Hardie Diana R, Newman Howard, Reid Joanna, Hsiao Nei-Yuan, van Zyl Gert, Hans Lucia, Odayar Jasantha, Korsman Stephen
Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
National Health Laboratory Service, Cape Town, South Africa.
Afr J Lab Med. 2024 May 28;13(1):2364. doi: 10.4102/ajlm.v13i1.2364. eCollection 2024.
Understanding factors that impact HIV viral load (VL) accuracy in resource-limited settings is key to quality improvement.
We evaluated whether testing delay and specimen storage between 25 °C and 30 °C before testing affected results.
Between November 2019 and June 2023, 249 individuals on antiretroviral therapy, or with newly diagnosed HIV, were recruited from clinics in Cape Town and Gqeberha, South Africa, and three plasma preparation tubes were collected. One tube was tested within 24 h, while the others were stored uncentrifuged at ambient temperatures before testing. Centrifugation and testing of matched samples were performed on Day 4 and Day 7 after collection.
Time delay and ambient storage had minimal impact in specimens with a Day 1 VL of > 100 copies/mL. When grouped by Day 1 VL range, 96% - 100% of specimens at Day 4 and 93% - 100% at Day 7 had VLs within 0.5 log copies/mL of the first result. The greatest variability at Days 4 and 7 was observed when the Day 1 VL was < 100 copies/mL. However, there was no trend of increasing difference over time. Of Day 1 specimens with undetectable VL, or VL < 50 copies/mL, 80% had concordant results at Day 4 and 78% at Day 7.
These results show that VL is stable in plasma preparation tubes for 7 days when stored at room temperature. There is significant variability in specimens with low VL, but variability is not affected by testing delay.
Ideal HIV VL testing conditions are frequently unachievable in resource-limited settings. Data are needed on whether this impacts on the validity of test results. Our results provide reassurance that storage at ambient temperature for up to 7 days before testing does not substantially affect the VL result.
了解在资源有限的环境中影响艾滋病毒病毒载量(VL)准确性的因素是质量改进的关键。
我们评估了检测延迟以及检测前在25°C至30°C之间的标本储存是否会影响结果。
在2019年11月至2023年6月期间,从南非开普敦和伊丽莎白港的诊所招募了249名接受抗逆转录病毒治疗或新诊断为艾滋病毒的个体,并采集了三支血浆制备管。一支试管在24小时内进行检测,而其他试管在检测前未离心并在环境温度下储存。采集后第4天和第7天对匹配样本进行离心和检测。
对于第1天病毒载量>100拷贝/毫升的标本,时间延迟和环境储存的影响最小。按第1天病毒载量范围分组时,第4天96% - 100%的标本和第7天93% - 100%的标本的病毒载量在第一个结果的0.5对数拷贝/毫升范围内。当第1天病毒载量<100拷贝/毫升时,在第4天和第7天观察到最大变异性。然而,差异没有随时间增加的趋势。对于第1天病毒载量不可检测或病毒载量<50拷贝/毫升的标本,80%在第4天结果一致,78%在第7天结果一致。
这些结果表明,血浆制备管中的病毒载量在室温下储存7天是稳定的。低病毒载量的标本存在显著变异性,但变异性不受检测延迟的影响。
在资源有限的环境中,理想的艾滋病毒病毒载量检测条件往往无法实现。需要有关这是否会影响检测结果有效性的数据。我们的结果让人放心,检测前在环境温度下储存长达7天不会实质性影响病毒载量结果。