Clinical performance validation of the STANDARD G6PD Test: A multi-country pooled analysis

Author:

Adissu Wondimagegn,Brito Marcelo,Garbin Eduardo,Macedo Marcela,Monteiro WueltonORCID,Mukherjee Sandip,Myburg JaneORCID,Alam Mohammad ShafiulORCID,Bancone GermanaORCID,Bansil Pooja,Pal Sampa,Sharma Abhijit,Zobrist Stephanie,Bryan Andrew,Chu Cindy S,Das SantasabujORCID,Domingo Gonzalo J,Hann Amanda,Kublin James,Lacerda Marcus VG,Layton Mark,Ley BenediktORCID,Murphy Sean C,Nosten FrancoisORCID,Pereira DhélioORCID,Price Ric N,Talukdar Arunansu,Yilma Daniel,Gerth-Guyette EmilyORCID

Abstract

AbstractIntroductionScreening for G6PD deficiency can inform disease management including malaria. Treatment with the antimalarial drugs primaquine and tafenoquine can be guided by point-of-care testing for G6PD deficiency.Methods and FindingsData from similar clinical studies evaluating the performance of the STANDARDG6PD Test (SD Biosensor, South Korea) conducted in Bangladesh, Brazil, Ethiopia, India, Thailand, the United Kingdom, and the United States were pooled. Test performance was assessed in a retrospective analysis on capillary and venous specimens. All study sites used spectrophotometry for reference G6PD testing, and either the HemoCue or complete blood count for reference hemoglobin measurement.The sensitivity of the STANDARDG6PD Test using the manufacturer thresholds for G6PD deficient and intermediate cases in capillary specimens from 4212 study participants was 100% (95% Confidence Interval (CI): 97.5%–100%) for G6PD deficient cases with <30% activity and 77% (95% CI 66.8%– 85.4%) for females with intermediate activity between 30%–70%. Specificity was 98.1% (95% CI 97.6%–98.5%) and 92.8% (95% CI 91.6%–93.9%) for G6PD deficient individuals and intermediate females, respectively. The majority (12/20) of G6PD intermediate females with false normal results had activity levels >60% on the reference assay. Negative predictive values for females with G6PD activity >60% was 99.6% (95% CI 99.1%–99.8%) on capillary specimens. Test sensitivity among 396P. vivaxmalaria cases was 100% (69.2%–100.0%) for both deficient and intermediate cases. In the study population, a high proportion of those classified as G6PD deficient or intermediate resulted from true normal cases. Despite this, the majority cases would receive the correct medication and no true G6PD deficient cases would be treated inappropriately.ConclusionsThe STANDARD G6PD Test enables safe access to drugs which are contraindicated for individuals with G6PD deficiency. Operational considerations will inform test uptake in specific settings.

Publisher

Cold Spring Harbor Laboratory

Reference47 articles.

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