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动脉内膜切除术与支架置入术及药物治疗的比较

Endarterectomy vs. stenting vs. medical therapy.

作者信息

Spence J David

机构信息

Stroke Prevention & Atherosclerosis Research Centre, Robarts Research Institute, Western University, London, ON, Canada

出版信息

Int J Stroke. 2016 Jul;11(5):500-1. doi: 10.1177/1747493016643552. Epub 2016 Apr 11.

Abstract

In recent trials, after deducting the risks in the 30-day periprocedural period, the long-term risk of stroke or death was similar with carotid stenting (CAS) and endarterectomy (CEA) for asymptomatic carotid stenosis (ACS) - approximately 0.5% per year. These findings may exacerbate the problem of inappropriate routine intervention in ACS, being justified on the basis of an invalid comparison of the risks in the medical arms of clinical trials conducted decades ago (˜ 2% per year) to the risks in modern trials of CAS vs. CEA with no medical arm. Intervention is regarded as justified if it can be carried out with a risk below 3%. The annual risk of ipsilateral stroke or death in ACS with intensive medical therapy is now ˜ 0.5% - similar to the long-term risk after the periprocedural period in recent trials of intervention. However, periprocedural risk was ˜ 3% for CAS and 1.7% for CEA. Thus with modern CAS and CEA, the risk remains much higher than with modern medical therapy, even with careful vetting of the surgeons and interventionalists. In real world practice, documented in registries, the risks are much higher. National differences - 90% of carotid intervention for ACS in the US vs. 0% in Denmark - bring into question the advisability and ethics of routine intervention. A moratorium on routine intervention for ACS should be respected except in ongoing randomized trials comparing CAS, CEA and modern intensive medical therapy. Patients with high-risk ACS can be identified for appropriate intervention.

摘要

在最近的试验中,扣除围手术期30天的风险后,对于无症状性颈动脉狭窄(ACS),颈动脉支架置入术(CAS)和颈动脉内膜切除术(CEA)的长期卒中或死亡风险相似——每年约0.5%。这些发现可能会加剧ACS中不适当的常规干预问题,其依据是将几十年前进行的临床试验中医疗组的风险(每年约2%)与现代CAS与CEA对比试验(无医疗组)中的风险进行无效比较。如果干预风险低于3%,则被认为是合理的。目前,强化药物治疗的ACS患者同侧卒中或死亡的年风险约为0.5%——与近期干预试验围手术期后的长期风险相似。然而,CAS的围手术期风险约为3%,CEA为1.7%。因此,对于现代的CAS和CEA,即使对外科医生和介入专家进行仔细审查,其风险仍远高于现代药物治疗。在登记处记录的实际临床实践中,风险要高得多。国家差异——美国90%的ACS颈动脉干预与丹麦的0%——使常规干预的可取性和伦理受到质疑。除了正在进行的比较CAS、CEA和现代强化药物治疗的随机试验外,应暂停对ACS的常规干预。高危ACS患者可被识别出来进行适当干预。

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