=1.},
note = {PMID: 34011358
PMCID: PMC8135182},
keywords = {Adamantane/administration \& dosage/analogs \& derivatives, Adolescent, Adult, Aged, Aminoquinolines/administration \& dosage, Benin, Burkina Faso, C580Y, Child, Combination treatment, Double-Blind Method, Drug Combinations, Exposure\textendashresponse, Falciparum/prevention \& control, Female, Ferroquine, Ferrous Compounds/administration \& dosage, Gabon, Humans, Infant, Kelch-13 mutation, Kenya, Malaria, Male, Metallocenes/administration \& dosage, Middle Aged, Mozambique, Parasite clearance, Peroxides/administration \& dosage, Pharmacokinetics/pharmacodynamics, Plasmodium falciparum/drug effects, Preschool, resistance, Uganda, Vietnam, Vomiting, Young Adult},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: For uncomplicated Plasmodium falciparum malaria,
highly efficacious single-dose treatments are expected to
increase compliance and improve treatment outcomes, and thereby
may slow the development of resistance. The efficacy and safety
of a single-dose combination of artefenomel (800 mg) plus
ferroquine (400/600/900/1200 mg doses) for the treatment of
uncomplicated P. falciparum malaria were evaluated in Africa
(focusing on children $łeq$ 5 years) and Asia. METHODS: The
study was a randomized, double-blind, single-dose, multi-arm
clinical trial in patients aged > 6 months to 5 years and 20
Asian patients. None of the treatment arms met the target
efficacy criterion for PCR-adjusted ACPR at Day 28 (lower limit
of 95% confidence interval [CI] > 90%). PCR-adjusted ACPR at
Day 28 [95% CI] in the PP Set ranged from 78.4% [64.7; 88.7%]
to 91.7% [81.6; 97.2%] for the 400 mg to 1200 mg ferroquine
dose. Efficacy rates were low in Vietnamese patients, ranging
from 20 to 40%. A clear relationship was found between drug
exposure (artefenomel and ferroquine concentrations at Day 7)
and efficacy (primary endpoint), with higher concentrations of
both drugs resulting in higher efficacy. Six distinct kelch-13
mutations were detected in parasite isolates from 10/272 African
patients (with 2 mutations known to be associated with
artemisinin resistance) and 18/20 Asian patients (all C580Y
mutation). Vomiting within 6 h of initial artefenomel
administration was common (24.6%) and associated with lower
drug exposures. CONCLUSION: The efficacy of
artefenomel/ferroquine combination was suboptimal in African
children aged $łeq$ 5 years, the population of interest, and
vomiting most likely had a negative impact on efficacy. Trial
registration ClinicalTrials.gov, NCT02497612. Registered 14 Jul
2015, https://clinicaltrials.gov/ct2/show/NCT02497612?term=NCT02497612&draw=2&rank=1. |
| Mehreen S Datoo, Magloire H Natama, Athanase Somé, Ousmane Traoré, Toussaint Rouamba, Duncan Bellamy, Prisca Yameogo, Daniel Valia, Moubarak Tegneri, Florence Ouedraogo, Rachidatou Soma, Seydou Sawadogo, Faizatou Sorgho, Karim Derra, Eli Rouamba, Benedict Orindi, Fernando Ramos Lopez, Amy Flaxman, Federica Cappuccini, Reshma Kailath, Sean Elias, Ekta Mukhopadhyay, Andres Noe, Matthew Cairns, Alison Lawrie, Rachel Roberts, Innocent Valéa, Hermann Sorgho, Nicola Williams, Gregory Glenn, Louis Fries, Jenny Reimer, Katie J Ewer, Umesh Shaligram, Adrian V S Hill, Halidou Tinto Efficacy of a low-dose candidate malaria vaccine, R21 in adjuvant Matrix-M, with seasonal administration to children in Burkina Faso: a randomised controlled trial Journal Article In: Lancet, vol. 397, no. 10287, pp. 1809–1818, 2021, ISSN: 1474-547X 0140-6736, (Copyright © 2021 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.
