Dagnaw Mequanente, Indracanti Meera, Geremew Bisrat Misganaw, Mekonnen Esubalew Asmare, Tekle Muluken, Muche Mulu, Gelaw Dagnachew Wassie, Amera Bogale Damtew
Department of Epidemiology, Institute of Public Health, Institute of Biotechnology, Department of Medical Biotechnology University of Gondar Gondar Ethiopia.
Department of Medical Biotechnology, School of Allied Health Sciences Malla Reddy University Hyderabad Telangana India.
Health Sci Rep. 2024 Feb 25;7(2):e1933. doi: 10.1002/hsr2.1933. eCollection 2024 Feb.
Adverse drug reactions (ADRs) are harmful and unintended reactions to medicines given at standard doses through a proper route of administration for the purpose of prophylaxis, diagnosis, or treatment.
The objective of this research paper was to assess median time to development of ADRs and associated factors among children HIV positive patients on antiretroviral treatment (ART) in North West Amhara Specialized Hospitals.
The adverse drug effect survival time was estimated using the Kaplan-Meier survival method and log-rank test curves was applied for analyze "time-to-event" data. Cox regression model was used to identify the associated factors. Adjusted hazard ratios with their respective 95% confidence intervals (CIs) were estimated and a value of less than 0.05 was used to declare the presence of a significant association.
The overall incidence of ADRs was 0.67 (95% CI: 3.74-4.44) per 10,000 person-year observation, with a median of 57 months. Adults are presenting with opportunistic Infections (OIs) experiences, baseline CD4 < 200 cells/µL counts, 1e, tenofovir disoproxil fumarate-lamivudine-efavirenz ART regimen, bedridden baseline functional status, World Health Organization (WHO) clinical stage II and III were notably associated with the incidence of ADRs development.
ADRs were uncommon in this study. predictors, such as OIs experiences, a low CD4 count, ART regimen, an advanced WHO stage, and bedridden functional status were significantly associated with ADRs.
药物不良反应(ADR)是指通过适当给药途径,以标准剂量使用药物进行预防、诊断或治疗时出现的有害且非预期的反应。
本研究论文的目的是评估西北阿姆哈拉专科医院接受抗逆转录病毒治疗(ART)的儿童HIV阳性患者发生药物不良反应的中位时间及相关因素。
采用Kaplan-Meier生存法估计药物不良反应的生存时间,并应用对数秩检验曲线分析“事件发生时间”数据。使用Cox回归模型确定相关因素。估计调整后的风险比及其各自的95%置信区间(CI),以小于0.05的值来判定存在显著关联。
每10000人年观察期内药物不良反应的总发生率为0.67(95%CI:3.74 - 4.44),中位时间为57个月。成人出现机会性感染(OI)经历、基线CD4计数<200个细胞/µL、替诺福韦酯-拉米夫定-依非韦伦抗逆转录病毒治疗方案、卧床的基线功能状态、世界卫生组织(WHO)临床分期II和III与药物不良反应的发生显著相关。
本研究中药物不良反应并不常见。机会性感染经历、低CD4计数、抗逆转录病毒治疗方案、WHO晚期以及卧床功能状态等预测因素与药物不良反应显著相关。