Abstract

BackgroundArtemether–lumefantrine (AL) is the recommended first-line artemisinin-based combination therapy (ACT) for the treatment of uncomplicated falciparum malaria in most of the malaria-endemic countries, including Tanzania. Recently, dihydroartemisinin–piperaquine (DP) has been recommended as the alternative anti-malarial to ensure effective case management in Tanzania. This study assessed the parasite clearance rate and efficacy of AL and DP among patients aged 6 months to 10 years with uncomplicated falciparum malaria in two sites with different malaria transmission intensity.MethodsThis was an open-label, randomized trial that was conducted at two sites of Muheza Designated District Hospital and Ujiji Health Centre in Tanga and Kigoma regions, respectively. Patients meeting inclusion criteria were enrolled, treated with either AL or DP and followed up for 28 (extended to 42) and 42 (63) days for AL and DP, respectively. Parasite clearance time was monitored in the first 72 h post treatment and the clearance rate constant and half-life were calculated using an established parasite clearance estimator. The primary outcome was parasitological cure on days 28 and 42 for AL and DP, respectively, while secondary outcome was extended parasitological cure on days 42 and 63 for AL and DP, respectively.ResultsOf the 509 children enrolled (192 at Muheza and 317 at Ujiji), there was no early treatment failure and PCR uncorrected cure rates on day 28 in the AL group were 77.2 and 71.2% at Muheza and Ujiji, respectively. In the DP arm, the PCR uncorrected cure rate on day 42 was 73.6% at Muheza and 72.5% at Ujiji. With extended follow-up (to day 42 for AL and 63 for DP) cure rates were lower at Ujiji compared to Muheza (AL: 60.2 and 46.1%, p = 0.063; DP: 57.6 and 40.3% in Muheza and Ujiji, respectively, p = 0.021). The PCR corrected cure rate ranged from 94.6 to 100% for all the treatment groups at both sites. Parasite clearance rate constant was similar in the two groups and at both sites (< 0.28/h); the slope half-life was < 3.0 h and all but only one patient cleared parasites by 72 h.ConclusionThese findings confirm high efficacy of the first- and the newly recommended alternative ACT for treatments for uncomplicated falciparum malaria in Tanzania. The high parasite clearance rate suggests absence of suspected artemisinin resistance, defined as delayed parasite clearance.Trial registration This trial is registered at ClinicalTrials.gov under registration number NCT02590627

Highlights

  • Artemether–lumefantrine (AL) is the recommended first-line artemisinin-based combination therapy (ACT) for the treatment of uncomplicated falciparum malaria in most of the malaria-endemic countries, including Tanzania

  • Recent studies have shown that artemisinin-based combination therapy (ACT) is still efficacious and safe for the treatment of uncomplicated falciparum malaria especially in Africa [1, 2], but emergence of resistant Plasmodium falciparum has been reported in Southeast Asian (SEA) countries [3,4,5] and might reverse the recent gains in malaria control, and jeopardize malaria elimination efforts

  • The findings of this study showed that both AL and DP are highly efficacious for the treatment of uncomplicated falciparum malaria in the study areas; with polymerase chain reaction (PCR) corrected adequate clinical and parasitological response (ACPR) of 97.4–100% on day 28 for AL and 97.0–99.1% on day 42 for DP

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Summary

Introduction

Artemether–lumefantrine (AL) is the recommended first-line artemisinin-based combination therapy (ACT) for the treatment of uncomplicated falciparum malaria in most of the malaria-endemic countries, including Tanzania. Dihydroartemisinin–piperaquine (DP) has been recommended as the alternative anti-malarial to ensure effective case management in Tanzania. Recent studies have shown that artemisinin-based combination therapy (ACT) is still efficacious and safe for the treatment of uncomplicated falciparum malaria especially in Africa [1, 2], but emergence of resistant Plasmodium falciparum has been reported in Southeast Asian (SEA) countries [3,4,5] and might reverse the recent gains in malaria control, and jeopardize malaria elimination efforts. DP was recommended in 2014 as an alternative drug for the treatment of uncomplicated falciparum malaria in Tanzania in order to improve case management [9]. Baseline data on the efficacy of DP is urgently needed to support future surveillance of its performance once it has been widely used in the country

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