Journal Article

Efficacy and safety of artemether-lumefantrine for the treatment of uncomplicated falciparum malaria in mainland Tanzania, 2018

Kamugisha, Erasmus, Chacky, Frank, Bishanga, Dunstan, Kitojo, Chonge, Bushukatale, Samwel, Mandara, Celine I., Ahmed, Maimuna, Greer, George, Nyinondi, Ssanyu S., Mahende, Muhidin K., Njau, Ritha, Warsame, Marian, Mandike, Renata, Reaves, Erik, Chiduo, Mercy G., Molteni, Fabrizio, Muro, Florida, Kavishe, Reginald A., Ishengoma, Deus S., Kabula, Bilali, Ngasala, Billy, Chadewa, Jasmine, Mohamed, Ally, Francis, Filbert, Makene, Twilumba, Mmbando, Bruno P.

2024

Overview

Background The use of artemisinin-based combination therapy (ACT) is recommended by the World Health Organization for the treatment of uncomplicated falciparum malaria. Artemether-lumefantrine (AL) is the most widely adopted first-line ACT for uncomplicated malaria in sub-Saharan Africa (SSA), including mainland Tanzania, where it was introduced in December 2006. The WHO recommends regular assessment to monitor the efficacy of the first-line treatment specifically considering that artemisinin partial resistance was reported in Greater Mekong sub-region and has been confirmed in East Africa (Rwanda and Uganda). The main aim of this study was to assess the efficacy and safety of AL for the treatment of uncomplicated falciparum malaria in mainland Tanzania. Methods A single-arm prospective anti-malarial drug efficacy trial was conducted in Kibaha, Mlimba, Mkuzi, and Ujiji (in Pwani, Morogoro, Tanga, and Kigoma regions, respectively) in 2018. The sample size of 88 patients per site was determined based on WHO 2009 standard protocol. Participants were febrile patients (documented axillary temperature ≥ 37.5 °C and/or history of fever during the past 24 h) aged 6 months to 10 years . Patients received a 6-dose AL regimen by weight twice a day for 3 days. Clinical and parasitological parameters were monitored during 28 days of follow-up to evaluate the drug efficacy and safety. Results A total of 653 children were screened for uncomplicated malaria and 349 (53.7%) were enrolled between April and August 2018. Of the enrolled children, 345 (98.9%) completed the 28 days of follow-up or attained the treatment outcomes. There were no early treatment failures, but recurrent infections were higher in Mkuzi (35.2%) and Ujiji (23%). By Kaplan–Meier analysis of polymerase chain reaction (PCR) uncorrected adequate clinical and parasitological response (ACPR) ranged from 63.4% in Mkuzi to 85.9% in Mlimba, while PCR-corrected ACPR on day 28 varied from 97.6% in Ujiji to 100% in Mlimba. The drug was well tolerated; the commonly reported adverse events were cough, runny nose, and abdominal pain. No serious adverse event was reported. Conclusion This study showed that AL had adequate efficacy and safety for the treatment of uncomplicated falciparum malaria. The high number of recurrent infections were mainly due to new infections, indicating the necessity of utilizing alternative artemisinin-based combinations, such as artesunate amodiaquine, which provide a significantly longer post-treatment prophylactic effect.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Adverse events / Amodiaquine / Amodiaquine - therapeutic use / Analysis / Antimalarials / Antimalarials - adverse effects / Artemether / Artemether - therapeutic use / Artemether lumefantrine / Artemether, Lumefantrine Drug Combination - adverse effects / Artemisinin / Artemisinins - adverse effects / Artesunate / Biomedical and Life Sciences / Biomedicine / Blood / Child / Children / Clinical trials / Combination therapy / Control / Cough / Dosage and administration / Drug Combinations / Drug dosages / Drug efficacy / Drug resistance / Drug therapy / Drugs / Entomology / Ethanolamines - adverse effects / Fever - drug therapy / Folkhälsovetenskap, global hälsa och socialmedicin / Human diseases / Humans / Identification and classification / Infectious Diseases / Leukocytes / Malaria / Malaria - drug therapy / Malaria, Falciparum - drug therapy / Malaria, Falciparum - prevention & control / Microbiology / Microscopy / Nucleotide sequence / Parasites / Parasitology / Patients / Pharmacovigilance / Plasmodium falciparum / Polymerase chain reaction / Prevention / Public Health / Public Health, Global Health and Social Medicine / Pyrimethamine / Reinfection - chemically induced / Reinfection - drug therapy / Risk factors / Safety / Tanzania / Therapeutic efficacy / Tropical Medicine / Vector-borne diseases