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经皮腔内血管成形术和支架置入术治疗颅内颈内动脉及其分支重度狭窄:Wingspan 支架与 Credo 支架的比较。

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.

机构信息

Department of Radiology, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.

School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan, ROC.

出版信息

J Chin Med Assoc. 2024 Sep 1;87(9):878-884. doi: 10.1097/JCMA.0000000000001131. Epub 2024 Jul 8.

Abstract

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.

摘要

背景

尽管 Wingspan 支架系统被广泛用于治疗严重的药物难治性颅内动脉狭窄(SMR-ICAS),但由于 Credo 支架系统可以将支架输送与球囊导管集成在一起,因此已获得批准。然而,这两种系统的治疗效果尚未进行比较。本初步研究旨在比较在前循环中使用 Wingspan 或 Credo 支架治疗的 SMR-ICAS 患者经皮血管成形术和支架置入术(PTAS)的结果。

方法

回顾性分析在前循环中狭窄>70%的 SMR-ICAS 患者,这些患者接受了 Wingspan 或 Credo 支架系统的 PTAS。我们评估了两种支架系统的技术成功率、安全性和结果。

结果

共分析了 29 例患者,其中 17 例患者接受 Wingspan 支架治疗,12 例患者接受 Credo 支架治疗。Wingspan 支架与 Credo 支架的结果如下: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(MRI)上的无症状栓塞性缺血性病变(13/17 [76%] vs 7/12 [58%],p = 0.42);1 年内支架内再狭窄率>50%(4/17 [24%] vs 2/12 [17%],p = 1.00)。在手术后 30 天内或 1 年随访期间,均未出现复发性中风或死亡。

结论

在治疗 SMR-ICAS 患者时,Credo 支架系统的技术成功率、安全性和结果与 Wingspan 支架系统相当。需要进一步的大规模研究来证实这些发现。

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