老年医学的药物警戒:南印度一家三级医院的etio -临床概况和药物不良反应严重程度的探索。

IF 1.1 Q4 PHARMACOLOGY & PHARMACY
Jerin James, Gowtham B, Kala P, Jamuna Rani, Sathyanarayanan V
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引用次数: 0

摘要

背景:由于生理和药代动力学特征的改变,世界范围内老年人口的增加需要关注药物管理。本研究旨在探讨老年患者药物不良反应(adr)的病因-临床特征及其严重程度,为加强药物警戒工作提供患病率、严重程度和影响因素的见解。方法:从2016年7月到2018年9月,在印度南部一家拥有1700张床位的三级医疗私立教学机构进行了一项为期两年的前瞻性观察研究。adr主要通过主动监测收集,辅以自发报告。收集到的不良反应根据性别、年龄、合并症和受影响的生理系统进行分类,以便进行详细分析。使用WHO-UMC量表进行因果关系评估,使用Hartwig和Siegel标准评估严重程度。采用SPSS 16.0软件进行统计分析,数据以百分比和比例表示。结果:研究期间共记录了206例不良反应,其中55例报告发生在老年人群中。老年人中女性32例(58.1%),男性23例(41.9%)。使用WHO-UMC因果关系评估量表进行的因果关系评估显示,大多数不良反应属于“可能”类别,占病例的69% (n=38)。皮肤表现最常见,共38例。β -内酰胺类抗菌剂,如哌拉西林-他唑巴坦、氨苄西林-舒巴坦和头孢曲松是最常见的。采用Hartwig和Siegel严重程度标准评估不良反应的严重程度。此外,48例被归类为轻度,对应于Hartwig和Siegel量表的1级和2级。6例为中度,分别为3级和4级,1例为重度。结论:本研究强调了提高老年人群药物警惕性以有效预防和管理不良反应的必要性。通过确定不良反应的etio-临床特征,医疗保健提供者可以制定有针对性的干预措施,以改善治疗结果,并确保在这一弱势人群中更安全的用药实践。加强患者教育和细致的病史记录是减少不良反应发生率的关键,从而促进老年患者更好的健康结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacovigilance in Geriatrics: Exploration of Etio-Clinical Profile and Severity of Adverse Drug Reactions at a Tertiary Hospital in South India.

Background: The increasing geriatric population worldwide necessitates focused attention on medication management due to altered physiological and pharmacokinetic profiles. This study aims to explore the etio-clinical profile of Adverse Drug Reactions (ADRs) in geriatric patients and their severity, providing insights into the prevalence, severity, and contributing factors to enhance pharmacovigilance efforts.

Methodology: A prospective observational study was conducted over two years, from July 2016 to September 2018, at a 1700-bed tertiary care private teaching institution in South India. ADRs were primarily collected through active surveillance, supplemented by spontaneous reporting. The collected ADRs were categorized based on gender, age, comorbidities, and the affected physiological systems to facilitate a detailed analysis. Causality assessment was performed using the WHO-UMC scale, and severity was evaluated using Hartwig and Siegel's criteria. Statistical analysis was conducted using SPSS software version 16.0, with data presented in percentages and proportions.

Results: A total of 206 ADRs were documented during the study period, with 55 cases reported within the geriatric population. Among the geriatric, 32 (58.1%) were females and 23 (41.9%) were males. The causality assessment, performed using the WHO-UMC causality assessment scale, revealed that the majority of the ADRs fell into the 'likely' category, accounting for 69% (n=38) of the cases. Cutaneous manifestations were the most prevalent, observed in 38 patients. Beta-lactam antimicrobials, such as piperacillin-tazobactam, ampicillin-sulbactam, and ceftriaxone, were the most commonly involved. The severity of the ADRs was assessed using the Hartwig and Siegel severity criteria. Additionally, 48 cases were classified as mild, corresponding to levels 1 and 2 on the Hartwig and Siegel scale. Furthermore, 6 cases were classified as moderate, corresponding to levels 3 and 4 on the scale, and one was severe.

Conclusion: The study highlights the critical need for vigilant pharmacovigilance in the geriatric population to prevent and manage ADRs effectively. By identifying the etio-clinical profiles of ADRs, healthcare providers can develop targeted interventions to improve therapeutic outcomes and ensure safer medication practices in this vulnerable demographic. Enhanced patient education and meticulous history-taking are pivotal in reducing the incidence of ADRs, thereby promoting better health outcomes for elderly patients.

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来源期刊
Current drug safety
Current drug safety PHARMACOLOGY & PHARMACY-
CiteScore
2.10
自引率
0.00%
发文量
112
期刊介绍: Current Drug Safety publishes frontier articles on all the latest advances on drug safety. The journal aims to publish the highest quality research articles, reviews and case reports in the field. Topics covered include: adverse effects of individual drugs and drug classes, management of adverse effects, pharmacovigilance and pharmacoepidemiology of new and existing drugs, post-marketing surveillance. The journal is essential reading for all researchers and clinicians involved in drug safety.
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