Volume 16 Supplement 3
Pancreatic stone protein: a new predictor of outcome in patients with peritonitis
© Gukasjan et al.; licensee BioMed Central Ltd. 2012
Published: 14 November 2012
Infection and sepsis are serious postoperative complications, which have to be recognized and treated by appropriate therapeutic options in the ICU. Pancreatic stone protein (PSP/reg) is synthesized and secreted by the pancreas, the stomach and the small intestine. In this study we evaluated whether PSP/reg predicts sepsis-related postoperative complications and death in patients with peritonitis.
A prospective cohort study of postoperative patients admitted to the ICU in an adult surgical teaching hospital in Germany. Ninety-one consecutive postoperative patients with proven diagnosis of secondary peritonitis admitted to the ICU were included in the study. Blood samples were taken within 3 hours from admission to the ICU for analysis of PSP/reg, white blood cell counts (WCC), C-reactive protein (CRP), IL-6, and procalcitonin (PCT). The Mannheim Peritonitis Index and APACHE II clinical scores were also determined. Univariate and multivariate analyses were performed to determine the diagnostic accuracy and independent predictors of death in the ICU.
Univariate analysis demonstrated that PSP/reg has the highest diagnostic accuracy for complications such as organ failure and is the best predictor for death in the ICU. PSP/reg had the highest overall efficacy in predicting death with an odds ratio (OR) of 4.0 versus PCT (OR 3.2), IL-6 (OR 2.8), CRP (OR 1.3), and WCC (OR 1.4). By multivariate analysis, PSP/reg was the only independent predictor of death.
Patients with sepsis-related complications showed elevated serum-PSP/reg levels. PSP/reg demonstrated a high diagnostic accuracy to discriminate the severity of peritonitis and to predict death in the ICU. This test could be used in clinical diagnosis and therapeutic decision-making in the ICU.
This study was supported by the Gebert Rüf Foundation, Switzerland.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.