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验证SeptiCyte RAPID以区分脓毒症与非感染性全身炎症。

Validation of SeptiCyte RAPID to Discriminate Sepsis from Non-Infectious Systemic Inflammation.

作者信息

Balk Robert, Esper Annette M, Martin Greg S, Miller Russell R, Lopansri Bert K, Burke John P, Levy Mitchell, Opal Steven, Rothman Richard E, D'Alessio Franco R, Sidhaye Venkataramana K, Aggarwal Neil R, Greenberg Jared A, Yoder Mark, Patel Gourang, Gilbert Emily, Parada Jorge P, Afshar Majid, Kempker Jordan A, van der Poll Tom, Schultz Marcus J, Scicluna Brendon P, Klein Klouwenberg Peter M C, Liebler Janice, Blodget Emily, Kumar Santhi, Navalkar Krupa, Yager Thomas D, Sampson Dayle, Kirk James T, Cermelli Silvia, Davis Roy F, Brandon Richard B

机构信息

Rush Medical College and Rush University Medical Center, Chicago, IL 60612, USA.

Grady Memorial Hospital and Emory University School of Medicine, Atlanta, GA 30322, USA.

出版信息

J Clin Med. 2024 Feb 20;13(5):1194. doi: 10.3390/jcm13051194.

Abstract

(1) SeptiCyte RAPID is a molecular test for discriminating sepsis from non-infectious systemic inflammation, and for estimating sepsis probabilities. The objective of this study was the clinical validation of SeptiCyte RAPID, based on testing retrospectively banked and prospectively collected patient samples. (2) The cartridge-based SeptiCyte RAPID test accepts a PAXgene blood RNA sample and provides sample-to-answer processing in ~1 h. The test output (SeptiScore, range 0-15) falls into four interpretation bands, with higher scores indicating higher probabilities of sepsis. Retrospective (N = 356) and prospective (N = 63) samples were tested from adult patients in ICU who either had the systemic inflammatory response syndrome (SIRS), or were suspected of having/diagnosed with sepsis. Patients were clinically evaluated by a panel of three expert physicians blinded to the SeptiCyte test results. Results were interpreted under either the Sepsis-2 or Sepsis-3 framework. (3) Under the Sepsis-2 framework, SeptiCyte RAPID performance for the combined retrospective and prospective cohorts had Areas Under the ROC Curve (AUCs) ranging from 0.82 to 0.85, a negative predictive value of 0.91 (sensitivity 0.94) for SeptiScore Band 1 (score range 0.1-5.0; lowest risk of sepsis), and a positive predictive value of 0.81 (specificity 0.90) for SeptiScore Band 4 (score range 7.4-15; highest risk of sepsis). Performance estimates for the prospective cohort ranged from AUC 0.86-0.95. For physician-adjudicated sepsis cases that were blood culture (+) or blood, urine culture (+)(+), 43/48 (90%) of SeptiCyte scores fell in Bands 3 or 4. In multivariable analysis with up to 14 additional clinical variables, SeptiScore was the most important variable for sepsis diagnosis. A comparable performance was obtained for the majority of patients reanalyzed under the Sepsis-3 definition, although a subgroup of 16 patients was identified that was called septic under Sepsis-2 but not under Sepsis-3. (4) This study validates SeptiCyte RAPID for estimating sepsis probability, under both the Sepsis-2 and Sepsis-3 frameworks, for hospitalized patients on their first day of ICU admission.

摘要

(1)SeptiCyte RAPID是一种用于区分脓毒症与非感染性全身炎症以及评估脓毒症概率的分子检测方法。本研究的目的是基于对回顾性保存和前瞻性收集的患者样本进行检测,对SeptiCyte RAPID进行临床验证。(2)基于试剂盒的SeptiCyte RAPID检测接受PAXgene血液RNA样本,并在约1小时内提供从样本到结果的处理。检测输出(SeptiScore,范围0 - 15)分为四个解读区间,分数越高表明脓毒症概率越高。对重症监护病房(ICU)中患有全身炎症反应综合征(SIRS)或疑似患有/被诊断为脓毒症的成年患者的回顾性样本(N = 356)和前瞻性样本(N = 63)进行了检测。由三位对SeptiCyte检测结果不知情的专家医生组成的小组对患者进行临床评估。结果根据脓毒症-2或脓毒症-3框架进行解读。(3)在脓毒症-2框架下,回顾性和前瞻性队列合并后的SeptiCyte RAPID性能的受试者工作特征曲线下面积(AUC)范围为0.82至0.85,SeptiScore第1区间(分数范围0.1 - 5.0;脓毒症风险最低)的阴性预测值为0.91(敏感性0.94),SeptiScore第4区间(分数范围7.4 - 15;脓毒症风险最高)的阳性预测值为0.81(特异性0.90)。前瞻性队列的性能估计值范围为AUC 0.86 - 0.95。对于经医生判定为血培养阳性或血、尿培养均阳性的脓毒症病例,43/48(90%)的SeptiCyte分数落在第3或第4区间。在包含多达14个其他临床变量的多变量分析中,SeptiScore是脓毒症诊断的最重要变量。在脓毒症-3定义下对大多数重新分析的患者获得了类似的性能,尽管识别出了16名患者的亚组,这些患者在脓毒症-2定义下被判定为脓毒症,但在脓毒症-3定义下不是。(4)本研究验证了SeptiCyte RAPID在脓毒症-2和脓毒症-3框架下,对入住ICU第一天的住院患者估计脓毒症概率的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41c3/10931699/d4c274a0e13f/jcm-13-01194-g001.jpg

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