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University of Colorado Dept. of Surgery Grand Rounds Prophylactic Antibiotics in Severe Acute Pancreatitis Eduardo Gonzalez, PGY2

Mortality from Acute Pancreatitis SAP 1 - >30% necrosis - SBP<90, scr>2.0, PaO2<60 - >500ml GI blood loss - abscess, or pseudocyst. 30% mortality 2 2 3 weeks after presentation Infection is most common cause of death in necrotizing pancreatitis (NP) 1.Bradley et al. Ann Chir 1993;47:537 541 2.Widdison et al. Br J Surg 1993;80:148 154.

Infection in Necrotizing Pancreatitis Bacterial contamination present, in ANP surgical specimens with no abscess 1 24% at 7d from presentation 74% at >14d from presentation Infection in ANP correlates with degree of necrosis E. coli, Klebsiella, Enterococcus, Pseudomonas 75% specimens monomicrobial Approaches to decrease infection in ANP: enteral feeding CT-guided aspiration antibiotics necrosectomy Banks et al, Am J Gastroenterol. 2006;101(10):2379 Berger et al, Gastroenterology. 1986;91(2):433 Horvath et al. Surg Endosc. 2001;15(10):1221. Jacobson et al. Clin Gastroenterol Hepatol. 2007;5(8):946.

Role of Antibiotics in SAP RCT s 1970s (Craig et al, Ann Intern Med. 1975; Howes et al, J Surg Res. 1975, Finch et al, Ann Surg. 1976) mild pancreatitis, ampicillin, no significant effect on mortality. Pederzoli P. A randomized multicenter clinical trial of antibiotic prophylaxis of septic complications in acute necrotizing pancreatitiswith imipenem. Surg Gynecol Obstet 1993 Sainio V, Early antibiotic treatment in acute necrotizing pancreatitis. Lancet 1995 Schwarz M, Ergebnisse einer kontrollierten Dtsch Med Wochenschr 1997 Nordback, Early treatment with antibiotics reduces the need for surgery in acute necrotizing pancreatitis a single-center randomized study. J Gastrointest Surg. 2001

Isenmann R, Prophylactic antibiotic treatment in patients with predicted severe acute pancreatitis a placebo controlled, double-blind trial. Gastroenterology 2004 Dellinger EP, Early antibiotic treatment for severe acute necrotizing pancreatitis: randomized, double-blind, placebo-controlled study. Ann Surg 2007 Røkke O, Early treatment of severe pancreatitis with imipenem: a prospective randomized clinical trial. Scand J Gastroenterol 2007 Cochrane Database Syst Rev 2010 Villatoro E, Mulla M, Larvin M. Antibiotic therapy for prophylaxis against infection of pancreatic necrosis in acute pancreatitis.

Pederzoli P, Bassi C, Vesentini S, Campedelli A. A randomized multicenter clinical trial of antibiotic prophylaxis of septic complications in acute necrotizing pancreatitiswith imipenem. Surg Gynecol Obstet 1993;176:480 3. RCT 74 patients with SAP and PN proven on CT. 6 Italian centers. Imipenem 500mg iv q8 for 14 days 33 patients - intensive medical treatment with no prophylactic antibiotics. 41 patients - intensive medical treatment with prophylactic antibiotics Pancreatic sepsis detected by (percutaneous CT or ultrasound-guided needle aspiration and intraoperative samples). The incidence of pancreatic sepsis was much less in treated patients (12.2 vs. 30.3%, p < 0.01).

Isenmann R, Rünzi M, Kron M, Kahl S, Kraus D, Jung N, et al. Prophylactic antibiotic treatment in patients with predicted severe acute pancreatitis a placebo controlled, double-blind trial. Gastroenterology 2004;126:997 1004. RCT, Randomized, placebo-controlled, double-blind trial 76 patients with severe AP and PN on CT Ciprofloxacin 400mg iv bd, and Metronidazole 500mg iv bd, 21d treatment 41 patients - supportive treatment and prophylactic antibiotics -15 patients with clinical deterioration, switch in antibiotics 35 patients supportive treatment and placebo. - 20 patients with clinical deterioration, switch in antibiotics Study medication was given for 3 23 days (med 12 days)

Isenmann R, Rünzi M, Kron M, Kahl S, Kraus D, Jung N, et al. Prophylactic antibiotic treatment in patients with predicted severe acute pancreatitis a placebo controlled, double-blind trial. Gastroenterology 2004;126:997 1004. Infected PN CIP/MET 12% Vs. 9% Placebo (p 0.585). Mortality 5% CIP/MET Vs. 7% Placebo Underpowered for oratlity, no reported secondary outcomes shock, and renal insufficiency, need for resection

Dellinger EP, Tellado JM, Soto NE, Ashles SW, Barie PS, Dugernier T, et al. Early antibiotic treatment for severe acute necrotizing pancreatitis: randomized, double-blind, placebo-controlled study. Ann Surg 2007;245:674 83. RCT, placebo-controlled, double-blind. 100 patients with severe AP and proven pancreatic necrosis on CT, Multicenter (US and Europe) Meropenem 1g q8h, recommended 14 (range 7 21) 50 patients - supportive treatment and meropenem 50 received supportive treatment and placebo. 31 patients treatment group, and 32 in placebo, received the study drug for less than 14 days.

Dellinger EP, Tellado JM, Soto NE, Ashles SW, Barie PS, Dugernier T, et al. Early antibiotic treatment for severe acute necrotizing pancreatitis: randomized, double-blind, placebo-controlled study. Ann Surg 2007;245:674 83. Pancreatic or peripancreatic infections Meropenem 18% Vs. 12% Placebo (p=0.40) Mortality Meropenem 20% Vs. 18% Placebo (p=0.799). Surgical intervention Meropenem 26% Vs. 20% (p=0.476). >50% patients on each arm interrupted antibiotics or received nonstudy antibiotics

Jacobson et al. Clin Gastroenterol Hepatol. 2010;5(8):946.

Cochrane Database Syst Rev 2010 Antibiotic therapy for prophylaxis against infection of pancreatic necrosis in acute pancreatitis. Mortality p=0.07

Cochrane Database Syst Rev 2010 Antibiotic therapy for prophylaxis against infection of pancreatic necrosis in acute pancreatitis. Pancreatic Necrosis p=0.42

Cochrane Database Syst Rev 2010 Antibiotic therapy for prophylaxis against infection of pancreatic necrosis in acute pancreatitis. Non-pancreatic Infections p=0.08

Cochrane Database Syst Rev 2010 Antibiotic therapy for prophylaxis against infection of pancreatic necrosis in acute pancreatitis. Fungal Infection p=0.9

Conclusions on Antibiotics for Severe Acute Pancreatitis A mortality benefit, p=0.07, reported as a trend, cannot disregard potential clinical benefit Benefit in non-pancreatic infection can lead to long term mortality benefit and has not been followed Heterogeneity of the methods and patients in the previous studies make it difficult combine their results Beta-lactams have yielded the best result vs. FQ/MET Most antibiotic courses studied have included 14-23 days No increase in incidence of fungal infection Reports of increased incidence of bacterial resistance have not been assoc. with antibiotic use.