Barath Sitaram, Patel Ramesh, Mittal Gaurav Kumar, Mohindru Rishabh, Sharma Jai Bharat, Jain Dilip
Department of Radiology, Geetanjali Medical College and Hospital, Udaipur, IND.
Department of Cardiology, Geetanjali Medical College and Hospital, Udaipur, IND.
Cureus. 2024 Dec 15;16(12):e75763. doi: 10.7759/cureus.75763. eCollection 2024 Dec.
Background Carotid artery stenting is a well-established alternative treatment to carotid endarterectomy for carotid artery stenosis for preventing stroke. This study assessed the procedural and clinical outcomes in patients undergoing carotid artery stenting in a tertiary care center in India. Methods A total of 39 patients underwent carotid artery stenting from January 2022 to December 2023, with different embolic protection devices and carotid stents. All the patients had symptomatic carotid artery stenosis with at least 50% stenosis as per the North American Symptomatic Carotid Endarterectomy Trial (NASCET) criteria. Procedural and technical success was assessed, and patients were followed for 20 ± 7 months for survival, new-onset stroke, and quality of life. Results The mean age was 64.8 ± 9.1 years and 25 (64.1%) of the patients were males. A total of 26 (66.7%) patients were hypertensive and 21 (53.9%) patients had a history of diabetes mellitus. Out of 39 patients, 2 (5.1%) had recurrent transient ischemic attacks while the rest (37; 94.9%) had a subacute and chronic ischemic stroke. A total of 37 (94.9%) patients had carotid artery stenosis of more than 70%. In this study, 9 (23.1%) patients had a history of sub-acute ischemic stroke of a 1 to 3-week duration. Two patients underwent bilateral staged stenting over a gap of one month. The overall procedural success rate was 39 (100%) and none of the patients had access site-related major complications. Out of the total 41 implants, 21 (51.2%) were self-expanding carotid WALLSTENT (Boston Scientific, Marlborough, Massachusetts, US) and 20 (48.8%) implants were Protégé RX tapered self-expanding carotid stent (Medtronic, Dublin, Ireland). A FilterWire EZ (Boston Scientific) embolic protection device was used in 23 (56.1%) cases and Spider FX (Medtronic) in 18 (43.9%) cases. None of our patients had an intraprocedural death. One patient had postprocedural ipsilateral third nerve palsy, which was resolved partially on the next day of carotid angioplasty. We used dual-antiplatelet drug therapy post-procedure for a month followed by a single antiplatelet drug lifelong. All patients were followed for a minimum of six months and a maximum of 30 months. A total of three (7.7%) patients have died, and 2 (5.1%) patients had a new-onset ischemic stroke with one on the same side of the carotid stenting. A total of 31 (79.5%) patients were doing well and in the recovery phase while those two patients who had a recurrent stroke were bedridden. None of the patients had clinically significant restenosis that needed revascularization of the carotid artery over a mean follow-up period. Conclusion Carotid artery stenting is an effective method to reduce the recurrence of ischemic stroke in significant symptomatic carotid stenosis patients. Experience in neuro-interventional procedures at our center leads to an acceptable rate of peri-procedural stroke, recurrence, and mortality in carotid artery stenting procedures.
颈动脉支架置入术是一种成熟的替代颈动脉内膜切除术治疗颈动脉狭窄以预防中风的方法。本研究评估了印度一家三级医疗中心接受颈动脉支架置入术患者的手术过程和临床结果。
2022年1月至2023年12月,共有39例患者接受了颈动脉支架置入术,使用了不同的栓塞保护装置和颈动脉支架。根据北美症状性颈动脉内膜切除术试验(NASCET)标准,所有患者均有症状性颈动脉狭窄,狭窄程度至少为50%。评估手术和技术成功率,并对患者进行20±7个月的随访,观察生存情况、新发中风及生活质量。
患者平均年龄为64.8±9.1岁,25例(64.1%)为男性。共有26例(66.7%)患者患有高血压,21例(53.9%)患者有糖尿病史。39例患者中,2例(5.1%)有反复短暂性脑缺血发作,其余37例(94.9%)有亚急性和慢性缺血性中风。共有37例(94.9%)患者颈动脉狭窄超过70%。本研究中,9例(23.1%)患者有1至3周病程的亚急性缺血性中风病史。2例患者在间隔一个月的时间内接受了双侧分期支架置入术。总体手术成功率为39例(100%),无患者发生与穿刺部位相关的严重并发症。在总共41枚植入物中,21枚(51.2%)为自膨式颈动脉WALLSTENT(美国波士顿科学公司,马尔伯勒,马萨诸塞州),20枚(48.8%)植入物为Protégé RX锥形自膨式颈动脉支架(美敦力公司,都柏林,爱尔兰)。23例(56.1%)使用了FilterWire EZ(波士顿科学公司)栓塞保护装置,18例(43.9%)使用了Spider FX(美敦力公司)。我们的患者均未发生术中死亡。1例患者术后出现同侧动眼神经麻痹,在颈动脉血管成形术后第二天部分缓解。术后我们使用双联抗血小板药物治疗一个月后改为终身单一抗血小板药物治疗。所有患者至少随访6个月,最长随访30个月。共有3例(7.7%)患者死亡,2例(5.1%)患者发生新发缺血性中风,其中1例发生在颈动脉支架置入同侧。共有31例(79.5%)患者情况良好,处于恢复期,而另外2例复发中风的患者卧床不起。在平均随访期内,无患者发生需要颈动脉血管再通的具有临床意义的再狭窄。
颈动脉支架置入术是降低有显著症状性颈动脉狭窄患者缺血性中风复发的有效方法。我们中心的神经介入手术经验使颈动脉支架置入术的围手术期中风、复发和死亡率处于可接受水平。