Mas Jean-Louis, Trinquart Ludovic, Leys Didier, Albucher Jean-François, Rousseau Hervé, Viguier Alain, Bossavy Jean-Pierre, Denis Béatrice, Piquet Philippe, Garnier Pierre, Viader Fausto, Touzé Emmanuel, Julia Pierre, Giroud Maurice, Krause Denis, Hosseini Hassan, Becquemin Jean-Pierre, Hinzelin Grégoire, Houdart Emmanuel, Hénon Hilde, Neau Jean-Philippe, Bracard Serge, Onnient Yannick, Padovani Raymond, Chatellier Gilles
Hôpitaux Sainte-Anne, Université Paris Descartes, Paris, France.
Lancet Neurol. 2008 Oct;7(10):885-92. doi: 10.1016/S1474-4422(08)70195-9. Epub 2008 Sep 5.
Carotid stenting is a potential alternative to carotid endarterectomy but whether this technique is as safe as surgery and whether the long-term protection against stroke is similar to that of surgery are unclear. We previously reported that in patients in the Endarterectomy Versus Angioplasty in Patients with Symptomatic Severe Carotid Stenosis (EVA-3S) trial, the rate of any stroke or death within 30 days after the procedure was higher with stenting than with endarterectomy. We now report the results up to 4 years.
In this follow-up study of a multicentre, randomised, open, assessor-blinded, non-inferiority trial, we compared outcome after stenting with outcome after endarterectomy in 527 patients who had carotid stenosis of at least 60% that had recently become symptomatic. The primary endpoint of the EVA-3S trial was the rate of any periprocedural stroke or death (ie, within 30 days after the procedure). The prespecified main secondary endpoint was a composite of any periprocedural stroke or death and any non-procedural ipsilateral stroke during up to 4 years of follow-up. Other trial outcomes were any stroke or periprocedural death, any stroke or death, and the above endpoints restricted to disabling or fatal strokes. This trial is registered with ClinicalTrials.gov, number NCT00190398.
262 patients were randomly assigned to endarterectomy and 265 to stenting. The cumulative probability of periprocedural stroke or death and non-procedural ipsilateral stroke after 4 years of follow-up was higher with stenting than with endarterectomy (11.1%vs 6.2%, hazard ratio [HR] 1.97, 95% CI 1.06-3.67; p=0.03). The HR for periprocedural disabling stroke or death and non-procedural fatal or disabling ipsilateral stroke was 2.00 (0.75-5.33; p=0.17). A hazard function analysis showed the 4-year differences in the cumulative probabilities of outcomes between stenting and endarterectomy were largely accounted for by the higher periprocedural (within 30 days of the procedure) risk of stenting compared with endarterectomy. After the periprocedural period, the risk of ipsilateral stroke was low and similar in both treatment groups. For any stroke or periprocedural death, the HR was 1.77 (1.03-3.02; p=0.04). For any stroke or death, the HR was 1.39 (0.96-2.00; p=0.08).
The results of this study suggest that carotid stenting is as effective as carotid endarterectomy for middle-term prevention of ipsilateral stroke, but the safety of carotid stenting needs to be improved before it can be used as an alternative to carotid endarterectomy in patients with symptomatic carotid stenosis.
颈动脉支架置入术是颈动脉内膜切除术的一种潜在替代方法,但该技术是否与手术一样安全,以及其预防卒中的长期效果是否与手术相似尚不清楚。我们之前报道过,在症状性严重颈动脉狭窄患者的内膜切除术与血管成形术(EVA-3S)试验中,接受支架置入术的患者术后30天内任何卒中或死亡的发生率高于接受内膜切除术的患者。我们现在报告长达4年的结果。
在这项多中心、随机、开放、评估者盲法、非劣效性试验的随访研究中,我们比较了527例近期出现症状且颈动脉狭窄至少60%的患者接受支架置入术与内膜切除术后的结局。EVA-3S试验的主要终点是围手术期任何卒中或死亡的发生率(即术后30天内)。预先设定的主要次要终点是围手术期任何卒中或死亡与随访长达4年期间任何非手术同侧卒中的复合终点。其他试验结局包括任何卒中或围手术期死亡、任何卒中或死亡,以及上述仅限于致残性或致命性卒中的终点。该试验已在ClinicalTrials.gov注册,注册号为NCT00190398。
262例患者被随机分配接受内膜切除术,265例接受支架置入术。随访4年后,支架置入术组围手术期卒中或死亡以及非手术同侧卒中的累积概率高于内膜切除术组(11.1%对6.2%,风险比[HR]1.97,95%CI 1.06 - 3.67;p = 0.03)。围手术期致残性卒中或死亡以及非手术致命性或致残性同侧卒中的HR为2.00(0.75 - 5.33;p = 0.17)。风险函数分析表明,支架置入术与内膜切除术之间结局累积概率的4年差异在很大程度上是由于支架置入术围手术期(术后30天内)的风险高于内膜切除术。围手术期之后,两个治疗组同侧卒中的风险都较低且相似。对于任何卒中或围手术期死亡,HR为1.77(1.03 - 3.02;p = 0.04)。对于任何卒中或死亡,HR为1.39(0.96 - 2.00;p = 0.08)。
本研究结果表明,颈动脉支架置入术在中期预防同侧卒中方面与颈动脉内膜切除术一样有效,但在可作为有症状颈动脉狭窄患者内膜切除术的替代方法之前,颈动脉支架置入术的安全性需要提高。