Indomethacin with or without prophylactic pancreatic stent placement to prevent pancreatitis after ERCP: a randomised non-inferiority trial.


Journal

Lancet (London, England)
ISSN: 1474-547X
Titre abrégé: Lancet
Pays: England
ID NLM: 2985213R

Informations de publication

Date de publication:
11 Jan 2024
Historique:
received: 12 07 2023
revised: 11 10 2023
accepted: 18 10 2023
medline: 15 1 2024
pubmed: 15 1 2024
entrez: 14 1 2024
Statut: aheadofprint

Résumé

The combination of rectally administered indomethacin and placement of a prophylactic pancreatic stent is recommended to prevent pancreatitis after endoscopic retrograde cholangiopancreatography (ERCP) in high-risk patients. Preliminary evidence suggests that the use of indomethacin might eliminate or substantially reduce the need for stent placement, a technically complex, costly, and potentially harmful intervention. In this randomised, non-inferiority trial conducted at 20 referral centres in the USA and Canada, patients (aged ≥18 years) at high risk for post-ERCP pancreatitis were randomly assigned (1:1) to receive rectal indomethacin alone or the combination of indomethacin plus a prophylactic pancreatic stent. Patients, treating clinicians, and outcomes assessors were masked to study group assignment. The primary outcome was post-ERCP pancreatitis. To declare non-inferiority, the upper bound of the two-sided 95% CI for the difference in post-ERCP pancreatitis (indomethacin alone minus indomethacin plus stent) would have to be less than 5% (non-inferiority margin) in both the intention-to-treat and per-protocol populations. This trial is registered with ClinicalTrials.gov (NCT02476279), and is complete. Between Sept 17, 2015, and Jan 25, 2023, a total of 1950 patients were randomly assigned. Post-ERCP pancreatitis occurred in 145 (14·9%) of 975 patients in the indomethacin alone group and in 110 (11·3%) of 975 in the indomethacin plus stent group (risk difference 3·6%; 95% CI 0·6-6·6; p=0·18 for non-inferiority). A post-hoc intention-to-treat analysis of the risk difference between groups showed that indomethacin alone was inferior to the combination of indomethacin plus prophylactic stent (p=0·011). The relative benefit of stent placement was generally consistent across study subgroups but appeared more prominent among patients at highest risk for pancreatitis. Safety outcomes (serious adverse events, intensive care unit admission, and hospital length of stay) did not differ between groups. For preventing post-ERCP pancreatitis in high-risk patients, a strategy of indomethacin alone was not as effective as a strategy of indomethacin plus prophylactic pancreatic stent placement. These results support prophylactic pancreatic stent placement in addition to rectal indomethacin administration in high-risk patients, in accordance with clinical practice guidelines. US National Institutes of Health.

Sections du résumé

BACKGROUND BACKGROUND
The combination of rectally administered indomethacin and placement of a prophylactic pancreatic stent is recommended to prevent pancreatitis after endoscopic retrograde cholangiopancreatography (ERCP) in high-risk patients. Preliminary evidence suggests that the use of indomethacin might eliminate or substantially reduce the need for stent placement, a technically complex, costly, and potentially harmful intervention.
METHODS METHODS
In this randomised, non-inferiority trial conducted at 20 referral centres in the USA and Canada, patients (aged ≥18 years) at high risk for post-ERCP pancreatitis were randomly assigned (1:1) to receive rectal indomethacin alone or the combination of indomethacin plus a prophylactic pancreatic stent. Patients, treating clinicians, and outcomes assessors were masked to study group assignment. The primary outcome was post-ERCP pancreatitis. To declare non-inferiority, the upper bound of the two-sided 95% CI for the difference in post-ERCP pancreatitis (indomethacin alone minus indomethacin plus stent) would have to be less than 5% (non-inferiority margin) in both the intention-to-treat and per-protocol populations. This trial is registered with ClinicalTrials.gov (NCT02476279), and is complete.
FINDINGS RESULTS
Between Sept 17, 2015, and Jan 25, 2023, a total of 1950 patients were randomly assigned. Post-ERCP pancreatitis occurred in 145 (14·9%) of 975 patients in the indomethacin alone group and in 110 (11·3%) of 975 in the indomethacin plus stent group (risk difference 3·6%; 95% CI 0·6-6·6; p=0·18 for non-inferiority). A post-hoc intention-to-treat analysis of the risk difference between groups showed that indomethacin alone was inferior to the combination of indomethacin plus prophylactic stent (p=0·011). The relative benefit of stent placement was generally consistent across study subgroups but appeared more prominent among patients at highest risk for pancreatitis. Safety outcomes (serious adverse events, intensive care unit admission, and hospital length of stay) did not differ between groups.
INTERPRETATION CONCLUSIONS
For preventing post-ERCP pancreatitis in high-risk patients, a strategy of indomethacin alone was not as effective as a strategy of indomethacin plus prophylactic pancreatic stent placement. These results support prophylactic pancreatic stent placement in addition to rectal indomethacin administration in high-risk patients, in accordance with clinical practice guidelines.
FUNDING BACKGROUND
US National Institutes of Health.

