Prospective Evaluation of Adverse Drug Reactions in Hospitalized Older Adults in Ethiopia.

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Mengist Awoke Yizengaw, Behailu Terefe Tesfaye, Dula Dessalegn Bosho, Gebremichael Tesfay Desta, Mohammed S Salahudeen
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引用次数: 0

Abstract

Background: Older adults are vulnerable to adverse drug reactions (ADRs), particularly in low-income settings, yet data on ADR prevalence in Africa, including Ethiopia, remain limited. Objective: This study aimed to evaluate the incidence, severity, and preventability of ADRs among hospitalized older adults, as well as all-cause inpatient mortality. Methods: A cross-sectional observational study was conducted at Jimma Medical Center, located in Jimma town, Ethiopia, from 6 September 2021 to 26 December 2022. The study participants were older adults (n = 162) admitted to the medical wards. ADRs were assessed using the Naranjo ADR probability scale, severity was classified according to the modified Hartwig and Siegel criteria, and preventability was determined using the Schumock and Thornton criteria. Results: The median age of participants was 65 years (interquartile range: 60-70). During their hospital stay, 84 patients (51.9%) experienced at least one ADR. A total of 123 ADRs (76 ADRs per 100 admissions) were captured. Most ADRs (93.5%) were classified as mild to moderate in severity, and 84.5% (n = 105) were considered preventable. Endocrine and metabolic systems (48.8%) and diuretics (43.9%) were the most frequently affected organ systems and drug class linked to ADRs, respectively. Furosemide (41.5%) and aspirin (10.6%) were the most frequently implicated medications, commonly causing hypokalemia (35.3%) and dyspepsia (53.8%), respectively. The observed all-cause in-patient mortality rate was 6.8% (5 deaths per 1000 patient-days). The use of potentially inappropriate medications (PIMs) (aOR: 4.747, p = 0.003) and presence of digestive system disorders (aOR: 8.784, p = 0.038) were associated with an increased risk of ADRs, while a history of recent traditional medicine use (aOR: 0.285, p = 0.042) was linked to a lower risk. Conclusions: More than half of the hospitalized older adults experienced ADRs, most of which were mild to moderate in severity and considered preventable. Regular medication review for screening and minimizing PIM use in older adults may play a crucial role in lowering ADR occurrence. The borderline but statistically significant association between a history of traditional medicine use and lower occurrence of ADRs requires cautious interpretation and further investigation to explore possible explanations. Nearly seven deaths per hundred hospitalized patients were recorded.

埃塞俄比亚住院老年人药物不良反应的前瞻性评价
背景:老年人容易发生药物不良反应(ADR),特别是在低收入环境中,但非洲(包括埃塞俄比亚)的ADR患病率数据仍然有限。目的:本研究旨在评估住院老年人不良反应的发生率、严重程度和可预防性,以及全因住院死亡率。方法:于2021年9月6日至2022年12月26日在位于埃塞俄比亚Jimma镇的Jimma医疗中心进行了一项横断面观察研究。研究参与者是住院的老年人(n = 162)。采用Naranjo ADR概率量表评估不良反应,根据修改后的Hartwig和Siegel标准对严重程度进行分级,采用Schumock和Thornton标准确定可预防性。结果:参与者的中位年龄为65岁(四分位数范围:60-70岁)。在住院期间,84例患者(51.9%)至少出现一次不良反应。共收集了123份adr(每100名患者中有76份adr)。大多数adr(93.5%)的严重程度为轻度至中度,84.5% (n = 105)被认为是可预防的。内分泌和代谢系统(48.8%)和利尿剂(43.9%)分别是与adr相关的最常受影响的器官系统和药物类别。速尿(41.5%)和阿司匹林(10.6%)是最常见的相关药物,分别引起低钾血症(35.3%)和消化不良(53.8%)。观察到的全因住院死亡率为6.8%(每1000病人日死亡5例)。使用潜在不适当药物(pim) (aOR: 4.747, p = 0.003)和存在消化系统疾病(aOR: 8.784, p = 0.038)与不良反应风险增加相关,而近期使用传统药物的历史(aOR: 0.285, p = 0.042)与风险较低相关。结论:超过一半的住院老年人经历了不良反应,其中大多数严重程度为轻至中度,被认为是可以预防的。定期进行药物审查以筛查和减少老年人PIM的使用可能在降低不良反应发生方面发挥关键作用。传统药物使用史与不良反应发生率较低之间存在边缘性但具有统计学意义的关联,需要谨慎解释,并进一步调查以探索可能的解释。每100名住院病人中有近7人死亡。
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来源期刊
Journal of Personalized Medicine
Journal of Personalized Medicine Medicine-Medicine (miscellaneous)
CiteScore
4.10
自引率
0.00%
发文量
1878
审稿时长
11 weeks
期刊介绍: Journal of Personalized Medicine (JPM; ISSN 2075-4426) is an international, open access journal aimed at bringing all aspects of personalized medicine to one platform. JPM publishes cutting edge, innovative preclinical and translational scientific research and technologies related to personalized medicine (e.g., pharmacogenomics/proteomics, systems biology). JPM recognizes that personalized medicine—the assessment of genetic, environmental and host factors that cause variability of individuals—is a challenging, transdisciplinary topic that requires discussions from a range of experts. For a comprehensive perspective of personalized medicine, JPM aims to integrate expertise from the molecular and translational sciences, therapeutics and diagnostics, as well as discussions of regulatory, social, ethical and policy aspects. We provide a forum to bring together academic and clinical researchers, biotechnology, diagnostic and pharmaceutical companies, health professionals, regulatory and ethical experts, and government and regulatory authorities.
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