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Pre-referral Rectal Artesunate Treatment by Community-Based Treatment Providers in Ghana, Guinea-Bissau, Tanzania, and Uganda (Study 18): A Cluster-Randomized Trial
Background. If malaria patients who cannot be treated orally are several hours from facilities for injections, rectal artesunate prior to hospital referral can prevent death and disability. The goal is to reduce death from malaria by having rectal artesunate treatment available and used. How best to...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5146703/ https://www.ncbi.nlm.nih.gov/pubmed/27941110 http://dx.doi.org/10.1093/cid/ciw631 |
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author | Warsame, Marian Gyapong, Margaret Mpeka, Betty Rodrigues, Amabelia Singlovic, Jan Babiker, Abdel Mworozi, Edison Agyepong, Irene Ansah, Evelyn Azairwe, Robert Biai, Sidu Binka, Fred Folb, Peter Gyapong, John Kimbute, Omari Machinda, Zena Kitua, Andrew Lutalo, Tom Majaha, Melkzedik Mamadu, Jao Mrango, Zakayo Petzold, Max Rujumba, Joseph Ribeiro, Isabela Gomes, Melba |
author_facet | Warsame, Marian Gyapong, Margaret Mpeka, Betty Rodrigues, Amabelia Singlovic, Jan Babiker, Abdel Mworozi, Edison Agyepong, Irene Ansah, Evelyn Azairwe, Robert Biai, Sidu Binka, Fred Folb, Peter Gyapong, John Kimbute, Omari Machinda, Zena Kitua, Andrew Lutalo, Tom Majaha, Melkzedik Mamadu, Jao Mrango, Zakayo Petzold, Max Rujumba, Joseph Ribeiro, Isabela Gomes, Melba |
author_sort | Warsame, Marian |
collection | PubMed |
description | Background. If malaria patients who cannot be treated orally are several hours from facilities for injections, rectal artesunate prior to hospital referral can prevent death and disability. The goal is to reduce death from malaria by having rectal artesunate treatment available and used. How best to do this remains unknown. Methods. Villages remote from a health facility were randomized to different community-based treatment providers trained to provide rectal artesunate in Ghana, Guinea-Bissau, Tanzania, and Uganda. Prereferral rectal artesunate treatment was provided in 272 villages: 109 through community-based health workers (CHWs), 112 via trained mothers (MUMs), 25 via trained traditional healers (THs), and 26 through trained community-chosen personnel (COMs); episodes eligible for rectal artesunate were established through regular household surveys of febrile illnesses recording symptoms eligible for prereferral treatment. Differences in treatment coverage with rectal artesunate in children aged <5 years in MUM vs CHW (standard-of-care) villages were assessed using the odds ratio (OR); the predictive probability of treatment was derived from a logistic regression analysis, adjusting for heterogeneity between clusters (villages) using random effects. Results. Over 19 months, 54 013 children had 102 504 febrile episodes, of which 32% (31 817 episodes) had symptoms eligible for prereferral therapy; 14% (4460) children received treatment. Episodes with altered consciousness, coma, or convulsions constituted 36.6% of all episodes in treated children. The overall OR of treatment between MUM vs CHW villages, adjusting for country, was 1.84 (95% confidence interval [CI], 1.20–2.83; P = .005). Adjusting for heterogeneity, this translated into a 1.67 higher average probability of a child being treated in MUM vs CHW villages. Referral compliance was 81% and significantly higher with CHWs vs MUMs: 87% vs 82% (risk ratio [RR], 1.1 [95% CI, 1.0–1.1]; P < .0001). There were more deaths in the TH cluster than elsewhere (RR, 2.7 [95% CI, 1.4–5.6]; P = .0040). Conclusions. Prereferral episodes were almost one-third of all febrile episodes. More than one-third of patients treated had convulsions, altered consciousness, or coma. Mothers were effective in treating patients, and achieved higher coverage than other providers. Treatment access was low. Clinical Trials Registration. ISRCTN58046240. |
format | Online Article Text |
id | pubmed-5146703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-51467032016-12-12 Pre-referral Rectal Artesunate Treatment by Community-Based Treatment Providers in Ghana, Guinea-Bissau, Tanzania, and Uganda (Study 18): A Cluster-Randomized Trial Warsame, Marian Gyapong, Margaret Mpeka, Betty Rodrigues, Amabelia Singlovic, Jan Babiker, Abdel Mworozi, Edison Agyepong, Irene Ansah, Evelyn Azairwe, Robert Biai, Sidu Binka, Fred Folb, Peter Gyapong, John Kimbute, Omari Machinda, Zena Kitua, Andrew Lutalo, Tom Majaha, Melkzedik Mamadu, Jao Mrango, Zakayo Petzold, Max Rujumba, Joseph Ribeiro, Isabela Gomes, Melba Clin Infect Dis Malaria in Highly Endemic Areas: Improving Control through Diagnosis, Artemisinin Combination Therapy, and Rectal Artesunate Treatment Background. If malaria patients who cannot be treated orally are several hours from facilities for injections, rectal artesunate prior to hospital referral can prevent death and disability. The goal is to reduce death from malaria by having rectal