Pre-referral rectal artesunate to prevent death and disability in severe malaria: a placebo-controlled trial

被引:148
|
作者
Gomes, M. F. [1 ]
Faiz, M. A. [2 ]
Gyapong, J. O. [3 ]
Warsame, M. [4 ]
Agbenyega, T. [5 ]
Babiker, A. [6 ]
Baiden, F. [7 ]
Yunus, E. B. [8 ]
Binka, F. [9 ]
Clerk, C. [10 ]
Folb, P. [11 ]
Hassan, R. [8 ]
Hossain, M. A. [8 ]
Kimbute, O. [12 ]
Kitua, A. [12 ]
Krishna, S. [13 ]
Makasi, C. [12 ]
Mensah, N. [14 ]
Mrango, Z. [12 ]
Olliaro, P. [1 ]
Peto, R. [15 ]
Peto, T. J. [16 ]
Rahman, M. R. [17 ]
Ribeiro, I. [18 ]
Samad, R. [8 ]
White, N. J. [19 ]
机构
[1] WHO, UNICEF UNDP World Bank, Special Programme Res & Training Trop Dis, CH-1211 Geneva 27, Switzerland
[2] Govt Peoples Repub Bangladesh, Minist Hlth & Family Welf, Dhaka, Bangladesh
[3] Ghana Hlth Serv, Hlth Res Unit, Accra, Ghana
[4] WHO, Global Malaria Programme, CH-1211 Geneva, Switzerland
[5] Kwame Nkrumah Univ Sci & Technol, Sch Med Sci, Kumasi, Ghana
[6] MRC, HIV Clin Trials Ctr, London, England
[7] WHO, Representat Off, Dar Es Salaam, Tanzania
[8] Chittagong Med Coll, Malaria Res Grp, Chittagong, Bangladesh
[9] Univ Ghana, Sch Publ Hlth, Accra, Ghana
[10] Dodowa Hlth Res Ctr, Dodowa, Ghana
[11] MRC, Cape Town, South Africa
[12] Natl Inst Med Res, Dar Es Salaam, Tanzania
[13] Univ London St Georges Hosp, Sch Med, London SW17 0RE, England
[14] Navrongo Hlth Res Ctr, Navrongo, Ghana
[15] Univ Oxford, Clin Trial Serv Unit, Oxford, England
[16] MRC Labs, Banjul, Gambia
[17] Begum Khaleda Zia Med Coll, Dhaka, Bangladesh
[18] DNDi, Rio De Janeiro, Brazil
[19] Mahidol Univ, Fac Trop Med, Bangkok 10700, Thailand
基金
英国医学研究理事会; 英国惠康基金;
关键词
SEVERE FALCIPARUM-MALARIA; ANTIMALARIAL-DRUG RESISTANCE; CEREBRAL MALARIA; CHILDREN; EFFICACY; QUININE;
D O I
10.1016/S0140-6736(08)61734-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Most malaria deaths occur in rural areas. Rapid progression from illness to death can be interrupted by prompt, effective medication. Antimalarial treatment cannot rescue terminally ill patients but could be effective if given earlier. If patients who cannot be treated orally are several hours from facilities for injections, rectal artesunate can be given before referral and acts rapidly on parasites. We investigated whether this intervention reduced mortality and permanent disability. Methods In Bangladesh, Ghana, and Tanzania, patients with suspected severe malaria who could not be treated orally were allocated randomly to a single artesunate (n=8954) or placebo (n=8872) suppository by taking the next numbered box, then referred to clinics at which injections could be given. Those with antimalarial injections or negative blood smears before randomisation were excluded, leaving 12068 patients (6072 artesunate, 5996 placebo) for analysis. Primary endpoints were mortality, assessed 7-30 days later, and permanent disability, reassessed periodically. All investigators were masked to group assignment. Analysis was by intention to treat. This study is registered in all three countries, numbers ISRCTN83979018, 46343627, and 76987662. Results Mortality was 154 of 6072 artesunate versus 177 of 5996 placebo (2.5% vs 3 . 0%, p=0 . 1). Two versus 13 (0 . 03% vs 0 . 22%, p=0 . 0020) were permanently disabled; total dead or disabled: 156 versus 190 (2 . 6% vs 3.2%, p=0 . 0484). There was no reduction in early mortality (56 vs 51 deaths within 6 h; median 2 h). In patients reaching clinic within 6 h (median 3 h), pre-referral artesunate had no significant effect on death after 6 h or permanent disability (71/4450 [1.6%] vs 82/4426 [1.9%], risk ratio 0.86 [95% Cl 0.63-1.18], p=0.35). In patients still not in clinic after more than 6 h, however, half were still not there after more than 15 h, and pre-referral rectal artesurate significantly reduced death or permanent disability (29/1566 [1.9%] vs 57/1519 [3.8%], risk ratio 0.49 [95% CI 0.32-0.77], p=0 . 0013). Interpretation If patients with severe malaria cannot be treated orally and access to injections will take several hours, a single inexpensive artesunate suppository at the time of referral substantially reduces the risk of death or permanent disability. Funding UNICEF/UNDP/World Bank Special Programme for Research and Training in Tropical Diseases (WHO/TDR); WHO Global Malaria Programme (WHO/GMP); Sall Family Poundation; the European Union (QLRT-2000-01430); the UK Medical Research Council; USAID; Irish Aid; the Karolinska Institute; and the University of Oxford Clinical Trial Service Unit (CTSU).
引用
收藏
页码:557 / 566
页数:10
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