Eur J Vasc Endovasc Surg. 2013 Nov;46(5):510-8. doi: 10.1016/j.ejvs.2013.07.020. Epub 2013 Sep 17.
ACST-2 is currently the largest trial ever conducted to compare carotid artery stenting (CAS) with carotid endarterectomy (CEA) in patients with severe asymptomatic carotid stenosis requiring revascularization.
Patients are entered into ACST-2 when revascularization is felt to be clearly indicated, when CEA and CAS are both possible, but where there is substantial uncertainty as to which is most appropriate. Trial surgeons and interventionalists are expected to use their usual techniques and CE-approved devices. We report baseline characteristics and blinded combined interim results for 30-day mortality and major morbidity for 986 patients in the ongoing trial up to September 2012.
A total of 986 patients (687 men, 299 women), mean age 68.7 years (SD ± 8.1) were randomized equally to CEA or CAS. Most (96%) had ipsilateral stenosis of 70-99% (median 80%) with contralateral stenoses of 50-99% in 30% and contralateral occlusion in 8%. Patients were on appropriate medical treatment. For 691 patients undergoing intervention with at least 1-month follow-up and Rankin scoring at 6 months for any stroke, the overall serious cardiovascular event rate of periprocedural (within 30 days) disabling stroke, fatal myocardial infarction, and death at 30 days was 1.0%.
Early ACST-2 results suggest contemporary carotid intervention for asymptomatic stenosis has a low risk of serious morbidity and mortality, on par with other recent trials. The trial continues to recruit, to monitor periprocedural events and all types of stroke, aiming to randomize up to 5,000 patients to determine any differential outcomes between interventions.
ISRCTN21144362.
ACST-2 是迄今为止比较颈动脉支架置入术(CAS)与颈动脉内膜切除术(CEA)治疗需要血运重建的严重无症状性颈动脉狭窄患者的最大规模临床试验。
当血运重建被认为明确需要时,当 CEA 和 CAS 均可行但对哪种方法更合适存在较大不确定性时,患者将被纳入 ACST-2 研究。手术医师和介入医师预计将使用其常规技术和经 CE 批准的器械。我们报告了截至 2012 年 9 月正在进行的试验中 986 例患者的基线特征和 30 天死亡率及主要并发症的盲法联合中期结果。
共 986 例患者(687 例男性,299 例女性),平均年龄 68.7 岁(标准差 ± 8.1),随机等分为 CEA 或 CAS 组。大多数(96%)患者同侧狭窄为 70%-99%(中位数 80%),对侧狭窄为 50%-99%,占 30%,对侧闭塞占 8%。所有患者均接受了适当的药物治疗。对于至少 1 个月随访和 6 个月时进行任何卒中性 Rankin 评分的 691 例接受介入治疗的患者,围手术期(30 天内)致残性卒中、致死性心肌梗死和 30 天死亡的总体严重心血管事件发生率为 1.0%。
ACST-2 的早期结果表明,当代无症状性狭窄的颈动脉介入治疗具有较低的严重发病率和死亡率风险,与其他近期试验相当。该试验继续招募患者,监测围手术期事件和所有类型的卒中,旨在随机纳入多达 5000 例患者,以确定两种干预方法之间的任何差异结果。
ISRCTN21144362。