The pediatric sepsis biomarker risk model

被引:150
作者
Wong, Hector R. [1 ,2 ,3 ]
Salisbury, Shelia [3 ]
Xiao, Qiang [4 ]
Cvijanovich, Natalie Z. [5 ]
Hall, Mark [6 ]
Allen, Geoffrey L. [7 ]
Thomas, Neal J. [8 ]
Freishtat, Robert J. [9 ]
Anas, Nick [10 ]
Meyer, Keith [11 ]
Checchia, Paul A. [12 ]
Lin, Richard [13 ]
Shanley, Thomas P. [14 ]
Bigham, Michael T. [15 ]
Sen, Anita [16 ]
Nowak, Jeffrey [17 ]
Quasney, Michael [18 ]
Henricksen, Jared W. [19 ]
Chopra, Arun [20 ]
Banschbach, Sharon [1 ,2 ]
Beckman, Eileen [1 ,2 ]
Harmon, Kelli [1 ,2 ]
Lahni, Patrick [1 ,2 ]
Lindsell, Christopher J. [21 ]
机构
[1] Cincinnati Childrens Hosp, Div Crit Care Med, Med Ctr, Cincinnati, OH USA
[2] Cincinnati Childrens Res Fdn, Cincinnati, OH USA
[3] Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH USA
[4] EMD Millipore Corp, St Charles, MO USA
[5] Childrens Hosp & Res Ctr Oakland, Oakland, CA USA
[6] Nationwide Childrens Hosp, Columbus, OH USA
[7] Childrens Mercy Hosp, Kansas City, MO 64108 USA
[8] Penn State Hershey Childrens Hosp, Hershey, PA USA
[9] Childrens Natl Med Ctr, Washington, DC 20010 USA
[10] Childrens Hosp Orange Cty, Orange, CA 92668 USA
[11] Miami Childrens Hosp, Miami, FL USA
[12] Texas Childrens Hosp, Houston, TX 77030 USA
[13] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[14] Univ Michigan, CS Mott Childrens Hosp, Ann Arbor, MI 48109 USA
[15] Akron Childrens Hosp, Akron, OH USA
[16] Columbia Univ, Med Ctr, Morgan Stanley Childrens Hosp, New York, NY USA
[17] Childrens Hosp & Clin Minnesota, Minneapolis, MN USA
[18] Childrens Hosp Wisconsin, Milwaukee, WI 53201 USA
[19] Primary Childrens Med Ctr, Salt Lake City, UT 84103 USA
[20] St Christophers Hosp Children, Philadelphia, PA 19133 USA
[21] Univ Cincinnati, Coll Med, Dept Emergency Med, Cincinnati, OH USA
来源
CRITICAL CARE | 2012年 / 16卷 / 05期
基金
美国国家卫生研究院;
关键词
SEPTIC SHOCK; EXPRESSION; MORTALITY; STRATIFICATION; IDENTIFICATION; REGRESSION; CHILDREN; TRIALS;
D O I
10.1186/cc11652
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Introduction: The intrinsic heterogeneity of clinical septic shock is a major challenge. For clinical trials, individual patient management, and quality improvement efforts, it is unclear which patients are least likely to survive and thus benefit from alternative treatment approaches. A robust risk stratification tool would greatly aid decision-making. The objective of our study was to derive and test a multi-biomarker-based risk model to predict outcome in pediatric septic shock. Methods: Twelve candidate serum protein stratification biomarkers were identified from previous genome-wide expression profiling. To derive the risk stratification tool, biomarkers were measured in serum samples from 220 unselected children with septic shock, obtained during the first 24 hours of admission to the intensive care unit. Classification and Regression Tree (CART) analysis was used to generate a decision tree to predict 28-day all-cause mortality based on both biomarkers and clinical variables. The derived tree was subsequently tested in an independent cohort of 135 children with septic shock. Results: The derived decision tree included five biomarkers. In the derivation cohort, sensitivity for mortality was 91% (95% CI 70 - 98), specificity was 86% (80 - 90), positive predictive value was 43% (29 - 58), and negative predictive value was 99% (95 - 100). When applied to the test cohort, sensitivity was 89% (64 - 98) and specificity was 64% (55 - 73). In an updated model including all 355 subjects in the combined derivation and test cohorts, sensitivity for mortality was 93% (79 - 98), specificity was 74% (69 - 79), positive predictive value was 32% (24 - 41), and negative predictive value was 99% (96 - 100). False positive subjects in the updated model had greater illness severity compared to the true negative subjects, as measured by persistence of organ failure, length of stay, and intensive care unit free days. Conclusions: The pediatric sepsis biomarker risk model (PERSEVERE; PEdiatRic SEpsis biomarkEr Risk modEl) reliably identifies children at risk of death and greater illness severity from pediatric septic shock. PERSEVERE has the potential to substantially enhance clinical decision making, to adjust for risk in clinical trials, and to serve as a septic shock-specific quality metric.
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页数:9
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