The Incidence of Adverse Drug Reaction Among Adult Patients on Antiretroviral Therapy in Ethiopia: Frailty Model

IF 1.5 Q4 INFECTIOUS DISEASES HIV AIDS-Research and Palliative Care Pub Date : 2022-04-01 DOI:10.2147/HIV.S358351
M. Menza
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引用次数: 1

Abstract

Introduction Adverse drug reactions are a major global public health concern and an important cause of hospitalization, discontinuation of the drug, morbidity and mortality. Even though the prevalence in Ethiopia was declining at a moderate rate, still, far too many people are suffering and dying unnecessarily due to adverse drug reactions. Objective The aim of this study was to determine the incidence of adverse drug reaction and its predictors among adult patients on antiretroviral therapy. Methods A retrospective follow-up study was conducted at Nigist Elleni Mohamed Memorial Comprehensive Specialized Hospital, Southern Ethiopia. Data were extracted from patients’ medical records. The Weibull model with gamma frailty distribution was fitted. Statistical significance was employed at a 5% level of significance and adjusted hazard ratio with 95% confidence interval was used. Results Out of the total 376 participants followed for 1988 person years of observations, 96 developed adverse reaction with the incidence rate of 4.820/100 per (95%CI: 4.102–5.317). The univariate frailty was statistically significant (theta=0.306, 95%CI: 0.102–0.521). Baseline CD4 count (AHR: 0.997, 95%CI: 0996–0.998), fair adherence (AHR: 2.358, 95%CI: 1.133–4.904), poor adherence (AHR: 3.069, 95%CI: 1.730–5.445), HIV/TB coinfection (AHR: 2.069, 95%CI: 1.115–3.843), WHO stage II (3.128, 95%CI: 1.414–6.916), WHO stage III (AHR: 2.709, 95%CI: 1.048–7.025) and WHO stage IV (1.516, 10.352) were associated with the incidence adverse reaction. Conclusion Most of the ADR cases occurred within two years after initiation of ART. Advanced clinical stage, TB coinfection, CD4 count, and poor adherence were predictors of ADRs. Continuous counseling for clients in advanced clinical stage and patients with TB coinfection need to get close follow-up to prevent the associated ADRs by the concerned parties.
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埃塞俄比亚接受抗逆转录病毒治疗的成人患者药物不良反应发生率:脆弱性模型
药物不良反应是一个主要的全球公共卫生问题,也是住院、停药、发病率和死亡率的重要原因。尽管埃塞俄比亚的流行率正在以适度的速度下降,但仍有太多的人因药物不良反应而遭受不必要的痛苦和死亡。目的了解成人抗逆转录病毒治疗患者药物不良反应的发生率及其预测因素。方法回顾性随访研究在埃塞俄比亚南部Nigist Elleni Mohamed纪念综合专科医院进行。数据从患者的医疗记录中提取。拟合了具有脆性分布的Weibull模型。统计学意义采用5%显著性水平,校正风险比采用95%置信区间。结果在随访的376名参与者中,有96名出现不良反应,发生率为4.820/100 /人(95%CI: 4.102-5.317)。单因素脆弱性有统计学意义(θ =0.306, 95%CI: 0.102 ~ 0.521)。基线CD4计数(AHR: 0.997, 95%CI: 0996-0.998)、一般依从性(AHR: 2.358, 95%CI: 1.133-4.904)、不良依从性(AHR: 3.069, 95%CI: 1.330 - 5.445)、HIV/TB合并感染(AHR: 2.069, 95%CI: 1.115-3.843)、WHO II期(3.128,95%CI: 1.414-6.916)、WHO III期(AHR: 2.709, 95%CI: 1.048-7.025)、WHO IV期(1.516,10.352)与不良反应发生率相关。结论不良反应多发生在抗逆转录病毒治疗开始后2年内。晚期临床阶段、结核病合并感染、CD4计数和不良依从性是不良反应的预测因素。对临床晚期患者和结核合并感染患者进行持续咨询,需要密切随访,防止相关方发生相关不良反应。
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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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