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一项在加拿大开展的前瞻性多中心研究,旨在评估基于口腔液的HIV自我检测的性能和可用性。

A prospective multi-site study to evaluate the performance and usability of an oral fluid-based HIV self-test in Canada.

作者信息

Galli Richard A, Maraj Darshanand, McBain Kristin, Lo Hog Tian Jason M, McFarland Abbey, Tharao Wangari, Nkala Nontobeko P, Chan Arlene, da Silva Mark, Thomas Rejean, Vassal Anne-Fanny, Lepage Martin, Ireland Laurie, Payne Mike, Starr Jared, Fraser Chris, Selfridge Marion, Loutfy Mona, Halpenny Roberta, Jeyarajah Nirubini, Tran Vanessa, Mazzulli Tony, Rourke Sean B

机构信息

MAP Centre for Urban Health Solutions, Unity Health Toronto, Toronto, ON, Canada.

University of Toronto, Toronto, ON, Canada.

出版信息

BMC Public Health. 2025 Jan 11;25(1):125. doi: 10.1186/s12889-024-21228-8.

Abstract

BACKGROUND

Blood and oral fluid-based HIV self-tests are important for reaching the undiagnosed living with HIV. The study objectives were to evaluate the oral fluid-based OraQuick® HIV Self-Test (HIV-ST) performance in comparison to laboratory reference testing; determine if laypersons can correctly perform the HIV-ST; document if intended users can successfully interpret pre-made contrived positive, negative, and invalid results; and document if intended users can understand the key messages in the product labeling.

METHODS

This prospective study enrolled consenting adult intended users of HIV self-testing from six community health centres in four Canadian provinces between June 2022 and January 2024. Positive and negative agreement was determined by comparing the results of the HIV self-tests with the results of the laboratory-based "gold standard" Abbott Alinity HIV Antigen/Antibody Combo test. Descriptive statistics were used to summarize usability self-test procedure steps.

RESULTS

Overall, 951 participants were recruited and consented with 911 available for all analyses. With respect to sociodemographics: 84% of participants were between 18-45 years of age, 73% had at least a college education, 48% were Cis-male, 45% were employed; and 26% identified as White, 23% as African, Caribbean or Black, 5% as Indigenous [First Nations, Métis or Inuit], 33% as Asian, and 6% as LatinX. Primary efficacy analysis on the 911 who completed HIV-ST revealed a single confirmed positive participant and a negative percent agreement of 100% (880/880, 95% CI: 99.9-100%) with the comparator method. For usability determination, the average success rate for "critical" steps for completing the test was 94.1%. Approximately 97% of participants found the instructions easy to follow and 98% of participants reported they would use the test again. Of the 465 participants who interpreted the strong positive, weak positive, negative, and invalid pre-made contrived results, the average of correct interpretations ranged from 59-97% CONCLUSIONS: A licensed oral fluid-based HIV self-test in Canada can present an accurate, easy-to-use, and less invasive alternative to blood-based HIV testing. The addition of an oral-fluid self-test along with the current licensed blood-based HIV self-test could help reach the undiagnosed with HIV in Canada and positively impact HIV testing rates overall by offering individuals a choice of self-testing devices.

摘要

背景

基于血液和口腔液的HIV自我检测对于发现未被诊断的HIV感染者至关重要。本研究的目的是评估基于口腔液的奥芮可HIV自我检测(HIV-ST)与实验室参考检测相比的性能;确定外行人是否能够正确进行HIV-ST检测;记录目标用户是否能够成功解读预先制作的人为设定的阳性、阴性和无效结果;以及记录目标用户是否能够理解产品标签中的关键信息。

方法

这项前瞻性研究于2022年6月至2024年1月期间,从加拿大四个省份的六个社区卫生中心招募了同意参与HIV自我检测的成年目标用户。通过将HIV自我检测结果与基于实验室的“金标准”雅培Alinity HIV抗原/抗体联合检测结果进行比较,确定阳性和阴性一致性。使用描述性统计来总结可用性自我检测程序步骤。

结果

总体而言,共招募了951名参与者并获得其同意,其中911名可用于所有分析。在社会人口统计学方面:84%的参与者年龄在18至45岁之间,73%至少拥有大学学历,48%为顺性别男性,45%有工作;26%为白人,23%为非洲、加勒比或黑人,5%为原住民[第一民族、梅蒂斯或因纽特人],33%为亚洲人,6%为拉丁裔。对完成HIV-ST检测的911名参与者进行的主要疗效分析显示,有一名确诊阳性参与者,与对照方法的阴性百分比一致性为100%(880/880,95%置信区间:99.9-100%)。对于可用性测定,完成检测的“关键”步骤的平均成功率为94.1%。约97%的参与者认为说明易于遵循,98%的参与者表示他们会再次使用该检测。在465名解读了预先制作的强阳性、弱阳性、阴性和无效人为设定结果的参与者中,正确解读的平均比例在59%-97%之间。结论:加拿大一种获得许可的基于口腔液的HIV自我检测可以提供一种准确、易用且侵入性较小的替代血液HIV检测的方法。除了目前获得许可的基于血液的HIV自我检测外,增加一种基于口腔液的自我检测可以帮助发现加拿大未被诊断的HIV感染者,并通过为个人提供自我检测设备的选择,对总体HIV检测率产生积极影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8444/11724549/8cb37ac1e27a/12889_2024_21228_Fig1_HTML.jpg

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