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Prospective Validation of a Risk Prediction Model to Identify High-Risk Patients for Medication Errors at Hospital Admission

机译:风险预测模型的预期验证识别医院入院治疗中的高危患者

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Background: Pharmacy-led medication reconciliation in elective surgery patients is often performed at the preoperative screening (POS). Because of the time lag between POS and admission, changes in medication may lead to medication errors at admission (MEAs). In a previous study, a risk prediction model for MEA was developed. Objective: To validate this risk prediction model to identify patients at risk for MEAs in a university hospital setting. Methods: The risk prediction model was derived from a cohort of a Dutch general hospital and validated within a comparable cohort from a Dutch University Medical Centre. MEAs were assessed by comparing the POS medication list with the reconciled medication list at hospital admission. This was considered the gold standard. For every patient, a risk score using the risk prediction model was calculated and compared with the gold standard. The risk prediction model was assessed with receiver operating characteristic (ROC) analysis. Results: Of 368 included patients, 167 (45.4%) had at least 1 MEA. ROC analysis revealed significant differences in the area under the curve of 0.535 ( P = 0.26; validation cohort) versus 0.752 ( P < 0.0001; derivation cohort). The sensitivity in this validating cohort was 66%, with a specificity of 40%. Conclusion and Relevance: The risk prediction model developed in a general hospital population is not suitable to identify patients at risk for MEA in a university hospital population. However, number of medications is a common risk factor in both patient populations and should, thus, form the basis of an adapted risk prediction model.
机译:背景:选修外科患者的药房导致药物和解通常在术前筛选(POS)中进行。由于POS和入学之间的时间延迟,药物的变化可能导致入院(MEA)的药物误差。在先前的研究中,开发了MEA的风险预测模型。目的:验证这种风险预测模型,以确定大学医院环境中测量风险的患者。方法:风险预测模型来自荷兰综合医院的队列,并在荷兰大学医疗中心的可比队列中验证。通过将POS药物清单与医院入院的和解药物清单进行比较来评估MEA。这被认为是金标准。对于每个患者,使用风险预测模型进行风险评分并与金标准进行比较。通过接收器操作特征(ROC)分析评估风险预测模型。结果:368名包括患者,167名(45.4%)至少有1个MEA。 ROC分析显示了0.535(P = 0.26;验证队)的曲线下面积的显着差异与0.752(P <0.0001;衍生队)。该验证队列的敏感性为66%,特异性为40%。结论与相关性:综合医院人口中发育的风险预测模型不适合识别大学医院人口MEA风险的患者。然而,药物数量是患者群体中的常见危险因素,因此应该构成适应风险预测模型的基础。

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