PMID: 33964223
PMCID: PMC8121760). @article{Datoo2021-dk,
title = {Efficacy of a low-dose candidate malaria vaccine, R21 in adjuvant Matrix-M, with seasonal administration to children in Burkina Faso: a randomised controlled trial},
author = {Mehreen S Datoo and Magloire H Natama and Athanase Som\'{e} and Ousmane Traor\'{e} and Toussaint Rouamba and Duncan Bellamy and Prisca Yameogo and Daniel Valia and Moubarak Tegneri and Florence Ouedraogo and Rachidatou Soma and Seydou Sawadogo and Faizatou Sorgho and Karim Derra and Eli Rouamba and Benedict Orindi and Fernando Ramos Lopez and Amy Flaxman and Federica Cappuccini and Reshma Kailath and Sean Elias and Ekta Mukhopadhyay and Andres Noe and Matthew Cairns and Alison Lawrie and Rachel Roberts and Innocent Val\'{e}a and Hermann Sorgho and Nicola Williams and Gregory Glenn and Louis Fries and Jenny Reimer and Katie J Ewer and Umesh Shaligram and Adrian V S Hill and Halidou Tinto},
doi = {10.1016/S0140-6736(21)00943-0},
issn = {1474-547X 0140-6736},
year = {2021},
date = {2021-05-15},
urldate = {2021-05-15},
journal = {Lancet},
volume = {397},
number = {10287},
pages = {1809--1818},
publisher = {Elsevier BV},
abstract = {BACKGROUND: Stalled progress in controlling Plasmodium
falciparum malaria highlights the need for an effective and
deployable vaccine. RTS,S/AS01, the most effective malaria
vaccine candidate to date, demonstrated 56% efficacy over 12
months in African children. We therefore assessed a new
candidate vaccine for safety and efficacy. METHODS: In this
double-blind, randomised, controlled, phase 2b trial, the
low-dose circumsporozoite protein-based vaccine R21, with two
different doses of adjuvant Matrix-M (MM), was given to children
aged 5-17 months in Nanoro, Burkina Faso-a highly seasonal
malaria transmission setting. Three vaccinations were
administered at 4-week intervals before the malaria season, with
a fourth dose 1 year later. All vaccines were administered
intramuscularly into the thigh. Group 1 received 5 $mu$g R21
plus 25 $mu$g MM, group 2 received 5 $mu$g R21 plus 50 $mu$g
MM, and group 3, the control group, received rabies
vaccinations. Children were randomly assigned (1:1:1) to groups
1-3. An independent statistician generated a random allocation
list, using block randomisation with variable block sizes, which
was used to assign participants. Participants, their families,
and the local study team were all masked to group allocation.
Only the pharmacists preparing the vaccine were unmasked to
group allocation. Vaccine safety, immunogenicity, and efficacy
were evaluated over 1 year. The primary objective assessed
protective efficacy of R21 plus MM (R21/MM) from 14 days after
the third vaccination to 6 months. Primary analyses of vaccine
efficacy were based on a modified intention-to-treat population,
which included all participants who received three vaccinations,
allowing for inclusion of participants who received the wrong
vaccine at any timepoint. This trial is registered with
ClinicalTrials.gov, NCT03896724. FINDINGS: From May 7 to June
13, 2019, 498 children aged 5-17 months were screened, and 48
were excluded. 450 children were enrolled and received at least
one vaccination. 150 children were allocated to group 1, 150
children were allocated to group 2, and 150 children were
allocated to group 3. The final vaccination of the primary
series was administered on Aug 7, 2019. R21/MM had a favourable
safety profile and was well tolerated. The majority of adverse
events were mild, with the most common event being fever. None
of the seven serious adverse events were attributed to the
vaccine. At the 6-month primary efficacy analysis, 43 (29%) of
146 participants in group 1, 38 (26%) of 146 participants in
group 2, and 105 (71%) of 147 participants in group 3 developed
clinical malaria. Vaccine efficacy was 74% (95% CI 63-82) in
group 1 and 77% (67-84) in group 2 at 6 months. At 1 year,
vaccine efficacy remained high, at 77% (67-84) in group 1.
Participants vaccinated with R21/MM showed high titres of
malaria-specific anti-Asn-Ala-Asn-Pro (NANP) antibodies 28 days
after the third vaccination, which were almost doubled with the
higher adjuvant dose. Titres waned but were boosted to levels
similar to peak titres after the primary series of vaccinations
after a fourth dose administered 1 year later. INTERPRETATION:
R21/MM appears safe and very immunogenic in African children,
and shows promising high-level efficacy. FUNDING: The European
\& Developing Countries Clinical Trials Partnership, Wellcome
Trust, and National Institute for Health Research Oxford
Biomedical Research Centre.},
note = {Copyright © 2021 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.
