Management of severe paediatric malaria in resource-limited settings

被引:0
作者
Kathryn Maitland
机构
[1] Wellcome Trust Centre for Clinical Tropical Medicine,
[2] and Department of Paediatrics,undefined
[3] Faculty of Medicine,undefined
[4] Kilifi Clinical Trials Facility,undefined
[5] KEMRI-Wellcome Trust Research Programme,undefined
来源
BMC Medicine | / 13卷
关键词
Malaria; Africa; Children; Mortality; Clinical Trial; Treatment; Bacterial Infection; Supportive Care;
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摘要
Over 90% of the world’s severe and fatal Plasmodium falciparum malaria is estimated to affect young children in sub-Sahara Africa, where it remains a common cause of hospital admission and inpatient mortality. Few children will ever be managed on high dependency or intensive care units and, therefore, rely on simple supportive treatments and parenteral anti-malarials. There has been some progress on defining best practice for antimalarial treatment with the publication of the AQUAMAT trial in 2010, involving 5,425 children at 11 centres across 9 African countries, showing that in artesunate-treated children, the relative risk of death was 22.5% (95% confidence interval (CI) 8.1 to 36.9) lower than in those receiving quinine. Human trials of supportive therapies carried out on the basis of pathophysiology studies, have so far made little progress on reducing mortality; despite appearing to reduce morbidity endpoints, more often than not they have led to an excess of adverse outcomes. This review highlights the spectrum of complications in African children with severe malaria, the therapeutic challenges of managing these in resource-poor settings and examines in-depth the results from clinical trials with a view to identifying the treatment priorities and a future research agenda.
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[81]  
Mehta U(2007)Malaria-induced renal damage: facts and myths Pediatr Nephrol 81 2483-4239
[82]  
Allen E(2012)A systematic review of RIFLE criteria in children, and its application and association with measures of mortality and morbidity Kidney Int 364 1037-3939
[83]  
Dlamini SS(2011)Mortality after fluid bolus in African children with severe infection N Engl J Med 12 S98-902
[84]  
Tsoka J(2007)A quantitative ultrastructural study of renal pathology in fatal Plasmodium falciparum malaria Trop Med Int Health 4 80-221S
[85]  
Bredenkamp B(2012)Formulation, process development and evaluation of artemether and lumefantrine soft gelatin capsule J Phar Bioallied Sciences 22 1408-319
[86]  
Mthembu DJ(1993)Blackwater fever after ingestion of mefloquine Three cases. Presse Med 347 211-331
[87]  
White NJ(1996)Blackwater fever after halofantrine Lancet 19 817-1322
[88]  
Sharp BL(2005)Management of severe malaria: interventions and controversies Infect Dis Clin North Am 100 1274-353
[89]  
Chizema-Kawesha E(2006)Muscle cell injury, haemolysis and dark urine in children with falciparum malaria in Papua New Guinea Trans R Soc Trop Med Hyg 23 205-684
[90]  
Miller JM(1996)Blackwater fever in southern Vietnam: a prospective descriptive study of 50 cases Clin Infect Dis 12 101-1097