Predictors of Severity of Postoperative Pancreatic Fistula After Pancreatoduodenectomy

Predictors of Severity of Postoperative Pancreatic Fistula After Pancreatoduodenectomy.

Pancreaticoduodenectomy is one of the commonly performed procedure for periampullary carcinoma/distal cholangio carcinoma/head of pancreas carcinoma. Postoperative pancreatic fistula remains the most important postoperative complication following pancreatic surgery. It's severity ranges from biochemical leak to grade C POPF which can lead to mortality. Radiological and biochemical parameters in early postoperative period predicts the severity of POPF after pancreatoduodenectomy. In this study, we will be evaluating the biochemical parameters and imaging findings as predictors of the severity of postoperative pancreatic fistula after pancreatoduodenectomy in early postoperative period.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

(a) Aim and Objective - The aim of this study is to evaluate the biochemical parameters and imaging findings as predictors of the severity of postoperative pancreatic fistula after pancreatoduodenectomy in early postoperative period

Methodology:

  1. Study population: All those operated for pancreatoduodenectomy during the period of December 2021 to May 2023 will be enrolled in this study, meeting the inclusion and exclusion criteria. On an average 3-4 cases are operated per month in ILBS.
  2. Study design: Prospective observational study.
  3. Study period: From the date of clearance by the Institutional Ethics Committee, till May 2023.
  4. Sample size with justification: All consecutive patients undergoing pancreatoduodenectomy for the above-mentioned study period (expected sample size 40)
  5. Intervention: none.
  6. Monitoring and assessment:

1) Definitions: International study group on pancreatic fistula definition of Post-Operative Pancreatic Fistula POPF) will be used which are as follows: drain output of any measurable volume of fluid on or after postoperative day 3 with an amylase content greater than 3 times the serum amylase activity

Variables to be assessed:

Patient characteristics - Age, Sex, Height, Weight, BMI, Serum albumin levels, Pancreatic parenchymal thickness- at spleno-portal confluence, Indication of Pancreatoduodenectomy -Peri ampullary mass, head of pancreatic mass, distal cholangiocarcinoma Operative Parameters - Duration of surgery, Blood Loss, Pancreatic consistency, Intraoperative remnant pancreatic parenchymal thickness at pancreatojejunostomy site/ spleno portal confluence.

Postoperative measurements -

  1. Drain Fluid amylase (POD 1,3 & 5) & serum amylase
  2. Serum Procalcitonin, C-reactive protein and albumin (POD 5)
  3. Remnant pancreatic parenchymal thickness & change in thickness at pancreaticojejunostomy site/splenoportal confluence on NCCT abdomen (POD 5)
  4. Presence & location of intra-abdominal collection by NCCT abdomen (POD 5)
  5. Interventions required if any for management of complications

Statistical Analysis: Data will be entered into Excel Worksheet and statistical analyses will be performed by SPSS Statistics version 22 (IBM Corp., Armonk, NY). Statistical data will be represented as frequencies (%) where the continuous variables will be expressed as medians and interquartile range (IQR). Continuous variables will be compared with the student t test and Mann-Whitney test as appropriate. Differences between proportions derived from categorical data will be compared with Chi-square or Fischer's exact test. Variables will be correlated with clinical outcomes. ROC curve will be used for biochemical markers and imaging findings Repeated analyses of measures will be applied wherever applicable.

Adverse effects: None

Study Type

Observational

Enrollment (Actual)

50

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Delhi
      • New Delhi, Delhi, India, 110070
        • Institute of Liver and Biliary Sciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Consecutive patients undergoing pancreatoduodenectomy at ILBS

Description

Inclusion Criteria:

  • Consecutive patients undergoing Pancreatoduodenectomy at ILBS
  • Duct to mucosa pancreaticojejunostomy

Exclusion Criteria:

  • Refused for consent
  • Age < 18 yrs
  • Hepatopancreatoduodenectomy
  • Multi-visceral resection
  • Re-exploration before POD 5
  • Pancreaticogastrostomy
  • Dunking type of pancreaticojejunostomy

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Post whipple's procedure patients
no intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
change in pancreatic parenchymal thickness at pancreaticojejunostomy site/spleno-portal confluence on postoperative day 5 predicts the severity of postoperative pancreatic fistula after pancreatoduodenectomy in early postoperative period
Time Frame: Post operative day 5
Post operative day 5

Secondary Outcome Measures

Outcome Measure
Time Frame
Levels of C-reactive protein among the different grades of post operative pancreatic fistula
Time Frame: Post operative day 5
Post operative day 5
Levels of serum albumin among the different grades of postoperative pancreatic fistula.
Time Frame: Post operative day 5
Post operative day 5
Levels of serum procalcitonin among the different grades of postoperative pancreatic fistula.
Time Frame: Post operative day 5
Post operative day 5
Intra-abdominal collection among the different grades of postoperative pancreatic fistula by NCCT abdomen.
Time Frame: Post operative day 5
Post operative day 5
Location of intra-abdominal collection among the different grades of postoperative pancreatic fistula by NCCT abdomen.
Time Frame: Post operative day 5
Post operative day 5

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Dr Piyush Kumar Sinha, MCh, Institute of Liver and Biliary Sciences, New Delhi

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 16, 2022

Primary Completion (Actual)

March 3, 2024

Study Completion (Actual)

March 5, 2024

Study Registration Dates

First Submitted

March 14, 2022

First Submitted That Met QC Criteria

March 14, 2022

First Posted (Actual)

March 23, 2022

Study Record Updates

Last Update Posted (Actual)

May 7, 2024

Last Update Submitted That Met QC Criteria

May 6, 2024

Last Verified

October 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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