Admission chemokine (C-C motif) ligand 4 levels predict survival in pediatric septic shock

被引:24
作者
Nowak, Jeffrey E.
Wheeler, Derek S.
Harmon, Kelli K.
Wong, Hector R. [1 ]
机构
[1] Cincinnati Childrens Hosp, Med Ctr, Div Crit Care Med, Cincinnati, OH USA
基金
美国国家卫生研究院;
关键词
chemokine CCL4; biological markers; sepsis; shock; septic; pediatrics; clinical trials as topic; EXPRESSION; CHILDREN; SEPSIS;
D O I
10.1097/PCC.0b013e3181b8076c
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: Stratification with an effective outcome biomarker could improve the design of interventional trials in pediatric septic shock. The objective of this study was to test the usefulness of chemokine (C-C motif) ligand 4 as an outcome biomarker for mortality in pediatric septic shock. Design: A cross-sectional, observational study. Setting: Eighteen pediatric intensive care units in the United States. Patients: One hundred fifty-six pediatric patients with septic shock. Interventions: Serum samples were obtained within 24 hrs of admission to the pediatric intensive care unit. Serum levels of chemokine (C-C motif) ligand 4 were measured by enzyme-linked immunosorbent assay and compared with mortality in a training set of 34 patients. These data were used to generate a cutoff value whose usefulness was evaluated through prospective application-without post hoc modification-to a larger validation set of 122 patients. Measurements and Main Results: On inspection of the training set data, a cutoff value of 140 pg/mL was chosen. When applied to the validation set, serum chemokine (C-C motif) ligand 4 levels >140 pg/mL yielded a sensitivity of 92% and a specificity of 40% for mortality. A serum level of <140 pg/mL had a negative predictive value for mortality of 98%. Conclusions: A serum level of chemokine (C-C motif) ligand 4 of <140 pg/mL, when obtained within 24 hrs of admission, predicts a very high likelihood of survival in pediatric septic shock. Exclusion of patients with a chemokine (C-C motif) ligand 4 level of <140 pg/mL from interventional clinical trials in pediatric septic shock could create a study population in which survival benefit from the study agent could be more readily demonstrated. (Pediatr Crit Care Med 2010; 11: 213-216)
引用
收藏
页码:213 / 216
页数:4
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