<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>19(1)</volume><submitter>Marasini B</submitter><funding>Government of Nepal, Ministry of Health and population, Department of Health Services, Epidemiology and Disease Control Division.</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Glucose-6-phosphate dehydrogenase (G6PD) deficiency is currently a threat to malaria elimination due to risk of primaquine-induced haemolysis in G6PD deficient individuals. The World Health Organization (WHO) recommends G6PD screening before providing primaquine as a radical treatment against vivax malaria. However, evidence regarding the prevalence and causing mutations of G6PD deficiency in Nepal is scarce.&lt;h4>Methods&lt;/h4>A cross-sectional, population-based, prevalence study was carried out from May to October 2016 in 12 malaria-endemic districts of Nepal. The screening survey included 4067 participants whose G6PD status was determined by G6PD Care Start™ rapid diagnostic test and genotyping.&lt;h4>Results&lt;/h4>The prevalence of G6PD deficiency at the national level was 3.</pubmed_abstract><journal>Malaria journal</journal><pagination>287</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7425560</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>G6PD deficiency in malaria endemic areas of Nepal.</pubmed_title><pmcid>PMC7425560</pmcid><pubmed_authors>Koirala D</pubmed_authors><pubmed_authors>Iama S</pubmed_authors><pubmed_authors>Khanal P</pubmed_authors><pubmed_authors>Ghimire P</pubmed_authors><pubmed_authors>Lal BK</pubmed_authors><pubmed_authors>Neupane S</pubmed_authors><pubmed_authors>Penpitchaporn P</pubmed_authors><pubmed_authors>Acharya S</pubmed_authors><pubmed_authors>Gornsawun G</pubmed_authors><pubmed_authors>Jha SN</pubmed_authors><pubmed_authors>Magar RG</pubmed_authors><pubmed_authors>Awasthi KR</pubmed_authors><pubmed_authors>Marasini B</pubmed_authors><pubmed_authors>Bhandari S</pubmed_authors><pubmed_authors>Bajracharya B</pubmed_authors><pubmed_authors>Chaudhary A</pubmed_authors><pubmed_authors>Koirala M</pubmed_authors><pubmed_authors>Mahato RK</pubmed_authors><pubmed_authors>Bhattarai RK</pubmed_authors><pubmed_authors>Bancone G</pubmed_authors><pubmed_authors>Acharya BP</pubmed_authors><pubmed_authors>Thapa S</pubmed_authors></additional><is_claimable>false</is_claimable><name>G6PD deficiency in malaria endemic areas of Nepal.</name><description>&lt;h4>Background&lt;/h4>Glucose-6-phosphate dehydrogenase (G6PD) deficiency is currently a threat to malaria elimination due to risk of primaquine-induced haemolysis in G6PD deficient individuals. The World Health Organization (WHO) recommends G6PD screening before providing primaquine as a radical treatment against vivax malaria. However, evidence regarding the prevalence and causing mutations of G6PD deficiency in Nepal is scarce.&lt;h4>Methods&lt;/h4>A cross-sectional, population-based, prevalence study was carried out from May to October 2016 in 12 malaria-endemic districts of Nepal. The screening survey included 4067 participants whose G6PD status was determined by G6PD Care Start™ rapid diagnostic test and genotyping.&lt;h4>Results&lt;/h4>The prevalence of G6PD deficiency at the national level was 3.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Aug</publication><modification>2026-07-15T23:19:28.19Z</modification><creation>2025-04-07T11:42:46.662Z</creation></dates><accession>S-EPMC7425560</accession><cross_references><pubmed>32787970</pubmed><doi>10.1186/s12936-020-03359-6</doi></cross_references></HashMap>