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In vivo efficacy and safety of artemetherlumefantrine and amodiaquine­artesunate for uncomplicated Plasmodium falciparum malaria in Mozambique, 2018
Nhama, abel; Nhamússua, lídia; Macete, eusébio; Bassat, quique; Salvador, crizolgo; Enosse, sónia; Candrinho, baltazar; Carvalho, eva; Nhacolo, arsénio; Chidimatembue, arlindo; Saifodine, abuchahama; Zulliger, rose; Lucchi, naomi; Svigel, samaly s; Moriarty, leah f; Halsey, eric s; Mayor, alfredo; Aide, pedro.
Afiliação
  • Nhama, abel; s.af
  • Nhamússua, lídia; s.af
  • Macete, eusébio; s.af
  • Bassat, quique; s.af
  • Salvador, crizolgo; s.af
  • Enosse, sónia; s.af
  • Candrinho, baltazar; s.af
  • Carvalho, eva; s.af
  • Nhacolo, arsénio; s.af
  • Chidimatembue, arlindo; s.af
  • Saifodine, abuchahama; s.af
  • Zulliger, rose; s.af
  • Lucchi, naomi; s.af
  • Svigel, samaly s; s.af
  • Moriarty, leah f; s.af
  • Halsey, eric s; s.af
  • Mayor, alfredo; s.af
  • Aide, pedro; s.af
Malar. j. (Online) ; 20(390): 1-12, 2021. Mapas, Tab.
Article em En | AIM, RSDM | ID: biblio-1352541
Biblioteca responsável: MZ1.1
ABSTRACT

Background:

Artemisinin-based combination therapy (ACT) has been the recommended first-line treatment for uncomplicated malaria in Mozambique since 2006, with artemether­lumefantrine (AL) and amodiaquine­artesunate (AS­AQ) as the first choice. To assess efficacy of currently used ACT, an in vivo therapeutic efficacy study was conducted.

Methods:

The study was conducted in four sentinel sites Montepuez, Moatize, Mopeia and Massinga. Patients between 6 and 59 months old with uncomplicated Plasmodium falciparum malaria (2000­200,000 parasites/µl) were enrolled between February and September of 2018, assigned to either an AL or AS­AQ treatment arm, and monitored for 28 days. A Bayesian algorithm was applied to differentiate recrudescence from new infection using genotyping data of seven neutral microsatellites. Uncorrected and PCR-corrected efficacy results at day 28 were calculated.

Results:

Totals of 368 and 273 patients were enrolled in the AL and AS­AQ arms, respectively. Of these, 9.5% (35/368) and 5.1% (14/273) were lost to follow-up in the AL and AS­AQ arms, respectively. There were 48 and 3 recurrent malaria infections (late clinical and late parasitological failures) in the AL and AS­AQ arms, respectively. The day 28 uncorrected efficacy was 85.6% (95% confidence interval (CI) 81.3­89.2%) for AL and 98.8% (95% CI 96.7­99.8%) for AS­AQ, whereas day 28 PCR-corrected efficacy was 97.9% (95% CI 95.6­99.2%) for AL and 99.6% (95% CI 97.9­100%) for AS­AQ. Molecular testing confirmed that 87.4% (42/48) and 33.3% (1/3) of participants with a recurrent malaria infection in the AL and AS­AQ arms were new infections; an expected finding in a high malaria transmission area. Adverse events were documented in less than 2% of participants for both drugs.

Conclusion:

Both AL and AS­AQ have therapeutic efficacies well above the 90% WHO recommended threshold and remain well-tolerated in Mozambique. Routine monitoring of therapeutic efficacy should continue to ensure the treatments remain efficacious.
Assuntos

Texto completo: 1 Base de dados: AIM / RSDM Assunto principal: Malária Falciparum / Malária Tipo de estudo: Diagnostic_studies Limite: Child, preschool País como assunto: Africa Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: AIM / RSDM Assunto principal: Malária Falciparum / Malária Tipo de estudo: Diagnostic_studies Limite: Child, preschool País como assunto: Africa Idioma: En Ano de publicação: 2021 Tipo de documento: Article