Br J Surg. 2025 Mar 4;112(3). doi: 10.1093/bjs/znaf005.
There is low-certainty evidence on the impact of extended pharmacological prophylaxis on venous thromboembolism-associated morbidity and mortality. The aim of this study was to determine the efficacy and safety of extended prophylaxis after major abdominopelvic surgery for the prevention of clinically relevant venous thromboembolism after hospital discharge.
CArdiovaSCulAr outcomes after major abDominal surgEry (CASCADE) was a prospective, international, cohort study into which consecutive adult patients undergoing major abdominopelvic surgery were enrolled (January-May 2022). Extended prophylaxis was considered at least 28 days of anticoagulant prescription after surgery. The primary efficacy outcome was clinically relevant venous thromboembolism and the primary safety outcome was clinically relevant bleeding within 30 days after surgery (European Medicines Agency definitions). The independent association of these outcomes with extended prophylaxis was explored using mixed-effects logistic regression and propensity score weighting.
A total of 11 571 patients (median age of 58.0 years; 6399 (55.3%) women) from 29 countries were included. The extended prophylaxis prescription rate was 31.7% (3670 patients). The post-discharge venous thromboembolism and bleeding rates were 0.1% (12 patients) and 0.7% (85 patients) respectively. After weighting, extended prophylaxis was not significantly associated with increased bleeding risk (OR 1.07 (95% c.i. 0.64 to 1.81); P = 0.792) or decreased venous thromboembolism incidence, both in the overall cohort (OR 1.13 (95% c.i. 0.33 to 3.90); P = 0.848) and in a subgroup analysis of patients undergoing complex major surgery and with active cancer (OR: 1.36 (95% c.i. 0.33 to 5.57); P = 0.669).
In modern practice, the incidence of postoperative venous thromboembolism is low. Extended prophylaxis appears safe, yet the clinical efficacy remains uncertain. Further work is required to define patients who stand to benefit.
关于延长药物预防对静脉血栓栓塞相关发病率和死亡率的影响,证据的确定性较低。本研究的目的是确定大型腹部盆腔手术后延长预防措施预防出院后临床相关静脉血栓栓塞的有效性和安全性。
大型腹部手术后心血管结局(CASCADE)是一项前瞻性、国际性队列研究,纳入了连续接受大型腹部盆腔手术的成年患者(2022年1月至5月)。延长预防措施被认为是术后至少28天的抗凝药物处方。主要疗效结局是临床相关静脉血栓栓塞,主要安全性结局是术后30天内的临床相关出血(欧洲药品管理局定义)。使用混合效应逻辑回归和倾向评分加权法探讨了这些结局与延长预防措施之间的独立关联。
共纳入了来自29个国家的11571例患者(中位年龄58.0岁;6399例(55.3%)为女性)。延长预防措施的处方率为31.7%(3670例患者)。出院后静脉血栓栓塞和出血率分别为0.1%(12例患者)和0.7%(85例患者)。加权后,在整个队列中(比值比1.13(95%置信区间0.33至3.90);P = 0.848)以及在接受复杂大型手术和患有活动性癌症的患者亚组分析中(比值比:1.36(95%置信区间0.33至5.57);P = 0.669),延长预防措施与出血风险增加(比值比1.07(95%置信区间0.64至1.81);P = 0.792)或静脉血栓栓塞发生率降低均无显著关联。
在现代实践中,术后静脉血栓栓塞的发生率较低。延长预防措施似乎是安全的,但其临床疗效仍不确定。需要进一步开展工作来确定可能受益的患者。