Chena Woreda Health Office, Kaffa Zone, Ethiopia.
School of Public Health, College of Medicine and Health, Hawassa University, Hawassa, Ethiopia.
Pan Afr Med J. 2021 Feb 17;38:181. doi: 10.11604/pamj.2021.38.181.19915. eCollection 2021.
incidence of adverse drug reactions (ADR) associated with antiretroviral therapy (ART) was higher in developing countries. In two teaching hospital in Ethiopia: Debremarkose 23% and Yirgalem 73.2% of study participants reported at least one ADR. Since there was limited information about ADR in the study area; we aimed to determine its incidence-rate and predictors.
we conducted retrospective cohort study using medical records of HIV-infected patients enrolled on ART between 2006 and 2017 in government hospitals of Ethiopia. ADR was defined as report of at least one unwanted response to ART. We run descriptive and cox regression analysis (CRA).
incidence-rate of ADR was 4.1 per 100 person-years (py). Hazards of ADR among patients living at rural was almost two times than at urban; [Adjusted hazard ratio (AHR): 1.94(95% (CI): 1.18, 3.20)]. Stavudine (D4T)-Lamivudine (3TC)-Nevirapine (NVP) had about two times [AHR: 1.78(95%CI: 1.03, 3.08)], Zidovudine(AZT)-3TC-NVP had about two times [AHR: 2.34 (95%CI: 1.20, 4.57)], D4T-3TC-Efaviranze(EFV) had about three times [AHR: 2.86(95%CI: 1.38, 5.95)] and AZT-3TC-EFV had about two times [AHR: 2.16(95%CI: 1.21,3.90)] hazards of ADR than Tenofovir(TDF) based regimens. Being WHO clinical stage III had about two times hazard of ADR [AHR: 2.46 (95%CI: 1.22, 4.95)] and IV had about four times hazard of ADR [AHR: 4.32 (95%CI: 1.88, 9.93)] than stage I.
risk of ADR was higher among adult HIV-infected patients on ART living in rural, WHO clinical stage III and IV, and patients on AZT and D4T based regimen. AZT should not be given as an alternative treatment, increase access of TDF regimens.
发展中国家抗逆转录病毒治疗(ART)相关不良药物反应(ADR)的发生率较高。在埃塞俄比亚的两所教学医院:Debremarkose 的发生率为 23%,Yirgalem 的发生率为 73.2%,研究参与者至少报告了一种 ADR。由于研究区域内有关 ADR 的信息有限;我们旨在确定其发生率和预测因素。
我们使用 2006 年至 2017 年在埃塞俄比亚政府医院接受 ART 的 HIV 感染患者的病历进行回顾性队列研究。ADR 定义为至少报告一种对 ART 的不良反应。我们进行描述性和 Cox 回归分析(CRA)。
ADR 的发生率为每 100 人年 4.1 例。农村地区患者的 ADR 风险几乎是城市地区的两倍;[调整后的危险比(AHR):1.94(95%置信区间(CI):1.18,3.20)]。司他夫定(D4T)-拉米夫定(3TC)-奈韦拉平(NVP)的风险约为两倍[AHR:1.78(95%CI:1.03,3.08)],齐多夫定(AZT)-3TC-NVP 的风险约为两倍[AHR:2.34(95%CI:1.20,4.57)],D4T-3TC-Efaviranze(EFV)的风险约为三倍[AHR:2.86(95%CI:1.38,5.95)],AZT-3TC-EFV 的风险约为两倍[AHR:2.16(95%CI:1.21,3.90)]。与基于替诺福韦(TDF)的方案相比,接受 AZT 和 D4T 方案的患者发生 ADR 的风险更高。世界卫生组织(WHO)临床分期 III 期患者发生 ADR 的风险约为两倍[AHR:2.46(95%CI:1.22,4.95)],IV 期患者发生 ADR 的风险约为四倍[AHR:4.32(95%CI:1.88,9.93)]。
在农村、WHO 临床分期 III 和 IV 以及接受 AZT 和 D4T 方案的 HIV 感染成年患者中,ART 治疗的 ADR 风险更高。AZT 不应作为替代治疗,应增加 TDF 方案的可及性。