Endoscopic sphincterotomy to prevent post-ERCP pancreatitis after self-expandable metal stent placement for distal malignant biliary obstruction (SPHINX): a multicentre, randomised controlled trial.

diagnostic and therapeutic endoscopy endoscopic retrograde pancreatography endoscopic sphincterotomy hepatobiliary cancer pancreatitis

Journal

Gut
ISSN: 1468-3288
Titre abrégé: Gut
Pays: England
ID NLM: 2985108R

Informations de publication

Date de publication:
10 Oct 2024
Historique:
received: 19 04 2024
accepted: 27 09 2024
medline: 11 10 2024
pubmed: 11 10 2024
entrez: 10 10 2024
Statut: aheadofprint

Résumé

Endoscopic retrograde cholangiopancreatography (ERCP) with fully covered self-expandable metal stent (FCSEMS) placement is the preferred approach for biliary drainage in patients with suspected distal malignant biliary obstruction (MBO). However, FCSEMS placement is associated with a high risk of post-ERCP pancreatitis (PEP). Endoscopic sphincterotomy prior to FCSEMS placement may reduce PEP risk. To compare endoscopic sphincterotomy to no sphincterotomy prior to FCSEMS placement. This multicentre, randomised, superiority trial was conducted in 17 hospitals and included patients with suspected distal MBO. Patients were randomised during ERCP to receive either endoscopic sphincterotomy (sphincterotomy group) or no sphincterotomy (control group) prior to FCSEMS placement. The primary outcome was PEP within 30 days. Secondary outcomes included procedure-related complications and 30-day mortality. An interim analysis was performed after 50% of patients (n=259) had completed follow-up. Between May 2016 and June 2023, 297 patients were included in the intention-to-treat analysis, with 156 in the sphincterotomy group and 141 in the control group. After the interim analysis, the study was terminated prematurely due to futility. PEP did not differ between groups, occurring in 26 patients (17%) in the sphincterotomy group compared with 30 patients (21%) in the control group (relative risk 0.78, 95% CI 0.49 to 1.26, p=0.37). There were no significant differences in bleeding, perforation, cholangitis, cholecystitis or 30-day mortality. This trial found that endoscopic sphincterotomy was not superior to no sphincterotomy in reducing PEP in patients with distal MBO. Therefore, there was insufficient evidence to recommend routine endoscopic sphincterotomy prior to FCEMS placement. NL5130.

Sections du résumé

BACKGROUND BACKGROUND
Endoscopic retrograde cholangiopancreatography (ERCP) with fully covered self-expandable metal stent (FCSEMS) placement is the preferred approach for biliary drainage in patients with suspected distal malignant biliary obstruction (MBO). However, FCSEMS placement is associated with a high risk of post-ERCP pancreatitis (PEP). Endoscopic sphincterotomy prior to FCSEMS placement may reduce PEP risk.
OBJECTIVE OBJECTIVE
To compare endoscopic sphincterotomy to no sphincterotomy prior to FCSEMS placement.
DESIGN METHODS
This multicentre, randomised, superiority trial was conducted in 17 hospitals and included patients with suspected distal MBO. Patients were randomised during ERCP to receive either endoscopic sphincterotomy (sphincterotomy group) or no sphincterotomy (control group) prior to FCSEMS placement. The primary outcome was PEP within 30 days. Secondary outcomes included procedure-related complications and 30-day mortality. An interim analysis was performed after 50% of patients (n=259) had completed follow-up.
RESULTS RESULTS
Between May 2016 and June 2023, 297 patients were included in the intention-to-treat analysis, with 156 in the sphincterotomy group and 141 in the control group. After the interim analysis, the study was terminated prematurely due to futility. PEP did not differ between groups, occurring in 26 patients (17%) in the sphincterotomy group compared with 30 patients (21%) in the control group (relative risk 0.78, 95% CI 0.49 to 1.26, p=0.37). There were no significant differences in bleeding, perforation, cholangitis, cholecystitis or 30-day mortality.
CONCLUSION CONCLUSIONS
This trial found that endoscopic sphincterotomy was not superior to no sphincterotomy in reducing PEP in patients with distal MBO. Therefore, there was insufficient evidence to recommend routine endoscopic sphincterotomy prior to FCEMS placement.
TRIAL REGISTRATION NUMBER BACKGROUND
NL5130.

