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住院期间老年患者药物不良反应预测风险模型的开发与验证:布莱顿药物不良反应风险(BADRI)模型

Development and validation of a risk model for predicting adverse drug reactions in older people during hospital stay: Brighton Adverse Drug Reactions Risk (BADRI) model.

作者信息

Tangiisuran Balamurugan, Scutt Greg, Stevenson Jennifer, Wright Juliet, Onder G, Petrovic M, van der Cammen T J, Rajkumar Chakravarthi, Davies Graham

机构信息

Discipline of Clinical Pharmacy, School of Pharmaceutical Sciences, Universiti Sains, Malaysia, Pulau Pinang, Malaysia.

Institute of Pharmaceutical Science, King's College London, London, United Kingdom.

出版信息

PLoS One. 2014 Oct 30;9(10):e111254. doi: 10.1371/journal.pone.0111254. eCollection 2014.

Abstract

BACKGROUND

Older patients are at an increased risk of developing adverse drug reactions (ADR). Of particular concern are the oldest old, which constitute an increasingly growing population. Having a validated clinical tool to identify those older patients at risk of developing an ADR during hospital stay would enable healthcare staff to put measures in place to reduce the risk of such an event developing. The current study aimed to (1) develop and (2) validate an ADR risk prediction model.

METHODS

We used a combination of univariate analysis and multivariate binary logistic regression to identify clinical risk factors for developing an ADR in a population of older people from a UK teaching hospital. The final ADR risk model was then validated in a European population (European dataset).

RESULTS

Six-hundred-ninety patients (median age 85 years) were enrolled in the development stage of the study. Ninety-five reports of ADR were confirmed by independent review in these patients. Five clinical variables were identified through multivariate analysis and included in our final model; each variable was attributed a score of 1. Internal validation produced an AUROC of 0.74, a sensitivity of 80%, and specificity of 55%. During the external validation stage the AUROC was 0.73, with sensitivity and specificity values of 84% and 43% respectively.

CONCLUSIONS

We have developed and successfully validated a simple model to use ADR risk score in a population of patients with a median age of 85, i.e. the oldest old. The model is based on 5 clinical variables (≥8 drugs, hyperlipidaemia, raised white cell count, use of anti-diabetic agents, length of stay ≥12 days), some of which have not been previously reported.

摘要

背景

老年患者发生药物不良反应(ADR)的风险增加。尤其值得关注的是高龄老人,这一群体的数量在不断增加。拥有一个经过验证的临床工具来识别住院期间有发生ADR风险的老年患者,将使医护人员能够采取措施降低此类事件发生的风险。本研究旨在(1)开发并(2)验证一个ADR风险预测模型。

方法

我们采用单因素分析和多因素二元逻辑回归相结合的方法,在一家英国教学医院的老年人群中识别发生ADR的临床风险因素。然后在欧洲人群(欧洲数据集)中对最终的ADR风险模型进行验证。

结果

690名患者(中位年龄85岁)纳入了本研究的开发阶段。这些患者中有95份ADR报告经独立审核确认。通过多因素分析确定了5个临床变量并纳入我们的最终模型;每个变量赋予1分。内部验证得出的曲线下面积(AUROC)为0.74,灵敏度为80%,特异度为55%。在外部验证阶段,AUROC为0.73,灵敏度和特异度值分别为84%和43%。

结论

我们已经开发并成功验证了一个简单的模型,用于在中位年龄为85岁的患者群体(即高龄老人)中使用ADR风险评分。该模型基于5个临床变量(≥8种药物、高脂血症、白细胞计数升高、使用抗糖尿病药物、住院时间≥12天),其中一些变量此前尚未见报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00a5/4214735/dcd022cfb054/pone.0111254.g001.jpg

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