医学
颈动脉内膜切除术
狭窄
颈动脉支架置入术
无症状的
冲程(发动机)
动脉内膜切除术
血运重建
血管成形术
颈内动脉
颈动脉疾病
外科
临床试验
随机对照试验
支架
心脏病学
内科学
心肌梗塞
工程类
机械工程
作者
Thomas G. Brott,James F. Meschia,Brajesh K. Lal,Ángel Chamorro,Virginia J. Howard,George Howard
出处
期刊:Stroke
[Ovid Technologies (Wolters Kluwer)]
日期:2023-05-01
卷期号:54 (5): 1452-1456
被引量:1
标识
DOI:10.1161/strokeaha.122.042172
摘要
The recently published SPACE-2 trial (Stent-Supported Percutaneous Angioplasty of the Carotid Artery Versus Endarterectomy-2) compared 3 treatments to prevent stroke in patients with asymptomatic carotid stenosis ≥70%: (1) carotid endarterectomy plus best medical treatment (BMT), (2) transfemoral carotid artery stenting plus BMT, or (3) BMT alone. Because of low enrollment, the findings of similar safety and efficacy for carotid endarterectomy, carotid artery stenting, or BMT alone were inconclusive. Publication of the CREST (Carotid Revascularization and Medical Management for Asymptomatic Carotid Stenosis Trial)-2 results should provide level A evidence that has been lacking for 2 to 3 decades, to guide treatment of asymptomatic patients with severe carotid stenosis. For symptomatic patients with ≥70% stenosis, no trials are underway to update the degree of benefit reported for carotid endarterectomy by NASCET (North American Carotid Endarterectomy Trial) and ECST (European Carotid Surgery Trial), published in 1991. Subsequently, the use of cigarettes has plummeted, and major improvements in medical treatments and in carotid revascularization have emerged. These advances have coincided with abrupt decline in the clinical end points necessary for treatment comparisons in procedural trials. One of the advances in the invasive management of carotid disease has been transcarotid artery revascularization, already with limited approval by the US Food and Drug Administration. Establishing safety and efficacy of transcarotid artery revascularization compared with carotid endarterectomy, carotid artery stenting, or BMT alone may be challenging because of enrollment, regulatory, and funding barriers to design and complete an adequately powered randomized trial.
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