<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Commons RJ</submitter><funding>Capability Systems Centre</funding><funding>Centers for Disease Control and Prevention</funding><funding>Conselho Nacional de Desenvolvimento Científico e Tecnológico</funding><funding>National Health and Medical Research Council</funding><funding>Bill and Melinda Gates Foundation</funding><funding>Wellcome Trust</funding><pagination>172-183</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7615564</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(2)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Primaquine is used to eliminate Plasmodium vivax hypnozoites, but its optimal dosing regimen remains unclear. We undertook a systematic review and individual patient data meta-analysis to investigate the efficacy and tolerability of different primaquine dosing regimens to prevent P vivax recurrence.&lt;h4>Methods&lt;/h4>For this systematic review and individual patient data meta-analysis, we searched MEDLINE, Web of Science, Embase, and Cochrane Central for prospective clinical studies of uncomplicated P vivax from endemic countries published between Jan 1, 2000, and June 8, 2023. We included studies if they had active follow-up of at least 28 days, and if they included a treatment group with daily primaquine given over multiple days, where primaquine was commenced within 7 da</pubmed_abstract><journal>The Lancet. Infectious diseases</journal><pubmed_title>Effect of primaquine dose on the risk of recurrence in patients with uncomplicated Plasmodium vivax: a systematic review and individual patient data meta-analysis.</pubmed_title><pmcid>PMC7615564</pmcid><funding_grant_id>1194702</funding_grant_id><funding_grant_id>093956/Z/10/Z</funding_grant_id><funding_grant_id>200909</funding_grant_id><funding_grant_id>223253/Z/21/Z</funding_grant_id><funding_grant_id>093956/Z/10/C</funding_grant_id><pubmed_authors>Green JA</pubmed_authors><pubmed_authors>Chau NH</pubmed_authors><pubmed_authors>Rijal KR</pubmed_authors><pubmed_authors>Lidia K</pubmed_authors><pubmed_authors>Karunajeewa H</pubmed_authors><pubmed_authors>von Seidlein L</pubmed_authors><pubmed_authors>Adhikari B</pubmed_authors><pubmed_authors>Price RN</pubmed_authors><pubmed_authors>Naadim MN</pubmed_authors><pubmed_authors>Taylor WRJ</pubmed_authors><pubmed_authors>Boyd SC</pubmed_authors><pubmed_authors>Ghimire P</pubmed_authors><pubmed_authors>Ladeia-Andrade S</pubmed_authors><pubmed_authors>Baird JK</pubmed_authors><pubmed_authors>Degaga TS</pubmed_authors><pubmed_authors>Nosten F</pubmed_authors><pubmed_authors>Mueller I</pubmed_authors><pubmed_authors>Zuluaga-Idarraga LM</pubmed_authors><pubmed_authors>Abreha T</pubmed_authors><pubmed_authors>Anstey NM</pubmed_authors><pubmed_authors>Longley RJ</pubmed_authors><pubmed_authors>Vieira JLF</pubmed_authors><pubmed_authors>Awab GR</pubmed_authors><pubmed_authors>Watson JA</pubmed_authors><pubmed_authors>Chu CS</pubmed_authors><pubmed_authors>Gonzalez-Ceron L</pubmed_authors><pubmed_authors>Guerin PJ</pubmed_authors><pubmed_authors>Woyessa A</pubmed_authors><pubmed_authors>Thanh PV</pubmed_authors><pubmed_authors>Erhart A</pubmed_authors><pubmed_authors>Assefa A</pubmed_authors><pubmed_authors>WorldWide Antimalarial Resistance Network (WWARN) Vivax Primaquine Dosing Efficacy, Tolerability and Safety Study Group</pubmed_authors><pubmed_authors>Simpson JA</pubmed_authors><pubmed_authors>Barber BE</pubmed_authors><pubmed_authors>Grigg MJ</pubmed_authors><pubmed_authors>Llanos-Cuentas A</pubmed_authors><pubmed_authors>Koh GC</pubmed_authors><pubmed_authors>Pereira DB</pubmed_authors><pubmed_authors>Ferreira MU</pubmed_authors><pubmed_authors>Dondorp AM</pubmed_authors><pubmed_authors>Cui L</pubmed_authors><pubmed_authors>Commons RJ</pubmed_authors><pubmed_authors>Thriemer K</pubmed_authors><pubmed_authors>William T</pubmed_authors><pubmed_authors>Hwang J</pubmed_authors><pubmed_authors>Lacerda MVG</pubmed_authors><pubmed_authors>Daher A</pubmed_authors><pubmed_authors>Pasaribu AP</pubmed_authors><pubmed_authors>Price DJ</pubmed_authors><pubmed_authors>Day NP</pubmed_authors><pubmed_authors>Rajasekhar M</pubmed_authors><pubmed_authors>Woodrow CJ</pubmed_authors><pubmed_authors>Sutanto I</pubmed_authors><pubmed_authors>Mekuria AH</pubmed_authors><pubmed_authors>Pukrittayakamee S</pubmed_authors><pubmed_authors>Nelwan EJ</pubmed_authors><pubmed_authors>Edler P</pubmed_authors><pubmed_authors>Sattabongkot J</pubmed_authors><pubmed_authors>Stepniewska K</pubmed_authors><pubmed_authors>White NJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effect of primaquine dose on the risk of recurrence in patients with uncomplicated Plasmodium vivax: a systematic review and individual patient data meta-analysis.</name><description>&lt;h4>Background&lt;/h4>Primaquine is used to eliminate Plasmodium vivax hypnozoites, but its optimal dosing regimen remains unclear. We undertook a systematic review and individual patient data meta-analysis to investigate the efficacy and tolerability of different primaquine dosing regimens to prevent P vivax recurrence.&lt;h4>Methods&lt;/h4>For this systematic review and individual patient data meta-analysis, we searched MEDLINE, Web of Science, Embase, and Cochrane Central for prospective clinical studies of uncomplicated P vivax from endemic countries published between Jan 1, 2000, and June 8, 2023. We included studies if they had active follow-up of at least 28 days, and if they included a treatment group with daily primaquine given over multiple days, where primaquine was commenced within 7 da</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2026-07-15T04:25:29.348Z</modification><creation>2026-07-01T03:06:57.099Z</creation></dates><accession>S-EPMC7615564</accession><cross_references><pubmed>37748496</pubmed><doi>10.1016/S1473-3099(23)00430-9</doi></cross_references></HashMap>