artesunate treatment available and used. How best to do this remains unknown. Methods. Villages remote from a health facility were randomized to different community-based treatment providers trained to provide rectal artesunate in Ghana, Guinea-Bissau, Tanzania, and Uganda. Prereferral rectal artesunate treatment was provided in 272 villages: 109 through community-based health workers (CHWs), 112 via trained mothers (MUMs), 25 via trained traditional healers (THs), and 26 through trained community-chosen personnel (COMs); episodes eligible for rectal artesunate were established through regular household surveys of febrile illnesses recording symptoms eligible for prereferral treatment. Differences in treatment coverage with rectal artesunate in children aged <5 years in MUM vs CHW (standard-of-care) villages were assessed using the odds ratio (OR); the predictive probability of treatment was derived from a logistic regression analysis, adjusting for heterogeneity between clusters (villages) using random effects. Results. Over 19 months, 54 013 children had 102 504 febrile episodes, of which 32% (31 817 episodes) had symptoms eligible for prereferral therapy; 14% (4460) children received treatment. Episodes with altered consciousness, coma, or convulsions constituted 36.6% of all episodes in treated children. The overall OR of treatment between MUM vs CHW villages, adjusting for country, was 1.84 (95% confidence interval [CI], 1.20–2.83; P = .005). Adjusting for heterogeneity, this translated into a 1.67 higher average probability of a child being treated in MUM vs CHW villages. Referral compliance was 81% and significantly higher with CHWs vs MUMs: 87% vs 82% (risk ratio [RR], 1.1 [95% CI, 1.0–1.1]; P < .0001). There were more deaths in the TH cluster than elsewhere (RR, 2.7 [95% CI, 1.4–5.6]; P = .0040). Conclusions. Prereferral episodes were almost one-third of all febrile episodes. More than one-third of patients treated had convulsions, altered consciousness, or coma. Mothers were effective in treating patients, and achieved higher coverage than other providers. Treatment access was low. Clinical Trials Registration. ISRCTN58046240. Oxford University Press 2016-12-15 2016-12-06 /pmc/articles/PMC5146703/ /pubmed/27941110 http://dx.doi.org/10.1093/cid/ciw631 Text en © 2016 World Health Organization; licensee Oxford Journals. http://creativecommons.org/licenses/by/3.0/igo/legalcode This is an open access article distributed under the terms of the Creative Commons Attribution IGO License (http://creativecommons.org/licenses/by/3.0/igo/legalcode), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. In any reproduction of this article there should not be any suggestion that WHO or this article endorse any specific organisation or products. The use of the WHO logo is not permitted. This notice should be preserved along with the article's original URL. |
spellingShingle | Malaria in Highly Endemic Areas: Improving Control through Diagnosis, Artemisinin Combination Therapy, and Rectal Artesunate Treatment Warsame, Marian Gyapong, Margaret Mpeka, Betty Rodrigues, Amabelia Singlovic, Jan Babiker, Abdel Mworozi, Edison Agyepong, Irene Ansah, Evelyn Azairwe, Robert Biai, Sidu Binka, Fred Folb, Peter Gyapong, John Kimbute, Omari Machinda, Zena Kitua, Andrew Lutalo, Tom Majaha, Melkzedik Mamadu, Jao Mrango, Zakayo Petzold, Max Rujumba, Joseph Ribeiro, Isabela Gomes, Melba Pre-referral Rectal Artesunate Treatment by Community-Based Treatment Providers in Ghana, Guinea-Bissau, Tanzania, and Uganda (Study 18): A Cluster-Randomized Trial |
title | Pre-referral Rectal Artesunate Treatment by Community-Based Treatment Providers in Ghana, Guinea-Bissau, Tanzania, and Uganda (Study 18): A Cluster-Randomized Trial |
title_full | Pre-referral Rectal Artesunate Treatment by Community-Based Treatment Providers in Ghana, Guinea-Bissau, Tanzania, and Uganda (Study 18): A Cluster-Randomized Trial |
title_fullStr | Pre-referral Rectal Artesunate Treatment by Community-Based Treatment Providers in Ghana, Guinea-Bissau, Tanzania, and Uganda (Study 18): A Cluster-Randomized Trial |
title_full_unstemmed | Pre-referral Rectal Artesunate Treatment by Community-Based Treatment Providers in Ghana, Guinea-Bissau, Tanzania, and Uganda (Study 18): A Cluster-Randomized Trial |
title_short | Pre-referral Rectal Artesunate Treatment by Community-Based Treatment Providers in Ghana, Guinea-Bissau, Tanzania, and Uganda (Study 18): A Cluster-Randomized Trial |
title_sort | pre-referral rectal artesunate treatment by community-based treatment providers in ghana, guinea-bissau, tanzania, and uganda (study 18): a cluster-randomized trial |
topic | Malaria in Highly Endemic Areas: Improving Control through Diagnosis, Artemisinin Combination Therapy, and Rectal Artesunate Treatment |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5146703/ https://www.ncbi.nlm.nih.gov/pubmed/27941110 http://dx.doi.org/10.1093/cid/ciw631 |
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