Precision phenotyping from routine laboratory parameters for out of hospital survival prediction in an all comers prospective PCI registry

利用常规实验室参数进行精准表型分析,预测所有接受前瞻性经皮冠状动脉介入治疗(PCI)患者出院后的生存率(基于前瞻性PCI注册研究)。

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Abstract

Out-of-hospital mortality in coronary artery disease (CAD) is particularly high and established adverse event prediction tools are yet to be available. Our study aimed to investigate whether precision phenotyping can be performed using routine laboratory parameters for the prediction of out-of-hospital survival in a CAD population treated by percutaneous coronary intervention (PCI). All patients treated by PCI and discharged alive in a tertiary center between January 2016 - December 2022 that have been included prospectively in the local registry were analyzed. 115 parameters from the PCI registry and 266 parameters derived from routine laboratory testing were used. An extreme gradient-boosted decision tree machine learning (ML) algorithm was trained and used to predict all-cause and cardiovascular-cause survival. A total of 4027 patients with 4981 PCI hospitalizations were randomly included in the 70% training dataset and 1729 patients with 2160 PCI hospitalizations were randomly included in the 30% validation dataset. All-cause and cardiovascular cause mortality was 17.5% and 12.2%. The integrated area under the receiver operator characteristic curve for prediction of all-cause and cardiovascular cause mortality by the ML on the validation dataset was 0.844 and 0.837, respectively (all p < 0.001). Parameters reflecting renal function (first and maximum serum creatinine), hematologic function (mean corpuscular hemoglobin concentration, platelet distribution width), and inflammatory status (lymphocyte per monocyte ratio) were among the most important predictors. Accurate out-of-hospital survival prediction in CAD can be achieved using routine laboratory parameters. ML outperformed clinical risk scores in predicting out-of-hospital mortality in a prospective all-comers PCI population and has the potential to precisely phenotype patients.

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