Concomitant assessment of PSP and NT-proCNP as predictive markers of sepsis in severe trauma patients under mechanical ventilation
KeywordsTrauma Patient Injury Severity Score Validation Cohort Aspiration Pneumonia Severe Trauma
area under the receiver operating characteristic curve
intensive care unit
amino terminal pro-C-type natriuretic peptide
pancreatic stone protein/regenerating protein.
In intensive care units (ICUs), a great deal of research is devoted to finding new biomarkers to help physicians in the prediction of outcome. The pancreatic stone protein/regenerating protein (PSP) [1, 2] and the amino terminal pro-C-type-natriuretic-peptide (NT-proCNP)  were assessed as markers of sepsis in patients with moderate trauma and as prognostic markers of mortality for PSP . The objective of this study was to analyze separately the roles of these two biomarkers in the prediction of sepsis in patients with severe trauma.
This retrospective observational study was conducted over the course of 24 months in a trauma ICU at a university hospital. Trauma patients who were under mechanical ventilation, had an Injury Severity Score of at least 25, and were at least 18 years old were included. Clinical exclusion criteria were aspiration pneumonia or gut perforation during trauma, immunosuppressive therapy, and death in the first 48 hours. Our institutional ethics committee ('Comité de Protection des Personnes') waived the need for signed consent as samples were obtained on residual blood after routine follow-up. They recommended delivering oral information about the study to the patient or their family.
Blood samples were collected at 8 a.m. on the first two days after injury. Every patient who had a frozen plasma sample available was retrospectively included. Plasma levels of PSP and NT-proCNP were measured by using the enzyme-linked immunosorbent assay (ELISA) technique.
The major limitations are that the study was conducted at only one center and only 61 patients participated. However, the homogenous severity of our patients has to be noticed.
Many studies are devoted to finding new biomarkers to predict sepsis in the ICU. In this pilot study, neither PSP nor NT-proCNP could help in the prediction of sepsis in patients with severe trauma. Our study illustrates the complexity of validating biomarkers for sepsis prediction in an independent cohort of patients. Validation cohorts should be designed in multicenter studies to confirm every result, whether positive or negative.
The authors would like to thank Anne Portier and Catherine Jouvene-Faure for technical assistance. This work was supported by funds from the Hospices Civils de Lyon. This project is part of Advanced Diagnostics for New Therapeutic Approaches, a program dedicated to personalized medicine, coordinated by Mérieux Alliance (Lyon, France).