用药物包被球囊或支架置入术干预股腘动脉后CLTI患者的临床结果。

IF 3.6 2区 医学 Q1 PERIPHERAL VASCULAR DISEASE Journal of Vascular Surgery Pub Date : 2025-07-01 Epub Date: 2025-02-18 DOI:10.1016/j.jvs.2025.02.010
Taira Kobayashi MD , Mitsuyoshi Takahara MD, PhD , Naoki Fujimura MD, PhD , Terutoshi Yamaoka MD, PhD , Daisuke Matsuda MD, PhD , Takanobu Okazaki MD, PhD , Shingo Mochizuki MD , Satoru Nagatomi MD , Masami Shingaki MD, PhD , Masayuki Endo MD, PhD , Kyosuke Hosokawa MD, PhD , Tadashi Furuyama MD, PhD , Tsunehiro Shintani MD, PhD , Yasuhito Sekimoto MD, PhD , Hidetoshi Uchiyama MD , Ryoichi Kyuragi MD, PhD , Susumu Watada MD, PhD , Koichi Morisaki MD, PhD , Hiroki Mitsuoka MD, PhD , Yohei Kawai MD, PhD , Shigeo Ichihashi MD, PhD
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引用次数: 0

摘要

背景:股腘动脉闭塞病变患者的血管内治疗(EVT)因其有效性而在世界范围内进行。然而,慢性肢体威胁缺血(CLTI)的病变是复杂的,是股浅动脉(SFA) EVT的主要关注点。尽管如此,对SFA EVT的详细研究,特别是最终装置作为药物包被球囊(DCB)或支架的选择,尚未在CLTI患者中进行。目的:比较使用DCB或支架的SFA EVT治疗CLTI患者的临床结果。方法:在日本21个中心进行多中心回顾性观察性研究。在治疗加权逆概率(IPTW)后,对接受初始SFA EVT与DCB或支架置入的患者进行比较,使用倾向评分来控制潜在的混杂因素(患者人口统计学、合并症、药物和手术细节)。主要结局指标为主要肢体不良事件(MALE)。我们采用了特定原因的风险模型,使用Fine和Gray的比例风险模型,其中死亡被视为一种竞争风险。次要结局指标也进行了评估:1)技术成功,2)血流缓慢,3)30天内死亡,4)30天内主要不良事件,5)再狭窄,6)靶病变血运重建术(TLR), 7)急性闭塞,8)伤口愈合,9)主要截肢,10)全因死亡率。结果:该研究包括900例CLTI患者,他们接受了EVT合并DCB (n=458)或支架植入术(n=442),中位随访时间为17.5个月(四分位数间距为6.2-31.9)。DCB组发生MALE的风险低于支架组,风险比为0.68(95%可信区间(CI), 0.52 - 0.89;P = .005)。随后对次要结局指标的分析表明,DCB组术后慢血流发生率较高,急性闭塞发生率较低(经Bonferroni校正后P均< 0.005)。结论:DCB血管成形术比支架置入术发生MALE的风险低。这些结果表明,在CLTI患者的初始SFA干预中,DCB可能更有益。
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Clinical outcomes in patients with chronic limb-threatening ischemia after femoropopliteal intervention with a drug-coated balloon or stenting

Objective

Endovascular treatment (EVT) for patients with an occlusive lesion of the femoropopliteal artery is performed worldwide due to its effectiveness. However, lesions in chronic limb-threatening ischemia (CLTI) are complex and a major concern in superficial femoral artery (SFA) EVT. Despite this, a detailed study of SFA EVT, and especially selection of the final device as a drug-coated balloon (DCB) or a stent, has not been performed in patients with CLTI. The aim of this stud was to compare the clinical outcomes of SFA EVT using a DCB or a stent in patients with CLTI.

Methods

A multicenter retrospective observational study was performed at 21 Japanese centers. Comparisons were made between patients undergoing initial SFA EVT with a DCB or stenting after inverse probability of treatment weighting using the propensity score to control for potential confounding (patient demographics, comorbidities, medications, and procedural details). The primary outcome measure was major adverse limb events (MALE). We adopted cause-specific hazard models, using Fine and Gray’s proportional hazards model in which death was treated as a competing risk. Secondary outcome measures were also evaluated: (1) technical success; (2) slow flow; (3) death within 30 days; (4) major adverse events within 30 days; (5) restenosis; (6) target lesion revascularization; (7) acute occlusion; (8) wound healing; (9) major amputation; and (10) all-cause mortality.

Results

The study included 900 CLTI cases that underwent EVT with a DCB (n = 458) or stenting (n = 442) and had a median follow-up period of 17.5 months (interquartile range, 6.2-31.9 months). The DCB group had a lower risk of MALE than the stent group, with a hazard ratio of 0.68 (95% confidence interval, 0.52-0.89; P = .005). Subsequent analysis for the secondary outcome measures demonstrated that the DCB group had a higher prevalence of postprocedural slow flow and a lower incidence rate of acute occlusion (both P < .005 after Bonferroni correction).

Conclusions

DCB angioplasty had a lower risk of MALE than stenting. These results suggest that a DCB might be more beneficial in initial SFA intervention in patients with CLTI.
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来源期刊
CiteScore
7.70
自引率
18.60%
发文量
1469
审稿时长
54 days
期刊介绍: Journal of Vascular Surgery ® aims to be the premier international journal of medical, endovascular and surgical care of vascular diseases. It is dedicated to the science and art of vascular surgery and aims to improve the management of patients with vascular diseases by publishing relevant papers that report important medical advances, test new hypotheses, and address current controversies. To acheive this goal, the Journal will publish original clinical and laboratory studies, and reports and papers that comment on the social, economic, ethical, legal, and political factors, which relate to these aims. As the official publication of The Society for Vascular Surgery, the Journal will publish, after peer review, selected papers presented at the annual meeting of this organization and affiliated vascular societies, as well as original articles from members and non-members.
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