Treiman Gerald S, Treiman Richard, Whiting John
Department of Surgery, University of Utah School of Medicine, Section of Vascular Surgery, Salt Lake City, Utah, USA.
J Vasc Surg. 2006 Mar;43(3):513-9. doi: 10.1016/j.jvs.2005.11.015.
To assess the long-term patency and clinical success of subintimal angioplasty in patients with limb-threatening ischemia.
From 1999 through 2004, 29 patients with superficial femoral artery (SFA) or popliteal artery occlusion and rest pain or tissue loss underwent subintimal angioplasty. Patients had subintimal wire placement followed by percutaneous transluminal angioplasty and stent placement. From 1 to 10 stents were placed. Technical success required stenosis less than 30% by arteriography, a velocity ratio less than 1.5 by duplex scan, and improvement of the ankle-brachial index greater than 0.15. Follow-up duplex scanning was performed every 3 months for 2 years and then every 6 months thereafter.
Initial success was obtained in 26 (90%) of the 29 patients, with an improvement in the mean ankle-brachial index of 0.25. Mean follow-up was 38 months (range, 28-54 months). During follow-up, 16 arteries reoccluded. Six of the 16 patients had recurrent symptoms, four required below-knee amputation, two required above-knee amputation, and four died with an intact limb. After treatment failure, two patients had attempted tissue plasminogen activator (TPA), and four had prosthetic tibial bypass. Overall, 15 patients died, and only 2 of the 14 who lived had a patent artery. One of the two required percutaneous transluminal angioplasty of the recanalized artery. By life-table analysis, success was 85%, 64%, 18%, and 9% at 1, 2, 3, and 4 years, respectively. Periprocedural complications occurred in four patients. Of the 13 patients with wounds, six died (four healed), two were alive with healed wounds, and five had limb loss. Of 16 patients with rest pain, 14 developed recurrent symptoms after reocclusion, 1 was alive without pain, and 1 underwent amputation.
Subintimal angioplasty is technically successful in most patients, with few complications. Most procedures provide short-term clinical success and have allowed for successful wound healing and temporary relief of rest pain. However, late arterial patency is poor, with a high rate of symptom recurrence. Many patients will have recurrent pain, and some will require major amputation. Nevertheless, limb-salvage rates are significantly better than arterial patency. Intermediate-term patency is higher than that commonly reported for prosthetic bypass, and despite the lack of durable long-term patency, the procedure offers an additional potentially effective therapeutic option in the treatment of patients with limb-threatening ischemia and femoropopliteal occlusion.
评估内膜下血管成形术治疗肢体威胁性缺血患者的长期通畅率及临床成功率。
1999年至2004年,29例股浅动脉(SFA)或腘动脉闭塞且存在静息痛或组织缺损的患者接受了内膜下血管成形术。患者先进行内膜下导丝置入,随后行经皮腔内血管成形术及支架置入。置入1至10枚支架。技术成功的标准为血管造影显示狭窄小于30%,双功超声扫描显示速度比小于1.5,踝肱指数改善大于0.15。术后每3个月进行一次双功超声扫描随访,持续2年,之后每6个月随访一次。
29例患者中有26例(90%)获得初始成功,平均踝肱指数改善0.25。平均随访时间为38个月(范围28 - 54个月)。随访期间,16条动脉再闭塞。16例患者中有6例出现复发症状,4例需要膝下截肢,2例需要膝上截肢,4例肢体完整但死亡。治疗失败后,2例患者尝试使用组织纤溶酶原激活剂(TPA),4例进行了人工血管胫动脉旁路移植术。总体而言,15例患者死亡,存活的14例患者中只有2例动脉通畅。其中1例需要对再通的动脉进行经皮腔内血管成形术。通过生命表分析,1年、2年、3年和4年的成功率分别为85%、64%、18%和9%。围手术期并发症发生在4例患者中。13例有伤口的患者中,6例死亡(4例伤口愈合),2例存活且伤口愈合,5例肢体缺失。16例有静息痛的患者中,14例在动脉再闭塞后出现复发症状,1例存活且无疼痛,1例接受了截肢手术。
内膜下血管成形术在大多数患者中技术成功,并发症少。大多数手术取得了短期临床成功,实现了伤口成功愈合并暂时缓解了静息痛。然而,后期动脉通畅率不佳,症状复发率高。许多患者会出现复发疼痛,部分患者需要进行大截肢。尽管如此,肢体挽救率明显高于动脉通畅率。中期通畅率高于人工血管旁路移植术的常见报道,尽管缺乏持久的长期通畅性,但该手术为治疗肢体威胁性缺血和股腘动脉闭塞患者提供了另一种潜在有效的治疗选择。