Sangha Rajbeer S, Naidech Andrew M, Corado Carlos, Ansari Sameer A, Prabhakaran Shyam
From the Departments of Neurology (R.S.S., A.M.N., C.C., S.P.) and Radiology (S.A.A.), Northwestern Memorial Hospital, Chicago, IL.
Stroke. 2017 Aug;48(8):2158-2163. doi: 10.1161/STROKEAHA.116.016254. Epub 2017 Jul 5.
Since the SAMMPRIS trial (Stenting and Aggressive Medical Management for Preventing Recurrent Stroke in Intracranial Stenosis), aggressive medical management (AMM), which includes dual antiplatelet therapy (DAPT) and high-dose statin (HDS) therapy, is recommended for patients with symptomatic intracranial atherosclerotic disease. However, limited data on the real-world application of this regimen exist. We hypothesized that recurrent stroke risk among patients treated with AMM is similar to the medical arm of the SAMMPRIS cohort.
Using a prospective registry, we identified all patients admitted between August 2012 and March 2015 with (1) confirmed ischemic stroke or transient ischemic attack; (2) independently adjudicated symptomatic intracranial atherosclerotic disease; and (3) follow-up at 30 days. We analyzed 30-day risk of recurrent ischemic stroke stratified by treatment: (1) AMM: DAPT plus HDS therapy, (2) HDS alone, and (3) DAPT alone. We also assessed 30-day risk among patients who met prespecified SAMMPRIS eligibility criteria.
Among 99 patients who met study criteria (51.5% male, 54.5% black, mean age 68.2±11.2 years), 49 (48.5%) patients were treated with AMM, 69 (69.7%) with DAPT, and 73 (73.7%) with HDS therapy. At 30 days, 20 (20.2%) patients had recurrent strokes in the territory of stenosis. Compared with the risk in the medical arm of SAMMPRIS (4.4%), the 30-day risk of recurrent stroke was 20.4% in AMM patients, 21.5% in HDS patients, 22.4% in DAPT patients, and 23.2% in SAMMPRIS-eligible patients (all <0.001).
Recurrent stroke risk within 30 days in patients with symptomatic intracranial atherosclerotic disease was higher than that observed in the medical arm of SAMMPRIS even in the subgroup receiving AMM. Replication of the SAMMPRIS findings requires further prospective study.
自SAMMPRIS试验(颅内狭窄支架置入与积极药物治疗预防复发性卒中)开展以来,对于有症状的颅内动脉粥样硬化疾病患者,推荐采用积极药物治疗(AMM),包括双联抗血小板治疗(DAPT)和大剂量他汀(HDS)治疗。然而,关于该治疗方案在现实世界应用的数据有限。我们假设接受AMM治疗的患者复发性卒中风险与SAMMPRIS队列的药物治疗组相似。
利用前瞻性登记系统,我们确定了2012年8月至2015年3月期间收治的所有患者,这些患者满足以下条件:(1)确诊为缺血性卒中或短暂性脑缺血发作;(2)经独立判定为有症状的颅内动脉粥样硬化疾病;(3)30天的随访。我们分析了按治疗分层的复发性缺血性卒中30天风险:(1)AMM:DAPT加HDS治疗;(2)单独使用HDS;(3)单独使用DAPT。我们还评估了符合预先设定的SAMMPRIS纳入标准的患者的30天风险。
在99例符合研究标准的患者中(男性占51.5%,黑人占54.5%,平均年龄68.2±11.2岁),49例(48.5%)患者接受AMM治疗,69例(69.7%)接受DAPT治疗,73例(73.7%)接受HDS治疗。在30天时,20例(20.2%)患者在狭窄区域出现复发性卒中。与SAMMPRIS药物治疗组的风险(4.4%)相比,AMM患者复发性卒中30天风险为20.4%,HDS患者为21.5%,DAPT患者为22.4%,符合SAMMPRIS纳入标准的患者为23.2%(均<0.001)。
有症状的颅内动脉粥样硬化疾病患者30天内的复发性卒中风险高于SAMMPRIS药物治疗组观察到的风险,即使在接受AMM治疗的亚组中也是如此。重复SAMMPRIS的研究结果需要进一步的前瞻性研究。