Key result
Continuing single-agent antithrombotic therapy shows no significant difference in blood loss during emergency cholecystectomy.
Why the study?
Optimal perioperative antithrombotic therapy management during emergency cholecystectomy for acute cholecystitis remains controversial, and whether continuing single-agent therapy increases hemorrhagic risk compared with no therapy was uncertain.
Does continuing single-agent antithrombotic therapy increase the risk of intraoperative blood loss > 100 mL compared with no antithrombotic therapy in patients undergoing emergency cholecystectomy for acute cholecystitis?
Cohort (n=1,018)
Yes
Does continuing single-agent antithrombotic therapy increase the risk of intraoperative blood loss > 100 mL compared with no antithrombotic therapy in patients undergoing emergency cholecystectomy for acute cholecystitis?
Answers are grounded in this paper and cite their sources.
Continuing single-agent antithrombotic therapy during emergency cholecystectomy for acute cholecystitis does not significantly increase the risk of intraoperative blood loss > 100 mL or perioperative bleeding complications compared to no antithrombotic therapy.
BACKGROUND/PURPOSE: Optimal perioperative antithrombotic therapy (ATT) management during emergency cholecystectomy for acute cholecystitis remains controversial. We examined whether continuing single-agent ATT is associated with hemorrhagic risk compared with no ATT. METHODS: This retrospective cohort study included 1018 patients (826 without ATT, 192 continued on single-agent ATT) at seven institutions (2020-2023). Propensity score overlap weighting balanced 12 baseline covariates. The primary outcome was intraoperative blood loss > 100 mL; risk ratios and 95% confidence intervals were estimated via modified Poisson regression, with upper confidence bound compared against a pre-specified risk ratio (1.5). RESULTS: The primary outcome occurred in 27.3% and 25.4% of the non-ATT and continued-ATT groups, respectively (risk ratio: 0.93, 95% confidence interval: 0.69-1.26). The upper bound of the confidence interval was within the pre-specified margin. No significant differences were observed in perioperative bleeding complications or hospital stay. Secondary outcomes, sensitivity analyses, and drug-specific subgroup analyses (including direct oral anticoagulants) yielded consistent results. CONCLUSIONS: Continuing single-agent ATT was comparable to no ATT regarding bleeding during cholecystectomy for acute cholecystitis. These findings suggest that emergency cholecystectomy can be performed without meaningful increases in hemorrhagic risk in patients for whom adequate preoperative ATT washout is not feasible.
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Tadokoro et al. (2026) conducted a cohort in Acute cholecystitis undergoing emergency cholecystectomy (n=1,018). Continued single-agent antithrombotic therapy (ATT) vs. No antithrombotic therapy (non-ATT) was evaluated on Intraoperative blood loss > 100 mL (RR 0.93, 95% CI 0.69-1.26). Continuing single-agent antithrombotic therapy was comparable to no therapy for intraoperative blood loss >100 mL during emergency cholecystectomy (25.4% vs 27.3%; RR 0.93; 95% CI 0.69-1.26).
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