Identifiants

pubmed: 39389757
pii: gutjnl-2024-332695
doi: 10.1136/gutjnl-2024-332695
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: JvH has received research support from Cook Medical and acted as lecturer for Cook Medical, Boston Scientific and Falk, and as consultant for Olympus, outside the submitted work. RPV received a research grant and acted as consultant for Boston Scientific, outside the submitted work. PF acted as a consultant for Cook Endoscopy and Olympus, outside the submitted work. RvW acted as a consultant for Boston Scientific, outside the submitted work. All other authors declare that they have no competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Anke M Onnekink (AM)

Department of Gastroenterology and Hepatology, Leiden University Medical Centre, Leiden, The Netherlands a.m.onnekink@lumc.nl.

Myrte Gorris (M)

Department of Gastroenterology and Hepatology, Amsterdam UMC, location University of Amsterdam, and Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam UMC, Amsterdam, The Netherlands.

Noor Lh Bekkali (NL)

Department of Gastroenterology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Philip Bos (P)

Department of Gastroenterology and Hepatology, Hospital Gelderse Vallei, Ede, The Netherlands.

Paul Didden (P)

Department of Gastroenterology and Hepatology, University Medical Centre Utrecht, Utrecht, The Netherlands.

J Enrique Dominguez-Muñoz (JE)

Department of Gastroenterology and Hepatology, University Hospital of Santiago de Compostela, Santiago de Compostela, Spain.

Pieter Friederich (P)

Department of Gastroenterology and Hepatology, Catharina Hospital, Eindhoven, The Netherlands.

Emo E van Halsema (EE)

Department of Gastroenterology and Hepatology, Leiden University Medical Centre, Leiden, The Netherlands.

Wouter L Hazen (WL)

Department of Gastroenterology and Hepatology, Elisabeth-TweeSteden Ziekenhuis, Tilburg, The Netherlands.

Nadine C van Huijgevoort (NC)

Department of Gastroenterology and Hepatology, Amsterdam UMC, location Vrije Universiteit, and, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam UMC, Amsterdam, The Netherlands.

Akin Inderson (A)

Department of Gastroenterology and Hepatology, Leiden University Medical Centre, Leiden, The Netherlands.

Maarten Ajm Jacobs (MA)

Department of Gastroenterology and Hepatology, Amsterdam UMC, location Vrije Universiteit, and, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam UMC, Amsterdam, The Netherlands.

Jan J Koornstra (JJ)

Department of Gastroenterology and Hepatology, University Medical Centre Groningen, Groningen, The Netherlands.

Sjoerd Kuiken (S)

Department of Gastroenterology and Hepatology, Onze Lieve Vrouwe Hospital, Amsterdam, The Netherlands.

Bob Ch Scheffer (BC)

Department of Gastroenterology and Hepatology, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands.

Hilbert Sloterdijk (H)

Department of Gastroenterology and Hepatology, Medical Centre Leeuwarden, Leeuwarden, The Netherlands.

Ellert J van Soest (EJ)

Department of Gastroenterology and Hepatology, Spaarne Gasthuis, Hoofddorp, The Netherlands.

Niels G Venneman (NG)

Department of Gastroenterology and Hepatology, Medisch Spectrum Twente, Enschede, The Netherlands.

Rogier P Voermans (RP)

Department of Gastroenterology and Hepatology, Amsterdam UMC, location University of Amsterdam, and Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam UMC, Amsterdam, The Netherlands.

Thomas R de Wijkerslooth (TR)

Department of Gastrointestinal Oncology, Netherlands Cancer Institute, Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.

Janneke Wonders (J)

Department of Gastroenterology and Hepatology, Haga Hospital, Den Haag, The Netherlands.

Roeland Zoutendijk (R)

Department of Gastroenterology and Hepatology, Sint Antonius Hospital, Nieuwegein, The Netherlands.

Serge Jlb Zweers (SJ)

Department of Gastroenterology and Hepatology, Maasstad Hospital, Rotterdam, The Netherlands.

Paul Fockens (P)

Department of Gastroenterology and Hepatology, Amsterdam UMC, location University of Amsterdam, and Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam UMC, Amsterdam, The Netherlands.

Robert C Verdonk (RC)

Department of Gastroenterology and Hepatology, Sint Antonius Hospital, Nieuwegein, The Netherlands.

Roy L J van Wanrooij (RLJ)

Department of Gastroenterology and Hepatology, Amsterdam UMC, location Vrije Universiteit, and, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam UMC, Amsterdam, The Netherlands.

Jeanin E Van Hooft (JE)

Department of Gastroenterology and Hepatology, Leiden University Medical Centre, Leiden, The Netherlands.

Classifications MeSH