The effect of chloroquine dose and primaquine on Plasmodium vivax recurrence: a WorldWide Antimalarial Resistance Network systematic review and individual patient pooled meta-analysis

Background: Chloroquine remains the mainstay of treatment for Plasmodium vivax malaria despite increasing reports of treatment failure. We did a systematic review and meta-analysis to investigate the effect of chloroquine dose and the addition of primaquine on the risk of recurrent vivax malaria acr...

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Autores:
Zuluaga Idarraga, Lina Marcela
Commons, Robert J.
Simpson, Julie A
Thriemer, Kamala
Humphreys, Georgina S.
Abreha, Tesfay
Alemu, Sisay G.
Añez, Arletta
Anstey, Nicholas M.
Awab, Ghulam R
Baird, J. Kevin
Barber, Bridget E.
Borghini-Fuhrer, Isabelle
Chu, Cindy S.
D’Alessandro, Umberto
Dahal, Prabin
Daher, André
de Vries, Peter J.
Erhart, Annette
Gomes, Margarete S. M.
Gonzalez Ceron, Lilia
Grigg, Matthew J.
Heidari, Aliehsan
Hwang, Jimee
Kager, Piet A.
Ketema, Tsige
Khan, Wasif A.
Lacerda, Marcus V. G.
Leslie, Toby
Ley, Benedikt
Lidia, Kartini
Monteiro, Wuelton M.
Nosten, Francois
Pereira, Dhelio B.
Phan, Giao T.
Phyo, Aung P.
Rowland, Mark
Saravu, Kavitha
Sibley, Carol H.
Siqueira, André M.
Stepniewska, Kasia
Sutanto, Inge
Taylor, Walter R. J.
Thwaites, Guy
Tran, Binh Q.
Tran, Hien T.
Valecha, Neena
Vieira, José Luiz F.
Wangchuk, Sonam
William, Timothy
Woodrow, Charles J.
Guerin, Philippe J.
White, Nicholas J.
Price, Ric N.
Tipo de recurso:
Review article
Fecha de publicación:
2018
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/48361
Acceso en línea:
https://hdl.handle.net/10495/48361
Palabra clave:
Antimaláricos
Antimalarials
Cloroquina
Chloroquine
Primaquina
Primaquine
Resistencia a Medicamentos
Drug Resistance
Quimioterapia Combinada
Drug Therapy, Combination
Malaria Vivax
Malaria, Vivax
Plasmodium vivax
Recurrencia
Recurrence
https://id.nlm.nih.gov/mesh/D000962
https://id.nlm.nih.gov/mesh/D002738
https://id.nlm.nih.gov/mesh/D011319
https://id.nlm.nih.gov/mesh/D004351
https://id.nlm.nih.gov/mesh/D004359
https://id.nlm.nih.gov/mesh/D016780
https://id.nlm.nih.gov/mesh/D010966
https://id.nlm.nih.gov/mesh/D012008
ODS 3: Salud y bienestar. Garantizar una vida sana y promover el bienestar de todos a todas las edades
Rights
openAccess
License
http://creativecommons.org/licenses/by/4.0/
Description
Summary:Background: Chloroquine remains the mainstay of treatment for Plasmodium vivax malaria despite increasing reports of treatment failure. We did a systematic review and meta-analysis to investigate the effect of chloroquine dose and the addition of primaquine on the risk of recurrent vivax malaria across different settings. Methods: A systematic review done in MEDLINE, Web of Science, Embase, and Cochrane Database of Systematic Reviews identified P vivax clinical trials published between Jan 1, 2000, and March 22, 2017. Principal investigators were invited to share individual patient data, which were pooled using standardised methods. Cox regression analyses with random effects for study site were used to investigate the roles of chloroquine dose and primaquine use on rate of recurrence between day 7 and day 42 (primary outcome). The review protocol is registered in PROSPERO, number CRD42016053310. Findings: Of 134 identified chloroquine studies, 37 studies (from 17 countries) and 5240 patients were included. 2990 patients were treated with chloroquine alone, of whom 1041 (34·8%) received a dose below the target 25 mg/kg. The risk of recurrence was 32·4% (95% CI 29·8–35·1) by day 42. After controlling for confounders, a 5 mg/kg higher chloroquine dose reduced the rate of recurrence overall (adjusted hazard ratio [AHR] 0·82, 95% CI 0·69–0·97; p=0·021) and in children younger than 5 years (0·59, 0·41–0·86; p=0·0058). Adding primaquine reduced the risk of recurrence to 4·9% (95% CI 3·1–7·7) by day 42, which is lower than with chloroquine alone (AHR 0·10, 0·05–0·17; p <0·0001). Interpretation: Chloroquine is commonly under-dosed in the treatment of vivax malaria. Increasing the recommended dose to 30 mg/kg in children younger than 5 years could reduce substantially the risk of early recurrence when primaquine is not given. Radical cure with primaquine was highly effective in preventing early recurrence and may also improve blood schizontocidal efficacy against chloroquine-resistant P vivax.