The Kirby Institute, UNSW Sydney, NSW, Australia.
Hospital Sungai Buloh, Sungai Buloh, Malaysia.
J Acquir Immune Defic Syndr. 2022 Nov 1;91(3):290-295. doi: 10.1097/QAI.0000000000003067.
Linkage studies have reported high rates of previously unascertained mortality among people living with HIV (PLHIV) who have been lost to follow-up (LTFU). We assessed survival outcomes among PLHIV who were LTFU in Thailand and Malaysia, through linkages to a national death registry or HIV database.
Data linkages with the national death registry or national HIV database were conducted in 2020 on all PLHIV who met LTFU criteria while enrolled in care at participating HIV clinical sites. LTFU was defined as having no documented clinical contact in the previous year, excluding transfers and deaths. Survival time was analyzed using the Cox regression, stratified by site.
Data linkages were performed for 489 PLHIV who had been LTFU at sites in Malaysia (n = 2) and Thailand (n = 4). There were 151 (31%) deaths after being LTFU; the mortality rate was 4.89 per 100 person-years. Risk factors for mortality after being LTFU were older age [41-50 years: hazard ratio (HR) = 1.99, 95% confidence interval (CI): 1.08 to 3.68; and older than 50 years: HR = 4.93, 95% CI: 2.63 to 9.22; vs. age 30 years or younger]; receiving NRTI + PI (HR = 1.87, 95% CI: 1.22 to 2.85 vs. NRTI + NNRTI); positive hepatitis C antibody (HR = 2.25, 95% CI: 1.40 to 3.62); and having previous AIDS illness (HR = 1.45, 95% CI: 1.03 to 2.05). An improved survival was seen with a higher CD4 count (CD4 351-500 cells/µL: HR = 0.40, 95%CI: 0.21-0.76; and CD4 >500 cells/µL: HR = 0.43, 95%CI: 0.25-0.75; vs. CD4 ≤200 cells/µL).
Almost one-third of PLHIV who were LTFU in this cohort had died while out of care, emphasizing the importance of efforts to reengage PLHIV after they have been LTFU and ensure they have access to ongoing ART.
失访(LTFU)的 HIV 感染者(PLHIV)的既往未确定死亡率在连锁研究中报告率较高。我们通过与国家死亡登记处或 HIV 数据库的链接,评估了泰国和马来西亚 LTFU 的 PLHIV 的生存结果。
2020 年,对所有符合参加 HIV 临床站点护理时 LTFU 标准的 PLHIV 进行了与国家死亡登记处或国家 HIV 数据库的数据链接。LTFU 定义为在过去一年中没有记录的临床接触,不包括转介和死亡。使用 Cox 回归分析,按地点分层分析生存时间。
对来自马来西亚(n=2)和泰国(n=4)的 LTFU 站点的 489 名 PLHIV 进行了数据链接。151 人(31%)在 LTFU 后死亡;死亡率为每 100 人年 4.89 人。LTFU 后死亡的危险因素包括年龄较大(41-50 岁:危险比(HR)=1.99,95%置信区间(CI):1.08 至 3.68;年龄大于 50 岁:HR=4.93,95%CI:2.63 至 9.22;与 30 岁或以下年龄);接受 NRTI+PI(HR=1.87,95%CI:1.22 至 2.85 与 NRTI+NNRTI);丙型肝炎抗体阳性(HR=2.25,95%CI:1.40 至 3.62);既往 AIDS 疾病(HR=1.45,95%CI:1.03 至 2.05)。CD4 计数较高时生存得到改善(CD4 351-500 个细胞/µL:HR=0.40,95%CI:0.21-0.76;CD4>500 个细胞/µL:HR=0.43,95%CI:0.25-0.75;与 CD4≤200 个细胞/µL 相比)。
在该队列中,近三分之一的 LTFU 的 PLHIV 在脱离护理期间死亡,这强调了努力重新接触 LTFU 并确保他们能够获得持续的 ART 的重要性。