Lee Joo Myung, Rhee Tae-Min, Hahn Joo-Yong, Hwang Doyeon, Park Jonghanne, Park Kyung Woo, Kim Hack-Lyoung, Kim Sang-Hyun, Chae In-Ho, Doh Joon-Hyung, Jeon Ki-Hyun, Choi Young Jin, Park Jin Sik, Choi Seung-Hyuck, Gwon Hyeon-Cheol, Koo Bon-Kwon, Alfonso Fernando, Kim Hyo-Soo
Division of Cardiology, Department of Internal Medicine, Heart Vascular Stroke Institute, Samsung Medical Center, Seoul, Republic of Korea.
Department of Internal Medicine and Cardiovascular Center, Seoul National University Hospital, Seoul, Republic of Korea.
Int J Cardiol. 2017 Mar 1;230:181-190. doi: 10.1016/j.ijcard.2016.12.176. Epub 2016 Dec 29.
Studies comparing the drug-eluting balloon (DEB) with contemporary drug-eluting stent (DES) in the treatment of in-stent restenosis (ISR) have been scarce. We compared that the efficacy and safety of contemporary DES versus DEB in unselected, real world patients of ISR occurred in bare-metal stent or DES.
Patient-level pooled analysis from nationwide multicenter registries was performed with 628 consecutive patients who underwent ISR treatment using 2nd or 3rd generation DES or DEB. Target lesion failure (TLF) and patient-oriented composite outcomes (POCO, composite of all-cause mortality, all-cause myocardial infarction, or any revascularization) at 1-year follow-up were compared between the DES and DEB groups.
A total of 628 patients with 697 ISR lesions were treated using newer generation DES (n=409) or DEB (n=219). About 55.1% presented with acute coronary syndrome, and 15.1% showed left ventricular dysfunction. The risks of TLF and POCO were significantly lower in the DES group, even after being adjusted by an inverse probability weighted model (TLF, 9.2% vs. 17.9%, HR 0.22, 95% CI 0.11-0.47; POCO, 12.4% vs. 24.1%, HR 0.25, 95% CI 0.13-0.48, all p-values<0.001), mainly driven by the significantly lower risk of target lesion revascularization (TLR) (7.6% vs. 13.0%, HR 0.21, 95% CI 0.09-0.49, p<0.001). Treatment of ISR with DEB independently predicted TLF (HR 1.87, 95% CI 1.05-3.02, p=0.034) along with multi-vessel disease, chronic kidney disease, type B2 or C lesion, and number of treated lesion>1.
In unselected patients of ISR, clinical outcome at one year was mainly dependent on difference in TLR and found to be better with contemporary DES than DEB.
比较药物洗脱球囊(DEB)与当代药物洗脱支架(DES)治疗支架内再狭窄(ISR)的研究较少。我们比较了当代DES与DEB在未选择的、现实世界中裸金属支架或DES发生ISR患者中的疗效和安全性。
对来自全国多中心注册研究的患者水平数据进行汇总分析,纳入628例连续接受第二代或第三代DES或DEB治疗ISR的患者。比较DES组和DEB组在1年随访时的靶病变失败(TLF)和以患者为导向的复合结局(POCO,全因死亡、全因心肌梗死或任何血运重建的复合结局)。
总共628例患有697处ISR病变的患者接受了新一代DES(n = 409)或DEB(n = 219)治疗。约55.1%的患者表现为急性冠状动脉综合征,15.1%的患者出现左心室功能障碍。DES组的TLF和POCO风险显著更低,即使在通过逆概率加权模型调整后也是如此(TLF,9.2%对17.9%,HR 0.22,95%CI 0.11 - 0.47;POCO,12.4%对24.1%,HR 0.25,95%CI 0.13 - 0.48,所有p值<0.001),主要是由于靶病变血运重建(TLR)风险显著更低(7.6%对13.0%,HR 0.21,95%CI 0.09 - 0.49,p<0.001)。DEB治疗ISR独立预测TLF(HR 1.87,95%CI 1.05 - 3.02,p = 0.034),同时还与多支血管病变、慢性肾脏病、B2或C型病变以及治疗病变数量>1有关。
在未选择的ISR患者中,1年时的临床结局主要取决于TLR的差异,发现当代DES比DEB的结局更好。