Topaz O, Rozenbaum E A, Luxenberg M G, Schumacher A
Cardiac Catheterization Laboratory, St. Paul Ramsey Medical Center, University of Minnesota Medical School, USA.
J Interv Cardiol. 1995 Dec;8(6):661-9. doi: 10.1111/j.1540-8183.1995.tb00916.x.
Laser-assisted coronary angioplasty can be successfully applied to lesions not ideal for balloon angioplasty. Patients with severely impaired left ventricular (LV) function and complex coronary artery stenoses who call for percutaneous revascularization are considered a high risk group for balloon angioplasty. In order to determine the feasibility, safety, and acute clinical outcome of a solid state, pulsed wave, mid-infrared (2.1 micron) laser facilitated angioplasty in these patients, data from 112 patients with 129 lesions were analyzed. Patients were identified according to angiographic LV function; group I included 22 patients with left ventricular ejection fraction (LVEF) < or = 40% (mean = 25% +/- 10%) and group II included 90 patients with LVEF > or = 40% (mean = 58% +/- 8%). No difference in age, gender, diabetes, hypertension, tobacco use, history of previous coronary artery bypass surgery (CABGS) or percutaneous transluminal coronary angioplasty was registered between the two groups. Multivessel disease, previous myocardial infarction (MI), and severe angina were more prevalent among group I patients (P = 0.03). No difference was found in lesion location, complexity, length, or calcification between the two groups; although group I had more eccentric lesions. Both groups were treated with the same laser energy level followed by adjunctive balloon angioplasty. One hundred percent procedural success was obtained in group I versus 93% in group II (P = NS). By Q.C.A. (independent core lab), minimal luminol diameter increased in group I from 0.9 +/- 0.5 mm preprocedure to 2.0 +/- 0.5, as compared to 0.8 +/- 0.5 mm to 1.9 +/- 0.5 mm (P = NS) in group II. Stenosis severity improved from 69% +/- 16% preprocedure to 37% +/- 13% postprocedure in group I, as compared to improvement from 78% +/- 16% to 37% +/- 12.7% in group II (P = NS). Overall complication rate was remarkably low, with no death or perforation in either group; emergency CABGS 0% in group I and 1.1% in group II; dissections 4.5% in group I and 8.8% in group II. There was no significant difference in complication rate between the two groups. The results of this study suggest that holmium:YAG laser facilitated coronary angioplasty can be safely performed in patients with severe LV dysfunction, achieving a remarkably high procedural success and low complication rate.
激光辅助冠状动脉成形术可成功应用于不适于球囊血管成形术的病变。左心室(LV)功能严重受损且冠状动脉复杂狭窄、需要经皮血管重建的患者被视为球囊血管成形术的高危人群。为了确定固态脉冲波中红外(2.1微米)激光辅助血管成形术在这些患者中的可行性、安全性和急性临床结果,分析了112例患者129处病变的数据。根据血管造影LV功能对患者进行分类;I组包括22例左心室射血分数(LVEF)≤40%(平均=25%±10%)的患者,II组包括90例LVEF≥40%(平均=58%±8%)的患者。两组在年龄、性别、糖尿病、高血压、吸烟、既往冠状动脉搭桥手术(CABGS)或经皮腔内冠状动脉成形术病史方面无差异。I组患者多支血管病变、既往心肌梗死(MI)和严重心绞痛更为常见(P=0.03)。两组在病变位置、复杂性、长度或钙化方面无差异;尽管I组偏心病变更多。两组均采用相同的激光能量水平治疗,随后进行辅助球囊血管成形术。I组手术成功率为100%,II组为93%(P=无统计学意义)。通过定量冠状动脉造影(独立核心实验室),I组最小管腔直径从术前的0.9±0.5毫米增加到2.0±0.5毫米,而II组从0.8±0.5毫米增加到1.9±0.5毫米(P=无统计学意义)。I组狭窄严重程度从术前的69%±16%改善到术后的37%±13%,而II组从78%±16%改善到37%±12.7%(P=无统计学意义)。总体并发症发生率极低,两组均无死亡或穿孔;I组急诊CABGS为0%,II组为1.1%;I组夹层为4.5%,II组为8.8%。两组并发症发生率无显著差异。本研究结果表明,钬:钇铝石榴石激光辅助冠状动脉成形术可在严重LV功能障碍患者中安全进行,手术成功率高,并发症发生率低。