The Utility of Sirolimus Eluting Balloons in the Setting of Chronic Limb Threatening Ischaemia in Asian Patients from Singapore - 12 Months Results of the PRISTINE Registry.

IF 2.8 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
T Y Tang, C Yap, S L Chan, S X Y Soon, C Sivanathan, A Gogna, A K Patel, T T Chong
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引用次数: 0

Abstract

Purpose: The aim of PRISTINE was to evaluate the 6 and 12 months safety and efficacy of the Selution Sustained Limus Release (SLR)™ sirolimus-coated balloon for treatment of complex lower limb occlusive lesions (TASC II C & D) in patients with chronic limb threatening ischemia (CLTI) from Singapore.

Methods: PRISTINE was a prospective, non-randomized, single arm, observational, multi-investigator, single-center clinical study. Complication-free survival at 30 days was the safety clinical endpoint. Immediate technical success (ability to cross and dilate the lesion and achieve residual angiographic stenosis < 30%), 6-month primary vessel patency, limb salvage, clinically driven target lesion revascularization (TLR) and amputation free survival (AFS) were the efficacy endpoints of interest.

Results: Seventy five patients were included. There were 50 (68.0%) males; mean age, 69.0 ± 10.7 years. CLTI severity was based on the Rutherford Scale (R5 = 51; R6 = 17). Significant co-morbidities included diabetes mellitus (n = 68; 91.0%) and end-stage renal failure (n = 28; 37.0%). 112 atherosclerotic lesions were treated (TASC II D = 58 (52%); 76 (67%) de novo). There was 100% technical success. Mean lesion length treated was 22.4 ± 13.9 cm. Primary vessel patencies at 6 and 12 months were 64/86 (74%) and 43/74 (58%) and freedom from clinically driven TLR were 72/86 (84%) and 55/74 (74%) respectively. AFS was 61/73 (84.0%; five deaths and seven major lower extremity amputation) at 6-months. Mean Rutherford score improved from 5.1 ± 0.55 at baseline to 1.1 ± 2.05 (p < 0.05) at one year and there was a wound healing rate of 38/48 (79%) at the same timepoint.

Conclusions: The Selution SLR™ drug eluting balloon is safe and efficacious in treating highly complex infra-inguinal atherosclerotic lesions in an otherwise challenging frail population of CLTI patients with a high incidence of diabetes and end-stage renal failure. It is associated with highly satisfactory acute technical and clinical success, 12-month target lesion patency and AFS.

Level of evidence: Level 2b, Individual Cohort Study.

Abstract Image

西罗莫司洗脱球囊在新加坡亚洲慢性肢体缺血患者中的应用--PRISTINE 登记 12 个月的结果。
目的:PRISTINE 的目的是评估 Selution Sustained Limus Release (SLR)™ 西罗莫司涂层球囊治疗复杂下肢闭塞性病变(TASC II C 和 D)的 6 个月和 12 个月的安全性和有效性:PRISTINE 是一项前瞻性、非随机、单臂、观察性、多研究者、单中心临床研究。30天无并发症存活率是安全临床终点。即时技术成功率(穿越和扩张病变的能力以及达到残余血管狭窄的能力 结果:共纳入 75 名患者。其中男性 50 人(68.0%),平均年龄(69.0 ± 10.7)岁。CLTI严重程度基于卢瑟福量表(R5 = 51;R6 = 17)。重要的并发症包括糖尿病(68 例;91.0%)和终末期肾衰竭(28 例;37.0%)。共治疗了112处动脉粥样硬化病变(TASC II D = 58(52%);76(67%)为新生病变)。技术成功率为 100%。治疗病变的平均长度为 22.4 ± 13.9 厘米。6个月和12个月时的原发性血管通畅率分别为64/86(74%)和43/74(58%),无临床驱动的TLR分别为72/86(84%)和55/74(74%)。6个月后,AFS为61/73(84.0%;5人死亡,7人下肢截肢)。平均卢瑟福评分从基线时的 5.1 ± 0.55 分提高到 1.1 ± 2.05 分(p 结论:卢瑟福评分从基线时的 5.1 ± 0.55 分提高到 1.1 ± 2.05 分(pSelution SLR™ 药物洗脱球囊治疗腹股沟下高度复杂的动脉粥样硬化病变既安全又有效,适用于糖尿病和终末期肾衰竭发病率高、体弱多病的 CLTI 患者。该疗法的急性技术和临床成功率、12 个月的目标病变通畅率和 AFS 均非常令人满意:2b级,个体队列研究。
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来源期刊
CiteScore
5.50
自引率
13.80%
发文量
306
审稿时长
3-8 weeks
期刊介绍: CardioVascular and Interventional Radiology (CVIR) is the official journal of the Cardiovascular and Interventional Radiological Society of Europe, and is also the official organ of a number of additional distinguished national and international interventional radiological societies. CVIR publishes double blinded peer-reviewed original research work including clinical and laboratory investigations, technical notes, case reports, works in progress, and letters to the editor, as well as review articles, pictorial essays, editorials, and special invited submissions in the field of vascular and interventional radiology. Beside the communication of the latest research results in this field, it is also the aim of CVIR to support continuous medical education. Articles that are accepted for publication are done so with the understanding that they, or their substantive contents, have not been and will not be submitted to any other publication.
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