Bansal Aasthaa, Mayer-Hamblett Nicole, Goss Christopher H, Chan Lingtak N, Heagerty Patrick J
The Comparative Health Outcomes, Policy, and Economic (CHOICE) Institute, School of Pharmacy, University of Washington, Box 357630, 1959 NE Pacific Ave, H-375B, Seattle, WA, USA, 98195.
Departments of Pediatrics and Biostatistics, University of Washington, Seattle, WA.
Epidemiology (Sunnyvale). 2019;9(2). doi: 10.4172/2161-1165.1000375. Epub 2019 Jun 17.
Effective transplantation recommendations in cystic fibrosis (CF) require accurate survival predictions, so that high-risk patients may be prioritized for transplantation. In practice, decisions about transplantation are made dynamically, using routinely updated assessments. We present a novel tool for evaluating risk prediction models that, unlike traditional methods, captures classification accuracy in identifying high-risk patients in a dynamic fashion.
Predicted risk is used as a score to rank incident deaths versus patients who survive, with the goal of ranking the deaths higher. The mean rank across deaths at a given time measures time-specific predictive accuracy; when assessed over time, it reflects time-varying accuracy.
Applying this approach to CF Registry data on patients followed from 1993-2011, we show that traditional methods do not capture the performance of models used dynamically in the clinical setting. Previously proposed multivariate risk scores perform no better than forced expiratory volume in 1 second as a percentage of predicted normal (FEV%) alone. Despite its value for survival prediction, FEV% has a low sensitivity of 45% over time (for fixed specificity of 95%), leaving room for improvement in prediction. Finally, prediction accuracy with annually-updated FEV% shows minor differences compared to FEV% updated every 2 years, which may have clinical implications regarding the optimal frequency of updating clinical information.
It is imperative to continue to develop models that accurately predict survival in CF. Our proposed approach can serve as the basis for evaluating the predictive ability of these models by better accounting for their dynamic clinical use.
囊性纤维化(CF)的有效移植建议需要准确的生存预测,以便对高风险患者进行移植优先排序。在实际操作中,移植决策是动态做出的,使用常规更新的评估。我们提出了一种评估风险预测模型的新工具,与传统方法不同,该工具以动态方式捕捉识别高风险患者的分类准确性。
将预测风险用作对死亡事件与存活患者进行排名的分数,目标是将死亡事件排名更高。给定时间点死亡事件的平均排名衡量特定时间的预测准确性;随时间评估时,它反映了随时间变化的准确性。
将这种方法应用于1993年至2011年随访的CF登记数据,我们发现传统方法无法捕捉临床环境中动态使用的模型的性能。先前提出的多变量风险评分并不比仅用1秒用力呼气量占预测正常值的百分比(FEV%)表现更好。尽管FEV%对生存预测有价值,但随着时间推移,其敏感性较低,为45%(固定特异性为95%),预测仍有改进空间。最后,与每2年更新一次的FEV%相比,每年更新一次FEV%的预测准确性差异较小,这可能对临床信息的最佳更新频率具有临床意义。
必须继续开发准确预测CF患者生存的模型。我们提出的方法可以通过更好地考虑模型的动态临床应用,作为评估这些模型预测能力的基础。