Department of Biostatistics, School of Public Health, College of Health Sciences, Mekelle University, P.O. Box: 1871, Mekelle, Ethiopia.
BMC Infect Dis. 2019 Feb 4;19(1):107. doi: 10.1186/s12879-019-3756-2.
Lost to follow-up (LTFU) negatively affects the treatment success of Anti-Retroviral Therapy (ART) and thus, increases Tuberculosis-Human Immunodeficiency Virus (TB/HIV) related morbidity, mortality and hospitalization. However, the incidence and predictors of loss to follow up (LTFU) among adults with TB/HIV co-infection have not yet well-investigated in Ethiopia. Therefore, this study was aimed at investigating the incidence and predictors of LTFU in the study setting in particular.
A facility based retrospective cohort study was employed among 305 (114 anemic and 191 normal) TB/HIV co-infected adults in two governmental hospitals (Mekelle Hospital and Ayder Comprehensive Specialized Hospital), Mekelle, Ethiopia from 2009 to 2016 and data were collected using checklist. Besides to descriptive statistics, a cox regression analysis was applied to identify statistically significant predictors of LTFU at 5% level of significance. Eventually, the Adjusted Hazard Ratio (AHR) and 95% Confidence Interval (CI) were estimated and interpreted for predictors of LTFU in the final cox model.
Generally, 45 of 305 (14.8%) of TB/HIV co-infected adults were LTFU with an incidence rate of 4.5 new LTFUs per 100 Person Years (PYs) and a median follow up time of 3.1 years (Interquartile Range (IQR): 0.8-5.3 Years). Hemoglobin level ≤ 11.0 g/dl (AHR = 2.660; 95%CI: 1.459-4.848), and any history of OI/s (AHR = 3.795; 95%CI: 1.165-12.364) were risk factors of LTFU. While, adverse drug events (AHR = 0.451; 95%CI: 0.216-0.941), TB treatment completion (AHR = 0.121; 95% CI: 0.057-0.254), and being on Isoniazid Preventive Therapy (IPT) (AHR = 0.085; 95%CI: 0.012-0.628) had protective effect against LTFU.
One in approximately seven TB/HIV co-infected adults had experienced of LTFU with an incidence rate 4.5 LTFUs per 100 PYs. The LTFU rate was higher among adults with low baseline hemoglobin level, no adverse drug events, presence of OI/s, failure to complete TB treatment, and being not on IPT. Therefore, it is advisable to treat anemia and active TB, and preventing the occurrence of OIs including TB using IPT to reduce the incidence of LTFU among TB/HIV co-infected adults.
失访(LTFU)会对抗逆转录病毒疗法(ART)的治疗效果产生负面影响,从而增加结核病-人类免疫缺陷病毒(TB/HIV)相关发病率、死亡率和住院率。然而,在埃塞俄比亚,TB/HIV 合并感染成人中 LTFU 的发生率及其预测因素尚未得到充分研究。因此,本研究旨在调查研究环境中 LTFU 的发生率及其预测因素。
采用 2009 年至 2016 年在两家政府医院(梅克尔医院和阿德尔综合专科医院)收治的 305 例(114 例贫血和 191 例正常)TB/HIV 合并感染成人进行基于设施的回顾性队列研究,并使用检查表收集数据。除了描述性统计外,还应用 Cox 回归分析确定 LTFU 的统计学显著预测因素,置信水平为 5%。最终,在最终的 Cox 模型中,对 LTFU 的预测因素进行了调整后的危险比(AHR)和 95%置信区间(CI)的估计和解释。
一般来说,305 例 TB/HIV 合并感染成人中有 45 例(14.8%)失访,失访率为每 100 人年(PY)新发生 4.5 例 LTFU,中位随访时间为 3.1 年(四分位间距(IQR):0.8-5.3 年)。血红蛋白水平≤11.0 g/dl(AHR=2.660;95%CI:1.459-4.848)和任何机会性感染/疾病史(AHR=3.795;95%CI:1.165-12.364)是 LTFU 的危险因素。而药物不良反应(AHR=0.451;95%CI:0.216-0.941)、结核病治疗完成(AHR=0.121;95%CI:0.057-0.254)和使用异烟肼预防治疗(IPT)(AHR=0.085;95%CI:0.012-0.628)对 LTFU 具有保护作用。
大约每 7 例 TB/HIV 合并感染成人中就有 1 例经历过 LTFU,失访率为每 100 PY 发生 4.5 例 LTFU。在基线血红蛋白水平较低、无药物不良反应、无机会性感染/疾病史、结核病治疗失败和未接受 IPT 的成人中,LTFU 发生率较高。因此,建议治疗贫血和活动性结核病,并通过使用 IPT 预防结核病等机会性感染,以降低 TB/HIV 合并感染成人的 LTFU 发生率。