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首页> 外文期刊>Journal of endovascular therapy: an official journal of the International Society of Endovascular Specialists >Paclitaxel-Coated Balloon for the Treatment of Infrainguinal Disease: 12-Month Outcomes in the All-Comers Cohort of BIOLUX P-III Global Registry
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Paclitaxel-Coated Balloon for the Treatment of Infrainguinal Disease: 12-Month Outcomes in the All-Comers Cohort of BIOLUX P-III Global Registry

机译:紫杉醇涂层气球用于治疗初级语言疾病:Biolux P-III全球注册表的全选式队列12个月的成果

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Purpose: To further investigate the safety and performance of the Passeo-18 Lux drug-coated balloon (DCB) for the treatment of atherosclerotic infrainguinal disease under real-world conditions. Materials and Methods: BIOLUX P-III is an international, prospective, observational registry (ClinicalTrials.gov identifier NCT02276313) conducted at 41 centers in Europe, Asia, and Australia with follow-up visits at 6, 12, and 24 months. Of 700 patients (mean age 70.0 +/- 10.2 years; 439 men) with 863 lesions in the all-comers cohort, 330 (47.1%) patients had diabetes and 234 (37.7%) had chronic limb-threatening ischemia. The majority (79.3%) of lesions were in the femoropopliteal segment; of all lesions, 645 (74.9%) were calcified and 99 (11.5%) had in-stent restenosis (ISR). The mean lesion length was 84.7 +/- 73.3 mm. The primary clinical endpoint was major adverse events (MAEs) within 6 months, a composite of device- and procedure-related mortality through 30 days, major target limb amputation, and clinically-driven target lesion revascularization (TLR). The primary performance endpoint was clinically-driven TLR within 12 months. Results: At 6 and 12 months, freedom from MAEs was 94.0% and 89.5% in the all-comers cohort: 95.0% and 91.2% in the femoropopliteal group and 95.3% and 88.0% in the ISR subgroup, respectively. Freedom from clinically-driven TLR at 12 months was 93.1% in the all-comers cohort, 93.9% in the femoropopliteal lesions, and 89.4% for ISR lesions. All-cause mortality was 6.1% in the all-comers cohort: 5.9% in both the femoropopliteal and ISR subgroups. There were no device- or procedure-related deaths at up to 12 months. The Rutherford category improved in >80% of all subgroups at 12 months. Conclusion: In a real-world patient population, the safety and performance of the Passeo-18 Lux DCB for the treatment of atherosclerotic infrainguinal lesions are maintained, with good performance outcomes and low complication rates at 12 months.
机译:目的:进一步调查Passeo-18 Lux药物涂层气球(DCB)的安全性和性能,用于治疗现实世界条件下的动脉粥样硬化缺陷症疾病。材料和方法:Biolux P-III是一个国际,前瞻性的观察性注册表(Clinicaltrials.gov标识符NCT02276313)在欧洲,亚洲和澳大利亚的41个中心进行,随访时间为6,12和24个月。 700名患者(平均年龄为70.0岁+/- 10.2岁; 439名男性)在全选煤会上有863个病变,330名(47.1%)患者患有糖尿病,234名(37.7%)患有慢性肢体威胁性缺血。大多数(79.3%)病变在股份质上的部分;在所有病变中,钙化645(74.9%),99(11.5%)有支架再狭窄(ISR)。平均病变长度为84.7 +/- 73.3毫米。主要临床终点是6个月内主要不良事件(MAES),通过30天,主要目标肢体截肢和临床驱动的靶病变血运重建(TLR)的综合患者和程序相关死亡率的复合物。主要性能终点在12个月内是临床驱动的TLR。结果:在6和12个月,MAE的自由分别为MAE的自由为94.0%和89.5%,分别为95.0%和91.2%,分别在ISR子组中95.3%和88.0%。在临床驱动的TLR中自由于12个月为93.1%,股骨头造质病变93.9%,ISR病变为89.4%。全型死亡率为6.1%,在股骨头造盘和ISR亚群中的5.9%。在12个月内没有设备或程序相关的死亡。 Rutherford类别在12个月内改善了所有子组的80%。结论:在真实世界的患者人口中,维持PASSEO-18 LUX DCB的安全性和性能,维持治疗动脉粥样硬化的疾病病变,在12个月内具有良好的性能结果和低并发症率。

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