使用Ranger紫杉醇包被球囊治疗慢性肢体缺血患者:来自新加坡的短期安全性和有效性结果

Mervin Lim, T. Chong, S. L. Chan, S. Yap, Ankur Patel, K. H. Tay, T. Tang
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Data were retrieved from the Vascular Quality Initiative database recently set up at this institution. Primary lesion patency, amputation-free survival (AFS), freedom from target-lesion revascularization (TLR), and complete wound healing were the efficacy endpoints of interest at 6 months post intervention. Results. A total of 84 patients (87 limbs; 229 lesions) were enrolled. Fifty-one of the 84 patients (60.7%) were men. Baseline characteristics included diabetes mellitus in 76/84 patients (90.5%), chronic renal impairment in 25/84 patients (29.8%), and Rutherford category 6 foot wounds in 22/87 limbs (24.7%). TASC D lesions were present in 63/229 lesions (27.9%) and moderate/severe vessel wall calcification was present in 167/229 lesions (72.9%). Immediate technical success was achieved in 218/229 lesions (95.2%) with no device-related mortality at 30 days. Primary patency rates at 3 months and 6 months were 76/82 (92.7%) and 69/81 (85.2%), respectively. 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引用次数: 1

摘要

慢性肢体威胁缺血,又称临界肢体缺血(CLI),是外周动脉疾病(PAD)的最晚期,患者下肢主要截肢和死亡的风险较高。血管内优先入路已成为这些患者首选的血运重建策略。该研究的目的是评估Ranger紫杉醇包被球囊(PCB;波士顿科学公司)在CLI的设置。方法。这是一项单中心、单臂、多研究者的前瞻性研究,研究对象是2019年7月至2019年11月在新加坡新加坡总医院使用Ranger PCB进行血管内血运重建术的CLI患者。数据从该机构最近建立的血管质量倡议数据库中检索。原发病变通畅、无截肢生存(AFS)、无靶病变血运重建术(TLR)和伤口完全愈合是干预后6个月的疗效终点。结果。共84例患者(87肢;229个病变)被纳入。84例患者中男性51例(60.7%)。基线特征包括糖尿病76/84例(90.5%),慢性肾功能损害25/84例(29.8%),卢瑟福6类足创伤22/87例(24.7%)。63/229例病变中存在TASC D病变(27.9%),167/229例病变中存在中重度血管壁钙化(72.9%)。218/229个病变(95.2%)立即获得技术成功,30天无器械相关死亡率。3个月和6个月的原发性通畅率分别为76/82(92.7%)和69/81(85.2%)。使用Ranger气囊治疗和不使用Ranger气囊治疗的6个月膝下(BTK)病变的原发性通畅率分别为89/94(94.7%)和34/41 (82.9%)(P= 0.03)。6个月AFS发生率为68/78 (87.2%),TLR解除率为73/81(90.1%)。6个月伤口完全愈合率为28/50(56.0%)。结论。使用Ranger PCB显示出良好的结果和短期通畅率,特别是在BTK地区,这是一个具有挑战性的患者队列。等待延长随访以评估气囊的长期安全性和有效性。
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Use of the Ranger Paclitaxel-Coated Balloon in Patients With Chronic Limb-Threatening Ischemia: Short-Term Safety and Efficacy Results From Singapore
Chronic limb-threatening ischemia, also known as critical limb ischemia (CLI), is the most advanced stage of peripheral arterial disease (PAD), and patients have high risk of major lower-limb amputation and mortality. An endovascular-first approach has become the preferred revascularization strategy for these patients. The aim of the study was to evaluate the safety and short-term efficacy of the Ranger paclitaxel-coated balloon (PCB; Boston Scientific) in the setting of CLI. Methods. This was a single-center, single-arm, multi-investigator, prospective study of CLI patients who underwent endovascular revascularization using the Ranger PCB from July 2019 to November 2019 at Singapore General Hospital in Singapore. Data were retrieved from the Vascular Quality Initiative database recently set up at this institution. Primary lesion patency, amputation-free survival (AFS), freedom from target-lesion revascularization (TLR), and complete wound healing were the efficacy endpoints of interest at 6 months post intervention. Results. A total of 84 patients (87 limbs; 229 lesions) were enrolled. Fifty-one of the 84 patients (60.7%) were men. Baseline characteristics included diabetes mellitus in 76/84 patients (90.5%), chronic renal impairment in 25/84 patients (29.8%), and Rutherford category 6 foot wounds in 22/87 limbs (24.7%). TASC D lesions were present in 63/229 lesions (27.9%) and moderate/severe vessel wall calcification was present in 167/229 lesions (72.9%). Immediate technical success was achieved in 218/229 lesions (95.2%) with no device-related mortality at 30 days. Primary patency rates at 3 months and 6 months were 76/82 (92.7%) and 69/81 (85.2%), respectively. Six-month primary patency rates of below-the-knee (BTK) lesions treated with and without Ranger balloons were 89/94 (94.7%) and 34/41 (82.9%), respectively (P=.03). Six-month AFS occurred in 68/78 (87.2%) and freedom from TLR occurred in 73/81 (90.1%). Six-month complete wound healing rate was respectable, at 28/50 (56.0%). Conclusion. Use of the Ranger PCB showed favorable outcomes and short-term patency rates, especially in the BTK region, in what is an otherwise challenging patient cohort. Extended follow-up is awaited to evaluate the long-term safety and efficacy of the balloon.
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