AI Article Synopsis

  • The study aimed to assess the effects of allogeneic red blood cell transfusion (ABT) on postoperative outcomes in patients with resectable pancreatic ductal adenocarcinoma (PDAC).
  • Out of 128 patients, 24 received ABT, and results showed those who received ABT had significantly lower recurrence-free survival (RFS) and disease-specific survival (DSS) rates compared to those who did not.
  • After adjusting for certain risk factors, the ABT group maintained poorer RFS (median of 9.8 vs 15.8 months) and DSS rates (median of 19.4 vs 40.0 months), indicating ABT may negatively affect survival outcomes for PDAC patients

Article Abstract

Objective: We aimed to investigate the real impact of allogeneic red blood cell transfusion (ABT) on postoperative outcomes in resectable pancreatic ductal adenocarcinoma (PDAC) patients.

Methods: Of 128 patients undergoing resectable PDAC surgery at our facility, 24 (18.8%) received ABT. Recurrence-free survival (RFS) and disease-specific survival (DSS), before and after propensity score matching (PSM), were compared among patients who did and did not receive ABT.

Results: In the entire cohort, ABT was significantly associated with decreased RFS (P = 0.002) and DSS (P = 0.014) before PSM. Cox regression analysis identified ABT (risk ratio, 1.884; 95% confidence interval, 1.015-3.497; P = 0.045) as an independent prognostic factor for RFS. Univariate and multivariate analysis identified preoperative hemoglobin value, preoperative total bilirubin value, and intraoperative blood loss as significant independent risk factors for ABT. Using these 3 variables, PSM analysis created 16 pairs of patients. After PSM, the ABT group had significantly poorer RFS rates than the non-ABT group (median, 9.8 vs 15.8 months, P = 0.022). Similar tendencies were found in DSS rates (median, 19.4 vs 40.0 months, P = 0.071).

Conclusions: This study revealed certain negative effects of intraoperative ABT on postoperative survival outcomes in patients with resectable PDAC.

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Source
http://dx.doi.org/10.1097/MPA.0000000000001913DOI Listing

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