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Anti-malarial treatment outcomes in Ethiopia: a systematic review and meta-analysis

BACKGROUND: Ethiopia is among countries with a high malaria burden. There are several studies that assessed the efficacy of anti-malarial agents in the country and this systematic review and meta-analysis was performed to obtain stronger evidence on treatment outcomes of malaria from the existing li...

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Autores principales: Gebreyohannes, Eyob Alemayehu, Bhagavathula, Akshaya Srikanth, Seid, Mohammed Assen, Tegegn, Henok Getachew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496337/
https://www.ncbi.nlm.nih.gov/pubmed/28673348
http://dx.doi.org/10.1186/s12936-017-1922-9
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author Gebreyohannes, Eyob Alemayehu
Bhagavathula, Akshaya Srikanth
Seid, Mohammed Assen
Tegegn, Henok Getachew
author_facet Gebreyohannes, Eyob Alemayehu
Bhagavathula, Akshaya Srikanth
Seid, Mohammed Assen
Tegegn, Henok Getachew
author_sort Gebreyohannes, Eyob Alemayehu
collection PubMed
description BACKGROUND: Ethiopia is among countries with a high malaria burden. There are several studies that assessed the efficacy of anti-malarial agents in the country and this systematic review and meta-analysis was performed to obtain stronger evidence on treatment outcomes of malaria from the existing literature in Ethiopia. METHODS: A systematic literature search using the preferred reporting items for systematic review and meta-analysis (PRISMA) statement was conducted on studies from Pubmed, Google Scholar, and ScienceDirect databases to identify published and unpublished literature. Comprehensive meta-analysis software was used to perform all meta-analyses. The Cochrane Q and the I (2) were used to evaluate heterogeneity of studies. Random effects model was used to combine studies showing heterogeneity of Cochrane Q p < 0.10 and I (2) > 50. RESULTS: Twenty-one studies were included in the final analysis with a total number of 3123 study participants. Treatment outcomes were assessed clinically and parasitologically using World Health Organization guidelines. Adequate clinical and parasitological response was used to assess treatment success at the 28th day. Overall, a significant high treatment success of 92.9% (95% CI 89.1–96.6), p < 0.001, I (2) = 98.39% was noticed. However, treatment success was higher in falciparum malaria patients treated with artemether–lumefantrine than chloroquine for Plasmodium vivax patients [98.1% (97.0–99.2), p < 0.001, I (2) = 72.55 vs 94.7% (92.6–96.2), p < 0.001, I (2) = 53.62%]. Seven studies reported the adverse drug reactions to anti-malarial treatment; of 822 participants, 344 of them were exposed to adverse drug reactions with a pooled event rate of 39.8% (14.1–65.5), p = 0.002. CONCLUSIONS: On the basis of this review, anti-malarial treatment success was high (92.9%) and standard regimens showed good efficacy against Plasmodium falciparum (98.1%) and P. vivax (94.7%) infections in Ethiopia, but associated with high rates of adverse drug reactions (ADRs). However, these ADRs were not serious enough to discontinue anti-malarial treatment. The results of this study suggest that the current anti-malarial medications are effective and safe; however, greater priority should be placed on the discovery of new anti-malarial drugs to achieve successful outcomes as resistance seems inevitable since cases of anti-malarial drug resistance have been reported from other areas of the world. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-017-1922-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-54963372017-07-05 Anti-malarial treatment outcomes in Ethiopia: a systematic review and meta-analysis Gebreyohannes, Eyob Alemayehu Bhagavathula, Akshaya Srikanth Seid, Mohammed Assen Tegegn, Henok Getachew Malar J Research BACKGROUND: Ethiopia is among countries with a high malaria burden. There are several studies that assessed the efficacy of anti-malarial agents in the country and this systematic review and meta-analysis was performed to obtain stronger evidence on treatment outcomes of malaria from the existing literature in Ethiopia. METHODS: A systematic literature search using the preferred reporting items for systematic review and meta-analysis (PRISMA) statement was conducted on studies from Pubmed, Google Scholar, and ScienceDirect databases to identify published and unpublished literature. Comprehensive meta-analysis software was used to perform all meta-analyses. The Cochrane Q and the I (2) were used to evaluate heterogeneity of studies. Random effects model was used to combine studies showing heterogeneity of Cochrane Q p < 0.10 and I (2) > 50. RESULTS: Twenty-one studies were included in the final analysis with a total number of 3123 study participants. Treatment outcomes were assessed clinically and parasitologically using World Health Organization guidelines. Adequate clinical and parasitological response was used to assess treatment success at the 28th day. Overall, a significant high treatment success of 92.9% (95% CI 89.1–96.6), p < 0.001, I (2) = 98.39% was noticed. However, treatment success was higher in falciparum malaria patients treated with artemether–lumefantrine than chloroquine for Plasmodium vivax patients [98.1% (97.0–99.2), p < 0.001, I (2) = 72.55 vs 94.7% (92.6–96.2), p < 0.001, I (2) = 53.62%]. Seven studies reported the adverse drug reactions to anti-malarial treatment; of 822 participants, 344 of them were exposed to adverse drug reactions with a pooled event rate of 39.8% (14.1–65.5), p = 0.002. CONCLUSIONS: On the basis of this review, anti-malarial treatment success was high (92.9%) and standard regimens showed good efficacy against Plasmodium falciparum (98.1%) and P. vivax (94.7%) infections in Ethiopia, but associated with high rates of adverse drug reactions (ADRs). However, these ADRs were not serious enough to discontinue anti-malarial treatment. The results of this study suggest that the current anti-malarial medications are effective and safe; however, greater priority should be placed on the discovery of new anti-malarial drugs to achieve successful outcomes as resistance seems inevitable since cases of anti-malarial drug resistance have been reported from other areas of the world. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-017-1922-9) contains supplementary material, which is available to authorized users. BioMed Central 2017-07-03 /pmc/articles/PMC5496337/ /pubmed/28673348 http://dx.doi.org/10.1186/s12936-017-1922-9 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Gebreyohannes, Eyob Alemayehu
Bhagavathula, Akshaya Srikanth
Seid, Mohammed Assen
Tegegn, Henok Getachew
Anti-malarial treatment outcomes in Ethiopia: a systematic review and meta-analysis
title Anti-malarial treatment outcomes in Ethiopia: a systematic review and meta-analysis
title_full Anti-malarial treatment outcomes in Ethiopia: a systematic review and meta-analysis
title_fullStr Anti-malarial treatment outcomes in Ethiopia: a systematic review and meta-analysis
title_full_unstemmed Anti-malarial treatment outcomes in Ethiopia: a systematic review and meta-analysis
title_short Anti-malarial treatment outcomes in Ethiopia: a systematic review and meta-analysis
title_sort anti-malarial treatment outcomes in ethiopia: a systematic review and meta-analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496337/
https://www.ncbi.nlm.nih.gov/pubmed/28673348
http://dx.doi.org/10.1186/s12936-017-1922-9
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