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在柬埔寨的现场环境中评估 CareStart™葡萄糖-6-磷酸脱氢酶(G6PD)快速诊断检测,以及在社区层面评估来自 Primaquine 的感知风险。

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.

机构信息

Armed Forces Research Institute of Medical Sciences, Bangkok, Thailand.

The George Washington University, School of Nursing, Washington, DC, United States of America.

出版信息

PLoS One. 2020 Jan 31;15(1):e0228207. doi: 10.1371/journal.pone.0228207. eCollection 2020.

Abstract

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.

摘要

背景

伯氨喹啉是一种已批准的根治间日疟原虫疟疾的药物,但如果给葡萄糖-6-磷酸脱氢酶缺乏症(G6PDd)患者使用,可能会导致危及生命的溶血。因此,需要可靠的即时护理 G6PD 诊断检测方法。

目的

评估 CareStart™快速诊断检测(RDT)在医疗保健工作者(HCWs)和乡村疟疾工作者(VMWs)手中的性能,并更好地了解用户对基于 RDT 结果的伯氨喹啉治疗风险和益处的看法。

方法

本研究招募了 105 名 HCWs 和 VMWs(以下简称受训者),他们在柬埔寨的 84 个村庄对 1543 名健康成年男性志愿者进行了检测。受训者接受了 G6PD 筛查、伯氨喹啉病例管理方面的培训,并完成了培训前后的调查问卷。每位受训者在研究人员的观察下在现场最多测试了 16 名志愿者。

结果

在 1542 名可评估的 G6PD 志愿者中,有 251 名(16.28%)的定量酶活性低于调整后的男性中位数(8.30 U/g Hb)的 30%。受训者、现场专家研究人员(98.01%)和实验室检测(95.62%)在检测 G6PDd 方面的检测敏感性没有显著差异(p = 0.229);然而,受训者(96.62%)、现场专家研究人员(98.14%)和实验室专家(98.99%)的检测特异性不同(p < 0.001)。受训者、现场专家和实验室检测的阴性预测值无统计学差异:分别为 99.44%、99.61%和 99.15%。培训后知识评分显著提高,98.7%的人愿意为间日疟原虫疟疾开具伯氨喹啉处方,比培训前的 40.6%有所提高(p < 0.001)。

结论

本研究表明,不同背景的医务人员能够准确使用 CareStart™RDT 来识别男性患者的 G6PDd,这可能使伯氨喹啉的处方更安全;然而,需要进行药物警戒以解决可能的 G6PDd 误诊问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75f7/6994100/3d70ef116e16/pone.0228207.g001.jpg

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