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首页> 外文期刊>British Journal of Clinical Pharmacology >Evaluation of accuracy of IHI Trigger Tool in identifying adverse drug events: a prospective observational study
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Evaluation of accuracy of IHI Trigger Tool in identifying adverse drug events: a prospective observational study

机译:IHI触发工具准确性评估识别不良药物事件的触发工具:预期观察研究

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Aims Adverse drug events (ADEs) can seriously compromise the safety and quality of care provided to hospitalized patients, requiring the adoption of accurate methods to monitor them. We sought to prospectively evaluate the accuracy of the triggers proposed by the Institute for Healthcare Improvement (IHI) for identifying ADEs. Methods A prospective study was conducted in a public university hospital in 2015 with patients over the age of 18. Triggers proposed by IHI and clinical alterations suspected to be ADEs were searched daily. The number of days in which the patient was hospitalized was considered as unit of measure to evaluate the accuracy of each trigger. Results A total of 300 patients were included in this study. Mean age was 56.3 years (standard deviation (SD) 16.0), and 154 (51.3%) were female. The frequency of patients with ADEs was 24.7% and with at least one trigger was 53.3%. From those patients who had at least one trigger, the most frequent triggers were antiemetics (57.5%) and ‘abrupt medication stop’ (31.8%). The sensitivity of triggers ranged from 0.3 to 11.8% and the positive predictive value ranged from 1.2 to 27.3%. Specificity and negative predictive value were greater than 86%. Most patients identified by the presence of triggers did not have ADEs (64.4%). No triggers were identified in 40 (38.5%) ADEs. Conclusions IHI Trigger Tool did not show good accuracy in detecting ADEs in this prospective study. The adoption of combined strategies could enhance effectiveness in identifying patient safety flaws. Further discussion might contribute to improve trigger usefulness in clinical practice.
机译:AIMS不良药物事件(ADES)可以严重损害所提供给住院患者的安全和质量,要求采用准确的方法监测它们。我们试图探讨医疗改善研究所提出的触发器(IHI)的准确性来识别识别ades。方法采用18岁的公立大学医院在公立大学医院进行了预期研究。每天都在检测IHI和临床改动所提出的触发器和临床改动。患者住院的天数被认为是评估每个触发器的准确性的衡量单位。结果本研究共纳入300名患者。平均年龄为56.3岁(标准差(SD)16.0),154名(51.3%)是女性。患者患者的频率为24.7%,至少一个触发为53.3%。从那些至少有一个触发的那些患者中,最常见的触发器是助药(57.5%)和“突然的药物停止”(31.8%)。触发器的敏感性范围为0.3〜11.8%,阳性预测值范围为1.2〜27.3%。特异性和消极预测值大于86%。大多数通过触发器存在鉴定的患者没有ades(64.4%)。在40(38.5%)的ades中没有发现触发器。结论IHI触发器工具在对该潜在研究中检测到探测的良好准确性。采用合并策略可以提高识别患者安全缺陷的有效性。进一步的讨论可能有助于改善临床实践中的触发有用性。

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