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利用新型生物标志物组学改善长期再入院和死亡率预测。

Improving the prediction of long-term readmission and mortality using a novel biomarker panel.

机构信息

Department of Epidemiology, Dartmouth Geisel School of Medicine, Hanover, New Hampshire, USA.

Department of Biomedical Data Science, Geisel School of Medicine, Lebanon, New Hampshire, USA.

出版信息

J Card Surg. 2021 Nov;36(11):4213-4223. doi: 10.1111/jocs.15954. Epub 2021 Sep 2.

Abstract

OBJECTIVE

Several short-term readmission and mortality prediction models have been developed using clinical risk factors or biomarkers among patients undergoing coronary artery bypass graft (CABG) surgery. The use of biomarkers for long-term prediction of readmission and mortality is less well understood. Given the established association of cardiac biomarkers with short-term adverse outcomes, we hypothesized that 5-year prediction of readmission or mortality may be significantly improved using cardiac biomarkers.

MATERIALS AND METHODS

Plasma biomarkers from 1149 patients discharged alive after isolated CABG surgery from eight medical centers were measured in a cohort from the Northern New England Cardiovascular Disease Study Group between 2004 and 2007. We assessed the added predictive value of a biomarker panel with a clinical model against the clinical model alone and compared the model discrimination using the area under the receiver operating characteristic (AUROC) curves.

RESULTS

In our cohort, 461 (40%) patients were readmitted or died within 5 years. Long-term outcomes were predicted by applying the STS ASCERT clinical model with an AUROC of 0.69. The biomarker panel with the clinical model resulted in a significantly improved AUROC of 0.74 (p value <.0001). Across 5 years, the hazard ratio for patients in the second to fifth quintile predicted probabilities from the biomarker augmented STS ASCERT model ranged from 2.2 to 7.9 (p values <.001).

CONCLUSIONS

We report that a panel of biomarkers significantly improved prediction of long-term readmission or mortality risk following CABG surgery. Our findings suggest biomarkers help clinical care teams better assess the long-term risk of readmission or mortality.

摘要

目的

已有研究利用临床风险因素或生物标志物开发了用于预测冠状动脉旁路移植术(CABG)患者短期再入院和死亡率的模型。但生物标志物在预测长期再入院和死亡率方面的应用尚不清楚。鉴于心脏生物标志物与短期不良结局的明确关联,我们假设使用心脏生物标志物可显著提高对再入院或死亡率的 5 年预测效果。

材料和方法

2004 年至 2007 年期间,来自 8 个医疗中心的 1149 例接受单纯 CABG 手术后存活出院的患者的血浆生物标志物在北方新英格兰心血管疾病研究组的队列中进行了测量。我们评估了在临床模型的基础上增加生物标志物组的预测价值,并比较了使用接收者操作特征曲线(ROC)下面积(AUROC)的模型区分度。

结果

在我们的队列中,461 例(40%)患者在 5 年内再次入院或死亡。应用 STS ASCERT 临床模型的 AUROC 为 0.69,可预测长期结局。将临床模型与生物标志物组结合后,AUROC 显著提高至 0.74(p 值<.0001)。在 5 年内,生物标志物增强型 STS ASCERT 模型预测概率处于第二至第五五分位数的患者的风险比为 2.2 至 7.9(p 值<.001)。

结论

我们报告称,一组生物标志物可显著提高对 CABG 术后长期再入院或死亡率风险的预测效果。我们的研究结果表明,生物标志物有助于临床护理团队更好地评估再入院或死亡率的长期风险。

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