首页> 外文期刊>The Lancet >Carotid artery stenting compared with endarterectomy in patients with symptomatic carotid stenosis (International Carotid Stenting Study): an interim analysis of a randomised controlled trial.
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Carotid artery stenting compared with endarterectomy in patients with symptomatic carotid stenosis (International Carotid Stenting Study): an interim analysis of a randomised controlled trial.

机译:有症状的颈动脉狭窄患者的颈动脉支架置入术与动脉内膜切除术的比较(国际颈动脉支架研究):一项随机对照试验的中期分析。

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BACKGROUND: Stents are an alternative treatment to carotid endarterectomy for symptomatic carotid stenosis, but previous trials have not established equivalent safety and efficacy. We compared the safety of carotid artery stenting with that of carotid endarterectomy. METHODS: The International Carotid Stenting Study (ICSS) is a multicentre, international, randomised controlled trial with blinded adjudication of outcomes. Patients with recently symptomatic carotid artery stenosis were randomly assigned in a 1:1 ratio to receive carotid artery stenting or carotid endarterectomy. Randomisation was by telephone call or fax to a central computerised service and was stratified by centre with minimisation for sex, age, contralateral occlusion, and side of the randomised artery. Patients and investigators were not masked to treatment assignment. Patients were followed up by independent clinicians not directly involved in delivering the randomised treatment. The primary outcome measure of the trial is the 3-year rate of fatal or disabling stroke in any territory, which has not been analysed yet. The main outcome measure for the interim safety analysis was the 120-day rate of stroke, death, or procedural myocardial infarction. Analysis was by intention to treat (ITT). This study is registered, number ISRCTN25337470. FINDINGS: The trial enrolled 1713 patients (stenting group, n=855; endarterectomy group, n=858). Two patients in the stenting group and one in the endarterectomy group withdrew immediately after randomisation, and were not included in the ITT analysis. Between randomisation and 120 days, there were 34 (Kaplan-Meier estimate 4.0%) events of disabling stroke or death in the stenting group compared with 27 (3.2%) events in the endarterectomy group (hazard ratio [HR] 1.28, 95% CI 0.77-2.11). The incidence of stroke, death, or procedural myocardial infarction was 8.5% in the stenting group compared with 5.2% in the endarterectomy group (72 vs 44 events; HR 1.69, 1.16-2.45, p=0.006). Risks of any stroke (65 vs 35 events; HR 1.92, 1.27-2.89) and all-cause death (19 vs seven events; HR 2.76, 1.16-6.56) were higher in the stenting group than in the endarterectomy group. Three procedural myocardial infarctions were recorded in the stenting group, all of which were fatal, compared with four, all non-fatal, in the endarterectomy group. There was one event of cranial nerve palsy in the stenting group compared with 45 in the endarterectomy group. There were also fewer haematomas of any severity in the stenting group than in the endarterectomy group (31 vs 50 events; p=0.0197). INTERPRETATION: Completion of long-term follow-up is needed to establish the efficacy of carotid artery stenting compared with endarterectomy. In the meantime, carotid endarterectomy should remain the treatment of choice for patients suitable for surgery. FUNDING: Medical Research Council, the Stroke Association, Sanofi-Synthelabo, European Union.
机译:背景:对于有症状的颈动脉狭窄,支架术是替代颈动脉内膜切除术的替代疗法,但先前的试验尚未建立等效的安全性和有效性。我们比较了颈动脉支架置入术和颈动脉内膜切除术的安全性。方法:国际颈动脉支架研究(ICSS)是一项多中心,国际,随机对照试验,对结果进行盲法裁决。将有症状的颈动脉狭窄患者按1:1比例随机分配以接受颈动脉支架置入术或颈动脉内膜切除术。随机化是通过电话或传真到中央计算机服务部门进行的,并按性别,年龄,对侧闭塞和随机化动脉的一侧最小化,由中心进行分层。患者和研究者并未隐瞒治疗任务。患者由不直接参与随机治疗的独立临床医生随访。该试验的主要结局指标是在任何地区的3年致命或致残性卒中发生率,尚未进行分析。临时安全性分析的主要结局指标是中风,死亡或程序性心肌梗塞的120天发生率。分析是按意向治疗(ITT)进行的。该研究已注册,编号ISRCTN25337470。结果:该试验招募了1713例患者(支架组,n = 855;动脉内膜切除术组,n = 858)。随机分组后,支架置入组中的两名患者和动脉内膜切除术组中的一名患者在随机分组后立即退出,未纳入ITT分析。在随机分组与120天之间,支架置入组发生34例(Kaplan-Meier估计为4.0%)致中风或死亡致残事件,而动脉内膜切除术组发生27例(3.2%)致残事件(危险比[HR] 1.28,95%CI 0.77-2.11)。支架置入术组中风,死亡或程序性心肌梗塞的发生率为8.5%,而动脉内膜切除术组为5.2%(72 vs 44事件; HR 1.69,1.16-2.45,p = 0.006)。支架置入组的任何卒中风险(65 vs 35事件; HR 1.92,1.27-2.89)和全因死亡(19 vs 7事件; HR 2.76,1.16-6.56)的风险均高于动脉内膜切除术组。支架置入组记录了3例程序性心肌梗塞,均是致命的,而内膜切除术组则记录了4例非致命性心肌梗塞。支架置入组发生颅神经麻痹1例,而动脉内膜切除术组发生45例。与支架内切除术组相比,支架置入组中任何严重程度的血肿也更少(31 vs 50事件; p = 0.0197)。解释:与颈动脉内膜切除术相比,需要完成长期随访才能确定颈动脉支架置入术的疗效。同时,对于适合手术的患者,颈动脉内膜切除术应仍然是治疗的选择。资金:欧盟萨诺菲-Synthelabo中风协会医学研究理事会。

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