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
MAP Centre for Urban Health Solutions, Unity Health Toronto, Toronto, ON, Canada.
University of Toronto, Toronto, ON, Canada.
BMC Public Health. 2025 Jan 11;25(1):125. doi: 10.1186/s12889-024-21228-8.
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.
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.
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.
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。
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。
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。