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Monitoring of efficacy, tolerability and safety of artemether-lumefantrine and artesunate-amodiaquine for the treatment of uncomplicated Plasmodium falciparum malaria in Lambaréné, Gabon: an open-label clinical trial

Authors :
Michael Ramharter
Bayode Romeo Adegbite
Mirabeau Mbong-Ngwese
Albert Lalremruata
Peter G. Kremsner
Fabrice Lotola-Mougueni
Fridia A. Obone Atome
Abdou R. Safiou
Selidji T Agnandji
Andrea Kreidenweiss
Benjamin Mordmüller
Yabo Josiane Honkpehedji
Ghyslain Mombo-Ngoma
Jean Claude Dejon-Agobé
Thirumalaisamy P. Velavan
Frejus J. Zinsou
Jean Ronald Edoa
J. F. J. Kun
Ayola A. Adegnika
Bertrand Lell
Erik Koehne
Graduate School
APH - Aging & Later Life
APH - Global Health
AII - Infectious diseases
Infectious diseases
Source :
Malaria journal, 18(1):424. BioMed Central, Malaria Journal, Vol 18, Iss 1, Pp 1-9 (2019), Malaria Journal
Publication Year :
2019

Abstract

Background Malaria remains a major public health problem, affecting mainly low-and middle-income countries. The management of this parasitic disease is challenged by ever increasing drug resistance. This study, investigated the therapeutic efficacy, tolerability and safety of artemether–lumefantrine (AL) and artesunate–amodiaquine (AS–AQ), used as first-line drugs to treat uncomplicated malaria in Lambaréné, Gabon. Methods A non-randomized clinical trial was conducted between October 2017 and March 2018 to assess safety, clinical and parasitological efficacy of fixed-doses of AL and AS–AQ administered to treat uncomplicated Plasmodium falciparum malaria in children aged from 6 months to 12 years. After 50 children were treated with AL, another 50 children received ASAQ. The 2009 World Health Organization protocol for monitoring of the efficacy of anti‑malarial drugs was followed. Molecular markers msp1 and msp2 were used to differentiate recrudescence and reinfection. For the investigation of artemisinin resistant markers, gene mutations in Pfk13 were screened. Results Per-protocol analysis on day 28 showed a PCR corrected cure rate of 97% (95% CI 86–100) and 95% (95% CI 84–99) for AL and AS–AQ, respectively. The most frequent adverse event in both groups was asthenia. No mutations in the kelch-13 gene associated with artemisinin resistance were identified. All participants had completed microscopic parasite clearance by day 3 post-treatment. Conclusion This study showed that AL and AS–AQ remain efficacious, well-tolerated, and are safe to treat uncomplicated malaria in children from Lambaréné. However, a regular monitoring of efficacy and a study of molecular markers of drug resistance to artemisinin in field isolates is essential. Trial registration ANZCTR, ACTRN12616001600437. Registered 18 November, http://www.anzctr.org.au/TrialSearch.aspx?searchTxt=ACTRN12616001600437p&isBasic=True

Details

Language :
English
ISSN :
12616001 and 14752875
Database :
OpenAIRE
Journal :
Malaria journal, 18(1):424. BioMed Central, Malaria Journal, Vol 18, Iss 1, Pp 1-9 (2019), Malaria Journal
Accession number :
edsair.doi.dedup.....aba32c4a5378296d23d2ed211b49a504