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

作者：Nowak Jeffrey E; Wheeler Derek S; Harmon Kelli K; Wong Hector R^*

来源：Pediatric Critical Care Medicine, 2010, 11(2): 213-216.

DOI：10.1097/PCC.0b013e3181b8076c

• chemokine CCL4
• biological markers
• sepsis
• shock
• septic
• pediatrics
• clinical trials as topic

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)

• 出版日期2010-3