Prophylactic Antibiotics in Severe Acute Pancreatitis: Antibiotics are good. Karen Lo R 3 University of Colorado Oct 11, 2010

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Prophylactic Antibiotics in Severe Acute Pancreatitis: Antibiotics are good Karen Lo R 3 University of Colorado Oct 11, 2010

Overview Pancreas: The History Pancreas: The Organ The Disease Pathogenesis The Prognosis The Argument over Antibiotics

History of the Pancreas Herophilus (335-280 BC) identified the pancreas Ruphos gave the name "pancreas meaning all flesh". Galen (129-199 199 AD) taught the pancreas was a cushion to protect the blood vessels behind it

History of Pancreatitis 1889 Fritz published paper on acute pancreatitis 1901 Opie postulated that a stone impacted at ampulla of Vater could cause pancreatitis

Pancreas: fundamentals The pancreas is both Endocrine organ made up of the islets of Langerhans Exocrine organ consisting of acinar and ductal cells.

Pathogenesis of Pancreatitis Inflammation of the pancreas Insult usually due to alcohol or gallstones Acute pancreatitis begins with injury to acinar cells. Insult induces activation on digestive enzymes including zymogens, such as trypsinogen, which induces auto digestions

Pancreatitis

Ranson s s Criteria: Prognosis On admission Glucose over 200 Age over 55 LD over 350 AST over 250 WBC over 16 After 48 hours Hct drop by more 10% BUN increase by 5 US Ca under 8 Arterial po2 under 60 Base Deficit greater than 4 6 L of fluid sequestration

CT Severity Index: prognosis Balthazar 0 pt Grade A - Normal pancreas 1 pt Grade B - Focal or diffuse gland enlargement 2 pt Grade C - Intrinsic gland abnormality recognized by haziness on the scan 3 pt Grade D - Single ill-defined collection or phlegmon 4 pt Grade E - Two or more ill-defined collections or the presence of gas in or nearby the pancreas Necrosis: 1/3 2 pt 1/3-1/2 4 pt Over 1/2 6 pt

Acute Pancreatitis: epidemiology About 210,000 people in the US are hospitalized for Acute Pancreatitis (AP) 25% of people presenting with AP have Severe Acute Pancreatitis (SAP) SAP has 10-20% mortality

Severe Acute Pancreatitis Definition: Presence of organ failure and /or local pancreatic necrosis, pseudocyst and abscess Ranson s s greater 3, APACHE II* greater than 8 CRP greater 210 on days 2-42

Severe Acute Pancreatitis Course: Day 1-14: 1 14: Systemic inflammatory response syndrome progressing to multiple organ dysfunction syndrome Day 14-21: infection of pancreatic necrosis

Risk of peripancreatic infection directly related to degree of pancreatic necrosis Approximately 40% of patients with pancreatic necrosis develop infected necrosis Infection rates: Pancreatic necrosis greater 30% 15-30% Pancreatic necrosis greater 50% 40-70%

Pancreatic infections Infection of pancreatic necrosis though to be caused by translocation of gut flora. Infection rate proportional to extent of necrosis. Complications due to infections are responsible for up to 80% of Deaths

Pancreatitis Bugs Infections in Necrotizing pancreatitis are gut derived: E Coli 25-35% Enterococcus 25% Klebsiella 15% Pseudomonas 7-11% 7 75% are monomicrobial

Severe Acute Pancreatitis and antibiotics, your friend

Historically In 1970s clinical trials showed no benefit of prophylactic antibiotics. WHY? Ampicillin was the most commonly used drug in these studies Failed to reach minimal inhibitory concentration in Pancreatic tissue

Pederzoli 1993 Randomized Multi center study N=74 with pancreatic necrosis on CT scan Randomized: Inipenem for 14 days or no antibiotics RESULTS: Less Pancreatic Sepsis in Antibiotic arm 12% vs 30% (p<0.01)

Sainio 1995 N=60 pt with pancreatitis. Randomized to: 30 patients were assigned cefuroxime (4.5 g/day IV) from admission. 30 patients no antibiotic treatment until clinical or microbiologically verified infection or after a rise in C-reactive C protein.

Sainio 1995 Less infectious complications in the antibiotic group (mean per patient 1.0 vs 1.8, p = 0.01). Mortality was lower in antibiotic group (1 vs 7 in the antibiotic group; p = 0.03). Conclusion: Antibiotics given early in necrotizing pancreatitis is beneficial and may reduce mortality, probably by decreasing the frequency of sepsis.

Cochrane 2003 strong evidence that intravenous antibiotic prophylactic therapy for 10 to 14 days decreased the risk of superinfection of necrotic tissue and mortality in patients with severe acute pancreatitis with proven pancreatic necrosis at CT.

