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Double Purse-string Telescoped Pancreaticogastrostomy is Not Superior in Preventing Pancreatic Fistula Development in High-risk Anastomosis: a 6-year Single-center Case-control Study

Overview
Specialty General Surgery
Date 2021 Nov 16
PMID 34782930
Citations 1
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Abstract

Purpose: The double purse-string telescoped pancreaticogastrostomy (PG) technique has been suggested as an alternative approach to reduce the risk of postoperative pancreatic fistula (POPF). Its efficacity in high-risk situations has not yet been explored. This study compared the incidence of clinically relevant POPF (CR-POPF) between patients with high-risk anastomosis undergoing PG and those undergoing pancreaticojejunostomy (PJ).

Methods: From 2013 to 2019, 198 consecutive patients with high-risk anastomosis, an updated alternative fistula risk score > 20%, and who underwent pancreatoduodenectomy with the PJ (165) or PG (33) technique were included. Optimal mitigation strategy (external stenting/octreotide omission) was applied for all patients. The primary endpoint was the incidence of CR-POPF.

Results: The mean ua-FRS was 33%. CR-POPF (grade B/C) was found in 42 patients (21%) and postoperative hemorrhage in 30 (15%); the mortality rate was 4%. CR-POPF rates were comparable between the PJ (19%) and PG (33%) groups (P = 0.062). The PG group had a higher rate of POPF grade C (24% vs. 10%; P = 0.036), longer operative time (P = 0.019), and a higher transfusion rate (P < 0.001), even after a matching process on ua-FRS. In the multivariate analysis, the type of anastomosis (P = 0.88), body mass index (P = 0.47), or main pancreatic duct diameter (P = 0.7) did not influence CR-POPF occurrence.

Conclusions: For patients with high-risk anastomosis, the double purse-string telescoped PG technique was not superior to the PJ technique for preventing CR-POPF.

Citing Articles

Application of 3D Printing to Design and Manufacture Pancreatic Duct Stent and Animal Experiments.

Xiang F, Yao C, Guan G, Luo F Bioengineering (Basel). 2024; 11(10).

PMID: 39451380 PMC: 11504459. DOI: 10.3390/bioengineering11101004.

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