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Enhanced Recovery After Minimally Invasive Pancreaticoduodenectomy

Enhanced Recovery After Minimally Invasive Pancreaticoduodenectomy With Stented Pancreaticogastrostomy and Roux-en-y Gastro-enterostomy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02671357
Acronym
ERAMIP
Enrollment
210
Registered
2016-02-02
Start date
2016-03-31
Completion date
2019-06-30
Last updated
2020-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic Neoplasms; Periampullary Neoplasms

Keywords

pancreatic surgery; neoplasms

Brief summary

This prospective observational cohort study aims to improve the postoperative course after minimally invasive pancreaticoduodenectomy (MIP) with stented pancreaticogastrostomy (sPG) for pancreatic head or peri-ampullary neoplasms. Patients are submitted to an enhanced recovery after surgery (ERAS) program with early enteral nutrition (EEN).

Detailed description

Pancreaticoduodenectomy (PD) is the standard of care for patients with malignant or benign disease of the pancreatic head or peri-ampullary region. The postoperative course after PD is strongly dependent of the occurrence of pancreatic fistula (POPF) and/or delayed gastric emptying (DGE). In a recent multicentre randomized controlled trial, the investigators have shown pancreaticogastrostomy (PG; without a stent in the pancreatic duct) to be associated with 8% POPF rate, significantly lower than pancreaticojejunostomy (20%) (1). Since then, PG reconstruction is considered the standard of care in PD, which is also underlined in more recent systematic reviews. In patients without POPF after PD, the length of hospital stay is determined by the occurrence of DGE, which is poorly understood and currently lacks any effective treatment. Patients who developed DGE after PD with PG anastomosis (n=18; 20%) had a significantly (p=0.014) longer (mean + sem) length of hospital stay (LOS) of 26.3 + 1.58 days, as compared to 22.4 + 1.27 days for patients without DGE (n=69). These figures are observed in the investigators' center as part of the multicentre RCT. Enhanced recovery after surgery (ERAS) or fast-track (FT) programs are able to reduce postoperative length of hospital stay (LOS). Indeed recently, ERAS or FT programs have been implemented successfully in PD (2). Patients were discharged 4 days earlier in the ERAS group, without a negative effect on the clinical outcome. Still, many surgeons are reluctant to implement ERAS programs because they fear compromising patient safety. In efforts to improve the outcomes of PD, many surgical techniques have been evaluated to restore the pancreatic digestive continuity after PD. However, the best way to ensure this and whether or not to perform the procedure via standard open or minimally invasive, i.e. 2- or 3-dimensional laparoscopic (3D-LPD) or 3-dimensional robotic surgery (RPD), is still under debate. The investigators have passed the learning curve of 50 3D-LPD and hypothesize the implementation of ERAS and EEN in 3D-LPD can improve short-term outcomes.

Interventions

PROCEDUREERAMIP

3D-LPD with stented umbrella-pancreaticogastrostomy & Roux-en-Y reconstruction of the biliary limb of the hepatico-jejunostomy onto the efferent limb of the gastro-enterostomy (RY-GES)

Sponsors

University Hospital, Gasthuisberg
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Patients, male or female, who undergo MIP + sPG for a pancreatic or peri-ampullary tumor * Patients with and without pre-operative biliary drainage (for obstructive jaundice) * Patients fit for minimally invasive pancreaticoduodenectomy (MIP) * Informed consent signed

Exclusion criteria

* Pregnancy * MIP for pancreatic trauma * MIP for complications of endoscopic retrograde cholangio-pancreaticography (ERCP) * Reconstruction of the portal vein or superior mesenteric vein * Any arterial reconstruction at the time of surgery

Design outcomes

Primary

MeasureTime frameDescription
The incidence of severe complicationsFrom date of pancreaticoduodenectomy until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 3 monthsSevere complications are classified according to the Clavien-Dindo Classification, i.e. Therapy Oriented Severity Grading Score of postoperative complications (TOSGS grade 3 or more): complication that needs interventional therapy under local or general anaesthesia

Secondary

MeasureTime frameDescription
Postoperative in-hospital, 30-day and 90-day mortalityFrom date of pancreaticoduodenectomy until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 3 monthPostoperative mortality rate

Other

MeasureTime frameDescription
Clinical postoperative pancreatic fistula (POPF) rateFrom date of pancreaticoduodenectomy until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 3 monthsThe incidence of POPF will be registered and defined according to the ISGPF
Postoperative bleeding (PPH) rateFrom date of discharge from hospital until date of re-admission to hospital within 2 weeks after discharge, assessed up to 3 monthsThe incidence of PPH will be registered and defined according to the ISGPF
Length of postoperative hospital stay (LOS)From date of pancreaticoduodenectomy until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 3 months. Readmissions within 30days after discharge will be added to the duration of LOS.Length of hospital stay (days) will be registered starting from the day of surgery until discharge
Delayed gastric emptying (DGE) rateFrom date of pancreaticoduodenectomy until the date of discharge from hospital or date of death from any cause, whichever came first, assessed up to 3 monthsThe incidence of DGE will be registered and defined according to the ISGPF

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026