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Extracorporeal Shock-Wave Lithotripsy and Endoscopy for the Treatment of Pain in Chronic Pancreatitis: A Sham-Controlled, Randomized Trial

  • Rupjyoti Talukdar
  • , Søren S. Olesen
  • , Misbah Unnisa
  • , Akshay Bedarkar
  • , Subhaleena Sarkar
  • , Manu Tandan
  • , Nitin Jagtap
  • , Santosh Darisetty
  • , Sekhramantri Kiran
  • , Vinod Koppoju
  • , Sundeep Lakhtakia
  • , Mohan Ramchandani
  • , Rakesh Kalapala
  • , Rajesh Gupta
  • , Vikesh K. Singh
  • , Guduru Venkat Rao
  • , Duvvur Nageshwar Reddy
  • , Asbjørn M. Drewes

Research output: Contribution to journalArticlepeer-review

Abstract

Background: No randomized controlled trials have substantiated endoscopic decompression of the pancreatic duct in patients with painful chronic pancreatitis. Objective: To investigate the pain-relieving effect of pancreatic duct decompression in patients with chronic pancreatitis and intraductal stones. Design: 24-week, parallel-group, randomized controlled trial (ClinicalTrials.gov: NCT03966781) Setting: Asian Institute of Gastroenterology in India from February 2021 to July 2022. Participants: 106 patients with chronic pancreatitis. Intervention: Combined extracorporeal shock-wave lithotripsy (ESWL) and endoscopic retrograde pancreatography (ERP) compared with sham procedures. Measurements: The primary end point was pain relief on a 0- to 10-point visual analog scale (VAS) at 12 weeks. Secondary outcomes were assessed after 12 and 24 weeks and included 30% pain relief, opioid use, pain-free days, questionaries, and complications to interventions. Results: 52 patients in the ESWL/ERP group and 54 in the sham group were included. At 12 weeks, the ESWL/ERP group showed better pain relief compared with the sham group (mean difference in change, -0.7 [95% CI, -1.3 to 0] on the VAS; P= 0.039). The difference between groups was not sustained at the 24-week follow-up, and no differences were seen for 30% pain relief at 12- or 24-week follow-up. The number of pain-free days was increased (median difference, 16.2 days [CI, 3.9 to 28.5 days]), and the number of days using opioids was reduced (median difference, -5.4 days [CI, -9.9 to -0.9 days]) in the ESWL/ERP group compared with the sham group at 12-week follow-up. Safety outcomes were similar between groups. Limitation: Single-center study and limited duration of follow-up. Conclusion: In patients with chronic pancreatitis and intraductal stones, ESWL with ERP provided modest short-term pain relief.

Original languageEnglish (US)
Pages (from-to)749-758
Number of pages10
JournalAnnals of internal medicine
Volume177
Issue number6
DOIs
StatePublished - Jun 1 2024

ASJC Scopus subject areas

  • Internal Medicine

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