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可生物降解聚合物涂层西罗莫司洗脱支架系统的九个月临床结果:一项多中心“真实世界”经验。

Nine-Months Clinical Outcome of Biodegradable Polymer Coated Sirolimus-eluting Stent System: A Multi-Centre "Real-World" Experience.

作者信息

Sarma Raghava, Prajapati Jayesh, Raheem Asif, Thakkar Kamlesh, Kothari Shivani, Thakkar Ashok

机构信息

Interventional Cardiologist, Lalitha Super Specialties Hospital (P) Ltd., Heart and Brain Centre , Kothapet, Guntur, Andhra Pradesh, India .

Interventional Cardiologist, Apollo Hospitals , Plot No.1 A, Bhat GIDC Estate, Gandhinagar, Gujarat, India .

出版信息

J Clin Diagn Res. 2015 Aug;9(8):OC23-6. doi: 10.7860/JCDR/2015/14060.6403. Epub 2015 Aug 1.

Abstract

BACKGROUND

The main culprit in first-generation drug eluting stents is 'durable' polymer, whose continuous presence may impair arterial healing and ultimately have a negative impact on late outcomes. The main enigma behind the biodegradable polymer usage is its degradation after elution of drug. This reduces adverse events in unselected patients with complex coronary artery lesions treated with biodegradable polymer coated sirolimus-eluting stents.

AIM

The aim of the INDOLIMUS-G Registry was to evaluate safety and efficacy of the Indolimus (Sahajanand Medical Technologies Pvt. Ltd., Surat, India) sirolimus-eluting stents in large cohorts of unselected patients with complex coronary artery lesions.

MATERIALS AND METHODS

It is a multi-centre, non-randomized retrospective registry with a clear aim of evaluating safety and efficacy of the Indolimus sirolimus-eluting stents in consecutive patients enrolled between April 2012 and May 2014. The primary end-point of the study was major adverse cardiac events (MACE), which is a composite of cardiac death, myocardial infarction (MI), target lesion revascularization (TLR), target vessel revascularization (TVR) and stent thrombosis (ST) at the end of follow-up. Clinical follow-up were scheduled at the end of 30-days, 6-months, and 9-months period.

RESULTS

The mean age of enrolled patients was 52.6 ± 11.0 years. A total of 1137 lesions were intervened successfully with 1242 stents (1.09 ± 0.30 stent per lesion). The average stent length and diameter was 27.42 ± 9.01 mm and 3.12 ± 0.36 mm respectively. There were 740 (73.40%) male patients, indicating their high prevalence. Diabetes, hypertension and totally occluded lesions were found in 372 (36.90%), 408 (40.47%) and 170 (16.86%) patients, respectively. This showed that study also included high risk complex lesions and not ideal recruited lesions. The incidence of MACE at 30-days, 6-months and 9-months were 3 (0.30%), 18 (1.80%) and 22 (2.20%) respectively. At 9-months, TLR was found in 6 (0.50%) patients. There were 2 (0.20%) cases of ST, 10 (1.0%) cases of MI and 4 (0.40%) cases of cardiac death at 9-month follow-up.

CONCLUSION

The lower incidence of MACE, TLR and ST at 9-month follow-up clearly delineates safety and efficacy of Indolimus SES in large cohorts of unselected patients with complex coronary lesions.

摘要

背景

第一代药物洗脱支架的主要问题在于“持久”聚合物,其持续存在可能会损害动脉愈合,最终对远期预后产生负面影响。可生物降解聚合物应用背后的主要谜团在于其在药物洗脱后发生降解。这减少了在接受可生物降解聚合物涂层西罗莫司洗脱支架治疗的未选择的复杂冠状动脉病变患者中的不良事件。

目的

INDOLIMUS - G注册研究的目的是评估吲哚莫司(印度苏拉特萨哈贾南德医疗技术有限公司)西罗莫司洗脱支架在大量未选择的复杂冠状动脉病变患者中的安全性和有效性。

材料与方法

这是一项多中心、非随机的回顾性注册研究,明确旨在评估2012年4月至2014年5月期间连续入选患者中吲哚莫司西罗莫司洗脱支架的安全性和有效性。该研究的主要终点是主要不良心脏事件(MACE),它是随访结束时心脏死亡、心肌梗死(MI)、靶病变血运重建(TLR)、靶血管血运重建(TVR)和支架血栓形成(ST)的复合终点。临床随访安排在30天、6个月和9个月结束时进行。

结果

入选患者的平均年龄为52.6±11.0岁。共成功干预了1137处病变,使用了1242枚支架(每处病变1.09±0.30枚支架)。平均支架长度和直径分别为27.42±9.01毫米和3.12±0.36毫米。有740名(73.40%)男性患者,表明男性患病率较高。分别在372名(36.90%)、408名(40.47%)和170名(16.86%)患者中发现糖尿病、高血压和完全闭塞病变。这表明该研究也纳入了高风险复杂病变,而非理想的入选病变。30天、6个月和9个月时MACE发生率分别为3例(0.30%)、18例(1.80%)和22例(2.20%)。在9个月时,6名(0.50%)患者发生TLR。在9个月随访时,有2例(0.20%)ST病例、10例(1.0%)MI病例和4例(0.40%)心脏死亡病例。

结论

9个月随访时较低的MACE、TLR和ST发生率清楚地表明了吲哚莫司西罗莫司洗脱支架在大量未选择的复杂冠状动脉病变患者中的安全性和有效性。

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Biodegradable coating for drug-eluting stents--more than a facelift?
Eur Heart J. 2008 Aug;29(16):1930-1. doi: 10.1093/eurheartj/ehn304. Epub 2008 Jun 26.

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