Evaluation of the CareStart™ glucose-6-phosphate dehydrogenase (G6PD) rapid diagnostic test in the field settings and assessment of perceived risk from primaquine at the community level in Cambodia

Background Primaquine is an approved radical cure treatment for Plasmodium vivax malaria but treatment can result in life-threatening hemolysis if given to a glucose-6-phosphate dehydrogenase deficient (G6PDd) patient. There is a need for reliable point-of-care G6PD diagnostic tests. Objectives To evaluate the performance of the CareStart™ rapid diagnostic test (RDT) in the hands of healthcare workers (HCWs) and village malaria workers (VMWs) in field settings, and to better understand user perceptions about the risks and benefits of PQ treatment guided by RDT results. Methods This study enrolled 105 HCWs and VMWs, herein referred to as trainees, who tested 1,543 healthy adult male volunteers from 84 villages in Cambodia. The trainees were instructed on G6PD screening, primaquine case management, and completed pre and post-training questionnaires. Each trainee tested up to 16 volunteers in the field under observation by the study staff. Results Out of 1,542 evaluable G6PD volunteers, 251 (16.28%) had quantitative enzymatic activity less than 30% of an adjusted male median (8.30 U/g Hb). There was no significant difference in test sensitivity in detecting G6PDd between trainees (97.21%), expert study staff in the field (98.01%), and in a laboratory setting (95.62%) (p = 0.229); however, test specificity was different for trainees (96.62%), expert study staff in the field (98.14%), and experts in the laboratory (98.99%) (p < 0.001). Negative predictive values were not statistically different for trainees, expert staff, and laboratory testing: 99.44%, 99.61%, and 99.15%, respectively. Knowledge scores increased significantly post-training, with 98.7% willing to prescribe primaquine for P.vivax malaria, an improvement from 40.6% pre-training (p < 0.001). Conclusion This study demonstrated ability of medical staff with different background to accurately use CareStart™ RDT to identify G6PDd in male patients, which may enable safer prescribing of primaquine; however, pharmacovigilance is required to address possible G6PDd misclassifications.

[1]  P. Newton,et al.  Comparison of glucose-6 phosphate dehydrogenase status by fluorescent spot test and rapid diagnostic test in Lao PDR and Cambodia , 2018, Malaria Journal.

[2]  R. Price,et al.  Methods for the field evaluation of quantitative G6PD diagnostics: a review , 2017, Malaria Journal.

[3]  S. Meshnick,et al.  Single dose primaquine to reduce gametocyte carriage and Plasmodium falciparum transmission in Cambodia: An open-label randomized trial , 2017, PloS one.

[4]  H. Win,et al.  Haemolysis in G6PD Heterozygous Females Treated with Primaquine for Plasmodium vivax Malaria: A Nested Cohort in a Trial of Radical Curative Regimens , 2017, PLoS medicine.

[5]  S. Siv,et al.  Plasmodium vivax Malaria in Cambodia , 2016, The American journal of tropical medicine and hygiene.

[6]  L. Amoah,et al.  Prevalence of G6PD deficiency and Plasmodium falciparum parasites in asymptomatic school children living in southern Ghana , 2016, Malaria Journal.

[7]  F. Nosten,et al.  Validation of G6PD Point-of-Care Tests among Healthy Volunteers in Yangon, Myanmar , 2016, PloS one.

[8]  A. Dondorp,et al.  Establishing research priorities for malaria elimination in the context of the emergency response to artemisinin resistance framework-the Cambodian approach , 2016, Malaria Journal.

[9]  L. Canier,et al.  Field Trial Evaluation of the Performances of Point-of-Care Tests for Screening G6PD Deficiency in Cambodia , 2014, PloS one.

[10]  M. Kahn,et al.  Comparison of Quantitative and Qualitative Tests for Glucose-6-Phosphate Dehydrogenase Deficiency , 2014, The American journal of tropical medicine and hygiene.

[11]  Sinuon Muth,et al.  G6PD deficiency in Plasmodium falciparum and Plasmodium vivax malaria-infected Cambodian patients , 2013, Malaria Journal.

[12]  P. Harnyuttanakorn,et al.  PREVALENCE OF G 6 PD DEFICIENCY IN MALARIA ENDEMIC AREA : CASE STUDY IN BONGTI SUB-DISTRICT , SAI YOK DISTRICT , KANCHANABURI PROVINCE , THAILAND , 2013 .

[13]  G. Shanks Control and elimination of Plasmodium vivax. , 2012, Advances in parasitology.

[14]  J. Baird,et al.  Performance of the CareStart™ G6PD Deficiency Screening Test, a Point-of-Care Diagnostic for Primaquine Therapy Screening , 2011, PloS one.

[15]  Organización Mundial de la Salud Guidelines for the treatment of malaria , 2010 .