Suppr超能文献

经皮冠状动脉介入治疗器械再狭窄倾向的差异。球囊血管成形术、定向旋切术、支架植入术和准分子激光血管成形术的定量血管造影比较。CARPORT、MERCATOR、MARCATOR、PARK和BENESTENT试验组。

Differences in restenosis propensity of devices for transluminal coronary intervention. A quantitative angiographic comparison of balloon angioplasty, directional atherectomy, stent implantation and excimer laser angioplasty. CARPORT, MERCATOR, MARCATOR, PARK, and BENESTENT Trial Groups.

作者信息

Foley D P, Melkert R, Umans V A, de Jaegere P P, Strikwerda S, de Feyter P J, Serruys P W

机构信息

Department of Interventional Cardiology, Erasmus University, Rotterdam, The Netherlands.

出版信息

Eur Heart J. 1995 Oct;16(10):1331-46. doi: 10.1093/oxfordjournals.eurheartj.a060740.

Abstract

With the increasing clinical application of new devices for percutaneous coronary revascularization, maximization of the acute angiographic result has become widely recognized as a key factor in maintained clinical and angiographic success. What is unclear, however, is whether the specific mode of action of different devices might exert an additional independent effect on late luminal renarrowing. The purpose of this study was to investigate such a difference in the degree of provocation of luminal renarrowing (or 'restenosis propensity') by different devices, among 3660 patients, who had 4342 lesions successfully treated by balloon angioplasty (n = 3797), directional coronary atherectomy (n = 200), Palmaz-Schatz stent implantation (n = 229) or excimer laser coronary angioplasty (n = 116) and who also underwent quantitative angiographic analysis pre- and post-intervention and at 6-month follow-up. To allow valid comparisons between the groups, because of significant differences in coronary vessel size (balloon angioplasty = 2.62 +/- 0.55 mm, directional coronary atherectomy = 3.28 +/- 0.62 mm, excimer laser coronary angioplasty = 2.51 +/- 0.47 mm, Palmaz-Schatz = 3.01 +/- 0.44 mm; P < 0.0001), the comparative measurements of interest selected were the 'relative loss' in luminal diameter (RLoss = loss/vessel size) to denote the restenosis process, and the 'relative lumen at follow-up' (RLfup = minimal luminal diameter at follow up/vessel size) to represent the angiographic outcome. For consistency, lesion severity pre-intervention was represented by the 'relative lumen pre' (RLpre = minimal luminal diameter pre/vessel size) and the luminal increase at intervention was measured as 'relative gain' (relative gain = gain/ vessel size). Differences in restenosis propensity between devices was evaluated by univariate and multivariate analysis. Multivariate models were constructed to determine relative loss and relative lumen at follow-up, taking account of relative lumen pre-intervention, lesion location, relative gain, vessel size and the device used. In addition, model-estimated relative loss and relative lumen at follow-up at given relative lumen pre-intervention relative gain and vessel size, were compared among the four groups. Significant differences were detected among the groups both with respect to these estimates, as well as in the degree of influence of progressively increasing relative gain, on the extent of renarrowing (relative loss) and angiographic outcome (relative lumen at follow-up), particularly at higher levels of luminal increase (relative gain). Specifically, lesions treated by balloon angioplasty or Palmaz-Schatz stent implantation (the predominantly 'dilating' interventions) were associated with more favourable angiographic profiles than directional atherectomy or excimer laser (the mainly 'debulking' interventions). Significant effects of lesion severity and location, as well as the well known influence of luminal increase on both luminal renarrowing and late angiographic outcome were also noted. These findings indicate that propensity to restenosis after apparently successful intervention is influenced not only by the degree of luminal enlargement achieved at intervention, but by the device used to achieve it. In view of the clinical implications of such findings, further evaluation in larger randomized patient populations is warranted.

摘要

随着经皮冠状动脉血运重建新器械在临床应用的不断增加,使急性血管造影结果最大化已被广泛认为是维持临床和血管造影成功的关键因素。然而,尚不清楚的是,不同器械的具体作用方式是否可能对晚期管腔再狭窄产生额外的独立影响。本研究的目的是在3660例患者中,调查不同器械引起管腔再狭窄程度(或“再狭窄倾向”)的差异,这些患者有4342处病变通过球囊血管成形术(n = 3797)、定向冠状动脉斑块旋切术(n = 200)、Palmaz-Schatz支架植入术(n = 229)或准分子激光冠状动脉血管成形术(n = 116)成功治疗,并且在干预前后及6个月随访时均接受了定量血管造影分析。为了在各组之间进行有效的比较,由于冠状动脉血管大小存在显著差异(球囊血管成形术= 2.62±0.55 mm,定向冠状动脉斑块旋切术= 3.28±0.62 mm,准分子激光冠状动脉血管成形术= 2.51±0.47 mm,Palmaz-Schatz = 3.01±0.44 mm;P < 0.0001),所选择的感兴趣的比较测量指标是管腔直径的“相对损失”(RLoss =损失/血管大小)以表示再狭窄过程,以及“随访时的相对管腔”(RLfup =随访时的最小管腔直径/血管大小)以代表血管造影结果。为保持一致性,干预前病变严重程度用“干预前相对管腔”(RLpre =干预前最小管腔直径/血管大小)表示,干预时管腔增加量用“相对增益”(相对增益=增益/血管大小)测量。通过单因素和多因素分析评估器械之间再狭窄倾向的差异。构建多因素模型以确定随访时的相对损失和相对管腔,同时考虑干预前相对管腔、病变位置、相对增益、血管大小和所使用的器械。此外,在给定的干预前相对管腔、相对增益和血管大小的情况下,比较四组模型估计的随访时相对损失和相对管腔。在这些估计值以及相对增益逐渐增加对再狭窄程度(相对损失)和血管造影结果(随访时相对管腔)的影响程度方面,各组之间均检测到显著差异,特别是在管腔增加量(相对增益)较高时。具体而言,通过球囊血管成形术或Palmaz-Schatz支架植入术治疗的病变(主要是“扩张”干预)与比定向斑块旋切术或准分子激光(主要是“减容”干预)更有利的血管造影表现相关。还注意到病变严重程度和位置的显著影响,以及管腔增加对管腔再狭窄和晚期血管造影结果的众所周知的影响。这些发现表明,明显成功干预后再狭窄的倾向不仅受干预时实现的管腔扩大程度影响,还受用于实现该扩大的器械影响。鉴于这些发现的临床意义,有必要在更大的随机患者群体中进行进一步评估。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验