Department of Surgery, Wilhelmina Hospital Assen, Assen, The Netherlands.
Eur J Vasc Endovasc Surg. 2010 Jul;40(1):27-34. doi: 10.1016/j.ejvs.2010.03.011. Epub 2010 Apr 15.
Subclavian artery aneurysms (SAAs) are rare and may cause life- and limb-threatening complications. Therapeutic options greatly differ as do access alternatives. The aim of the study was to assess its clinical presentation, diagnostics and therapeutic options as reported in the literature.
A literature search was performed of the Medline, Cochrane and EMBASE databases. All articles, published until September 2009, describing treatment of an SAA were included.
A total of 191 reports, of which 126 met the inclusion criteria, were identified and were published from June 1915 until September 2009. Of these, 394 SAAs were described in 381 patients, with a mean age of 52+/-16 years. The median diameter was 40 mm (range: 10-180 mm). The aetiology appeared to change in time towards more exogenous causes. Fifty-one percent of the SAAs presented with a pulsating mass, shoulder pain and/or non-specific chest pain. Embolisation, rupture and thrombosis were present in 16%, 9% and 6% of patients, respectively, and their incidence was related to the anatomical localisation of the SAA. Open surgery and endovascular repair had a complication rate of 26% and 28%, respectively (p=0.49). Cardiopulmonary complications were restricted to open repair. Mortality rates for open and endovascular techniques were similar (5%). The mortality rates for conventional elective and emergency procedures were 3% and 13%, respectively, and for endovascular repair 4% and 8%, respectively.
The profiles of diagnostic and treatment options of SAAs are changing. Although guidelines considering timing of intervention may not be conducted from available literature, intervention appears to be indicated, especially in distal SAAs, due to the risk of thrombo-embolic complications. Endovascular repair and hybrid procedures appear to be the preferred treatment modalities, due to a lower rate of cardiopulmonary complications.
锁骨下动脉动脉瘤(SAAs)较为罕见,但可能引起危及生命和肢体的并发症。治疗方案差异很大,治疗途径也各不相同。本研究旨在评估文献中报道的 SAA 的临床表现、诊断和治疗方法。
对 Medline、Cochrane 和 EMBASE 数据库进行文献检索。纳入所有直至 2009 年 9 月描述 SAA 治疗的文章。
共 191 篇报道,其中 126 篇符合纳入标准,这些报道于 1915 年 6 月至 2009 年 9 月发表。其中,381 例患者的 394 个 SAA 被描述,平均年龄为 52+/-16 岁。中位数直径为 40mm(范围:10-180mm)。病因似乎随时间变化,向更多的外在原因发展。51%的 SAA 表现为搏动性肿块、肩部疼痛和/或非特异性胸痛。栓塞、破裂和血栓形成分别在 16%、9%和 6%的患者中出现,其发生率与 SAA 的解剖位置有关。开放性手术和血管内修复的并发症发生率分别为 26%和 28%(p=0.49)。心肺并发症仅限于开放性修复。开放性和血管内技术的死亡率相似(5%)。传统择期和急诊手术的死亡率分别为 3%和 13%,血管内修复的死亡率分别为 4%和 8%。
SAA 的诊断和治疗方案的特征正在发生变化。尽管根据现有文献,可能无法制定介入时机的指南,但由于血栓栓塞并发症的风险,介入似乎是必要的,尤其是在远端 SAA 中。由于心肺并发症发生率较低,血管内修复和杂交手术似乎是首选的治疗方式。