Objective: Cochrane 2006 To determine the effectiveness and safety of prophylactic antibiotics in CT proven acute pancreatitis complicated by pancreatic necrosis. Methods: 5 RC Studies with 294 patients

Cochrane 2006 Beta lactam prophylaxis had: Significantly less mortality 6.3% vs 16.7% Significantly less infected pancreatic necrosis 15.6% vs 29.2%

Arguments against Prophylaxis antibiotics Resistant organisms Fungal infection Cost

Cochrane 2010 7 Randomized controlled studies 404 patients Objective: Pancreatic necrosis may complicate severe acute pancreatitis, and is detectable by computed tomography (CT). If it becomes infected mortality increases, but the use of prophylactic antibiotics raises concerns about antibiotic resistance and fungal infection.

Cochrane 2010 Results: Fungal infections were not significantly different. Insufficient data were provided concerning antibiotic resistance.

Arguments against Prophylaxis antibiotics Resistant organisms Fungal infection Cost

Arguments against Prophylaxis antibiotics and why they are just wrong Resistant organisms- Fungal infection- Cost- Nope Nope unable to determine Xu s 2008 meta analysis 8 RCT: Prophylactic antibiotic treatment is associated with a significant reduction of pancreatic or peripancreaticinfection,, non-pancreatic infection, and length of hospital stay

Cochrane 2010 Mortality lower in antibiotic group 8.4% vs. 14.4% Non-pancreatic infection lower in antibiotic groups 23.7% vs. 36%

Cochrane 2010 Furthermore: Imipenem (beta lactam) use had significant decrease in pancreatic infections were found. Final recommendation: further research is needed

About the antibiotic haters

Isenmann study 2004 RCT that concluded that no benefit in prophylaxis antibiotics. HOWEVER: Underpowered Had people in the control arm on antibiotics Used ciprofloxacin and metronidazole

Dellinger study 2007 International, multi-institutional institutional double blind placebo-controlled controlled study 100 patients CT confirmed necrotizing pancreatitis However Patients in study arm were included up to 120 hours after onset of symptoms 46% patients in control arm on antibiotics The calculated number of patients (n = 240) was not reached.

Acute pancreatitis is the most terrible of all the calamities that occur in connection to the abdominal viscera. The suddenness of its onset, the illimitable agony which accompanies it, and the mortality attendant upon it, render it the most formidable of catastrophes. Lord Moynihan, 1925

References Bassi C et al. Controlled clinical trial of pefloxacin versus imipenem in severe acute pancreatitis. Gastroenterology. 1998;115:1513-7 Bassi, C., M. Larvin,, et al. (2003). "Antibiotic therapy for prophylaxis against infection of pancreatic necrosis in acute pancreatitis." Cochrane Database Syst Rev(4): CD002941. Bradley EL, A clinically based classification system for acute pancreatits.. Summary of the ISAP, Atlanta, 1992. Arch Surg 1993;128(5):586-90 90 Dellinger EP et al. Early antibiotic treatment for severe acute necrotizing pancreatitis: randomized, double-blind, blind, placebo-controlled controlled study. Ann Surg. 2007;245(5):674-83. Dervenis C et al. Diagnosis, objective assessment of severity, and management of acute pancreatitis. Santorini. Int J Pancreatol. 1999;25(3):195-210 210 Isenman R et al. Prophylactic antibiotic treatment in patients with predicted severe acute pancreatitis: placebo-controlled controlled double blind trial. Gastroent.. 2004;126:997-1004 1004 Manes G et al. Prophylaxis with meropenem of septic complications s in acute pancreatitis: randomized controlled trial versus imipenem. Pancreas. 2003;27(4):e79-83 Maravi-Poma E et al. Early antibiotic treatment prophylaxis of septic complications c in severe acute necrotizing pancreatitis: a prospective randomized multicenter study comparing two regimens with imipenem-cilastin cilastin.. Int Care Med. 2003;29:1974-80 Pederzoli P et al. A randomized multicenter clinical trial of antibiotic prophylaxis of septic complications in acute necrotizing pancreatitis with imipenem. Surg Gynecol Obstet. 1993;176:480-3 Rokke,, O., T. B. Harbitz,, et al. (2007). "Early treatment of severe pancreatitis with imipenem: ipenem: a prospective randomized clinical trial." Scand J Gastroenterol 42(6): 771-6. Sainio V et al. Early antibiotic treatment in acute necrotizing pancreatitis atitis.. Lancet 1995;346:663-7 Villatoro E et al. Antibiotic therapy for prophylaxis against infectino of pancreatic necrosis in acute pancreatitis. Cochrane Database Syst Rev. 2006.CD002941 Villatoro,, E., M. Mulla,, et al. "Antibiotic therapy for prophylaxis against infection of pancreatic necrosis in acute pancreatitis." Cochrane Database Syst Rev 5: : CD002941. Waele JJD et al. Emergence of antibiotic resistance in infected pancreatic necrosis. Arch Surg 2004;139:1371-1375 1375. Xu, T. and Q. Cai (2008). "Prophylactic antibiotic treatment in acute necrotizing pancreatitis: results from a meta-analysis." analysis." Scand J Gastroenterol 43(10): 1249-58.