IHI全球触发工具在药物不良事件识别中的性能评估:一项前瞻性观察研究

Narayana Goruntla, Krishna Yasaswini Nitturi, Krishnapriya Pujari, L. Jayanthi, V. R. Gurram, K. Veerabhadrappa, Pradeepkumar Bhupalam
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引用次数: 0

摘要

目的:本研究旨在评估医疗保健改善研究所(IHI)全球触发工具在识别药物不良事件方面的表现。研究设计:前瞻性观察研究。研究地点和持续时间:该研究在一篇原创研究文章的普通医学部门进行。Goruntla等人。;JPRI,33(31A):146-1562021;文章编号:JPRI.69737 147二级护理转诊医院,位于印度安得拉邦Anantapur区Bathalapalli的资源有限的农村地区。这项研究为期六个月,从2019年6月到2019年11月。方法:使用预先设计的数据收集表来收集研究参与者的数据。所需数据来自患者病例表、实验室报告、治疗图表、每日护理记录、每日医生记录和直接患者访谈。IHI开发的全球触发工具用于快速审查住院病历,并为识别ADE提供线索。描述性统计用于表示人口统计学、临床特征、ADE概况、IHI触发因素和临床改变的结果。ADE的发生率以每1000个患者日的ADE来衡量。IHI全局触发工具在检测ADE方面的性能通过敏感性、特异性、阳性预测值和阴性预测值来衡量。结果:共有192名患者参与了这项研究。其中,检测到225个触发因素和123个ADE。用IHI方法估计的住院患者ADE的发生率估计为:;每1000个患者日20.2个ADE,每100个入院64.0ADE,占ADE入院人数的56.2%。大多数ADE可能与药物(60;48.7%)、2级严重程度(49;39.8%)和不可预防(52;42.2%)有关。大多数IHI全局触发因素对检测ADE具有高灵敏度、特异性、阳性预测值和阴性预测值。结论:研究表明,IHI触发器工具中的大多数触发器在识别ADE方面显示出良好的准确性。因此,使用IHI触发工具来识别ADE可以帮助提高患者的安全性。因此,该研究建议将IHI全球触发工具纳入常规ADE筛查技术,以提高检测率并提高药物安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Performance of IHI Global Trigger Tool in Identification of Adverse Drug Events: A Prospective Observational Study
Aims: The study aims to evaluate the performance of the Institute for Healthcare Improvement (IHI) global trigger tool in the identification of adverse drug events. Study design: Prospective observational study. Place and duration of study: The study was conducted in a General Medicine department of a Original research Article Goruntla et al.; JPRI, 33(31A): 146-156, 2021; Article no.JPRI.69737 147 secondary care referral hospital located in rural, resource-limited settings of Bathalapalli, Anantapur district, Andhra Pradesh, India. The study was conducted for a period of six months, from June 2019 to November 2019. Methodology: A pre-designed data collection form was used to collect the data from the study participants. The required data was obtained from the patient case sheet, lab reports, treatment charts, daily nursing notes, daily physician notes, and direct patient interviews. The global trigger tool developed by IHI was used for the rapid review of inpatient medical records and to generate clues for the identification of ADEs. Descriptive statistics were used to represent the findings of demographics, clinical characteristics, ADE profiles, IHI triggers, and clinical alterations. ADE incidence was shown in a measure of ADE per 1000 patient days. IHI global trigger tool performance in detecting ADE was measured by sensitivity, specificity, positive predictive value, and negative predictive value. Results: A total of 192 patients were enrolled in the study. Among them, 225 triggers and 123 ADEs were detected. The incidence of ADEs in the inpatients estimated by the IHI method was estimated as; 20.2 ADEs per 1000 patient days,64.0ADEs per 100 admissions, 56.2percent of admissions with ADE. Majority of ADEs are shown possible relationship with drug (60; 48.7%), level-2 severity (49; 39.8%), and not preventable (52; 42.2%). Most IHI global triggers showed high sensitivity, specificity, positive predictive value, and negative predictive value for detecting ADEs. Conclusion: The study shows that most of the triggers in the IHI Trigger tool have shown good accuracy in identifying ADEs. Thus, using the IHI Trigger Tool to identify ADEs can help to improve patient safety. Therefore, the study recommends incorporating IHI global trigger tool in routine, conventional ADE screening techniques to improve the detection rate and promote drug safety.
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