Central Clinical Hospital of Ministry of Home Affairs and Administration

Warsaw, Poland

Central Clinical Hospital of Ministry of Home Affairs and Administration

Warsaw, Poland
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Piascik M.,Central Clinical Hospital of Ministry of Home Affairs and Administration | Rydzewska G.,Central Clinical Hospital of Ministry of Home Affairs and Administration | Milewski J.,Central Clinical Hospital of Ministry of Home Affairs and Administration | Olszewski S.,Central Clinical Hospital of Ministry of Home Affairs and Administration | And 3 more authors.
Pancreas | Year: 2010

Objectives: A randomized controlled trial was conducted to clarify whether continuous regional arterial infusion (CRAI) of protease inhibitor and antibiotic could reduce mortality rate of severe acute pancreatitis (SAP). Methods: Seventy-eight patients with SAP were included in the study. Thirty-nine patients were treated with CRAI, 31 patients completed the study; and another group of 39 patients was treated without CRAI therapy. Groups were well matched in clinical characteristics. The CRAI patients were treated continuously with nafamostat mesylate 240 mg/d and imipenem 1 g/d for 5 days via one of the arteries perfusing the pancreas. Later, imipenem was given intravenously (0.5 g every 8 hours) for 9 days. The non-CRAI patients received imipenem (0.5 g every 8 hours) intravenously for 14 days. Statistical analysis of the intention-to-treat (ITT) group was performed. Results: Lack of septic complications was observed in 23 patients with CRAI therapy and 20 non-CRAI patients (not significant). The additional antibiotics were applied in 8 of CRAI patients and in 18 non-CRAI (ITT, P = 0.02). Mortality rate was 5.1% in CRAI and 23.1% in non-CRAI group (ITT, P = 0.02). Urgent surgical intervention was necessary in 10.3% CRAI patients and in 33.3% non-CRAI (ITT, P = 0.01). Conclusions: The results show that CRAI of protease inhibitor and antibiotic is effective in preventing complications and in reducing mortality rate in SAP. Copyright © 2010 by Lippincott Williams & Wilkins.

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