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Preoperative Inflammatory Biomarkers and Postoperative Day 1 Drain Amylase Value Predict Pancreatic Fistula After Pancreaticoduodenectomy

C

Campus Bio-Medico University of Rome

Status

Completed

Conditions

Pancreatic Fistula
Inflammatory Response
Pancreas Cancer

Treatments

Procedure: Surgical Drain Management

Study type

Observational

Funder types

Other

Identifiers

NCT04361682
27/19 OSS ComEt CBM

Details and patient eligibility

About

Particularly, pancreatic fistula is the most common and serious complication after pancreaticoduodenectomy (PD) and is reported in up to 40% of cases. The aim of this retrospective single-center study was to investigate the utility of the combination of preoperative inflammation biomarkers (PIBs) with postoperative day 1 drains amylase (POD1-d.a.) levels in predicting grade C Pancreatic Fistula (PF).

Full description

Data from a prospective collected database of 317 consecutive PDs performed at the University Campus Bio-Medico di Roma during the years 2005-2019, have been retrospectively analyzed. Local Ethical Committee approved the study.

Patients undergoing PD for periampullary neoplasms were included in the study. All patients underwent to PD with pancreaticojejunostomy reconstruction. Two surgical drains were always placed at the end of the surgery.

Data regarding PIBs, as full blood count including white blood cell (WBC) count, lymphocytes, neutrophils and platelets counts, neutrophil-to-lymphocyte ratio (NLR), derived neutrophil-to-lymphocyte ratio (d-NLR), platelet-to-lymphocyte ratio (PLR) and POD1-d.a. levels were collected and Positive Predictive Values (PPV) and Negative Predictive Values (NPV) were computed to investigate the probability to develop PF combining PIBs and drains amylase values.

Enrollment

227 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients underwent pancreaticoduodenectomy (PD) for periampullary neoplasms
  • Patients underwent PD with pancreaticojejunostomy reconstruction.
  • Patient with data of blood count in first postoperative day

Exclusion criteria

  • None of the above criteria

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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