Billing et al. [16] demonstrated the reliability of MPI in 2003 patients from 7 centres in Europe. With a threshold index score of 26, the sensitivity was 86 (range 54-98) per cent, specificity 74 (range 58-97) per cent and accuracy 83 (range 70-94) per cent in predicting PF-6463922 death. For patients with a score less than 21 the mean mortality rate was 2.3 (range 0-11) per cent, for score 21-29 22.5 (range 10.6-50) per cent and for score greater than 29 59.1 (range 41-87) per cent. In this study the Mannheim peritonitis index provided an easy and reliable means of risk evaluation and classification for patients with peritoneal inflammation. In 2008 Panhofer et al. [17] published

a retrospective single-centre cohort study in patients who developed tertiary peritonitis, proposing a combination of both MPI and APACHE II, concluding that combination of prognostic scores was very Fludarabine supplier useful to detect tertiary peritonitis. Hypothesizing that intrinsic risk factors were a better predictor of mortality rather than the type of infection, Inui at al. [18] recently investigated the utility of Charlson Comorbidity Index and multiple organ dysfunction

(MOD). They reviewed retrospectively 452 patients with IAI who had been treated over 8 years (June 1999-June 2007). Charlson Comorbidity Index and Multiple Organ Dysfunction (MOD) scores were evaluated at admission and on postoperative day 7. When patients with appendicitis were excluded, there was no difference in selleckchem mortality or complications between patients with CA-IAI and HA-IAI. Statistical analysis demonstrated that catheter-related bloodstream infection, cardiac event, and age > or = 65 were independent risk factors for mortality. Among patients who failed initial therapy, a non-appendiceal source of infection and a Charlson score > or = 2 were determined to be independent risk factors. Non-appendiceal source of infection

and MOD score > or = 4 on postoperative day 7 were found to be independent predictors for re-intervention. Diagnosis In the patient with abdominal sepsis Selleck Rucaparib early detection and treatment is essential to minimize complications [19]. Complicated intra-abdominal infections diagnosis is mainly a clinical diagnosis. Abdominal pain, which may be acute or insidious. Initially, the pain may be dull and poorly localized (visceral peritoneum) and often progresses to steady, severe, and more localized pain (parietal peritoneum). Systemic manifestations are SIRS manifestations: Core body temperature > 38°C or < 36°C, heart rate > 90 beats per minute, respiratory rate > 20 breaths per minute (not ventilated) or PaCO2 < 32 mm Hg (ventilated), WBC > 12,000, < 4,000 or > 10% immature forms (bands) [20]. Hypotension and hypoperfusion signs such as lactic acidosis, oliguria, and acute alteration of mental status are indicative of evolution to severe sepsis.