Identifiants

pubmed: 38219767
pii: S0140-6736(23)02356-5
doi: 10.1016/S0140-6736(23)02356-5
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT02476279']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Investigateurs

B Joseph Elmunzer (BJ)
Lydia D Foster (LD)
Jose Serrano (J)
Gregory A Coté (GA)
Steven A Edmundowicz (SA)
Sachin Wani (S)
Raj Shah (R)
Ji Young Bang (JY)
Shyam Varadarajulu (S)
Vikesh K Singh (VK)
Mouen Khashab (M)
Richard S Kwon (RS)
James M Scheiman (JM)
Field F Willingham (FF)
Steven A Keilin (SA)
Georgios I Papachristou (GI)
Amitabh Chak (A)
Adam Slivka (A)
Daniel Mullady (D)
Vladimir Kushnir (V)
James Buxbaum (J)
Rajesh Keswani (R)
Timothy B Gardner (TB)
Nauzer Forbes (N)
Amit Rastogi (A)
Andrew Ross (A)
Joanna Law (J)
Patrick Yachimski (P)
Yen-I Chen (YI)
Alan Barkun (A)
Zachary L Smith (ZL)
Bret Petersen (B)
Andrew Y Wang (AY)
John R Saltzman (JR)
Rebecca L Spitzer (RL)
Collins Ordiah (C)
Cathie Spino (C)
Peter D R Higgins (PDR)
Erin Forster (E)
Robert A Moran (RA)
Brian Brauer (B)
Erik J Wamsteker (EJ)
Qiang Cai (Q)
Emad Qayed (E)
Royce Groce (R)
Somashekar G Krishna (SG)
Ashley Faulx (A)
Brooke Glessing (B)
Mordechai Rabinovitz (M)
Gabriel Lang (G)
Aziz Aadam (A)
Srinadh Komanduri (S)
Jefferey Adler (J)
Stuart Gordon (S)
Rachid Mohamed (R)
Mojtaba Olyaee (M)
April Wood-Williams (A)
Emily K Depue Brewbaker (EK)
Andre Thornhill (A)
Mariana Gould (M)
Kristen Clasen (K)
Jama Olsen (J)
Violette C Simon (VC)
Ayesha Kamal (A)
Sarah L Volk (SL)
Ambreen A Merchant (AA)
Ali Lahooti (A)
Nancy Furey (N)
Gulsum Anderson (G)
Thomas Hollander (T)
Alejandro Vazquez (A)
Thomas Y Li (TY)
Steven M Hadley (SM)
Millie Chau (M)
Robinson Mendoza (R)
Tida Tangwongchai (T)
Casey L Koza (CL)
Olivia Geraci (O)
Lizbeth Nunez (L)
Alexander M Waters (AM)
Valerie Durkalski-Mauldin (V)

Informations de copyright

Copyright © 2024 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The following authors have received honoraria, consulting fees, or research support from companies that manufacture prophylactic pancreatic stents or indomethacin within the last 2 years: SAE (consulting fees from Olympus, honoraria from Boston Scientific), NF (consulting fees and payment or honoraria for lectures or receipt of equipment or materials from Boston Scientific and Pentax), FFW (consulting fees from Cook/Boston Scientific), SV (consulting fees from Boston Scientific/Olympus), JYB (consulting fees from Boston Scientific/Olympus), MK (consulting fees from Boston Scientific), RK (consulting fees from Boston Scientific), Y-IC (consulting fees, honoraria, research grants, and travel payments from Boston Scientific), AB (financial interest in Olympus), ARo (payment or honoraria for lectures or presentations and travel from Boston Scientific), and study group members SGK (honoraria and grant support from Taewoong Medical) and SG (consulting fees and honoraria from Boston Scientific). All other authors declare no competing interests.

