Yang Wei, Liu Jinlin, Lin Kai, et al. Clinical value of low molecular weight heparin bridging therapy for patients undergoing inguinal hernia repair who with long‑term oral antiplatelet agentsJ. Chinese Journal of Digestive Surgery, 2025, 24(9): 1180-1185. DOI: 10.3760/cma.j.cn115610-20250713-00467
Citation: Yang Wei, Liu Jinlin, Lin Kai, et al. Clinical value of low molecular weight heparin bridging therapy for patients undergoing inguinal hernia repair who with long‑term oral antiplatelet agentsJ. Chinese Journal of Digestive Surgery, 2025, 24(9): 1180-1185. DOI: 10.3760/cma.j.cn115610-20250713-00467

Clinical value of low molecular weight heparin bridging therapy for patients undergoing inguinal hernia repair who with long‑term oral antiplatelet agents

  • Objective To investigate the clinical value of low molecular weight heparin bridging therapy for patients undergoing inguinal hernia repair who with long‑term oral antiplatelet agents.
    Methods The propensity score matching and retrospective cohort study was conducted. The clinical data of 126 patients undergoing tension‑free inguinal hernia repair who with long‑term oral antiplatelet agents and admitted to Sichuan Academy of Medical Sciences & Sichuan Provincial People′s Hospital (Affiliated Hospital of University of Electronic Science and Technology of China) from January 2017 to January 2025 were collected. There were 120 males and 6 females, aged (74±9)years. Of the 126 patients, 77 patients who discontinued antiplatelet agents alone before inguinal hernia repair were set as the drug withdrawal group, and 49 patients who discontinued antiplatelet agents with low molecular weight heparin bridging therapy before inguinal hernia repair were set as the bridging group. Observation indicators: (1) propensity score matching and comparison of general data of patients between the two groups after matching; (2) intraoperative and postopera-tive conditions; (3) follow‑up. Comparison of measurement data with normal distribution between groups was conducted using the independent sample t test. Comparison of measurement data with skewed distribution between groups was conducted using the Mann‑Whitney U test. Comparison of count data between groups was conducted using the chi‑square test or Fisher exact probability. Propensity score matching was performed using the 1∶1 nearest neighbor matching method. The caliper value was set as 0.1.
    Results (1) Propensity score matching and comparison of general data of patients between the two groups after matching. Of the 126 patients, 90 patients were success-fully matched, with 45 cases in each of the drug withdrawal group and the bridging group. After propensity score matching, the elimination of hernia ring size, activated partial thromboplasmin time and surgical method factors confounding bias ensured comparability. (2) Intraoperative and postoperative conditions. After propensity score matching, patients using plasma drainage tubes during the operation in the drug withdrawal group and the bridging group were 8 and 1, respec-tively, showing a significant difference between the two groups (P<0.05). The visual analogue scale scores of patients in the drug withdrawal group and the bridging group at 48 hours after surgery were 2(range, 1-2) and 2(range, 2-3), respectively, showing a significant difference between the two groups (Z=-2.57, P<0.05). (3) Follow‑up. After propensity score matching, all 90 patients were followed up after surgery for 16.5(range, 9.0-30.0)days. During the follow‑up period, there was no significant difference in pain, seroma, incisional infection, readmission within 30 days after surgery getween two groups (P>0.05). No serious thrombotic events occurred in either group of patients, and no patient died.
    Conclusion Compared with patients who discontinued antiplatelet agents alone before surgery, preoperative low molecular weight heparin bridging therapy after discontinua-tion of medication is safe and feasible for patients undergoing inguinal hernia repair who with long-term oral antiplatelet agents, in additon to less plasma drainage tubes using during the operation and without more risk of bleeding, but more postoperative pain.
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