• Pediatr Crit Care Me · Mar 2010

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

    • Jeffrey E Nowak, Derek S Wheeler, Kelli K Harmon, and Hector R Wong.
    • Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
    • Pediatr Crit Care Me. 2010 Mar 1;11(2):213-6.

    ObjectiveStratification 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.DesignA cross-sectional, observational study.SettingEighteen pediatric intensive care units in the United States.PatientsOne hundred fifty-six pediatric patients with septic shock.InterventionsSerum 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 ResultsOn 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 < or =140 pg/mL had a negative predictive value for mortality of 98%.ConclusionsA serum level of chemokine (C-C motif) ligand 4 of < or =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 < or =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.

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