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紫杉醇涂层球囊导管治疗小冠状动脉。

Treatment of small coronary arteries with a paclitaxel-coated balloon catheter.

机构信息

Institut für Klinische Forschung, Herz- und Kreislaufzentrum, Rotenburg an der Fulda, Germany.

出版信息

Clin Res Cardiol. 2010 Mar;99(3):165-74. doi: 10.1007/s00392-009-0101-6. Epub 2010 Jan 6.

DOI:10.1007/s00392-009-0101-6
PMID:20052480
Abstract

BACKGROUND

Treatment of lesions in small coronary arteries by percutaneous transluminal coronary intervention is limited by a high recurrence rate. We assessed the use of a paclitaxel-coated balloon in this indication.

METHODS

One-hundred eighteen patients with stenoses in small coronary vessels were treated by a paclitaxel-coated balloon (3 microg/mm(2)). The main inclusion criteria encompassed diameter stenosis of > or =70% and < or =22 mm in length with a vessel diameter of 2.25-2.8 mm. Follow-up angiography was performed at scheduled 6-month post-intervention or whenever driven by clinical or electrocardiographic signs of ischemia. The primary endpoint was angiographic in-segment late lumen loss.

RESULTS

Eighty-two of 118 patients (70%) with a vessel diameter of 2.35 +/- 0.19 mm were treated with the drug-coated balloon only, while 32 patients required additional stent deployment. The mean in-segment late lumen loss was 0.28 +/- 0.53 mm. In patients treated with the drug-coated balloon only, the in-segment late lumen loss was 0.16 +/- 0.38 mm. At 12 months, the rate of major adverse cardiac events was 15% which was primarily due to the need for target lesion revascularization in 14 patients (12%). In those with additional bare metal stent implantation geographical mismatch between coated-balloon dilatation and stent implantation was significantly associated with the occurrence of restenosis.

CONCLUSION

Treatment of coronary stenosis in small coronary vessels with the paclitaxel-coated balloon was well tolerated. It may offer an alternative to the implantation of a drug-eluting stent (ClinicalTrials.gov Identifier: NCT00404144).

摘要

背景

经皮腔内冠状动脉介入治疗小冠状动脉病变的复发率较高,受到限制。我们评估了紫杉醇涂层球囊在该适应证中的应用。

方法

118 例小冠状动脉狭窄患者接受紫杉醇涂层球囊(3μg/mm²)治疗。主要纳入标准包括直径狭窄>70%且<22mm,血管直径为 2.25-2.8mm。在预定的 6 个月介入后或出现临床或心电图缺血迹象时进行随访造影。主要终点是血管造影节段晚期管腔丢失。

结果

82 例血管直径为 2.35±0.19mm 的患者(70%)仅接受药物涂层球囊治疗,32 例患者需要额外植入支架。平均节段晚期管腔丢失为 0.28±0.53mm。仅接受药物涂层球囊治疗的患者,节段晚期管腔丢失为 0.16±0.38mm。12 个月时,主要不良心脏事件发生率为 15%,主要归因于 14 例患者(12%)需要靶病变血运重建。在那些接受裸金属支架植入术的患者中,涂层球囊扩张和支架植入术之间的地理不匹配与再狭窄的发生显著相关。

结论

紫杉醇涂层球囊治疗小冠状动脉狭窄是安全的,可能为药物洗脱支架的植入提供替代方案(ClinicalTrials.gov 标识符:NCT00404144)。

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