经皮腔内血管成形术和支架植入术治疗颅内颈动脉及其分支严重狭窄:Wingspan 支架与 Credo 支架的比较。

Te-Ming Lin, Chia-Hung Wu, Chih-Ping Chung, Kai-Wei Yu, Wei-An Tai, Chao-Bao Luo, Jiing-Feng Lirng, Feng-Chi Chang
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引用次数: 0

摘要

背景:尽管 Wingspan 支架系统已被广泛用于治疗严重的药物难治性颅内动脉狭窄(SMR-ICAS),但新的 Credo 支架系统因能在球囊导管内整合支架输送而获得批准。然而,这两种系统的治疗效果尚未进行比较。这项初步研究旨在比较在前循环中使用 Wingspan 或 Credo 支架治疗 SMR-ICAS 患者的经皮血管成形术和支架植入术(PTAS)的效果:分析了使用 Wingspan 或 Credo 支架系统进行经皮血管成形术和支架植入术(PTAS)的前循环狭窄超过 70% 的 SMR-ICAS 患者。我们评估了两种支架系统的技术成功率、安全性和疗效:结果:共分析了29例患者,其中17例使用Wingspan支架,12例使用Credo支架。Wingspan支架与Credo支架的疗效对比如下:技术成功率(16/17 [94%] vs. 11/12 [92%],P = 1.00);围手术期颅内出血(2/17 [12%] vs. 0/12 [0%],P = 0.50);围手术期磁共振成像显示无声栓塞性缺血性病变(13/17 [76%] vs. 7/12 [58%],p = 0.42);一年内支架内再狭窄显著(超过 50%)(4/17 [24%] vs. 2/12 [17%],p = 1.00)。术后 30 天内或一年随访期间未发现复发中风或死亡:结论:在治疗 SMR-ICAS 患者方面,Credo 支架系统的技术成功率、安全性和疗效与 Wingspan 支架系统相当。有必要进一步开展大规模研究,以证实这些研究结果。
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Percutaneous transluminal angioplasty and stenting for severe stenosis of the intracranial carotid artery and its branches: Comparison of the Wingspan stent vs the Credo stent.

Background: Despite the widespread use of the Wingspan stent system for treating severe medically refractory intracranial artery stenosis (SMR-ICAS), a new Credo stent system was approved because it could integrate stent delivery within the balloon catheter. However, the therapeutic outcomes of these two systems have not been compared. This preliminary study aimed to compare the results of percutaneous angioplasty and stenting (PTAS) in SMR-ICAS patients treated with either Wingspan or Credo stents within the anterior cerebral circulation.

Methods: SMR-ICAS patients with >70% stenosis in the anterior circulation who underwent PTAS using either the Wingspan or Credo stent system were retrospectively analyzed. We evaluated the technical success, safety, and outcomes of the two-stent systems.

Results: A total of 29 patients were analyzed, including 17 patients treated with Wingspan stents and 12 with Credo stents. The outcomes of the Wingspan stent vs Credo stent were as follows: technical success (16/17 [94%] vs 11/12 [92%], p = 1.00); periprocedural intracranial hemorrhage (2/17 [12%] vs 0/12 [0%], p = 0.50); silent embolic ischemic lesions on periprocedural magnetic resonance imaging (MRI) (13/17 [76%] vs 7/12 [58%], p = 0.42); and significant (>50%) in-stent restenosis in 1 year (4/17 [24%] vs 2/12 [17%], p = 1.00). No recurrent stroke or mortality was noted within 30 days after the procedures or during the 1-year follow-up period.

Conclusion: The technical success, safety, and outcomes of the Credo stent system were comparable to those of the Wingspan stent system in the management of SMR-ICAS patients. Further large-scale studies are warranted to substantiate these findings.

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