Görmez Selçuk, Erdim Refik, Erdoğmuş Onur, Civan Murat, Catakoğlu Alp Burak, Gülbaran Murat, Demiroğlu Cemşid, Aytekin Vedat
Department of Cardiology, Florence Nightingale Hospital, Istanbul, Turkey.
Anadolu Kardiyol Derg. 2008 Dec;8(6):431-6.
The purpose of this study was to compare treatment of saphenous vein graft (SVG) lesions with paclitaxel-eluting (PES) and sirolimus-eluting stents (SES) in daily practice with regard to short- and long-term clinical outcomes.
Between August 2002 and September 2006, a total of 71 patients with SVG lesions who were implanted PES or SES with percutaneous coronary intervention in our center were evaluated retrospectively. Forty-six patients with PES (PES group) were compared to twenty-five patients treated with SES (SES group) in terms of in-hospital, 30-day, six-months and 1-year clinical outcomes. Statistical analyses were performed using Chi-Square statistics or Fisher's exact and independent sample t test. Survival analysis was done using Kaplan-Meier method and log-rank test.
Baseline clinical characteristics were similar in both groups except for a tendency toward a lower age in the SES group. No statistically significant difference was found between two groups by means of lesion and procedural characteristics. All clinical outcomes at 30-day, 6-month and 1-year after the interventions were similar in both groups. Early stent thrombosis was detected in one patient (2.2%) of PES group (p=0.65). Late stent thrombosis was not observed in both groups. The rate of major adverse cardiac events at 1-year was 8.7% in the PES group and 16% in the SES group (p=0.44).
Short-and long-term clinical outcomes of PES and SES in the treatment of SVG lesions are similar. The results of our study showed that both drug-eluting stents are effective and safe in real-world patient with diseased SVGs.
本研究旨在比较在日常临床实践中,紫杉醇洗脱支架(PES)和西罗莫司洗脱支架(SES)治疗隐静脉桥(SVG)病变的短期和长期临床疗效。
回顾性分析2002年8月至2006年9月期间,在本中心接受经皮冠状动脉介入治疗并植入PES或SES的71例SVG病变患者。将46例接受PES治疗的患者(PES组)与25例接受SES治疗的患者(SES组)在住院期间、30天、6个月和1年的临床疗效方面进行比较。采用卡方检验、Fisher精确检验和独立样本t检验进行统计学分析。采用Kaplan-Meier法和对数秩检验进行生存分析。
除SES组年龄有稍低趋势外,两组基线临床特征相似。两组在病变和手术特征方面未发现统计学显著差异。两组干预后30天、6个月和1年的所有临床疗效相似。PES组有1例患者(2.2%)发生早期支架血栓形成(p = 0.65)。两组均未观察到晚期支架血栓形成。PES组1年时主要不良心脏事件发生率为8.7%,SES组为16%(p = 0.44)。
PES和SES治疗SVG病变的短期和长期临床疗效相似。我们的研究结果表明,两种药物洗脱支架在患有病变SVG的真实患者中都是有效且安全的。