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Impact of the addition of azithromycin to antimalarials used for seasonal malaria chemoprevention on antimicrobial resistance of Streptococcus pneumoniae

OBJECTIVE: A trial was conducted in Burkina Faso and Mali to investigate whether addition of azithromycin to the antimalarials used for seasonal malaria chemoprevention reduces mortality and hospital admissions of children. We tested the sensitivity of nasal isolates of Streptococcus pneumoniae obta...

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Autores principales: Hema‐Ouangraoua, Soumeya, Aziz Maiga, Abdoul, Cairns, Matthew, Zongo, Issaka, Frédéric, Nikiema, Serge Yerbanga, Rakiswendé, Tamboura, Boubou, Badji, Henry, Gore‐Langton, Georgia, Kuepfer, Irene, Tinto, Halidou, Sagara, Issaka, Dicko, Alassane, Sow, Samba O., Chandrahoman, Daniel, Greenwood, Brian, Bosco Ouedraogo, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687265/
https://www.ncbi.nlm.nih.gov/pubmed/31655020
http://dx.doi.org/10.1111/tmi.13321
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author Hema‐Ouangraoua, Soumeya
Aziz Maiga, Abdoul
Cairns, Matthew
Zongo, Issaka
Frédéric, Nikiema
Serge Yerbanga, Rakiswendé
Tamboura, Boubou
Badji, Henry
Gore‐Langton, Georgia
Kuepfer, Irene
Tinto, Halidou
Sagara, Issaka
Dicko, Alassane
Sow, Samba O.
Chandrahoman, Daniel
Greenwood, Brian
Bosco Ouedraogo, Jean
author_facet Hema‐Ouangraoua, Soumeya
Aziz Maiga, Abdoul
Cairns, Matthew
Zongo, Issaka
Frédéric, Nikiema
Serge Yerbanga, Rakiswendé
Tamboura, Boubou
Badji, Henry
Gore‐Langton, Georgia
Kuepfer, Irene
Tinto, Halidou
Sagara, Issaka
Dicko, Alassane
Sow, Samba O.
Chandrahoman, Daniel
Greenwood, Brian
Bosco Ouedraogo, Jean
author_sort Hema‐Ouangraoua, Soumeya
collection PubMed
description OBJECTIVE: A trial was conducted in Burkina Faso and Mali to investigate whether addition of azithromycin to the antimalarials used for seasonal malaria chemoprevention reduces mortality and hospital admissions of children. We tested the sensitivity of nasal isolates of Streptococcus pneumoniae obtained during this trial to azithromycin and other antibiotics. METHODS: Azithromycin or placebo was administered monthly, in combination with the antimalarials used for seasonal malaria chemoprevention, for four months, over the annual malaria transmission seasons of 2014, 2015, and 2016. Nasopharyngeal swabs were collected from 2773 Burkinabe and 2709 Malian children on seven occasions: in July and December each year prior to and after drug administration, and at a final survey in early 2018. Pneumococci were isolated from nasopharyngeal swabs and tested for sensitivity to azithromycin and other antibiotics. RESULTS: A total of 5482 samples were collected. In Burkina Faso, the percentage of pneumococcal isolates resistant to azithromycin among children who had received it increased from 4.9% (95% CI: 2.4%, 9.9%) before the intervention to 25.6% (95% CI: 17.6%, 35.7%) afterward. In Mali, the increase was from 7.6% (95% CI: 3.8%, 14.4%) to 68.5% (95% CI: 55.1%, 79.4%). The percentage of resistant isolates remained elevated (17.7% (95% CI: 11.1%, 27.1%) in Burkina Faso and 19.1% (95% CI: 13.5%, 26.3%) in Mali) among children who had received azithromycin 1 year after stopping the intervention. An increase in resistance to azithromycin was also observed in children who had received a placebo but it was less marked. CONCLUSION: Addition of azithromycin to the antimalarial combination used for seasonal malaria chemoprevention was associated with an increase in resistance of pneumococci to azithromycin and erythromycin, which persisted 1 year after the last administration of azithromycin.
