Pancreatitis
Conditions
Keywords
cholecystectomy
Brief summary
Randomized trial of laparoscopic cholecystectomy with cholangiogram on admission versus after resolution of pain for mild gallstone pancreatitis.
Detailed description
The purpose of this study is to perform a single-center randomized trial to compare laparoscopic cholecystectomy with intraoperative cholangiogram (IOC) within 24 hours of presentation versus after clinical resolution during index admission for mild gallstone pancreatitis on clinical and patient-reported outcomes. Additionally, this study aims to determine patients' values and preferences that influence decision-making regarding treatment options for gallstone pancreatitis. Hypothesis: During index admission for mild gallstone pancreatitis, early cholecystectomy within 24 hours of presentation regardless of symptoms or laboratory values versus after clinical resolution results in a shorter 30-day total hospital length of stay.
Interventions
The intervention will be laparoscopic cholecystectomy with intraoperative cholangiogram (IOC) on admission within 24 hours of presentation regardless of whether pain or tenderness are present or laboratory values are elevated.
The control will be laparoscopic cholecystectomy with IOC once the patient has met the following criteria: (a) a score of less than 2 on the Visual Analogue Pain Scale, (b) no tenderness on physical exam, and (c) decreased lipase to either less than half of the peak value or within normal range (73-393 U/L).
Sponsors
Study design
Eligibility
Inclusion criteria
* Diagnosis of gallstone pancreatitis. Patients will be considered to have gallstone pancreatitis if they have: 1. upper abdominal pain, nausea, vomiting, and epigastric tenderness 2. absence of ethanol abuse 3. elevated lipase level above the upper limit of normal (\>370 U/L) 4. imaging confirmation of gallstones or sludge * Low predicted mortality using the Bedside Index of Severity in Acute Pancreatitis (BISAP) -Diagnosis of mild pancreatitis (i.e.,no evidence of organ failure or local or systemic complications) * Scheduled for laparoscopic cholecystectomy prior to discharge * Lack of any very strong indicator for choledocholithiasis based on the American Society for Gastrointestinal Endoscopy (ASGE) guidelines * Clinical stability as denoted by admission to a non-monitored floor bed.
Exclusion criteria
* Pregnancy * Severe preexisting medical comorbidities precluding surgery, organ failure, local or systemic complications of acute pancreatitis * Chronic pancreatitis * Native language other than English and Spanish * Patient refusal to participate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 30-day hospital length of stay | 30 days |
Secondary
| Measure | Time frame |
|---|---|
| Initial hospital LOS | up to 30 days |
| Number of participants who underwent conversion to open cholecystectomy | 30 days |
| Change in patient reported outcomes as assessed by the Gastrointestinal Quality-of-Life Index (GIQLI) | baseline, 1 week |
| Time from admission to cholecystectomy | up to 10 days |
| Change in patient reported outcomes as assessed by the Patients' Experience of Surgery Questionnaire (PESQ) | baseline, 1 week |
| Change in health-related quality of life as assessed by the standard gamble | baseline, 1 week |
| Change in patient reported outcomes as assessed by the Gastrointestinal Quality-of-Life Index (GIQLI) and Patients' Experience of Surgery Questionnaire (PESQ) | baseline, 6 weeks |
Countries
United States