Multi-center Clinical Study of Early Antibios of Severe Acute Pancreatitis
- Conditions
- Pancreatitis,Acute Necrotizing
- Interventions
- Procedure: oral care by chlorhexidine gluconateProcedure: enteral nutrition
- Registration Number
- NCT01992198
- Lead Sponsor
- Erzhen Chen
- Brief Summary
Strategy of antibiotic therapy in SAP,De-escalate (cefoperazone+metronidazole) or Escalate (meropenem) therapy,which one is better.
- Detailed Description
SAP is a serious and life-threatening disease and requires intensive and aggressive management of multiple organ failure and severe infectious complications that can develop in these patients. The most common cause of death in patients suffering from severe acute pancreatitis (SAP) is the infection of pancreatic necrosis by enteric bacteria with mortality rates of 30% (range 14- 62%),spurring the discussion of whether or not prophylactic antibiotic administration could be a beneficial approach. Pancreatic infections are more often monomicrobial, especially E. coli in the two first weeks (100% and 62.5%) of onset, with a shift from gram-negative to gram-positive as the pancreatitis progressed.
In order to evaluate the benefit of prophylactic antibiotic application, a number of randomized controlled clinical trials have been published over the past 15 years. Since the results were conflicting and most studies were of low methodological quality and/or statistically underpowered, meta-analyses have been performed to assess this important issue. However, their results ranged from absolutely no effect of antibiotic prophylaxis to positive effects regarding mortality, the incidence of infected pancreatic necrosis and the incidence of extra pancreatic infections.
In order to provide reliable evidence of the effect of antibiotherapy strategy in SAP, we performed a prospective randomized multicenter clinical trial.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 60
- severe Acute Pancreatitis according to Atlanta criteria revisited in 2012
- concurrent sepsis or (peri)pancreatic infection caused by a second disease
- patients with chronic organ failure (chronic renal failure needs kidney replacement, chronic heart failure, decompensate hepatic cirrhosis, chronic obstructive pulmonary disease)
- recurrent or endoscopic retrograde cholangiopancreatography (ERCP), or traumatic or operative pancreatitis
- pregnancy, malignancy or immunodeficiency
- a history of allergy to meropenem, cefoperazone and metronidazole
- a history of antibiotic administration within 48 h prior to enrollment
- possible death within 48 h after enrollment
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description cefoperazone + metronidazole Somatostatin cefoperaozone 2g q8h + MDZ 0.5g q8h Oral care Somatostatin 3-6mg per 24h enteral nutrition cefoperazone + metronidazole Meropenem cefoperaozone 2g q8h + MDZ 0.5g q8h Oral care Somatostatin 3-6mg per 24h enteral nutrition meropenem cefoperazone + metronidazole Meropenem 0.5g q6h or adapted with renal function. Oral care Somatostatin 3-6mg per 24h enteral nutrition meropenem oral care by chlorhexidine gluconate Meropenem 0.5g q6h or adapted with renal function. Oral care Somatostatin 3-6mg per 24h enteral nutrition meropenem enteral nutrition Meropenem 0.5g q6h or adapted with renal function. Oral care Somatostatin 3-6mg per 24h enteral nutrition meropenem Somatostatin Meropenem 0.5g q6h or adapted with renal function. Oral care Somatostatin 3-6mg per 24h enteral nutrition cefoperazone + metronidazole oral care by chlorhexidine gluconate cefoperaozone 2g q8h + MDZ 0.5g q8h Oral care Somatostatin 3-6mg per 24h enteral nutrition cefoperazone + metronidazole enteral nutrition cefoperaozone 2g q8h + MDZ 0.5g q8h Oral care Somatostatin 3-6mg per 24h enteral nutrition
- Primary Outcome Measures
Name Time Method pancreatic or peripancreatic infection 28-day
- Secondary Outcome Measures
Name Time Method cost of management of SAP 90-day Microbiology resistance 90-day sputum, urine and blood culture will be done once or twice per week if needed. bill or other culutre will be done when the patient is undergoing operation.
Trial Locations
- Locations (1)
Depatrment of EICU,Ruijin Hospital
🇨🇳Shanghai, Shanghai, China