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Prospective Testing and Redesign of a Temporal Biomarker Based Risk Model for Patients With Septic Shock: Implications for Septic Shock Biology

机译:感染性休克患者基于时间生物标志物的风险模型的前瞻性测试和重新设计:对感染性休克生物学的影响

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The temporal version of the pediatric sepsis biomarker risk model (tPERSEVERE) estimates the risk of a complicated course in children with septic shock based on biomarker changes from days 1 to 3 of septic shock. We validated tPERSEVERE performance in a prospective cohort, with an a priori plan to redesign tPERSEVERE if it did not perform well. Biomarkers were measured in the validation cohort (n=168) and study subjects were classified according to tPERSEVERE. To redesign tPERSEVERE, the validation cohort and the original derivation cohort (n=299) were combined and randomly allocated to training (n=374) and test (n=93) sets. tPERSEVERE was redesigned using the training set and CART methodology. tPERSEVERE performed poorly in the validation cohort, with an area under the curve (AUC) of 0.67 (95% CI: 0.58-0.75). Failure analysis revealed potential confounders related to clinical characteristics. The redesigned tPERSEVERE model had an AUC of 0.83 (0.79-0.87) and a sensitivity of 93% (68-97) for estimating the risk of a complicated course. Similar performance was seen in the test set. The classification tree segregated patients into two broad endotypes of septic shock characterized by either excessive inflammation or immune suppression.
机译:儿科败血症生物标志物风险模型(tPERSEVERE)的时态版本根据感染性休克的第1天到第3天的生物标志物变化,估计了感染性休克患儿复杂病程的风险。我们在前瞻性队列中验证了tPERSEVERE的性能,并通过先验计划重新设计了tPERSEVERE(如果效果不佳)。在验证队列(n = 168)中测量生物标志物,并根据tPERSEVERE对研究对象进行分类。为了重新设计tPERSEVERE,将验证队列和原始派生队列(n = 299)组合在一起,并随机分配给训练(n = 374)和测试(n = 93)集。使用培训集和CART方法对tPERSEVERE进行了重新设计。 tPERSEVERE在验证队列中表现不佳,曲线下面积(AUC)为0.67(95%CI:0.58-0.75)。失败分析显示与临床特征相关的潜在混杂因素。重新设计的tPERSEVERE模型的AUC为0.83(0.79-0.87),灵敏度为93%(68-97),用于估计复杂过程的风险。在测试集中看到了类似的性能。分类树将患者分为败血症性休克的两种广泛的内型,其特征是过度炎症或免疫抑制。

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