Efficacy of artesunate-amodiaquine, dihydroartemisinin-piperaquine and artemether-lumefantrine for the treatment of uncomplicated Plasmodium falciparum malaria in Maradi, Niger

被引:23
作者
Grandesso, Francesco [1 ]
Guindo, Ousmane [2 ]
Messe, Lynda Woi [2 ]
Makarimi, Rockyath [2 ]
Traore, Aliou [3 ]
Dama, Souleymane [3 ]
Laminou, Ibrahim Maman [4 ]
Rigal, Jean [5 ]
de Smet, Martin [6 ]
Oukem-Boyer, Odile Ouwe Missi [4 ]
Doumbo, Ogobara K. [3 ]
Djimde, Abdoulaye [3 ]
Etard, Jean-Francois [1 ,7 ]
机构
[1] Epicentre, 8 Rue St Sabin, F-75011 Paris, France
[2] Epictr Res Ctr, Maradi, Niger
[3] Univ Sci Tech & Technol Bamako, Fac Pharm, Malaria Res & Training Ctr, Dept Epidemiol Parasit Dis, POB 1805 Point G, Bamako, Mali
[4] Ctr Rech Med & Sanitaire, Parasitol Unit, Niamey, Niger
[5] Med Sans Frontieres, 8 Rue St Sabin, Paris, France
[6] Med Sans Frontieres, Rue Arbre Benit 46, B-1050 Brussels, Belgium
[7] Univ Montpellier, INSERM U1175, IRD UMI 233, Unit TransVIHMI, F-34000 Montpellier, France
关键词
Malaria; Efficacy; Antimalarial; Artemisinin; Resistance; Parasite clearance; Niger; ARTEMISININ RESISTANCE; COMBINATION; PHARMACOKINETICS;
D O I
10.1186/s12936-018-2200-1
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Malaria endemic countries need to assess efficacy of anti-malarial treatments on a regular basis. Moreover, resistance to artemisinin that is established across mainland South-East Asia represents today a major threat to global health. Monitoring the efficacy of artemisinin-based combination therapies is of paramount importance to detect as early as possible the emergence of resistance in African countries that toll the highest burden of malaria morbidity and mortality. Methods: A WHO standard protocol was used to assess efficacy of the combinations artesunate-amodiaquine (AS-AQ Winthrop (R)), dihydroartemisinin-piperaquine (DHA-PPQ, Eurartesim (R)) and artemether-lumefantrine (AM-LM, Coartem (R)) taken under supervision and respecting pharmaceutical recommendations. The study enrolled for each treatment arm 212 children aged 6-59 months living in Maradi (Niger) and suffering with uncomplicated falciparum malaria. The Kaplan-Meier 42-day PCR-adjusted cure rate was the primary outcome. A standardized parasite clearance estimator was used to assess delayed parasite clearance as surrogate maker of suspected artemisinin resistance. Results: No early treatment failures were found in any of the study treatment arms. The day-42 PCR-adjusted cure rate estimates were 99.5, 98.4 and 99.0% in the AS-AQ, DHA-PPQ and AM-LM arms, respectively. The reinfection rate (expressed also as Kaplan-Meier estimates) was higher in the AM-LM arm (32.4%) than in the AS-AQ (13.8%) and the DHA-PPQ arm (24.9%). The parasite clearance rate constant was 0.27, 0.26 and 0.25 per hour for AS-AQ, DHA-PPQ and AM-LM, respectively. Conclusions: All the three treatments evaluated largely meet WHO criteria (at least 95% efficacy). AS-AQ and AL-LM may continue to be used and DHA-PPQ may be also recommended as first-line treatment for uncomplicated falciparum malaria in Maradi. The parasite clearance rate were consistent with reference values indicating no suspected artemisinin resistance. Nevertheless, the monitoring of anti-malarial drug efficacy should continue.
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