Sarhaddi Deniz, Xu Kyle, Wisbeck Alex, Deigni Olivier, Kaswan Sumesh, Prada Christian, Lund Herluf
Division of Plastic and Reconstructive Surgery, Saint Louis University, Saint Louis, MO.
Saint Louis University School of Medicine, Saint Louis, MO.
Aesthet Surg J. 2019 Oct 15;39(11):1214-1221. doi: 10.1093/asj/sjz184.
It is well established that abdominoplasty confers a uniquely high risk of venous thromboembolism (VTE) complications. However, chemoprophylaxis is not routinely utilized due to the risk of bleeding complications. Fondaparinux, a factor Xa inhibitor FDA approved in 2001 for postoperative VTE prophylaxis, has emerged as a safe option for preventing VTE complications after high-risk surgeries.
The goal of this study was to examine the effectiveness and safety of fondaparinux for VTE chemoprophylaxis in patients undergoing abdominoplasty.
This is a single-center retrospective chart review from January 2008 to December 2014 of 492 patients who underwent abdominoplasty with or without an additional body procedure. Prior to 2011, no VTE chemoprophylaxis was utilized (n = 233). In 2011, the routine employment of postoperative chemoprophylaxis with fondaparinux was implemented (n = 259). Patient demographics and 2005 Caprini scores were evaluated. Primary outcomes included postoperative VTE and bleeding complications.
There were no statistical differences in patient demographics or median Caprini score. The treatment group demonstrated a statistically significant reduction in the rate of VTE compared with the nontreatment group (0% vs 2.1%, respectively, P = 0.02). There was no statistically significant difference in the rate of hematoma requiring reoperation between the nontreatment and treatment groups (1.7% vs 2.3%, P = 0.76) or blood loss requiring transfusion (0% vs 0.8%, P = 0.5).
Fondaparinux for VTE chemoprophylaxis after abdominoplasty is efficacious in decreasing the risk of VTE in this susceptible patient population without increasing the risk of postoperative bleeding complications.
腹壁成形术具有静脉血栓栓塞(VTE)并发症的独特高风险,这一点已得到充分证实。然而,由于存在出血并发症的风险,化学预防措施并未常规使用。磺达肝癸钠是一种2001年被美国食品药品监督管理局(FDA)批准用于术后VTE预防的Xa因子抑制剂,已成为高危手术后预防VTE并发症的一种安全选择。
本研究的目的是检验磺达肝癸钠对接受腹壁成形术患者进行VTE化学预防的有效性和安全性。
这是一项单中心回顾性病历审查,研究对象为2008年1月至2014年12月期间492例行腹壁成形术(有或无其他身体手术)的患者。2011年之前,未采用VTE化学预防措施(n = 233)。2011年,开始常规使用磺达肝癸钠进行术后化学预防(n = 259)。评估了患者的人口统计学特征和2005年卡普里尼评分。主要结局包括术后VTE和出血并发症。
患者人口统计学特征或中位卡普里尼评分无统计学差异。与未治疗组相比,治疗组的VTE发生率有统计学显著降低(分别为0%和2.1%,P = 0.02)。未治疗组和治疗组之间需要再次手术的血肿发生率(1.7%对2.3%,P = 0.76)或需要输血的失血量(0%对0.8%,P = 0.5)无统计学显著差异。
腹壁成形术后使用磺达肝癸钠进行VTE化学预防,在该易感患者群体中可有效降低VTE风险,且不增加术后出血并发症的风险。