Two fixed-dose artemisinin combinations for drug-resistant falciparum and vivax malaria in Papua, Indonesia: an open-label randomised comparison

被引:212
作者
Ratcliff, A.
Siswantoro, H.
Kenangalem, E.
Maristela, R.
Wuwung, R. M.
Laihad, F.
Ebsworth, E. P.
Anstey, N. M.
Tjitra, E.
Price, R. N.
机构
[1] Menzies Sch Hlth Res, Int Hlth Programme, Darwin, NT 0811, Australia
[2] Charles Darwin Univ, Darwin, NT, Australia
[3] Natl Inst Hlth Res & Dev, Minist Hlth, Jakarta, Indonesia
[4] NIHRD, MSHR, Malaria Res Programme, Timika, Indonesia
[5] Dist Minist Hlth, Timika, Papua, Indonesia
[6] PT Freeport, Publ Hlth & Malaria Control Dept, Tembagapura, Papua, Indonesia
[7] Int SOS, Tembagapura, Papua, Indonesia
[8] Directorate Gen Ctr Dis Control & Environm Hlth, Minist Hlth, Jakarta, Indonesia
[9] John Radcliffe Hosp, Nuffield Dept Clin Med, Ctr Vaccinol & Trop Med, Oxford OX3 9DU, England
基金
英国惠康基金;
关键词
D O I
10.1016/S0140-6736(07)60160-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The burden of Plasmodium vivax infections has been underappreciated, especially in southeast Asia where chloroquine resistant strains have emerged. Our aim was to compare the safety and efficacy of dihydroartemisinin-piperaquine with that of artemether-lumefantrine in patients with uncomplicated malaria caused by multidrug-resistant P falciparum and P vivax. Methods 774 patients in southern Papua, Indonesia, with slide-confirmed malaria were randomly assigned to receive either artemether-lumefantrine or dihydroartemisinin-piperaquine and followed up for at least 42 days. The primary endpoint was the overall cumulative risk of parasitological failure at day 42 with a modified intention-to-treat analysis. This trial is registered with ClinicalTrials.gov, trial number 00157833. Findings Of the 754 evaluable patients enrolled, 466 had infections with P falciparum, 175 with P vivax, and 113 with a mixture of both species. The overall risk of failure at day 42 was 43% (95% CI 38-48) for artemether-lumefantrine and 19% (14-23) for dihydroartemisinin-piperaquine (hazard ratio=3.0, 95% CI 2.2-4. 1, p<0.0001). After correcting for reinfections, the risk of recrudescence of P falciparum was 4.4% (2.6-6.2) with no difference between regimens. Recurrence of vivax occurred in 38% (33-44) of patients given artemether-lumefantrine compared with 10% (6.9-14.0) given dihydroartemisinin-piperaquine (p<0.0001). At the end of the study, patients receiving dihydroartemisinin-piperaquine were 2.0 times (1.2-3.6) less likely to be anaemic and 6.6 times (2.8-16) less likely to carry vivax gametocytes than were those given artemether-lumefantrine. Interpretation Both dihydroartemisinin-piperaquine and artemether-lumefantrine were safe and effective for the treatment of multidrug-resistant uncomplicated malaria. However, dihydroartemisinin-piperaquine provided greater post-treatment prophylaxis than did artemether-lumefantrine, reducing P falciparum reinfections and P vivax recurrences, the clinical public-health importance of which should not be ignored.
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收藏
页码:757 / 765
页数:9
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