Görge G, Haude M, Ge J, Voegele E, Gerber T, Rupprecht H J, Meyer J, Erbel R
Department of Cardiology, University Hospital, Essen, Germany.
J Am Coll Cardiol. 1995 Sep;26(3):725-30. doi: 10.1016/0735-1097(95)00211-l.
We sought to characterize the differences seen after low or high pressure coronary artery stent deployment as assessed by intravascular ultrasound.
Until 1992, the success of stent deployment was assessed by angiographic criteria only, but in 1993 the procedure was expanded to include postprocedural single-use intravascular ultrasound imaging. Ultrasound criteria for successful stent deployment were 1) symmetry, 2) minimal lumen diameter > 3.0 mm, 3) no echo-free spaces between the stent and the vessel, and 4) no uncovered dissections.
We used mechanical 4.8F or 3.5F 20- or 30-MHz monorail single-use intravascular ultrasound catheters.
Fifty-two patients were included, 28 treated in 1991 and 1992 (group A) and 24 treated in 1993 or 1994 (group B); 87% of patients underwent elective stent implantation. The number of echocardiographic studies per patient increased from 1 +/- 0.1 (mean +/- SD) in group A to 2.0 +/- 0.85 in group B. Mean maximal balloon size increased from 3.3 +/- 0.33 to 3.73 +/- 0.24 mm and maximal inflation pressure from 6.9 +/- 1.1 to 15.8 +/- 2.4 bar (p < 0.001). The eccentricity index was 0.915 +/- 0.04 in group B versus 0.87 +/- 0.05 in group A. Minimal lumen diameter measured by echocardiography increased from 2.55 +/- 0.41 mm in group A to 3.14 +/- 0.37 mm in group B. The final mean values per cross-sectional area as a percent of calculated balloon area were similar in group A (67.5 +/- 23%) and group B (66.5 +/- 22.9%). No major acute complications occurred in either group; subacute thrombosis developed in two patients, both in group A.
Intravascular ultrasound data confirm that high pressure stent deployment leads to increased minimal lumen area. Despite high pressure stent deployment, homogeneous stent geometry and optimal stent expansion were not observed in all patients.
我们试图通过血管内超声来描述冠状动脉支架在低压或高压下植入后所观察到的差异。
直到1992年,支架植入的成功仅通过血管造影标准来评估,但在1993年该方法扩展到包括术后一次性血管内超声成像。成功植入支架的超声标准为:1)对称性,2)最小管腔直径>3.0mm,3)支架与血管之间无无回声间隙,4)无未覆盖的夹层。
我们使用机械4.8F或3.5F、20或30MHz的单轨一次性血管内超声导管。
纳入52例患者,1991年和1992年治疗28例(A组),1993年或1994年治疗24例(B组);87%的患者接受了择期支架植入。每位患者的超声心动图检查次数从A组的1±0.1(均值±标准差)增加到B组的2.0±0.85。平均最大球囊尺寸从3.3±0.33增加到3.73±0.24mm,最大充气压力从6.9±1.1增加到15.8±2.4巴(p<0.001)。B组的偏心指数为0.915±0.04,而A组为0.87±0.05。超声心动图测量的最小管腔直径从A组的2.55±0.41mm增加到B组的3.14±0.37mm。A组(67.5±23%)和B组(66.5±22.9%)每个横截面积相对于计算出的球囊面积的最终平均值相似。两组均未发生重大急性并发症;两名患者发生亚急性血栓形成,均在A组。
血管内超声数据证实,高压支架植入可导致最小管腔面积增加。尽管采用了高压支架植入,但并非所有患者都观察到均匀的支架几何形状和最佳的支架扩张效果。