PORSCH: POstopeRative Standardization of Care: THe Implementation of Best Practice After Pancreatic Resection

Sponsor
St. Antonius Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT03400280
Collaborator
Dutch Cancer Society (Other)
1,600
17
2
25
94.1
3.8

Study Details

Study Description

Brief Summary

This Nationwide stepped-wedge cluster randomized trial is designed to evaluate if the implementation of a best practice algorithm for postoperative care results in a decrease in incidence of major complications and death after pancreatic resection as compared to current practice.

Condition or Disease Intervention/Treatment Phase
  • Other: Best practice algorithm for postoperative care
N/A

Detailed Description

Rationale

Pancreatic resection is a major abdominal operation with 50% chance of postoperative complications. A feared complication is severe pancreatic fistula, in which there is leakage of enzyme rich fluid into the abdominal cavity. Adequate complication management appears to be the most important factor in improving outcomes of patients undergoing pancreatic resection.

Objective

To investigate whether implementation of a best practice algorithm for postoperative care focusing on early detection and step-up management of postoperative pancreatic fistula results in a lower rate of major complications and death after pancreatic resection as compared to current practice

Study design

A nationwide stepped-wedge, cluster randomized, superiority trial. In this design all participating centers cross over from current practice to best practice according to the algorithm, but are randomized to determine the exact order. At the end of the trial, all centers will have implemented the best practice algorithm.

Study population

All centers performing pancreatic surgery in the Netherlands (i.e. the Dutch Pancreatic Cancer Group).

Intervention

Cluster level education on postoperative care according to a best practice algorithm, focusing on early detection and step-up management of postoperative pancreatic fistula. This algorithm is based on findings in Dutch observational cohort studies, systematic literature analyses, an inventory in current protocols on postoperative care and expert opinion. The proposed algorithm is validated in a multicenter cohort and consensus upon this algorithm is reached with pancreatic surgeons from all centers of the Dutch Pancreatic Cancer Group. The final algorithm was reviewed critically by the advisory committee of internationally respected experts in the field of pancreatology before implementation in this trial.

Comparison

Postoperative care according to current practice.

Endpoints

The primary outcome was measured in all patients undergoing pancreatic resection and is a composite of major complications (i.e. postpancreatectomy bleeding, new-onset organ failure and death). Secondary endpoints include the individual components of the primary endpoint and other clinical outcomes, number of patients receiving adjuvant chemotherapy, healthcare resource utilization and costs analysis. Follow-up will be 90 days after pancreatic resection.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
1600 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
Stepped-wedge cluster randomized trialStepped-wedge cluster randomized trial
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
POstopeRative Standardization of Care: THe Implementation of Best Practice After Pancreatic Resection. a Nationwide Stepped-Wedge Cluster Randomized Trial
Actual Study Start Date :
Jan 8, 2018
Anticipated Primary Completion Date :
Nov 9, 2019
Anticipated Study Completion Date :
Feb 9, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Best practice

Postoperative care according to a best practice algorithm for postoperative care focussing on early detection and minimally invasive management of postoperative pancreatic fistula.

Other: Best practice algorithm for postoperative care
See arm/group description

No Intervention: Current practice

Postoperative care according to current usual practice.

Outcome Measures

Primary Outcome Measures

  1. Composite primary endpoint [90 days after index pancreatic resection]

    The primary endpoint of this trial is a composite of the most severe complications associated to postoperative pancreatic fistula. This endpoint will be considered positive if one of the following complications occurs within 90 days after pancreatic resection: late postpancreatectomy bleeding, new-onset organ failure and/or death

Secondary Outcome Measures

  1. Postoperative mortality [90 days after index pancreatic resection]

    Measured as rate of death at 90-day follow-up

  2. New-onset organ failure [90 days after index pancreatic resection]

    Measured as organ failure occuring any time within 90 days after resection, not present at time of index pancreatic resection.

  3. Late postpancreatectomy bleeding [90 days after index pancreatic resection]

    Defined in accordance to the International Study Group on Pancreatic Surgery (ISGPS) definition as bleeding occurring any time after 24 hours after pancreatic resection.

  4. Postoperative morbidity [90 days after index pancreatic resection]

    Including complications according to the Clavien-Dindo system and pancreatectomy specific complications according to the ISGPS definitions (e.g. postpancreatectomy bleeding, postoperative pancreatic fistula, postoperative bile leak, postoperative chyle leak and delayed gastric emptying).

  5. Adjuvant chemotherapy [90 days after index pancreatic resection]

    Measured as number of patients receiving adjuvant chemotherapy at 90-day follow-up

  6. Success of implementation [90 days after index pancreatic resection]

    Measured as number of patients in whom the algorithm was not followed and timing of abdominal CT scans in both strategies.

  7. Cost-effectiveness [90 days after index pancreatic resection]

    Calculated by comparing health effects and medical costs related to both strategies up to 90 days after pancreatic resection.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria for Clusters:
  • All Dutch centers performing pancreatic surgery (i.e. performing at least 20 pancreatoduodenectomies a year)
Exclusion Criteria for Clusters:
  • None
Inclusion Criteria for Patients:
  • Patients underoging pancreatic resection for any indication
Exclusion Criteria for Patients:
  • None (i.e. complete enumeration)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Jeroen Bosch Ziekenhuis 's Hertogenbosch Netherlands
2 Academic Medical Center Amsterdam Netherlands
3 Onze Lieve Vrouwen Gasthuis Amsterdam Netherlands
4 VUmc Amsterdam Netherlands
5 Amphia ziekenhuis Breda Netherlands
6 Reinier de Graaf gasthuis Delft Netherlands
7 Catharina ziekenhuis Eindhoven Netherlands
8 Medisch Spectrum Twente Enschede Netherlands
9 UMCG Groningen Netherlands
10 Tjongerschans Heerenveen Netherlands
11 LUMC Leiden Netherlands
12 Maastricht UMC Maastricht Netherlands
13 Radboud UMC Nijmegen Netherlands
14 Erasmus MC Rotterdam Netherlands
15 Maasstad ziekenhuis Rotterdam Netherlands
16 RAKU (St. Antonius ziekenhuis & UMC Utrecht) Utrecht Netherlands
17 Isala klinieken Zwolle Netherlands

Sponsors and Collaborators

  • St. Antonius Hospital
  • Dutch Cancer Society

Investigators

  • Principal Investigator: Quintus Molenaar, MD, PhD, UMC Utrecht
  • Principal Investigator: Hjalmar C van Santvoort, MD, PhD, St. Antonius ziekenhuis

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
HC van Santvoort, Principal Investigator, St. Antonius Hospital
ClinicalTrials.gov Identifier:
NCT03400280
Other Study ID Numbers:
  • W17.057
  • UU2017-8272
First Posted:
Jan 17, 2018
Last Update Posted:
Jun 14, 2019
Last Verified:
Jun 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by HC van Santvoort, Principal Investigator, St. Antonius Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 14, 2019