Gurbel P A, Anderson R D
Division of Cardiology, Union Memorial Hospital, Baltimore, Maryland, USA.
Cathet Cardiovasc Diagn. 1997 Jan;40(1):109-16. doi: 10.1002/(sici)1097-0304(199701)40:1<109::aid-ccd21>3.0.co;2-m.
These preclinical studies investigate a new concept in coronary angioplasty and balloon catheter technology (the P100 catheter). The study sought to evaluate the morphology of experimental coronary arterial plaques dilated with the P100 in comparison to standard balloons, to determine the in vitro flow rates occurring during the inflation of the P100 in comparison to available perfusion catheters, and to assess the in vivo coronary flow velocity and the presence of ischemia during prolonged inflations with the P100. The development of myocardial ischemia is a major limitation of standard balloon angioplasty. To limit ischemia, autoperfusion catheters have been developed, in which blood flows through the balloon in the central catheter shaft. However, as the flow lumen profile is reduced to enhance the performance of these devices, so is the accompanying flow. An angioplasty catheter was designed to evaluate the feasibility of continuous autoperfusion around the dilatation balloon. The balloon surface was engineered to develop a helical trough for blood flow to occur during inflation. Arterial plaque morphology following angioplasty with the P100 (n = 8) and with standard balloons (n = 8) was evaluated in a swine model. In vitro flow rates during inflation of the P100 and available perfusion catheters were determined using 33% glycerol solution. In vivo coronary flow velocity was determined with a Doppler-tipped wire during 60-min continuous inflations with the P100, and 15-sec inflations with a standard balloon in 12 vessel segments in 7 dogs; using 3.0-3.5-mm-diameter balloons. All lesions were successfully dilated (< 50% luminal diameter stenosis) with the P100 and standard balloons. There were no morphologic differences in plaques dilated with P100 compared to standard balloons. In vitro flow rates with conventional 3.0-mm balloon perfusion catheters ranged from 27.1 +/- 2.1 ml/min (RX Flowtrack) to 38.7 +/- 0.9 ml/min (Stack Perfusion), P < .05. Flow with the P100 ranged from 54.8 +/- 4.3 ml/min (2.5-mm balloon) to 103.2 +/- 4.5 ml/min (3.5-mm balloon), P < .05. Distal average peak coronary flow velocity during prolonged P100 inflations varied from 69 +/- 7% of baseline at 5 min to 83 +/- 8% of baseline at 40 min, with an upward trend in velocity the longer the balloon was inflated. Hemodynamics remained stable. Experimental plaques are successfully dilated with a helical balloon by a mechanism that appears similar to the dilatation mechanism of standard balloons. These preclinical studies show that angioplasty and autoperfusion can be accomplished by a balloon that does not have complete surface area contact with the vessel wall. A gap created by the helix can thus provide a conduit for blood flow. Clinical studies will determine whether this innovation, which alters the tubular geometry of current angioplasty balloons, will provide autoperfusion and equivalent dilatation effects in human.
这些临床前研究探讨了冠状动脉血管成形术和球囊导管技术中的一个新概念(P100导管)。该研究旨在评估与标准球囊相比,用P100扩张的实验性冠状动脉斑块的形态,确定与现有灌注导管相比,P100充气过程中的体外流速,并评估P100长时间充气期间的体内冠状动脉流速和缺血情况。心肌缺血的发生是标准球囊血管成形术的一个主要限制。为了限制缺血,已开发出自灌注导管,血液通过中央导管轴内的球囊流动。然而,随着流动腔轮廓缩小以提高这些装置的性能,伴随的血流也减少了。设计了一种血管成形术导管来评估围绕扩张球囊进行连续自灌注的可行性。球囊表面经过设计,形成一个螺旋形凹槽,以便在充气时实现血流。在猪模型中评估了用P100(n = 8)和标准球囊(n = 8)进行血管成形术后的动脉斑块形态。使用33%甘油溶液测定P100和现有灌注导管充气期间的体外流速。在7只狗的12个血管节段中,使用直径3.0 - 3.5毫米的球囊,用带多普勒探头的导丝在P100连续充气60分钟和标准球囊充气15秒期间测定体内冠状动脉流速。所有病变用P100和标准球囊均成功扩张(管腔直径狭窄<50%)。与标准球囊相比,用P100扩张的斑块在形态上没有差异。传统3.0毫米球囊灌注导管的体外流速范围为27.1±2.1毫升/分钟(RX Flowtrack)至38.7±0.9毫升/分钟(Stack Perfusion),P < 0.05。P100的流速范围为54.8±4.3毫升/分钟(2.5毫米球囊)至103.2±4.5毫升/分钟(3.5毫米球囊),P < 0.05。P100长时间充气期间远端平均冠状动脉峰值流速从5分钟时基线的69±7%变化到40分钟时基线的83±8%,球囊充气时间越长,流速呈上升趋势。血流动力学保持稳定。实验性斑块通过一种类似于标准球囊扩张机制成功地用螺旋球囊扩张。这些临床前研究表明,血管成形术和自灌注可以通过与血管壁没有完全表面积接触的球囊来实现。螺旋形产生的间隙因此可以为血流提供一个通道。临床研究将确定这种改变当前血管成形术球囊管状几何形状的创新是否能在人体中提供自灌注和等效的扩张效果。