IMPEL

Prospective international audit of mechanical large-bowel obstruction.

IMPEL banner graphic

IMPEL is an international, time-bound prospective observational clinical snapshot audit that characterizes the epidemiology, diagnostic pathways, operative and non-operative management strategies, and short-term outcomes of mechanical large-bowel obstruction across real-world acute care settings. The platform supports benchmarking, defines variation in care, and preserves the structure required for decision-aligned comparative analyses in clinically coherent subgroups.

Last updated: 2026-05-05 Protocol v1.0 · 2026-01-28 ClinicalTrials.gov: NCT07458867

Leadership and governance

Study coordination and collaborative structure.

Gary Alan Bass

CESOR Director

Gary Alan Bass, MD, MSc, MBA, PhD, FICS, FEBS (Emergency Surgery)
Assistant Professor of Surgery and Assistant Professor of Biostatistics and Epidemiology, Perelman School of Medicine, University of Pennsylvania
gary.bass@pennmedicine.upenn.edu

Matteo Maria Cimino

Co-Lead Coordinator

Matteo Maria Cimino, MD
IRCCS Fondazione Ca' Granda Ospedale Maggiore Policlinico, Milan
cimino.matteo@gmail.com

Steering group

IMPEL is overseen through CESOR with representation from ESTES, ASGBI, ESCP, and ASCRS alongside senior emergency and colorectal surgery collaborators.

Why this study exists

Large-bowel obstruction is common, high-acuity, and marked by persistent pathway variation.

Mechanical large-bowel obstruction is associated with substantial morbidity, mortality, stoma burden, and resource use. Yet the contemporary evidence base remains dominated by retrospective studies, cancer-specific cohorts, and single-center series, with recommendations often extrapolated from heterogeneous populations.

IMPEL captures acute-care practice: how patients are diagnosed, decompressed, selected for surgery, diverted, resected, and followed. The result is a structured map of current care that supports benchmarking and design-first comparative analysis.

Core objective

Management pathways

Diagnostic strategy, operative timing, procedure choice, and stoma-related outcomes

Inclusion window

90 days

Consecutive eligible adults during a local 90-day study period

Short-term outcomes

30-day morbidity and mortality

With inpatient course, complications, reintervention, and critical-care use

Patient-centered follow-up

6-month stoma status

Persistence, reversal, and late complications after index obstruction care

Design

What IMPEL measures.

Prospective snapshot audit

International multicenter inclusion of consecutive adults with mechanical large-bowel obstruction using standardized prospective data capture and routinely collected clinical data only.

Diagnostic pathway detail

IMPEL records presenting physiology, imaging modality and timing, decompression attempts, endoscopic evaluation, and the interval from presentation to definitive management decisions.

Operative and non-operative strategy

The platform captures both operative and non-operative care, including urgency, approach, resection, anastomosis, stoma creation, staged strategies, and non-operative management patterns.

Outcomes beyond discharge

In-hospital course, critical care use, re-intervention, complications, discharge destination, and later stoma outcomes are captured to reflect the practical burden of emergency LBO care.

Decision-aligned analytic agenda

Core comparative questions already visible within the platform.

M1

Malignant left-sided obstruction

  • Immediate oncologic resection versus decompression-first care
  • Includes endoscopic stenting or diverting stoma where both strategies are feasible
  • Outcomes: DAOH90, 90-day mortality, and stoma-free survival
  • Question: does decompression-first care improve early recovery or simply defer risk?

M2

Sigmoid volvulus pathway selection

  • Endoscopic decompression-first versus upfront surgery
  • Restricted to patients without perforation, ischemia, or peritonitis and with dual feasibility
  • Outcomes: recurrence-free survival, emergency surgery, morbidity, and mortality
  • Question: is decompression-first a bridge or a recurrence-generating delay?

M3

High-risk and frail patients

  • Initial operative intervention versus initial non-operative or temporizing management
  • Conditional on the treating team documenting both pathways as feasible
  • Outcomes: 90-day mortality, DAOH90, critical-care use, and later intervention
  • Question: does restraint reflect good selection or modifiable therapeutic nihilism?

Spin-off work

Stoma burden and systems variation

  • Predictors of 6-month stoma persistence and non-reversal
  • Center-level resource and capability benchmarking
  • Variation in CT, endoscopy, colorectal surgery, and emergency OR access
  • Focus on modifiable process variation rather than unsupported causal claims

Stoma burden is part of the outcome, not an afterthought. IMPEL quantifies not only who survives the index admission, but how pathway selection shapes continuity restoration, later complications, and the medium-term consequences of emergency colorectal care.

That makes the platform more informative than a simple in-hospital audit and strengthens its benchmarking and comparative value.

For participating centers and collaborators

How to engage with the study.

IMPEL is intended for centers able to support consecutive case ascertainment, structured prospective data capture, local governance approval, and follow-up through six months for stoma outcomes using routine clinical data. Acute care surgeons, colorectal surgeons, endoscopists, methodologists, and implementation collaborators can engage through CESOR’s participation pathways.

For participating centers

Site interest and onboarding

Centers interested in participation should contact CESOR and submit structured intake through the participation pathway.

For analysts and collaborators

Methods, benchmarking, and secondary analyses

Collaborators with relevant methodological, colorectal, emergency surgery, or systems expertise should review CESOR participation pathways before initial outreach.