Comparing the Effects of EST and EPBD in Patients With Acute Biliary Pancreatitis
Acute Biliary Pancreatitis
About this trial
This is an interventional treatment trial for Acute Biliary Pancreatitis focused on measuring Endoscopic sphincterotomy, Endoscopic papillary balloon dilation, Metagenomics
Eligibility Criteria
Patients with age ≥ 20 years and acute biliary pancreatitis concomitant with either signs of acute cholangitis or bile duct obstruction will be enrolled in the study. They will be randomized into two treatment groups (sphincterotomy vs. balloon dilation).
Inclusion Criteria:
Patients diagnosed with acute gallstone pancreatitis and fulfill any two items from a to c, plus one item in d, and e:
- abdominal pain typical of pancreatitis;
- elevation of serum amylase and/or lipase up to three times above normal;
- imaging studies (abdominal ultrasound or abdominal computed tomography) showed evidence of pancreatitis
- common bile duct stones, acute cholangitis (Charcot's triad), total bilirubin (total bilirubin)> 4mg / dL, bile duct dilatation (diameter> 6mm with intact gallbladder, or> 10mm when the gallbladder has been removed) plus total bilirubin 1.8 ~ 4mg / dL;
- exclude other causes of acute pancreatitis.
Exclusion Criteria:
- septic shock
- serious coagulopathy (international normalized ratio 1.5, partial thromboplastin time greater than twice that of control, platelet count <50 x 1000 / Cumm)
- malignant tumors of the biliary and pancreatic tract
- severe cardiovascular or mental illness which can not cooperate with the exam and treatment;
- pregnant women
- patient who had ever received surgery or endoscopic treatment for biliopancreatic tract
Sites / Locations
- Kaohsiung Veterans General Hospital.Recruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Endoscopic papillary balloon dilation
Endoscopic sphincterotomy
For EPBD group, after selective cannulation of the common bile duct by the catheter, cholangiography will be performed to confirm the diagnosis of bile duct pathology. A 0.025-0.035-inch guidewire will then be inserted into the bile duct through the catheter. A dilating balloon (The controlled radial expansion (CRE) balloon dilation catheter, CRE balloon 5.5 cm (centimeter) in length, 1-1.2 cm/1.2-1.5 cm/1.5-2.0 cm in diameter) will be passed via the pre-positioned guidewire into the bile duct. Using fluoroscopic and endoscopic guidance, the balloon will be inflated with contrast medium up to the optimal size and duration (normally 5min (minutes)) after the waist on the balloon disappeared according to the patients' condition and tolerance.
For EST group,endoscopic sphincterotomy(EST) will be done as large as possible with a pull type sphincterotome (The TRUEtome, Biliary sphincterotomy sphincterotome, Single-use sphincterotome CleverCut2V) Other interventions: surgical intervention, endoscopic stenting, percutaneous transhepatic cholangiogram with balloon dilation