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      Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
      Oxford University Press
      rectal artesunate, coverage, CHWs, mothers, Africa

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          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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          Most cited references22

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          Artesunate versus quinine for treatment of severe falciparum malaria: a randomised trial.

          In the treatment of severe malaria, intravenous artesunate is more rapidly acting than intravenous quinine in terms of parasite clearance, is safer, and is simpler to administer, but whether it can reduce mortality is uncertain. We did an open-label randomised controlled trial in patients admitted to hospital with severe falciparum malaria in Bangladesh, India, Indonesia, and Myanmar. We assigned individuals intravenous artesunate 2.4 mg/kg bodyweight given as a bolus (n=730) at 0, 12, and 24 h, and then daily, or intravenous quinine (20 mg salt per kg loading dose infused over 4 h then 10 mg/kg infused over 2-8 h three times a day; n=731). Oral medication was substituted when possible to complete treatment. Our primary endpoint was death from severe malaria, and analysis was by intention to treat. We assessed all patients randomised for the primary endpoint. Mortality in artesunate recipients was 15% (107 of 730) compared with 22% (164 of 731) in quinine recipients; an absolute reduction of 34.7% (95% CI 18.5-47.6%; p=0.0002). Treatment with artesunate was well tolerated, whereas quinine was associated with hypoglycaemia (relative risk 3.2, 1.3-7.8; p=0.009). Artesunate should become the treatment of choice for severe falciparum malaria in adults.
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            Mortality and morbidity from malaria among children in a rural area of The Gambia, West Africa.

            Mortality and morbidity from malaria were measured among 3000 children under the age of 7 years in a rural area of The Gambia, West Africa. Using a post-mortem questionnaire technique, malaria was identified as the probable cause of 4% of infant deaths and of 25% of deaths in children aged 1 to 4 years. The malaria mortality rate was 6.3 per 1000 per year in infants and 10.7 per 1000 per year in children aged 1 to 4 years. Morbidity surveys suggested that children under the age of 7 years experienced about one clinical episode of malaria per year. Calculation of attributable fractions showed that malaria may be responsible for about 40% of episodes of fever in children. Although the overall level of parasitaemia showed little seasonal variation, the clinical impact of malaria was highly seasonal; all malaria deaths and a high proportion of febrile episodes were recorded during a limited period at the end of the rainy season.
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              Teaching mothers to provide home treatment of malaria in Tigray, Ethiopia: a randomised trial.

              No satisfactory strategy for reducing high child mortality from malaria has yet been established in tropical Africa. We compared the effect on under-5 mortality of teaching mothers to promptly provide antimalarials to their sick children at home, with the present community health worker approach. Of 37 tabias (cluster of villages) in two districts with hyperendemic to holoendemic malaria, tabias reported to have the highest malaria morbidity were selected. A census was done which included a maternity history to determine under-5 mortality. Tabias (population 70,506) were paired according to under-5 mortality rates. One tabia from each pair was allocated by random number to an intervention group and the other was allocated to the control group. In the intervention tabias, mother coordinators were trained to teach other local mothers to recognise symptoms of malaria in their children and to promptly give chloroquine. In both intervention and control tabias, all births and deaths of under-5s were recorded monthly. From January to December 1997, 190 of 6383 (29.8 per 1000) children under-5 died in the intervention tabias compared with 366 of 7294 (50.2 per 1000) in the control tabias. Under-5 mortality was reduced by 40% in the intervention localities (95% CI from 29.2-50.6; paired t test, p<0.003). For every third child who died, a structured verbal autopsy was undertaken to ascribe cause of mortality as consistent with malaria or possible malaria, or not consistent with malaria. Of the 190 verbal autopsies, 13 (19%) of 70 in the intervention tabias were consistent with possible malaria compared with 68 (57%) of 120 in the control tabias. A major reduction in under-5 mortality can be achieved in holoendemic malaria areas through training local mother coordinators to teach mothers to give under-5 children antimalarial drugs.
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                Author and article information

                Journal
                Clin Infect Dis
                Clin. Infect. Dis
                cid
                cid
                Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
                Oxford University Press
                1058-4838
                1537-6591
                15 December 2016
                06 December 2016
                06 December 2016
                : 63
                : Suppl 5 , Malaria in Highly Endemic Areas: Improving Control Through Diagnosis, Artemisinin Combination Therapy, and Rectal Artesunate Treatment
                : S312-S321
                Affiliations
                [1 ]Division of International Health, Karolinska Institutet , Stockholm, Sweden
                [2 ]Dodowa Health Research Centre , Ghana
                [3 ]Malaria Consortium , Kampala, Uganda
                [4 ]Projecto de Saude de Bandim , Guinea-Bissau
                [5 ]Special Programme for Research and Training in Tropical Diseases, World Health Organization , Geneva, Switzerland
                [6 ]Medical Research Council Clinical Trials Unit, London, United Kingdom
                [7 ]Makerere University Medical School , Kampala, Uganda
                [8 ]Greater Accra Regional Health Directorate
                [9 ]Dangme West District Health Directorate , Dodowa, Ghana
                [10 ]National Malaria Control Programme, World Health Organization Uganda Country Office , Kampala
                [11 ]University of Health and Allied Sciences, Ho, Ghana
                [12 ]Medical Research Council , Tygerberg, South Africa
                [13 ]University of Ghana , Accra
                [14 ]National Institute for Medical Research , Dar-es-Salaam
                [15 ]St Augustine University of Tanzania , Mwanza
                [16 ]Preparedness and Response Project, Lugogo House , Kampala, Uganda
                [17 ]Rakai Health Sciences Program, Rakai Project Centre , Entebbe, Uganda
                [18 ]National Institute for Medical Research, Gonja Field Station , Tanzania
                [19 ]Centre for Applied Biostatistics, Sahlgrenska Academy, University of Gothenburg , Sweden
                [20 ]College of Health Sciences, Makerere University , Kampala, Uganda
                [21 ]Drugs for Neglected Diseases, Geneva, Switzerland
                Author notes
                [a]

                Present affiliation: Global Malaria Programme, World Health Organization, Geneva, Switzerland.

                [b]

                Members of the Study 18 Research Group are listed in the Notes.

                Correspondence: M. Warsame, World Health Organization, 1211 Avenue Appia, Geneva 27, Switzerland ( warsamem@ 123456who.int ).
                Article
                ciw631
                10.1093/cid/ciw631
                5146703
                27941110
                69e34586-e38d-4e1f-913a-13d115c1af9c
                © 2016 World Health Organization; licensee Oxford Journals.

                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.

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                Categories
                Malaria in Highly Endemic Areas: Improving Control through Diagnosis, Artemisinin Combination Therapy, and Rectal Artesunate Treatment

                Infectious disease & Microbiology
                rectal artesunate,coverage,chws,mothers,africa
                Infectious disease & Microbiology
                rectal artesunate, coverage, chws, mothers, africa

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