Evidence map›Paper›PMID 30184203›Full record

ArticleInternational health2019

Addressing the gender-knowledge gap in glucose-6-phosphate dehydrogenase deficiency: challenges and opportunities.

Gonzalo J Domingo, Nicole Advani, Ari W Satyagraha, Carol H Sibley, Elizabeth Rowley, Michael Kalnoky, Jessica Cohen, Michael Parker, Maureen Kelley

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in International health, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05361486 (Health Care Provider Use of Plasmodium Vivax Radical Cure), which is not on this map. Cited by 51 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 3 pooled it
9.4field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05361486 completednot on this mapstarted 2023, after this paper: background citation

Health Care Provider Use of Plasmodium Vivax Radical Cure (RC) With Tafenoquine or Primaquine After Semi-quantitative G6PD Testing: A Feasibility Study in Peru

TypeobservationalSponsorMedicines for Malaria VentureRan2023 to 2024Enrolled187ConditionsMalaria, VivaxArmsTafenoquine (TQ)
3 · Its place in the literature

Who cites it

51 citing papers in PubMed, 3 syntheses or guidelines pooled it, 79 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Gonzalo J DomingoPATH, Seattle, WA, USA.
Nicole AdvaniPATH, Seattle, WA, USA.
Ari W SatyagrahaEijkman Institute for Molecular Biology, Jakarta, Indonesia.
Carol H SibleyWorldWide Antimalarial Resistance Network, University of Washington, Seattle, WA, USA.
Elizabeth RowleyPATH, Seattle, WA, USA.
Michael KalnokyPATH, Seattle, WA, USA.
Jessica CohenPATH, Seattle, WA, USA.
Michael ParkerThe Ethox Centre and Wellcome Centre for Ethics and Humanities, Nuffield Department of Population Health, University of Oxford, UK.
Maureen KelleyThe Ethox Centre and Wellcome Centre for Ethics and Humanities, Nuffield Department of Population Health, University of Oxford, UK.
Program for Appropriate Technology in Health · USUniversity of Oxford · GBEijkman Institute for Molecular Biology · IDUniversity of Washington · US

Funding

Medical Research Council MC_PC_16025Wellcome Trust 096527Wellcome Trust 200344Wellcome Trust 200344/Z/15/Z
6 · The paper itself

Abstract

Glucose-6-phosphate dehyrdgoenase (G6PD) deficiency is a common X-linked genetic trait, with an associated enzyme phenotype, whereby males are either G6PD deficient or normal, but females exhibit a broader range of G6PD deficiencies, ranging from severe deficiency to normal. Heterozygous females typically have intermediate G6PD activity. G6PD deficiency has implications for the safe treatment for Plasmodium vivax malaria. Individuals with this deficiency are at greater risk of serious adverse events following treatment with the only curative class of anti-malarials, 8-aminoquinolines, such as primaquine. Quantitative diagnostic tests for G6PD deficiency are complex and require sophisticated laboratories. The commonly used qualitative tests, do not discriminate intermediate G6PD activities. This has resulted in poor understanding of the epidemiology of G6PD activity in females and its corresponding treatment ramifications. New simple-to-use quantitative tests, and a momentum to eliminate malaria, create an opportunity to address this knowledge gap. While this will require additional resources for clinical studies, adequate operational research, and appropriate pharmacovigilance, the health benefits from this investment go beyond the immediate intervention for which the G6PD status is first diagnosed.

Indexed as

Glucosephosphate Dehydrogenase DeficiencyHealth Knowledge, Attitudes, PracticeAfricaAminoquinolinesAntimalarialsFemaleHumansMalaria, VivaxMalePrimaquineRisk FactorsSex Factors8-aminoquinolineAminoquinolinesAntimalarialsPrimaquine

Identifiers

PMID30184203
PMCPMC6314154
OpenAlexW2891104345

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.