Department of Neurosurgery, Xuanwu Hospital, China International Neuroscience Institute, Capital Medical University, National Center for Neurological Disorders, Beijing, China.
Peking University Clinical Research Institute, Peking University First Hospital, Beijing, China.
JAMA. 2023 Aug 22;330(8):704-714. doi: 10.1001/jama.2023.13390.
Prior trials of extracranial-intracranial (EC-IC) bypass surgery showed no benefit for stroke prevention in patients with atherosclerotic occlusion of the internal carotid artery (ICA) or middle cerebral artery (MCA), but there have been subsequent improvements in surgical techniques and patient selection.
To evaluate EC-IC bypass surgery in symptomatic patients with atherosclerotic occlusion of the ICA or MCA, using refined patient and operator selection.
DESIGN, SETTING, AND PARTICIPANTS: This was a randomized, open-label, outcome assessor-blinded trial conducted at 13 centers in China. A total of 324 patients with ICA or MCA occlusion with transient ischemic attack or nondisabling ischemic stroke attributed to hemodynamic insufficiency based on computed tomography perfusion imaging were recruited between June 2013 and March 2018 (final follow-up: March 18, 2020).
EC-IC bypass surgery plus medical therapy (surgical group; n = 161) or medical therapy alone (medical group; n = 163). Medical therapy included antiplatelet therapy and stroke risk factor control.
The primary outcome was a composite of stroke or death within 30 days or ipsilateral ischemic stroke beyond 30 days through 2 years after randomization. There were 9 secondary outcomes, including any stroke or death within 2 years and fatal stroke within 2 years.
Among 330 patients who were enrolled, 324 patients were confirmed eligible (median age, 52.7 years; 257 men [79.3%]) and 309 (95.4%) completed the trial. For the surgical group vs medical group, no significant difference was found for the composite primary outcome (8.6% [13/151] vs 12.3% [19/155]; incidence difference, -3.6% [95% CI, -10.1% to 2.9%]; hazard ratio [HR], 0.71 [95% CI, 0.33-1.54]; P = .39). The 30-day risk of stroke or death was 6.2% (10/161) in the surgical group and 1.8% (3/163) in the medical group, and the risk of ipsilateral ischemic stroke beyond 30 days through 2 years was 2.0% (3/151) and 10.3% (16/155), respectively. Of the 9 prespecified secondary end points, none showed a significant difference including any stroke or death within 2 years (9.9% [15/152] vs 15.3% [24/157]; incidence difference, -5.4% [95% CI, -12.5% to 1.7%]; HR, 0.69 [95% CI, 0.34-1.39]; P = .30) and fatal stroke within 2 years (2.0% [3/150] vs 0% [0/153]; incidence difference, 1.9% [95% CI, -0.2% to 4.0%]; P = .08).
Among patients with symptomatic ICA or MCA occlusion and hemodynamic insufficiency, the addition of bypass surgery to medical therapy did not significantly change the risk of the composite outcome of stroke or death within 30 days or ipsilateral ischemic stroke beyond 30 days through 2 years.
ClinicalTrials.gov Identifier: NCT01758614.
先前关于颅外-颅内(EC-IC)旁路手术的试验表明,对于颈内动脉(ICA)或大脑中动脉(MCA)粥样硬化闭塞的患者,该手术并不能预防卒中,但是,随后在手术技术和患者选择方面有所改进。
使用改良的患者和术者选择方法,评估症状性 ICA 或 MCA 粥样硬化闭塞患者的 EC-IC 旁路手术。
设计、地点和参与者:这是一项在中国 13 个中心进行的随机、开放标签、结局评估者设盲的试验。2013 年 6 月至 2018 年 3 月(最终随访:2020 年 3 月 18 日)共招募了 324 例短暂性脑缺血发作或非致残性缺血性卒中有症状的 ICA 或 MCA 闭塞患者,这些患者归因于基于计算机断层灌注成像的血液动力学不足。
EC-IC 旁路手术加药物治疗(手术组,n=161)或单纯药物治疗(药物组,n=163)。药物治疗包括抗血小板治疗和卒中危险因素控制。
主要结局是随机分组后 30 天内的卒中或死亡复合结局,以及 30 天至 2 年内的同侧缺血性卒中。共有 9 个次要结局,包括 2 年内的任何卒中或死亡以及 2 年内的致死性卒中。
在纳入的 330 例患者中,324 例患者被确认符合条件(中位年龄 52.7 岁;257 例男性[79.3%]),309 例(95.4%)完成了试验。手术组与药物组相比,主要复合结局无显著差异(8.6%[13/151] vs 12.3%[19/155];发生率差异,-3.6%[95% CI,-10.1%至 2.9%];危险比[HR],0.71[95% CI,0.33-1.54];P=0.39)。手术组 30 天内的卒中或死亡风险为 6.2%(10/161),药物组为 1.8%(3/163),30 天至 2 年内同侧缺血性卒中的风险分别为 2.0%(3/151)和 10.3%(16/155)。9 个预设次要终点中,没有一个具有统计学意义,包括 2 年内任何卒中或死亡(9.9%[15/152] vs 15.3%[24/157];发生率差异,-5.4%[95% CI,-12.5%至 1.7%];HR,0.69[95% CI,0.34-1.39];P=0.30)和 2 年内致死性卒中(2.0%[3/150] vs 0%[0/153];发生率差异,1.9%[95% CI,-0.2%至 4.0%];P=0.08)。
在有症状的 ICA 或 MCA 闭塞和血液动力学不足的患者中,旁路手术加药物治疗与 30 天内的卒中或死亡复合结局或 30 天至 2 年内同侧缺血性卒中的风险无显著差异。
ClinicalTrials.gov 标识符:NCT01758614。