Predictors of Survival Time Among HIV-Infected Adults After Initiating Anti-Retroviral Therapy in Kombolcha Town: A 5-Year Retrospective Cohort Study

IF 1.5 Q4 INFECTIOUS DISEASES HIV AIDS-Research and Palliative Care Pub Date : 2022-04-01 DOI:10.2147/HIV.S359495
Muhammed Siraj, Sisay Gedamu, Belachew Tegegne
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Abstract

Background Antiretroviral therapy (ART) enhances the survival of HIV-infected patients by reducing viral load and increasing CD4. As CD4 count increases, patients are more protected against opportunistic infections. In developing countries including Ethiopia, there were limited studies about the survival benefit of ART particularly no study in Kombolcha Town. Thus, this study was aimed to address the gap. Methods A hospital-based retrospective cohort study was employed in Kombolcha town among 510 patients’ records from January 2015 to December 2019. A systematic random sampling technique was used to select patient records. The collected data were checked, coded, and entered into Epidata version 4.6 and exported to Statistical Package for Social Sciences version 26 for data cleaning and analysis. Kaplan–Meier was used to estimate the probability of category of each predictor and a log rank test was used to compare survival curves. Bivariate and multivariate Cox-regression were employed using a 95% CI and variables with p-value <0.05 were declared as predictors of poor survival time. Results In this cohort, out of 510 HIV-infected patients, 39 (7.65%) were died, and 471 (92.35%) were censored. Fair drug adherence (AHR=6.88, 95% CI: 4.31–24.04), Poor drug adherence (AHR=9.58, 95% CI: 8.72–30.97), CD4 count <50 cell/µL (AHR=9.38, 95% CI: 1.48–59.31), CD4 count 50–99 cell/µL (AHR=9.67, 95% CI: 1.80–51.73), bedridden (AHR=9.5, 95% CI: 4.49–18.66), opportunistic infections (AHR=4.58, 95% CI: 1.20–5.65), weight <60kg (AHR=2.48, 95% CI:1.59, 10.38), WHO stage III (AHR=3.56, 95% CI: 1.71–17.89), WHO stage IV (AHR=4.42, 95% CI:1.75–25.93) were predictors of poor survival time. Conclusion The Kaplan–Meier result showed that the estimated median survival time of patients after ART initiation in Kombolcha town was higher (32 months) as compared to other studies. Poor drug adherence, WHO stage III & IV, Lower baseline CD4 count, presence of opportunistic infections, weight <60kg, and being bedridden were predictors of poor survival time. Thus, early initiation of ART ought to be encouraged among HIV-infected patients and good patient counseling on the level of adherence should be strengthened.
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在Kombolcha镇开始抗逆转录病毒治疗后hiv感染成人存活时间的预测因素:一项5年回顾性队列研究
抗逆转录病毒治疗(ART)通过降低病毒载量和增加CD4来提高hiv感染患者的生存率。随着CD4计数的增加,患者对机会性感染的保护更强。在包括埃塞俄比亚在内的发展中国家,关于抗逆转录病毒治疗的生存益处的研究有限,特别是在Kombolcha镇没有研究。因此,本研究旨在解决这一差距。方法对2015年1月至2019年12月康波查镇510例住院患者进行回顾性队列研究。采用系统随机抽样技术选取患者病历。对收集到的数据进行检查、编码,输入Epidata版本4.6,导出到Statistical Package for Social Sciences版本26进行数据清洗和分析。Kaplan-Meier法用于估计各预测因子类别的概率,log rank检验用于比较生存曲线。双变量和多变量cox回归采用95% CI, p值<0.05的变量被宣布为不良生存时间的预测因子。结果510例hiv感染者中死亡39例(7.65%),检出471例(92.35%)。一般的药物依从性(AHR=6.88, 95% CI: 4.31-24.04)、较差的药物依从性(AHR=9.58, 95% CI: 8.72-30.97)、CD4细胞计数<50细胞/µL (AHR=9.38, 95% CI: 1.48-59.31)、CD4细胞计数50 - 99细胞/µL (AHR=9.67, 95% CI: 1.80-51.73)、卧床(AHR=9.5, 95% CI: 4.49-18.66)、机会性感染(AHR=4.58, 95% CI: 1.20-5.65)、体重<60kg (AHR=2.48, 95% CI:1.59 - 10.38)、WHO III期(AHR=3.56, 95% CI: 1.71-17.89)、WHO IV期(AHR=4.42, 95% CI: 1.75-25.93)是不良生存时间的预测因子。结论Kaplan-Meier结果显示,与其他研究相比,Kombolcha镇患者开始抗逆转录病毒治疗后的估计中位生存时间(32个月)更高。较差的药物依从性、世卫组织III期和IV期、较低的基线CD4计数、机会性感染的存在、体重<60kg和卧床是生存时间较差的预测因素。因此,应鼓励艾滋病毒感染者尽早开始抗逆转录病毒治疗,并应加强对患者坚持治疗水平的良好咨询。
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来源期刊
CiteScore
3.00
自引率
6.70%
发文量
61
审稿时长
16 weeks
期刊介绍: About Dove Medical Press Dove Medical Press Ltd is part of Taylor & Francis Group, the Academic Publishing Division of Informa PLC. We specialize in the publication of Open Access peer-reviewed journals across the broad spectrum of science, technology and especially medicine. Dove Medical Press was founded in 2003 with the objective of combining the highest editorial standards with the ''best of breed'' new publishing technologies. We have offices in Manchester and London in the United Kingdom, representatives in Princeton, New Jersey in the United States, and our editorial offices are in Auckland, New Zealand. Dr Scott Fraser is our Medical Director based in the UK. He has been in full time clinical practice for over 20 years as well as having an active research interest.
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