Intravascular Ultrasound Assessment of Arterial Dissections Following Rotarex Atherectomy: Results of the iDissection Rotarex Study

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Abstract

Background

There are limited data on the mechanism of the Rotarex Rotational Excisional Atherectomy System in treating femoropopliteal arterial disease. The Rotarex iDissection study is a prospective, single center study evaluating the extent of excision and dissection in de novo and restenotic (not in-stent) lesions of the femoropopliteal arteries in symptomatic peripheral arterial disease patients.

Methods

Consecutive patients with symptomatic peripheral arterial disease were prospectively enrolled in the Rotarex iDissection study at a single US center after obtaining informed consent. The study was approved by a central ethics committee. Quantitative vascular angiography and intravascular ultrasound images were analyzed by an independent core laboratory. The Eagle Eye Platinum ST intravascular ultrasound (Phillips) was used to identify the depth (A, B, C for intima, media, and adventitia, respectively) and arc of dissections (1 and 2 for <180° and ≥180°, respectively) using the iDissection classification. Statistical significance was determined by a P value <.05.

Results

A total of 19 patients (20 procedures) were enrolled by 1 endovascular specialist. There were 57.9% men with mean age of 71.1 ± 9.6 years. Of the patients, 31.6% had diabetes mellitus, and 84.2% were current or past smokers. Thirty percent of treated vessels were chronic total occlusions. A total of 10 patients received stents (2 covered stents due to perforation, 6 due to National Heart, Lung, and Blood Institute Type C dissections, and 2 were primary stenting). Two distal embolizations occurred; one was attributed to the Rotarex, and both were treated with no adverse consequences. Angiographic baseline stenosis was 74.7% ± 25.6%; after Rotarex, 48.7% ± 14.8%; and after percutaneous transluminal angioplasty (PTA), 16.0% ± 6.2%. Baseline minimal lumen diameter was 1.0 ± 1.0 mm; after Rotarex, 2.4 ± 1.1 mm; and after PTA, 4.4 ± 1.0 mm. Angiographically, there was 1 type A dissection at baseline; 1 A, 1 B, and 2 C after Rotarex, and 3 A and 5 C after final adjunctive PTA. Intravascular ultrasound revealed a reference diameter of 6.2 ± 1.0 mm; 70% of patients had adventitial dissections. The mean arc of calcium was 221° ± 39.4° (moderate to severe calcium).

Conclusions

The Rotarex device is an effective atherectomy device in treating complex femoropopliteal arterial disease. A high frequency of adventitial dissections is seen with the Rotarex. The long-term outcomes of this finding need to be further studied.

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罗塔列克斯动脉粥样硬化切除术和球囊血管成形术后的动脉横断面血管内超声评估:前瞻性 iDissection Rotarex 研究结果
背景关于Rotarex旋转切除动脉粥样硬化切除术系统治疗股腘动脉疾病机制的数据很有限。Rotarex iDissection 研究是一项前瞻性的单中心研究,评估了无症状外周动脉疾病患者股腘动脉新发病变和再狭窄(非支架内)病变的切除和剥离范围。该研究获得了中心伦理委员会的批准。定量血管造影和血管内超声图像由独立的核心实验室进行分析。Eagle Eye Platinum ST 血管内超声(Phillips)采用 iDissection 分类法识别血管内膜、中膜和前壁的深度(分别为 A、B、C)和断裂弧度(分别为 1 和 2 表示 180°和≥180°)。统计意义由 P 值决定。其中男性占 57.9%,平均年龄为 71.1 ± 9.6 岁。其中,31.6%的患者患有糖尿病,84.2%的患者目前或曾经吸烟。接受治疗的血管中有 30% 为慢性全闭塞。共有10名患者接受了支架治疗(2名患者因穿孔而接受了覆盖支架治疗,6名患者因国家心肺血液研究所C型血管断裂而接受了覆盖支架治疗,2名患者接受了初级支架治疗)。发生了两次远端栓塞,其中一次是由 Rotarex 引起的,两次栓塞都得到了治疗,没有造成不良后果。血管造影基线狭窄率为74.7%±25.6%;Rotarex术后为48.7%±14.8%;经皮腔内血管成形术(PTA)后为16.0%±6.2%。基线最小管腔直径为 1.0 ± 1.0 毫米;Rotarex 治疗后为 2.4 ± 1.1 毫米;PTA 治疗后为 4.4 ± 1.0 毫米。血管造影显示,基线时有1处A型夹层;Rotarex治疗后有1处A型、1处B型和2处C型夹层;最终辅助PTA治疗后有3处A型和5处C型夹层。血管内超声显示的参考直径为 6.2 ± 1.0 毫米;70% 的患者有血管内膜剥离。结论Rotarex设备是治疗复杂股骨腘动脉疾病的有效动脉粥样硬化切除设备。使用Rotarex时出现临近面剥离的频率很高。这一发现的长期结果还需进一步研究。
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