The Gametocytocidal Efficacy of Different Single Doses of Primaquine with Dihydroartemisinin-piperaquine in Asymptomatic Parasite Carriers in The Gambia: A Randomized Controlled Trial

被引:26
|
作者
Okebe, Joseph [1 ]
Bousema, Teun [2 ,3 ]
Affara, Muna [1 ]
Di Tanna, Gian Luca [4 ]
Dabira, Edgard [1 ]
Gaye, Abdoulaye [1 ]
Sanya-Isijola, Frank [1 ]
Badji, Henry [1 ]
Correa, Simon [1 ]
Nwakanma, Davis [1 ]
Van Geertruyden, Jean-Pierre [5 ]
Drakeley, Chris [2 ]
D'Alessandro, Umberto [1 ,6 ,7 ]
机构
[1] MRC Unit, Dis Control & Eliminat Theme, Fajara, Gambia
[2] London Sch Hyg & Trop Med, Fac Infect & Trop Dis, Dept Immunol & Infect, London, England
[3] Radboud Univ Nijmegen, Med Ctr, Dept Med Microbiol, Nijmegen, Netherlands
[4] Queen Mary Univ London, Ctr Primary Care & Publ Hlth, Pragmat Clin Trials Unit, London, England
[5] Univ Antwerp, Fac Med & Hlth Sci, Epidemiol Global Hlth Inst, Antwerp, Belgium
[6] London Sch Hyg & Trop Med, Fac Infect & Trop Dis, Dept Dis Control, London, England
[7] Inst Trop Med, Dept Publ Hlth, Antwerp, Belgium
来源
EBIOMEDICINE | 2016年 / 13卷
基金
英国医学研究理事会;
关键词
Asymptomatic infection; Malaria; Primaquine; Plasmodium falciparum; Infectivity; Gametocyte carriage; Efficacy; Randomized trial; PLASMODIUM-FALCIPARUM GAMETOCYTES; DOUBLE-BLIND; MALARIA TRANSMISSION; CARRIAGE; CHILDREN; RISK; CLEARANCE; RATIONALE; INFECTION; HEMOLYSIS;
D O I
10.1016/j.ebiom.2016.10.032
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Asymptomatic low-density gametocyte carriers represent the majority of malaria-infected individuals. However, the impact of recommended treatment with single low dose of primaquine and an artemisinin-based combination therapy to reduce transmission in this group is unknown. Methods: This was a four-arm, open label, randomized controlled trial comparing the effect of dihydroartemisinin-piperaquine (DHAP) alone or combined with single dose of primaquine (PQ) at 0.20 mg/kg, 0.40 mg/kg, or 0.75 mg/kg on Plasmodium falciparum gametocytaemia, infectiousness to mosquitoes and hemoglobin change in asymptomatic, malaria-infected, glucose-6-phosphate dehydrogenase (G6PD) normal individuals. Randomization was done using a computer-generated sequence of uneven block sizes with codes concealed in sequentially numbered opaque envelopes. The primary endpoint was the prevalence of P. falciparum gametocytemia at day 7 of follow-up determined by quantitative nucleic acid sequence based assay and analysis was by intention to treat. The trial has been concluded (registration number: NCT01838902; https://clinicaltrials.gov/ct2/show/NCT01838902). Results: A total of 694 asymptomatic, malaria-infected individuals were enrolled. Gametocyte prevalence at day 7 was 37.0% (54/146; 95% CI 29.2-45.4), 19.0% (27/142; 95% CI 12.9-26.4), 17.2% (25/145; 95% CI 11.0-23.5) and 10.6% (15/141; 95% CI 6.1-16.9) in the DHAP alone, 0.20 mg/kg, 0.40 mg/kg, and 0.75 mg/kg PQ arms, respectively. The main adverse events reported include headache (130/471, 27.6%), cough (73/471, 15.5%), history of fever (61/471, 13.0%) and abdominal pain (57/471, 12.1%). There were five serious adverse events however, none was related to the interventions. Interpretation: A single course of PQ significantly reduces gametocyte carriage in malaria-infected asymptomatic, G6PD-normal individuals without increasing the risk of clinical anemia. The limited number of successful mosquito infections suggests that post-treatment transmission potential in this asymptomatic population is low. (C) 2016 The Authors. Published by Elsevier B.V.
引用
收藏
页码:348 / 355
页数:8
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