Auteurs

B Joseph Elmunzer (BJ)

Division of Gastroenterology & Hepatology, Medical University of South Carolina, Charleston, SC, USA. Electronic address: elmunzer@musc.edu.

Lydia D Foster (LD)

Data Coordination Unit, Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA.

Jose Serrano (J)

National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.

Gregory A Coté (GA)

Division of Gastroenterology & Hepatology, Oregon Health & Science University, Portland, OR, USA.

Steven A Edmundowicz (SA)

Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Sachin Wani (S)

Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Raj Shah (R)

Division of Gastroenterology and Hepatology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

Ji Young Bang (JY)

Orlando Health Digestive Health Institute, Orlando Health, Orlando, FL, USA.

Shyam Varadarajulu (S)

Orlando Health Digestive Health Institute, Orlando Health, Orlando, FL, USA.

Vikesh K Singh (VK)

Division of Gastroenterology, Johns Hopkins Medical Institutions, Baltimore, MD, USA.

Mouen Khashab (M)

Division of Gastroenterology, Johns Hopkins Medical Institutions, Baltimore, MD, USA.

Richard S Kwon (RS)

Division of Gastroenterology, University of Michigan Medical Center, Ann Arbor, MI, USA.

James M Scheiman (JM)

Division of Gastroenterology, University of Michigan Medical Center, Ann Arbor, MI, USA.

Field F Willingham (FF)

Division of Digestive Diseases, Emory University School of Medicine, Atlanta, GA, USA.

Steven A Keilin (SA)

Division of Digestive Diseases, Emory University School of Medicine, Atlanta, GA, USA.

Georgios I Papachristou (GI)

Division of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical Center, Columbus, OH, USA.

Amitabh Chak (A)

Division of Gastroenterology, University Hospitals Cleveland Medical Center, Cleveland, OH, USA.

Adam Slivka (A)

Division of Gastroenterology, Hepatology, and Nutrition, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.

Daniel Mullady (D)

Division of Gastroenterology, Washington University School of Medicine, St Louis, MO, USA.

Vladimir Kushnir (V)

Division of Gastroenterology, Washington University School of Medicine, St Louis, MO, USA.

James Buxbaum (J)

Division of Gastroenterology, University of Southern California, Los Angeles, CA, USA.

Rajesh Keswani (R)

Division of Gastroenterology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

Timothy B Gardner (TB)

Section of Gastroenterology and Hepatology, Dartmouth-Hitchcock Health, Lebanon, NH, USA.

Nauzer Forbes (N)

Division of Gastroenterology, University of Calgary, Calgary, AB, Canada.

Amit Rastogi (A)

Division of Gastroenterology and Hepatology, University of Kansas Medical Center, Kansas City, KS, USA.

Andrew Ross (A)

Division of Gastroenterology, Virginia Mason Medical Center, Seattle, WA, USA.

Joanna Law (J)

Division of Gastroenterology, Virginia Mason Medical Center, Seattle, WA, USA.

Patrick Yachimski (P)

Division of Gastroenterology, Hepatology, and Nutrition, Vanderbilt University Medical Center, Nashville, TN, USA.

Yen-I Chen (YI)

Division of Gastroenterology, McGill University, Montreal, QC, Canada.

Alan Barkun (A)

Division of Gastroenterology, McGill University, Montreal, QC, Canada.

Zachary L Smith (ZL)

Division of Gastroenterology, Medical College of Wisconsin, Milwaukee, WI, USA.

Bret Petersen (B)

Department of Gastroenterology, Mayo Clinic, Rochester, MN, USA.

Andrew Y Wang (AY)

Division of Gastroenterology, University of Virginia, Charlottesville, VA, USA.

John R Saltzman (JR)

Division of Gastroenterology, Hepatology and Endoscopy, Brigham and Women's Hospital, Boston, MA, USA.

Rebecca L Spitzer (RL)

Division of Gastroenterology & Hepatology, Medical University of South Carolina, Charleston, SC, USA.

Collins Ordiah (C)

Division of Gastroenterology & Hepatology, Medical University of South Carolina, Charleston, SC, USA.

Cathie Spino (C)

Department of Public Health, University of Michigan, Ann Arbor, MI, USA.

Valerie Durkalski-Mauldin (V)

Data Coordination Unit, Department of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA.

Classifications MeSH