PMID: 33964223
PMCID: PMC8121760},
keywords = {Adjuvants, Burkina Faso, Double-Blind Method, Falciparum/prevention \& control, Female, Hepatitis B Surface Antigens, Humans, Immunogenicity, Immunologic/administration \& dosage, Infant, Malaria, Malaria Vaccines/therapeutic use, Malaria/prevention \& control, Male, Nanoparticles/administration \& dosage, Proportional Hazards Models, Protozoan Proteins/immunology, Saponins/administration \& dosage, Treatment Outcome, Vaccine, Vaccines, Virus-Like Particle/therapeutic use},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Stalled progress in controlling Plasmodium
falciparum malaria highlights the need for an effective and
deployable vaccine. RTS,S/AS01, the most effective malaria
vaccine candidate to date, demonstrated 56% efficacy over 12
months in African children. We therefore assessed a new
candidate vaccine for safety and efficacy. METHODS: In this
double-blind, randomised, controlled, phase 2b trial, the
low-dose circumsporozoite protein-based vaccine R21, with two
different doses of adjuvant Matrix-M (MM), was given to children
aged 5-17 months in Nanoro, Burkina Faso-a highly seasonal
malaria transmission setting. Three vaccinations were
administered at 4-week intervals before the malaria season, with
a fourth dose 1 year later. All vaccines were administered
intramuscularly into the thigh. Group 1 received 5 $mu$g R21
plus 25 $mu$g MM, group 2 received 5 $mu$g R21 plus 50 $mu$g
MM, and group 3, the control group, received rabies
vaccinations. Children were randomly assigned (1:1:1) to groups
1-3. An independent statistician generated a random allocation
list, using block randomisation with variable block sizes, which
was used to assign participants. Participants, their families,
and the local study team were all masked to group allocation.
Only the pharmacists preparing the vaccine were unmasked to
group allocation. Vaccine safety, immunogenicity, and efficacy
were evaluated over 1 year. The primary objective assessed
protective efficacy of R21 plus MM (R21/MM) from 14 days after
the third vaccination to 6 months. Primary analyses of vaccine
efficacy were based on a modified intention-to-treat population,
which included all participants who received three vaccinations,
allowing for inclusion of participants who received the wrong
vaccine at any timepoint. This trial is registered with
ClinicalTrials.gov, NCT03896724. FINDINGS: From May 7 to June
13, 2019, 498 children aged 5-17 months were screened, and 48
were excluded. 450 children were enrolled and received at least
one vaccination. 150 children were allocated to group 1, 150
children were allocated to group 2, and 150 children were
allocated to group 3. The final vaccination of the primary
series was administered on Aug 7, 2019. R21/MM had a favourable
safety profile and was well tolerated. The majority of adverse
events were mild, with the most common event being fever. None
of the seven serious adverse events were attributed to the
vaccine. At the 6-month primary efficacy analysis, 43 (29%) of
146 participants in group 1, 38 (26%) of 146 participants in
group 2, and 105 (71%) of 147 participants in group 3 developed
clinical malaria. Vaccine efficacy was 74% (95% CI 63-82) in
group 1 and 77% (67-84) in group 2 at 6 months. At 1 year,
vaccine efficacy remained high, at 77% (67-84) in group 1.
Participants vaccinated with R21/MM showed high titres of
malaria-specific anti-Asn-Ala-Asn-Pro (NANP) antibodies 28 days
after the third vaccination, which were almost doubled with the
higher adjuvant dose. Titres waned but were boosted to levels
similar to peak titres after the primary series of vaccinations
after a fourth dose administered 1 year later. INTERPRETATION:
R21/MM appears safe and very immunogenic in African children,
and shows promising high-level efficacy. FUNDING: The European
& Developing Countries Clinical Trials Partnership, Wellcome
Trust, and National Institute for Health Research Oxford
Biomedical Research Centre. |
| Toussaint Rouamba, Sékou Samadoulougou, Mady Ouédraogo, Hervé Hien, Halidou Tinto, Fati Kirakoya-Samadoulougou Asymptomatic malaria and anaemia among pregnant women during high and low malaria transmission seasons in Burkina Faso: household-based cross-sectional surveys in Burkina Faso, 2013 and 2017 Journal Article In: Malar. J., vol. 20, no. 1, pp. 211, 2021, ISSN: 1475-2875. @article{Rouamba2021-gn,
title = {Asymptomatic malaria and anaemia among pregnant women during high and low malaria transmission seasons in Burkina Faso: household-based cross-sectional surveys in Burkina Faso, 2013 and 2017},
author = {Toussaint Rouamba and S\'{e}kou Samadoulougou and Mady Ou\'{e}draogo and Herv\'{e} Hien and Halidou Tinto and Fati Kirakoya-Samadoulougou},
doi = {10.1186/s12936-021-03703-4},
issn = {1475-2875},
year = {2021},
date = {2021-05-01},
urldate = {2021-05-01},
journal = {Malar. J.},
volume = {20},
number = {1},
pages = {211},
publisher = {Springer Science and Business Media LLC},
abstract = {BACKGROUND: Malaria in endemic countries is often asymptomatic
during pregnancy, but it has substantial consequences for both
the mother and her unborn baby. During pregnancy, anaemia is an
important consequence of malaria infection. In Burkina Faso, the
intensity of malaria varies according to the season, albeit the
prevalence of malaria and anaemia as well as their risk factors,
during high and low malaria transmission seasons is
underexplored at the household level. METHODS: Data of 1751
pregnant women from October 2013 to March 2014 and 1931 pregnant
women from April 2017 to June 2017 were drawn from two
cross-sectional household surveys conducted in 24 health
districts of Burkina Faso. Pregnant women were tested for
malaria in their household after consenting. Asymptomatic
carriage was defined as a positive result from malaria rapid
diagnostic tests in the absence of clinical symptoms of malaria.
