Colombo A, Hall P, Nakamura S, Almagor Y, Maiello L, Martini G, Gaglione A, Goldberg S L, Tobis J M
Centro Cuore Columbus, Milan, Italy.
Circulation. 1995 Mar 15;91(6):1676-88. doi: 10.1161/01.cir.91.6.1676.
The placement of stents in coronary arteries has been shown to reduce restenosis in comparison to balloon angioplasty. However, clinical use of intracoronary stents is impeded by the risk of subacute stent thrombosis and complications associated with the anticoagulant regimen. To reduce these complications, the hypothesis that systemic anticoagulation is not necessary when adequate stent expansion is achieved was prospectively evaluated on a consecutive series of patients who received intracoronary stents.
From March 1993 to January 1994, 359 patients underwent Palmaz-Schatz coronary stent insertion. After an initial successful angiographic result with < 20% stenosis by visual estimation had been achieved, intravascular ultrasound imaging was performed. Further balloon dilatation of the stent was guided by observation of the intravascular ultrasound images. All patients with adequate stent expansion confirmed by ultrasound were treated only with antiplatelet therapy (either ticlopidine for 1 month with short-term aspirin for 5 days or only aspirin) after the procedure. Clinical success (procedure success without early postprocedural events) at 2 months was achieved in 338 patients (94%). With an inflation pressure of 14.9 +/- 3.0 atm and a balloon-to-vessel ratio of 1.17 +/- 0.19, optimal stent expansion was achieved in 321 of the 334 patients (96%) who underwent intravascular ultrasound evaluation, with these patients receiving only antiplatelet therapy after the procedure. Despite the absence of anticoagulation, there were only two acute stent thromboses (0.6%) and one subacute stent thrombosis (0.3%) at 2-month clinical follow-up. Follow-up angiography at 3 to 6 months documented two additional occlusions (0.6%) at the stent site. At 6-month clinical follow-up, angiographically documented stent occlusion had occurred in 5 patients (1.6%). At 6-month clinical follow-up, there was a 5.7% incidence of myocardial infarction, a 6.4% rate of coronary bypass surgery, and a 1.9% incidence of death. Emergency intervention (emergency angioplasty or bailout stent) for a stent thrombosis event was performed in 3 patients (0.8%). The overall event rate was relatively high because of intraprocedural complications that occurred in 16 patients (4.5%). Intraprocedural complications, however, decreased to 1% when angiographically appropriately sized balloons were used for final stent dilations. There was one ischemic vascular complication that occurred at the time of the procedure and one ischemic vascular complication that occurred at the time of angiographic follow-up. By 6 months, repeat angioplasty for symptomatic restenosis was performed in 47 patients (13.1%).
The Palmaz-Schatz stent can be safely inserted in coronary arteries without subsequent anticoagulation provided that stent expansion is adequate and there are no other flow-limiting lesions present. The use of high-pressure final balloon dilatations and confirmation of adequate stent expansion by intravascular ultrasound provide assurance that anticoagulation therapy can be safely omitted. This technique significantly reduces hospital time and vascular complications and has a low stent thrombosis rate.
与球囊血管成形术相比,冠状动脉内支架置入已显示可减少再狭窄。然而,冠状动脉内支架的临床应用受到亚急性支架血栓形成风险以及与抗凝方案相关并发症的阻碍。为减少这些并发症,对一系列连续接受冠状动脉内支架置入的患者进行前瞻性评估,以验证在实现充分的支架扩张后无需全身抗凝的假设。
1993年3月至1994年1月,359例患者接受了Palmaz-Schatz冠状动脉支架置入术。在血管造影初步成功,目测狭窄<20%后,进行血管内超声成像。根据血管内超声图像观察指导对支架进行进一步球囊扩张。所有经超声证实支架充分扩张的患者术后仅接受抗血小板治疗(噻氯匹定治疗1个月并短期服用阿司匹林5天或仅服用阿司匹林)。2个月时338例患者(94%)获得临床成功(手术成功且无早期术后事件)。在接受血管内超声评估的334例患者中,321例(96%)在14.9±3.0个大气压的充盈压力和1.17±0.19的球囊与血管比率下实现了最佳支架扩张,这些患者术后仅接受抗血小板治疗。尽管未进行抗凝,在2个月临床随访时仅发生2例急性支架血栓形成(0.6%)和1例亚急性支架血栓形成(0.3%)。3至6个月的随访血管造影显示支架部位又有2例闭塞(0.6%)。在6个月临床随访时,血管造影记录有5例患者(1.6%)发生支架闭塞。在6个月临床随访时,心肌梗死发生率为5.7%,冠状动脉搭桥手术率为6.4%,死亡率为1.9%。3例患者(0.8%)因支架血栓形成事件进行了紧急干预(紧急血管成形术或补救支架置入)。由于16例患者(4.5%)发生术中并发症,总体事件发生率相对较高。然而,当使用血管造影尺寸合适的球囊进行最终支架扩张时,术中并发症降至1%。术中发生1例缺血性血管并发症,血管造影随访时发生1例缺血性血管并发症。到6个月时,47例患者(13.1%)因有症状的再狭窄接受了重复血管成形术。
只要支架扩张充分且不存在其他限流病变,Palmaz-Schatz支架可安全地置入冠状动脉且无需后续抗凝。使用高压最终球囊扩张并通过血管内超声确认支架充分扩张可确保安全省略抗凝治疗。该技术显著减少住院时间和血管并发症,且支架血栓形成率低。