Aurshina Afsha, Kibrik Pavel, Eisenberg Justin, Alsheekh Ahmad, Hingorani Anil, Marks Natalie, Ascher Enrico
Vascular Institute of New York, Brooklyn, USA.
Vascular. 2018 Apr;26(2):189-193. doi: 10.1177/1708538117724646. Epub 2017 Aug 18.
Objectives The use of postoperative anticoagulation is not uncommon for patients undergoing lower extremity arterial procedures as adjunctive therapy. Longer postoperative length of stay is necessary to achieve adequate therapeutic international normalized ratio with traditional protocols that call for the use of unfractionated heparin and warfarin therapy. We hypothesized the direct oral anticoagulants are an attractive alternative to provide adequate anticoagulation in patients who undergo lower extremity arterial procedures. Methods We retrospectively studied patients who had lower extremity arterial procedures between 2012 and 2015 to examine the safety and efficacy of the direct oral anticoagulants in a single institution. Patency, freedom from re-intervention, and major adverse limb event were evaluated. The direct oral anticoagulant agents used included dabigatran, rivaroxaban, and apixaban. The primary patency, adverse effects and freedom from re-intervention were then compared to a control group of patients who were treated with traditional heparin-warfarin therapy after lower extremity bypass procedures. Results Direct oral anticoagulants were utilized in a total of 23 patients (48% men; mean age 69 ± 11 years) during the study period. Indication for use of direct oral anticoagulant after procedure included use of polytetrafluoroethylene (PTFE) bypass graft below the knee joint or after lower extremity angioplasty with disadvantaged runoff. Mean follow-up of the drugs was 23 months (SD ± 16 months). At the end of follow-up, the direct oral anticoagulants have been discontinued in four patients, who are currently only on plavix. Among 82.6% of patients who were given direct oral anticoagulants for PTFE bypasses, graft patency, freedom from re-intervention, and major adverse limb event were 100%, 100%, and 0%, respectively. Patients (17.4%) treated with direct oral anticoagulants for disadvantaged runoff after balloon angioplasty of the lower extremity, patency, freedom from re-intervention, and major adverse limb event were 100%, 100%, and 0%, respectively. For the patients who underwent direct oral anticoagulant administration for disadvantaged runoff primary patency was 100%. One patient developed wound dehiscence which was unrelated to direct oral anticoagulant administration. Our control group consisted of 100 patients who were treated with heparin-warfarin therapy for 30 days after lower extremity bypass procedures. The graft patency, freedom from intervention, and major adverse limb event were 93%, 12%, and 0%, respectively. There was however no statistically significant difference in graft patency rate ( P = .34) or freedom from intervention ( P = .07) between the two groups. Conclusions The preliminary data suggest that there may be a role for using the direct oral anticoagulants with patients who undergo lower extremity arterial procedures for prevention of thrombosis and warrants further investigation.
目的 对于接受下肢动脉手术的患者,术后使用抗凝治疗作为辅助治疗并不罕见。采用传统方案使用普通肝素和华法林治疗时,需要更长的术后住院时间才能达到足够的治疗性国际标准化比值。我们推测直接口服抗凝剂是为接受下肢动脉手术的患者提供充分抗凝的一种有吸引力的替代方法。方法 我们回顾性研究了2012年至2015年间接受下肢动脉手术的患者,以考察单一机构中直接口服抗凝剂的安全性和有效性。评估通畅率、无需再次干预情况和主要肢体不良事件。使用的直接口服抗凝剂包括达比加群、利伐沙班和阿哌沙班。然后将主要通畅率、不良反应和无需再次干预情况与下肢旁路手术后接受传统肝素-华法林治疗的患者对照组进行比较。结果 在研究期间,共有23例患者(48%为男性;平均年龄69±11岁)使用了直接口服抗凝剂。术后使用直接口服抗凝剂的指征包括在膝关节以下使用聚四氟乙烯(PTFE)旁路移植物或在下肢血管成形术后血流不佳时使用。这些药物的平均随访时间为23个月(标准差±16个月)。随访结束时,4例患者已停用直接口服抗凝剂,目前仅服用氯吡格雷。在接受PTFE旁路手术并使用直接口服抗凝剂的患者中,82.6%的患者移植物通畅率、无需再次干预率和主要肢体不良事件发生率分别为100%、100%和0%。接受下肢球囊血管成形术后血流不佳并使用直接口服抗凝剂治疗的患者(17.4%),通畅率、无需再次干预率和主要肢体不良事件发生率分别为100%、100%和0%。对于因血流不佳接受直接口服抗凝剂治疗的患者,主要通畅率为100%。1例患者发生伤口裂开,与直接口服抗凝剂的使用无关。我们的对照组由100例下肢旁路手术后接受肝素-华法林治疗30天的患者组成。移植物通畅率、无需干预率和主要肢体不良事件发生率分别为93%、12%和0%。然而,两组之间的移植物通畅率(P = 0.34)或无需干预率(P = 0.07)无统计学显著差异。结论 初步数据表明,对于接受下肢动脉手术的患者,使用直接口服抗凝剂预防血栓形成可能有作用,值得进一步研究。