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spelling pubmed-76872652020-12-05 Impact of the addition of azithromycin to antimalarials used for seasonal malaria chemoprevention on antimicrobial resistance of Streptococcus pneumoniae Hema‐Ouangraoua, Soumeya Aziz Maiga, Abdoul Cairns, Matthew Zongo, Issaka Frédéric, Nikiema Serge Yerbanga, Rakiswendé Tamboura, Boubou Badji, Henry Gore‐Langton, Georgia Kuepfer, Irene Tinto, Halidou Sagara, Issaka Dicko, Alassane Sow, Samba O. Chandrahoman, Daniel Greenwood, Brian Bosco Ouedraogo, Jean Trop Med Int Health Original Research Papers OBJECTIVE: A trial was conducted in Burkina Faso and Mali to investigate whether addition of azithromycin to the antimalarials used for seasonal malaria chemoprevention reduces mortality and hospital admissions of children. We tested the sensitivity of nasal isolates of Streptococcus pneumoniae obtained during this trial to azithromycin and other antibiotics. METHODS: Azithromycin or placebo was administered monthly, in combination with the antimalarials used for seasonal malaria chemoprevention, for four months, over the annual malaria transmission seasons of 2014, 2015, and 2016. Nasopharyngeal swabs were collected from 2773 Burkinabe and 2709 Malian children on seven occasions: in July and December each year prior to and after drug administration, and at a final survey in early 2018. Pneumococci were isolated from nasopharyngeal swabs and tested for sensitivity to azithromycin and other antibiotics. RESULTS: A total of 5482 samples were collected. In Burkina Faso, the percentage of pneumococcal isolates resistant to azithromycin among children who had received it increased from 4.9% (95% CI: 2.4%, 9.9%) before the intervention to 25.6% (95% CI: 17.6%, 35.7%) afterward. In Mali, the increase was from 7.6% (95% CI: 3.8%, 14.4%) to 68.5% (95% CI: 55.1%, 79.4%). The percentage of resistant isolates remained elevated (17.7% (95% CI: 11.1%, 27.1%) in Burkina Faso and 19.1% (95% CI: 13.5%, 26.3%) in Mali) among children who had received azithromycin 1 year after stopping the intervention. An increase in resistance to azithromycin was also observed in children who had received a placebo but it was less marked. CONCLUSION: Addition of azithromycin to the antimalarial combination used for seasonal malaria chemoprevention was associated with an increase in resistance of pneumococci to azithromycin and erythromycin, which persisted 1 year after the last administration of azithromycin. John Wiley and Sons Inc. 2019-11-13 2019-12 /pmc/articles/PMC7687265/ /pubmed/31655020 http://dx.doi.org/10.1111/tmi.13321 Text en © 2020 The Authors Tropical Medicine & International Health Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Papers
Hema‐Ouangraoua, Soumeya
Aziz Maiga, Abdoul
Cairns, Matthew
Zongo, Issaka
Frédéric, Nikiema
Serge Yerbanga, Rakiswendé
Tamboura, Boubou
Badji, Henry
Gore‐Langton, Georgia
Kuepfer, Irene
Tinto, Halidou
Sagara, Issaka
Dicko, Alassane
Sow, Samba O.
Chandrahoman, Daniel
Greenwood, Brian
Bosco Ouedraogo, Jean
Impact of the addition of azithromycin to antimalarials used for seasonal malaria chemoprevention on antimicrobial resistance of Streptococcus pneumoniae
title Impact of the addition of azithromycin to antimalarials used for seasonal malaria chemoprevention on antimicrobial resistance of Streptococcus pneumoniae
title_full Impact of the addition of azithromycin to antimalarials used for seasonal malaria chemoprevention on antimicrobial resistance of Streptococcus pneumoniae
title_fullStr Impact of the addition of azithromycin to antimalarials used for seasonal malaria chemoprevention on antimicrobial resistance of Streptococcus pneumoniae
title_full_unstemmed Impact of the addition of azithromycin to antimalarials used for seasonal malaria chemoprevention on antimicrobial resistance of Streptococcus pneumoniae
title_short Impact of the addition of azithromycin to antimalarials used for seasonal malaria chemoprevention on antimicrobial resistance of Streptococcus pneumoniae
title_sort impact of the addition of azithromycin to antimalarials used for seasonal malaria chemoprevention on antimicrobial resistance of streptococcus pneumoniae
topic Original Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687265/
https://www.ncbi.nlm.nih.gov/pubmed/31655020
http://dx.doi.org/10.1111/tmi.13321
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