Anaemia was defined as haemoglobin level less than 11 g/dL in
the first and third trimester and less than 10.5 g/dL in the
second trimester of pregnancy. RESULTS: Prevalence of
asymptomatic malaria in pregnancy was estimated at 23.9% (95%
CI 20.2-28.0) during the high transmission season
(October-November) in 2013. During the low transmission season,
it was 12.7% (95% CI 10.9-14.7) between December and March in
2013-2014 and halved (6.4%; 95% CI 5.3-7.6) between April and
June 2017. Anaemia prevalence was estimated at 59.4% (95% CI
54.8-63.8) during the high transmission season in 2013. During
the low transmission season, it was 50.6% (95% CI 47.7-53.4)
between December and March 2013-2014 and 65.0% (95% CI
62.8-67.2) between April and June, 2017. CONCLUSION: This study
revealed that the prevalence of malaria asymptomatic carriage
and anaemia among pregnant women at the community level remain
high throughout the year. Thus, more efforts are needed to
increase prevention measures such as IPTp-SP coverage in order
to reduce anaemia and contribute to preventing low birth weight
and poor pregnancy outcomes.},
keywords = {Adult, Anemia/epidemiology/parasitology, Asymptomatic carriage, Asymptomatic Infections/epidemiology, Burkina Faso/epidemiology, Community, Cross-Sectional Studies, Female, Haemoglobin, Humans, Malaria/epidemiology/parasitology, Parasitic/epidemiology/parasitology, Plasmodium, Pregnancy, Pregnancy Complications, Pregnant, Pregnant Women, Prevalence, Young Adult},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: Malaria in endemic countries is often asymptomatic
during pregnancy, but it has substantial consequences for both
the mother and her unborn baby. During pregnancy, anaemia is an
important consequence of malaria infection. In Burkina Faso, the
intensity of malaria varies according to the season, albeit the
prevalence of malaria and anaemia as well as their risk factors,
during high and low malaria transmission seasons is
underexplored at the household level. METHODS: Data of 1751
pregnant women from October 2013 to March 2014 and 1931 pregnant
women from April 2017 to June 2017 were drawn from two
cross-sectional household surveys conducted in 24 health
districts of Burkina Faso. Pregnant women were tested for
malaria in their household after consenting. Asymptomatic
carriage was defined as a positive result from malaria rapid
diagnostic tests in the absence of clinical symptoms of malaria.
