<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Taylor WRJ</submitter><funding>World Health Organization</funding><funding>Wellcome Trust</funding><pagination>1750-1760</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6804333</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>220(11)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Hemoglobin (Hb) data are limited in Southeast Asian glucose-6-phosphate dehydrogenase (G6PD) deficient (G6PD-) patients treated weekly with the World Health Organization-recommended primaquine regimen (ie, 0.75 mg/kg/week for 8 weeks [PQ 0.75]).&lt;h4>Methods&lt;/h4>We treated Cambodians who had acute Plasmodium vivax infection with PQ0.75 and a 3-day course of dihydroartemisinin/piperaquine and determined the Hb level, reticulocyte count, G6PD genotype, and Hb type.&lt;h4>Results&lt;/h4>Seventy-five patients (male sex, 63) aged 5-63 years (median, 24 years) were enrolled. Eighteen were G6PD deficient (including 17 with G6PD Viangchan) and 57 were not G6PD deficient; 26 had HbE (of whom 25 were heterozygous), and 6 had ?-/?-thalassemia. Mean Hb concentrations at baseline (ie, day 0) were similar between G6PD deficient and G6PD normal patients (12.9 g/dL [range, 9?16.3 g/dL] and 13.26 g/dL [range, 9.6?16 g/dL], respectively; P = .46). G6PD deficiency (P = &lt;.001), higher Hb concentration at baseline (P = &lt;.001), higher parasitemia level at baseline (P = .02), and thalassemia (P = .027) influenced the initial decrease in Hb level, calculated as the nadir level minus the baseline level (range, -5.8-0 g/dL; mean, -1.88 g/dL). By day 14, the mean difference from the day 7 level (calculated as the day 14 level minus the day 7 level) was 0.03 g/dL (range, -0.25?0.32 g/dL). Reticulocyte counts decreased from days 1 to 3, peaking on day 7 (in the G6PD normal group) and day 14 (in the G6PD deficient group); reticulocytemia at baseline (P = .001), G6PD deficiency (P = &lt;.001), and female sex (P = .034) correlated with higher counts. One symptomatic, G6PD-deficient, anemic male patient was transfused on day 4.&lt;h4>Conclusions&lt;/h4>The first PQ0.75 exposure was associated with the greatest decrease in Hb level and 1 blood transfusion, followed by clinically insignificant decreases in Hb levels. PQ0.75 requires monitoring during the week after treatment. Safer antirelapse regimens are needed in Southeast Asia.&lt;h4>Clinical trials registration&lt;/h4>ACTRN12613000003774.</pubmed_abstract><journal>The Journal of infectious diseases</journal><pubmed_title>Hemolytic Dynamics of Weekly Primaquine Antirelapse Therapy Among Cambodians With Acute Plasmodium vivax Malaria With or Without Glucose-6-Phosphate Dehydrogenase Deficiency.</pubmed_title><pmcid>PMC6804333</pmcid><funding_grant_id>001</funding_grant_id><funding_grant_id>B9RJIXO</funding_grant_id><pubmed_authors>Muth S</pubmed_authors><pubmed_authors>Taylor WRJ</pubmed_authors><pubmed_authors>Souy P</pubmed_authors><pubmed_authors>Vanna C</pubmed_authors><pubmed_authors>Kerleguer A</pubmed_authors><pubmed_authors>Sothea K</pubmed_authors><pubmed_authors>Baird JK</pubmed_authors><pubmed_authors>Kim S</pubmed_authors><pubmed_authors>Char CM</pubmed_authors><pubmed_authors>Khieu V</pubmed_authors><pubmed_authors>Pantaleo A</pubmed_authors><pubmed_authors>Menard D</pubmed_authors><pubmed_authors>Topps N</pubmed_authors><pubmed_authors>Mukaka M</pubmed_authors><pubmed_authors>Tor P</pubmed_authors><pubmed_authors>Christophel E</pubmed_authors><pubmed_authors>Ly P</pubmed_authors><pubmed_authors>Kheng S</pubmed_authors><pubmed_authors>Kosal K</pubmed_authors><pubmed_authors>Bjorge S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Hemolytic Dynamics of Weekly Primaquine Antirelapse Therapy Among Cambodians With Acute Plasmodium vivax Malaria With or Without Glucose-6-Phosphate Dehydrogenase Deficiency.</name><description>&lt;h4>Background&lt;/h4>Hemoglobin (Hb) data are limited in Southeast Asian glucose-6-phosphate dehydrogenase (G6PD) deficient (G6PD-) patients treated weekly with the World Health Organization-recommended primaquine regimen (ie, 0.75 mg/kg/week for 8 weeks [PQ 0.75]).&lt;h4>Methods&lt;/h4>We treated Cambodians who had acute Plasmodium vivax infection with PQ0.75 and a 3-day course of dihydroartemisinin/piperaquine and determined the Hb level, reticulocyte count, G6PD genotype, and Hb type.&lt;h4>Results&lt;/h4>Seventy-five patients (male sex, 63) aged 5-63 years (median, 24 years) were enrolled. Eighteen were G6PD deficient (including 17 with G6PD Viangchan) and 57 were not G6PD deficient; 26 had HbE (of whom 25 were heterozygous), and 6 had ?-/?-thalassemia. Mean Hb concentrations at baseline (ie, day 0) were similar between G6PD deficient and G6PD normal patients (12.9 g/dL [range, 9?16.3 g/dL] and 13.26 g/dL [range, 9.6?16 g/dL], respectively; P = .46). G6PD deficiency (P = &lt;.001), higher Hb concentration at baseline (P = &lt;.001), higher parasitemia level at baseline (P = .02), and thalassemia (P = .027) influenced the initial decrease in Hb level, calculated as the nadir level minus the baseline level (range, -5.8-0 g/dL; mean, -1.88 g/dL). By day 14, the mean difference from the day 7 level (calculated as the day 14 level minus the day 7 level) was 0.03 g/dL (range, -0.25?0.32 g/dL). Reticulocyte counts decreased from days 1 to 3, peaking on day 7 (in the G6PD normal group) and day 14 (in the G6PD deficient group); reticulocytemia at baseline (P = .001), G6PD deficiency (P = &lt;.001), and female sex (P = .034) correlated with higher counts. One symptomatic, G6PD-deficient, anemic male patient was transfused on day 4.&lt;h4>Conclusions&lt;/h4>The first PQ0.75 exposure was associated with the greatest decrease in Hb level and 1 blood transfusion, followed by clinically insignificant decreases in Hb levels. PQ0.75 requires monitoring during the week after treatment. Safer antirelapse regimens are needed in Southeast Asia.&lt;h4>Clinical trials registration&lt;/h4>ACTRN12613000003774.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Oct</publication><modification>2021-02-21T00:35:34Z</modification><creation>2019-11-05T08:09:16Z</creation></dates><accession>S-EPMC6804333</accession><cross_references><pubmed>31549159</pubmed><doi>10.1093/infdis/jiz313</doi></cross_references></HashMap>