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

被引:4
作者
Cassidy-Seyoum, Sarah A. [1 ,2 ]
Chheng, Keoratha [3 ]
Chanpheakdey, Phal [3 ]
Meershoek, Agnes [2 ]
Hsiang, Michelle S. [4 ,5 ,6 ]
von Seidlein, Lorenz [3 ,7 ]
Tripura, Rupam [3 ,7 ]
Adhikari, Bipin [3 ,7 ]
Ley, Benedikt [1 ,8 ]
Price, Ric N. [1 ,3 ,7 ]
Lek, Dysoley [9 ,10 ]
Engel, Nora [2 ]
Thriemer, Kamala [1 ]
机构
[1] Charles Darwin Univ, Menzies Sch Hlth Res, Global & Trop Hlth Div, Darwin, Australia
[2] Maastricht Univ, Care & Publ Hlth Res Inst CAPHRI, Dept Hlth Eth & Soc, Maastricht, Netherlands
[3] Mahidol Univ, Fac Trop Med, Mahidol Oxford Res Unit, Bangkok, Thailand
[4] Univ Calif San Francisco, Inst Global Hlth Sci, Malaria Eliminat Initiat, San Francisco, CA USA
[5] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA USA
[6] Univ Calif San Francisco, Dept Pediat, Div Pediat Infect Dis, San Francisco, CA USA
[7] Univ Oxford, Ctr Trop Med & Global Hlth, Nuffield Dept Med, Oxford, England
[8] Charles Darwin Univ, Menzies Sch Hlth Res, Div Educ, Darwin, Australia
[9] Natl Ctr Parasitol Entomol & Malaria Control, Phnom Penh, Cambodia
[10] Natl Inst Publ Hlth, Sch Publ Hlth, Phnom Penh, Cambodia
来源
PLOS GLOBAL PUBLIC HEALTH | 2024年 / 4卷 / 07期
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
TAFENOQUINE; PRIMAQUINE; RELAPSE; MALARIA;
D O I
10.1371/journal.pgph.0003476
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
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.
引用
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页数:27
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