Implementation of Glucose-6-Phosphate Dehydrogenase (G6PD) testing for Plasmodium vivax case management, a mixed method study from Cambodia

Sarah A. Cassidy-Seyoum, Keoratha Chheng, Phal Chanpheakdey, Agnes Meershoek, Michelle S. Hsiang, Lorenz von Seidlein, Rupam Tripura, Bipin Adhikari, Benedikt Ley, Ric N. Price, Dysoley Lek, Nora Engel, Kamala Thriemer

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Plasmodium vivax remains a challenge for malaria elimination since it forms dormant liver stages (hypnozoites) that can reactivate after initial infection. 8-aminoquinolone drugs kill hypnozoites but can cause severe hemolysis in individuals with Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency. The STANDARD G6PD test (Biosensor) is a novel point-of-care diagnostic capable of identifying G6PD deficiency prior to treatment. In 2021, Cambodia implemented the Biosensor to facilitate radical cure treatment for vivax malaria. To assess the Biosensor’s implementation after its national rollout, a mixed-methods study was conducted in eight districts across three provinces in Cambodia. Interviews, focus group discussions, and observations explored stakeholders’ experiences with G6PD testing and factors influencing its implementation. Quantitative data illustrative of test implementation were gathered from routine surveillance forms and key proportions derived. Qualitative data were analyzed thematically. The main challenge to implementing G6PD testing was that only 49.2% (437/888) of eligible patients reached health centers for G6PD testing following malaria diagnosis by community health workers. Factors influencing this included road conditions and long distances to the health center, compounded by the cost of seeking further care and patients’ perceptions of vivax malaria and its treatment. 93.9% (790/841) of eligible vivax malaria patients who successfully completed referral (429/434) and directly presented to the health center (360/407) were G6PD tested. Key enabling factors included the test’s acceptability among health workers and their understanding of the rationale for testing. Only 36.5% (443/1213) of eligible vivax episodes appropriately received primaquine. 70.5% (165/234) of female patients and all children under 20 kilograms never received primaquine. Our findings suggest that access to radical cure requires robust infrastructure and income security, which would likely improve referral rates to health centers enabling access. Bringing treatment closer to patients, through community health workers and nuanced community engagement, would improve access to curative treatment of vivax malaria.
Original languageEnglish
Article numbere0003476
JournalPLOS Global Public Health
Volume4
Issue number7
DOIs
Publication statusPublished - 19 Jul 2024
Externally publishedYes

Funding

Funding: This research was supported by a grant from the Australian National Health and Medical Research Council (NHMRC) (1182950). SCS is funded through a Charles Darwin International PhD Scholarships (CDIPS), KT is a CSL Centenary Fellow, and RNP is supported by an NHMRC Investigator Grant (2008501).The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We are thankful to all study participants who shared their experiences and made this research possible. We also recognize the study team members who facilitated the logistics and implementation of the study. Essential to this study were also the primary translators who transcribed and translated the KIIs and FGDs from Khmer to English, including Phorn Nayelin. Finally, we acknowledge the support provided by CNM in facilitating the study and CNM\u2019s implementation partners, University Research Co (URC), Catholic Relief Service (CRS), and Clinton Health Access Initiative (CHAI), who supported data collection efforts.

FundersFunder number
University Research Co (URC), Catholic Relief Service
Catholic Relief Services
KIIs
CNM
Clinton Health Access Initiative
National Health and Medical Research Council1182950, 2008501

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