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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.
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.
Afiliación
  • Warsame M; Division of International Health, Karolinska Institutet, Stockholm, Sweden.
  • Gyapong M; Dodowa Health Research Centre, Ghana.
  • Mpeka B; Malaria Consortium, Kampala, Uganda.
  • Rodrigues A; Projecto de Saude de Bandim, Guinea-Bissau.
  • Singlovic J; Special Programme for Research and Training in Tropical Diseases, World Health Organization, Geneva, Switzerland.
  • Babiker A; Medical Research Council Clinical Trials Unit, London, United Kingdom.
  • Mworozi E; Makerere University Medical School, Kampala, Uganda.
  • Agyepong I; Greater Accra Regional Health Directorate.
  • Ansah E; Dangme West District Health Directorate, Dodowa, Ghana.
  • Azairwe R; National Malaria Control Programme, World Health Organization Uganda Country Office, Kampala.
  • Biai S; Projecto de Saude de Bandim, Guinea-Bissau.
  • Binka F; University of Health and Allied Sciences, Ho, Ghana.
  • Folb P; Medical Research Council, Tygerberg, South Africa.
  • Gyapong J; University of Ghana, Accra.
  • Kimbute O; National Institute for Medical Research, Dar-es-Salaam.
  • Machinda Z; St Augustine University of Tanzania, Mwanza.
  • Kitua A; Preparedness and Response Project, Lugogo House, Kampala, Uganda.
  • Lutalo T; Rakai Health Sciences Program, Rakai Project Centre, Entebbe, Uganda.
  • Majaha M; National Institute for Medical Research, Gonja Field Station, Tanzania.
  • Mamadu J; Projecto de Saude de Bandim, Guinea-Bissau.
  • Mrango Z; National Institute for Medical Research, Dar-es-Salaam.
  • Petzold M; Centre for Applied Biostatistics, Sahlgrenska Academy, University of Gothenburg, Sweden.
  • Rujumba J; College of Health Sciences, Makerere University, Kampala, Uganda.
  • Ribeiro I; Drugs for Neglected Diseases, Geneva, Switzerland.
  • Gomes M; Special Programme for Research and Training in Tropical Diseases, World Health Organization, Geneva, Switzerland.
Clin Infect Dis ; 63(suppl 5): S312-S321, 2016 Dec 15.
Article en En | MEDLINE | ID: mdl-27941110
ABSTRACT

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.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Malaria / Antimaláricos Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Child, preschool / Female / Humans / Infant / Male País/Región como asunto: Africa Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2016 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Malaria / Antimaláricos Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Child, preschool / Female / Humans / Infant / Male País/Región como asunto: Africa Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2016 Tipo del documento: Article País de afiliación: Suecia