Post-operative procalcitonin and C-reactive protein predict pancreatic fistula after laparoscopic pancreatoduodenectomy

BMC Surg. 2021 Mar 30;21(1):171. doi: 10.1186/s12893-021-01177-4.

Abstract

Background: Clinically relevant pancreatic fistula (CRPF) is a serious complication following laparoscopic pancreaticoduodenectomy (LPD). This study aimed to determine if C-reactive protein (CRP) and procalcitonin (PCT) serum levels could be used as early biomarkers to predict CRPF after LPD.

Methods: In this retrospective study, we collected peri-operative data of patients who underwent LPD between January 2019 and November 2019. We compared serum levels of white blood cells (WBC), CRP, and PCT on post-operative days (POD) 1, 2, 3, 5, and 7 between the CRPF and non-CRPF groups and analyzed the predictive risk factors for CRPF.

Results: Among the 186 patients included in this study, 18 patients (9.7%) developed CRPF, including 15 and 3 patients with grade B and C fistulas, respectively. The mean WBC, CRP, and PCT levels were higher on most PODs in the CRPF group compared to the non-CRPF group. Receiver operating characteristic (ROC) analysis indicated that CRP levels on POD 2, 5, and 7 can predict CRPF development after LPD, with the area under the curve (AUC) value reaching the highest level on POD 2 (AUC 0.794). PCT levels on POD 2, 3, 5, and 7 were highly predictive of CRPF after LPD. The highest AUC value was achieved on POD 3 [PCT > 2.10 ng/ml (AUC 0.951; sensitivity 88.2%, specificity 92.9%, P < 0.001)].

Conclusions: Both CRP and PCT levels can be used to predict CRPF development after LPD, with PCT having a higher predictive value.

Keywords: C-reactive protein; Laparoscopic pancreaticoduodenectomy; Pancreatic fistula; Procalcitonin.

MeSH terms

  • Biomarkers / blood
  • C-Reactive Protein* / metabolism
  • Humans
  • Laparoscopy / adverse effects
  • Pancreatic Fistula* / etiology
  • Pancreaticoduodenectomy* / adverse effects
  • Pancreaticoduodenectomy* / methods
  • Procalcitonin* / blood
  • Retrospective Studies

Substances

  • Biomarkers
  • Procalcitonin
  • C-Reactive Protein