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药物洗脱支架与裸金属支架用于初发冠状动脉狭窄的异质性重叠支架置入术后的临床结局

Clinical outcomes after heterogeneous overlap stenting with drug-eluting stents and bare-metal stents for de novo coronary artery narrowings.

作者信息

Aoki Jiro, Kirtane Ajay J, Dangas George D, Lansky Alexandra J, Morales Andy, Kimura Masashi, Kim Young-Hak, Moussa Issam, Weisz Giora, Kreps Edward M, Collins Michael, Frankin-Bond Theresa, Stone Gregg W, Moses Jeffrey W, Leon Martin B, Mehran Roxana

机构信息

Center for Interventional Vascular Therapy, Columbia University Medical Center, New York, NY, USA.

出版信息

Am J Cardiol. 2008 Jan 1;101(1):58-62. doi: 10.1016/j.amjcard.2007.07.049. Epub 2007 Nov 26.

DOI:10.1016/j.amjcard.2007.07.049
PMID:18157966
Abstract

When it is difficult to deliver multiple drug-eluting stents (DES) or when size constraints limit DES implantation, bare-metal stents (BMS) may be implanted contiguous to DES. However, the clinical outcomes after overlapping DES and BMS implantation are not known. From September 2004 to June 2006, 4,872 consecutive patients who underwent percutaneous coronary intervention consented to be enrolled in a prospective registry. Of these patients, 44 (0.9%) with de novo lesions were treated with DES and BMS overlap stenting. All patients were followed to 12 months for the assessment of clinical outcomes. The average implanted stent diameter was 2.68 +/- 0.30 mm for DES and 2.35 +/- 0.38 mm for BMS. Overlapping BMS were implanted distal to DES in all but 1 case. One patient (2.3%) experienced acute stent thrombosis and died 2 days after the procedure. No other patient died or had a myocardial infarction during 12 months. The target vessel revascularization rate at 12 months, however, was 31.8%, mainly driven by diffuse in-stent restenosis in the BMS segments. In conclusion, the incidence of DES and BMS overlap stenting is rare in daily practice, but this procedure is associated with a high rate of target vessel revascularization.

摘要

当难以植入多个药物洗脱支架(DES)或尺寸限制阻碍DES植入时,裸金属支架(BMS)可紧邻DES植入。然而,DES与BMS重叠植入后的临床结果尚不清楚。从2004年9月至2006年6月,4872例连续接受经皮冠状动脉介入治疗的患者同意纳入一项前瞻性注册研究。在这些患者中,44例(0.9%)新发病变患者接受了DES与BMS重叠支架植入治疗。所有患者均随访至12个月以评估临床结果。DES的平均植入支架直径为2.68±0.30mm,BMS为2.35±0.38mm。除1例患者外,所有患者的重叠BMS均植入于DES的远端。1例患者(2.3%)发生急性支架血栓形成,并在术后2天死亡。在12个月期间,无其他患者死亡或发生心肌梗死。然而,12个月时的靶血管血运重建率为31.8%,主要由BMS节段的弥漫性支架内再狭窄所致。总之,DES与BMS重叠支架植入在日常实践中发生率较低,但该操作与较高的靶血管血运重建率相关。

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