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Do population-level risk prediction models that use routinely collected health data reliably predict individual risks?

机译:使用常规收集的健康数据的人群风险预测模型是否可以可靠地预测个体风险?

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摘要

The objective of this study was to assess the reliability of individual risk predictions based on routinely collected data considering the heterogeneity between clinical sites in data and populations. Cardiovascular disease (CVD) risk prediction with QRISK3 was used as exemplar. The study included 3.6 million patients in 392 sites from the Clinical Practice Research Datalink. Cox models with QRISK3 predictors and a frailty (random effect) term for each site were used to incorporate unmeasured site variability. There was considerable variation in data recording between general practices (missingness of body mass index ranged from 18.7% to 60.1%). Incidence rates varied considerably between practices (from 0.4 to 1.3 CVD events per 100 patient-years). Individual CVD risk predictions with the random effect model were inconsistent with the QRISK3 predictions. For patients with QRISK3 predicted risk of 10%, the 95% range of predicted risks were between 7.2% and 13.7% with the random effects model. Random variability only explained a small part of this. The random effects model was equivalent to QRISK3 for discrimination and calibration. Risk prediction models based on routinely collected health data perform well for populations but with great uncertainty for individuals. Clinicians and patients need to understand this uncertainty.
机译:这项研究的目的是基于常规收集的数据,考虑到临床数据和人群之间的异质性,评估个人风险预测的可靠性。使用QRISK3进行心血管疾病(CVD)风险预测的范例。该研究包括来自临床实践研究数据链的392个地点的360万患者。使用带有QRISK3预测因子和每个站点的虚弱(随机效应)项的Cox模型来合并未测量的站点变异性。通用记录之间的数据记录存在很大差异(体重指数的缺失范围为18.7%至60.1%)。不同实践之间的发生率差异很大(每100个病人年0.4至1.3个CVD事件)。具有随机效应模型的个体CVD风险预测与QRISK3预测不一致。对于QRISK3预测风险为10%的患者,随机效应模型的95%预测风险范围在7.2%和13.7%之间。随机变异性只能解释其中的一小部分。随机效应模型等效于QRISK3进行判别和校准。基于常规收集的健康数据的风险预测模型对人群而言效果很好,但对个人而言却具有很大的不确定性。临床医生和患者需要了解这种不确定性。

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