Anaemia was defined as haemoglobin level less than 11 g/dL in
the first and third trimester and less than 10.5 g/dL in the
second trimester of pregnancy. RESULTS: Prevalence of
asymptomatic malaria in pregnancy was estimated at 23.9% (95%
CI 20.2-28.0) during the high transmission season
(October-November) in 2013. During the low transmission season,
it was 12.7% (95% CI 10.9-14.7) between December and March in
2013-2014 and halved (6.4%; 95% CI 5.3-7.6) between April and
June 2017. Anaemia prevalence was estimated at 59.4% (95% CI
54.8-63.8) during the high transmission season in 2013. During
the low transmission season, it was 50.6% (95% CI 47.7-53.4)
between December and March 2013-2014 and 65.0% (95% CI
62.8-67.2) between April and June, 2017. CONCLUSION: This study
revealed that the prevalence of malaria asymptomatic carriage
and anaemia among pregnant women at the community level remain
high throughout the year. Thus, more efforts are needed to
increase prevention measures such as IPTp-SP coverage in order
to reduce anaemia and contribute to preventing low birth weight
and poor pregnancy outcomes. |
| Massa Dit Achille Bonko, Palpouguini Lompo, Marc Christian Tahita, Francois Kiemde, Ibrahima Karama, Athanase M Somé, Petra F Mens, Sandra Menting, Halidou Tinto, Henk D F H Schallig Antibiotic susceptibility of Staphylococcus aureus and Streptococcus pneumoniae isolates from the nasopharynx of febrile children under 5 years in Nanoro, Burkina Faso Journal Article In: Antibiotics (Basel), vol. 10, no. 4, 2021, ISSN: 2079-6382, (PMID: 33920987
PMCID: PMC8071235). @article{Bonko2021-kv,
title = {Antibiotic susceptibility of Staphylococcus aureus and Streptococcus pneumoniae isolates from the nasopharynx of febrile children under 5 years in Nanoro, Burkina Faso},
author = {Massa Dit Achille Bonko and Palpouguini Lompo and Marc Christian Tahita and Francois Kiemde and Ibrahima Karama and Athanase M Som\'{e} and Petra F Mens and Sandra Menting and Halidou Tinto and Henk D F H Schallig},
doi = {10.3390/antibiotics10040444},
issn = {2079-6382},
year = {2021},
date = {2021-04-15},
urldate = {2021-04-15},
journal = {Antibiotics (Basel)},
volume = {10},
number = {4},
abstract = {(1) Background: nasopharynx colonization by resistant
Staphylococcus aureus and Streptococcus pneumoniae can lead to
serious diseases. Emerging resistance to antibiotics commonly
used to treat infections due to these pathogens poses a serious
threat to the health system. The present study aimed to determine
the antibiotic susceptibility of S. aureus and S. pneumoniae
isolates from the febrile children's nasopharynx under 5 years in
Nanoro (Burkina Faso). (2) Methods: bacterial isolates were
identified from nasopharyngeal swabs prospectively collected from
629 febrile children. Antibiotic susceptibility of S. aureus and
S. pneumoniae isolates was assessed by Kirby-Bauer method and
results were interpreted according to the Clinical and Laboratory
Standard Institute guidelines. (3) Results: bacterial
colonization was confirmed in 154 (24.5%) of children of whom
96.1% carried S. aureus, 3.2% had S. pneumoniae, and 0.6%
carried both bacteria. S. aureus isolates showed alarming
resistance to penicillin (96.0%) and S. pneumoniae was highly
resistant to tetracycline (100%) and
trimethoprim-sulfamethoxazole (83.3%), and moderately resistant
to penicillin (50.0%). Furthermore, 4.0% of S. aureus
identified were methicillin resistant. (4) Conclusion: this study
showed concerning resistance rates to antibiotics to treat
suspected bacterial respiratory tract infections. The work
highlights the necessity to implement continuous antibiotic
resistance surveillance.},
note = {PMID: 33920987
PMCID: PMC8071235},
keywords = {antibiotics, children; nasopharynx, resistance, Staphylococcus aureus, Streptococcus pneumoniae},
pubstate = {published},
tppubtype = {article}
}
(1) Background: nasopharynx colonization by resistant
Staphylococcus aureus and Streptococcus pneumoniae can lead to
serious diseases. Emerging resistance to antibiotics commonly
used to treat infections due to these pathogens poses a serious
threat to the health system. The present study aimed to determine
the antibiotic susceptibility of S. aureus and S. pneumoniae
isolates from the febrile children's nasopharynx under 5 years in
Nanoro (Burkina Faso). (2) Methods: bacterial isolates were
identified from nasopharyngeal swabs prospectively collected from
629 febrile children. Antibiotic susceptibility of S. aureus and
S. pneumoniae isolates was assessed by Kirby-Bauer method and
results were interpreted according to the Clinical and Laboratory
Standard Institute guidelines. (3) Results: bacterial
colonization was confirmed in 154 (24.5%) of children of whom
96.1% carried S. aureus, 3.2% had S. pneumoniae, and 0.6%
carried both bacteria. S. aureus isolates showed alarming
resistance to penicillin (96.0%) and S. pneumoniae was highly
resistant to tetracycline (100%) and
trimethoprim-sulfamethoxazole (83.3%), and moderately resistant
to penicillin (50.0%). Furthermore, 4.0% of S. aureus
identified were methicillin resistant. (4) Conclusion: this study
showed concerning resistance rates to antibiotics to treat
suspected bacterial respiratory tract infections. The work
highlights the necessity to implement continuous antibiotic
resistance surveillance. |