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Efficacy of Single-Dose Primaquine With Artemisinin Combination Therapy on Plasmodium falciparum Gametocytes and Transmission: An Individual Patient Meta-Analysis.
Stepniewska, Kasia; Humphreys, Georgina S; Gonçalves, Bronner P; Craig, Elaine; Gosling, Roly; Guerin, Philippe J; Price, Ric N; Barnes, Karen I; Raman, Jaishree; Smit, Menno R; D'Alessandro, Umberto; Stone, Will J R; Bjorkman, Anders; Samuels, Aaron M; Arroyo-Arroyo, Maria I; Bastiaens, Guido J H; Brown, Joelle M; Dicko, Alassane; El-Sayed, Badria B; Elzaki, Salah-Eldin G; Eziefula, Alice C; Kariuki, Simon; Kwambai, Titus K; Maestre, Amanda E; Martensson, Andreas; Mosha, Dominic; Mwaiswelo, Richard O; Ngasala, Billy E; Okebe, Joseph; Roh, Michelle E; Sawa, Patrick; Tiono, Alfred B; Chen, Ingrid; Drakeley, Chris J; Bousema, Teun.
Afiliación
  • Stepniewska K; WorldWide Antimalarial Resistance Network, Oxford, United Kingdom.
  • Humphreys GS; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
  • Gonçalves BP; Infectious Diseases Data Observatory, Oxford, United Kingdom.
  • Craig E; WorldWide Antimalarial Resistance Network, Oxford, United Kingdom.
  • Gosling R; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
  • Guerin PJ; Infectious Diseases Data Observatory, Oxford, United Kingdom.
  • Price RN; Green Templeton College, University of Oxford, Oxford, United Kingdom.
  • Barnes KI; Department of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Raman J; WorldWide Antimalarial Resistance Network, Oxford, United Kingdom.
  • Smit MR; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
  • D'Alessandro U; Infectious Diseases Data Observatory, Oxford, United Kingdom.
  • Stone WJR; Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California, USA.
  • Bjorkman A; Global Health Group, Malaria Elimination Initiative, University of California, San Francisco, California, USA.
  • Samuels AM; WorldWide Antimalarial Resistance Network, Oxford, United Kingdom.
  • Arroyo-Arroyo MI; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
  • Bastiaens GJH; Infectious Diseases Data Observatory, Oxford, United Kingdom.
  • Brown JM; WorldWide Antimalarial Resistance Network, Oxford, United Kingdom.
  • Dicko A; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
  • El-Sayed BB; Global and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Norther Territory, Australia.
  • Elzaki SG; Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
  • Eziefula AC; WorldWide Antimalarial Resistance Network, Oxford, United Kingdom.
  • Kariuki S; University of Cape Town/Medical Research Council Collaborating Centre for Optimising Antimalarial Therapy, University of Cape Town, Cape Town, South Africa.
  • Kwambai TK; Division of Clinical Pharmacology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
  • Maestre AE; University of Cape Town/Medical Research Council Collaborating Centre for Optimising Antimalarial Therapy, University of Cape Town, Cape Town, South Africa.
  • Martensson A; Centre for Emerging Zoonotic and Parasitic Diseases, National Institute for Communicable Diseases, National Health Laboratory Services, Johannesburg, South Africa.
  • Mosha D; Wits Research Institute for Malaria, Faculty of Health Sciences, University of Witwatersrand, Johannesburg, South Africa.
  • Mwaiswelo RO; Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
  • Ngasala BE; Medical Research Council Unit The Gambia, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Okebe J; Department of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Roh ME; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Sawa P; Department of Microbiology Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
  • Tiono AB; Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • Chen I; Centers for Disease Control and Prevention, Kisumu, Kenya.
  • Drakeley CJ; Grupo Salud y Comunidad, Facultad de Medicina, Universidad de Antioquia, Medellin, Colombia.
  • Bousema T; Department of Medical Microbiology, Radboud University Medical Center, Nijmegen, the Netherlands.
J Infect Dis ; 225(7): 1215-1226, 2022 04 01.
Article en En | MEDLINE | ID: mdl-32778875
ABSTRACT

BACKGROUND:

Since the World Health Organization recommended single low-dose (0.25 mg/kg) primaquine (PQ) in combination with artemisinin-based combination therapies (ACTs) in areas of low transmission or artemisinin-resistant Plasmodium falciparum, several single-site studies have been conducted to assess efficacy.

METHODS:

An individual patient meta-analysis to assess gametocytocidal and transmission-blocking efficacy of PQ in combination with different ACTs was conducted. Random effects logistic regression was used to quantify PQ effect on (1) gametocyte carriage in the first 2 weeks post treatment; and (2) the probability of infecting at least 1 mosquito or of a mosquito becoming infected.

RESULTS:

In 2574 participants from 14 studies, PQ reduced PCR-determined gametocyte carriage on days 7 and 14, most apparently in patients presenting with gametocytemia on day 0 (odds ratio [OR], 0.22; 95% confidence interval [CI], .17-.28 and OR, 0.12; 95% CI, .08-.16, respectively). Rate of decline in gametocyte carriage was faster when PQ was combined with artemether-lumefantrine (AL) compared to dihydroartemisinin-piperaquine (DP) (P = .010 for day 7). Addition of 0.25 mg/kg PQ was associated with near complete prevention of transmission to mosquitoes.

CONCLUSIONS:

Transmission blocking is achieved with 0.25 mg/kg PQ. Gametocyte persistence and infectivity are lower when PQ is combined with AL compared to DP.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Malaria Falciparum / Artemisininas / Antimaláricos Tipo de estudio: Systematic_reviews Límite: Animals / Humans Idioma: En Revista: J Infect Dis Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Malaria Falciparum / Artemisininas / Antimaláricos Tipo de estudio: Systematic_reviews Límite: Animals / Humans Idioma: En Revista: J Infect Dis Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido