Ishikawa Tetsuya, Nakano Yosuke, Mutoh Makoto
Division of Cardiology, Saitama Cardiovascular Respiratory Center, Japan.
Intern Med. 2012;51(19):2695-701. doi: 10.2169/internalmedicine.51.6704. Epub 2012 Oct 1.
We retrospectively analyzed the midterm clinical and angiographic outcomes after the implantation of paclitaxel- (PES, TAXUS Express) and sirolimus- (SES, Cypher Bx Velocity) eluting stents in Japanese patients with complex coronary lesions.
From August 2004 to May 2009, 1,335 nonrandomized de novo native complex coronary lesions treated with either a PES (357 cases) or SES were included. The inclusion criteria for patients with complex lesions were those with diabetes, those undergoing hemodialysis, and those with a low ejection fraction, as well as subjects who had lesions with severe calcification, ostiums of the right coronary and left circumflex arteries, and who underwent the side-branch bifurcation 2-stent technique. The subjects were evaluated for consistent predictors of cardiac events, binary restenosis and target lesion vascularization of the SES. The composite primary endpoint percentage (900-day cardiac death, nonfatal recurrent myocardial infarction, and definite stent thrombosis) after PES placement was 0.6%, which was not significantly different from that after SES placement (0.12%; p=0.290). The incidence of the secondary endpoint (binary restenosis; stenosis >50% of the diameter at the secondary angiographic examination performed within 550 days after the procedure) after PES placement (15.0%) was also not significantly different than that after SES placement (13.3%; p=0.498). There was no relationship between PES placement and binary restenosis upon angiographic follow-up of 989 lesions (odds ratio of 1.14; 95% confidence interval, 0.73-1.77; p=0.57).
For de novo native complex coronary stenosis, the midterm safety and efficacy of PES placement was statistically equivalent to that of SES placement in a clinical setting in Japan.
我们回顾性分析了日本复杂冠状动脉病变患者植入紫杉醇洗脱支架(PES,TAXUS Express)和西罗莫司洗脱支架(SES,Cypher Bx Velocity)后的中期临床和血管造影结果。
2004年8月至2009年5月,纳入1335例接受PES(357例)或SES治疗的非随机原发性天然复杂冠状动脉病变患者。复杂病变患者的纳入标准包括糖尿病患者、接受血液透析的患者、射血分数低的患者,以及有严重钙化病变、右冠状动脉和左旋支动脉开口病变的患者,以及接受边支分叉双支架技术的患者。评估这些受试者发生心脏事件、二元再狭窄和SES靶病变血管化的一致预测因素。PES置入后复合主要终点百分比(900天心脏死亡、非致命性复发性心肌梗死和明确的支架血栓形成)为0.6%,与SES置入后(0.12%;p=0.290)无显著差异。PES置入后次要终点(二元再狭窄;在术后550天内进行的二次血管造影检查中直径狭窄>50%)的发生率(15.0%)与SES置入后(13.3%;p=0.498)也无显著差异。在对989个病变进行血管造影随访时,PES置入与二元再狭窄之间无相关性(优势比为1.14;95%置信区间,0.73 - 1.77;p=0.57)。
对于原发性天然复杂冠状动脉狭窄,在日本临床环境中,PES置入的中期安全性和有效性在统计学上等同于SES置入。