De Bonis Michele, Lapenna Elisabetta, Buzzatti Nicola, La Canna Giovanni, Denti Paolo, Pappalardo Federico, Schiavi Davide, Pozzoli Alberto, Cioni Micaela, Di Giannuario Giovanna, Alfieri Ottavio
Department of Cardiac Surgery, IRCCS San Raffaele Hospital, Vita e Salute San Raffaele University, Milan, Italy
Department of Cardiac Surgery, IRCCS San Raffaele Hospital, Vita e Salute San Raffaele University, Milan, Italy.
Eur J Cardiothorac Surg. 2016 Sep;50(3):488-94. doi: 10.1093/ejcts/ezw093. Epub 2016 Mar 23.
Recurrent mitral regurgitation (MR) is common after surgical and percutaneous (MitraClip) treatment of functional MR (FMR). However, the Everest II trial suggested that, in patients with secondary MR and initially successful MitraClip therapy, the results were sustained at 4 years and were comparable with surgery in terms of late efficacy. The aim of this study was to assess whether both those findings were confirmed by our own experience.
We reviewed 143 patients who had an initial optimal result (residual MR ≤ 1+ at discharge) after MitraClip therapy (85 patients) or surgical edge-to-edge (EE) repair (58 patients) for severe secondary MR (mean ejection fraction 28 ± 8.5%). Patients with MR ≥ 2+ at hospital discharge were excluded. The two groups were comparable. Only age and logistic EuroSCORE were higher in the MitraClip group.
Follow-up was 100% complete (median 3.2 years; interquartile range 1.8;6.1). Freedom from cardiac death at 4 years (81 ± 5.2 vs 84 ± 4.6%, P = 0.5) was similar in the surgical and MitraClip group. The initial optimal MitraClip results did not remain stable. At 1 year, 32.5% of the patients had developed MR ≥ 2+ (P = 0.0001 compared with discharge). Afterwards, patients with an echocardiographic follow-up at 2 years (60 patients), 3 years (40 patients) and 4 years (21 patients) showed a significant increase in the severity of MR compared with the corresponding 1 year grade (all P < 0.01). Freedom from MR ≥ 3+ at 4 years was 75 ± 7.6% in the MitraClip group and 94 ± 3.3% in the surgical one (P = 0.04). Freedom from MR ≥ 2+ at 4 years was 37 ± 7.2 vs 82 ± 5.2%, respectively (P = 0.0001). Cox regression analysis identified the use of MitraClip as a predictor of recurrence of MR ≥ 2+ [hazard ratio (HR) 5.2, 95% confidence interval (CI) 2.5-10.8, P = 0.0001] as well as of MR ≥ 3 (HR 3.5, 95% CI 0.9-13.1, P = 0.05).
In patients with FMR and optimal mitral competence after MitraClip implantation, the recurrence of significant MR at 4 years is not uncommon. This study does not confirm previous observations reported in the Everest II randomized controlled trial indicating that, if the MitraClip therapy was initially successful, the results were sustained at 4 years. When compared with the surgical EE combined with annuloplasty, MitraClip therapy provides lower efficacy at 4 years.
在功能性二尖瓣反流(FMR)的外科手术和经皮治疗(MitraClip)后,二尖瓣反流复发很常见。然而,EVEREST II试验表明,在继发性二尖瓣反流且MitraClip治疗最初成功的患者中,4年时结果得以维持,且在晚期疗效方面与手术相当。本研究的目的是评估我们自己的经验是否证实了这两项发现。
我们回顾了143例因严重继发性二尖瓣反流(平均射血分数28±8.5%)接受MitraClip治疗(85例)或外科缘对缘(EE)修复(58例)且初始结果最佳(出院时残余二尖瓣反流≤1+)的患者。出院时二尖瓣反流≥2+的患者被排除。两组具有可比性。仅MitraClip组的年龄和逻辑EuroSCORE较高。
随访完成率为100%(中位时间3.2年;四分位间距1.8;6.1)。手术组和MitraClip组4年时的心源性死亡自由度相似(81±5.2%对84±4.6%,P = 0.5)。MitraClip最初的最佳结果未保持稳定。1年时,32.5%的患者二尖瓣反流发展至≥2+(与出院时相比,P = 0.0001)。之后,在2年(60例患者)、3年(40例患者)和4年(21例患者)进行超声心动图随访的患者中,二尖瓣反流严重程度与相应的1年分级相比显著增加(所有P<0.01)。MitraClip组4年时无二尖瓣反流≥3+的自由度为75±7.6%,手术组为94±3.3%(P = 0.04)。4年时无二尖瓣反流≥2+的自由度分别为37±7.2%和82±5.2%(P = 0.0001)。Cox回归分析确定使用MitraClip是二尖瓣反流≥2+复发的预测因素[风险比(HR)5.2,95%置信区间(CI)2.5 - 10.8,P = 0.0001]以及二尖瓣反流≥3+复发的预测因素(HR 3.5,95% CI 0.9 - 13.1,P = 0.05)。
在植入MitraClip后二尖瓣功能最佳的FMR患者中,4年时显著二尖瓣反流复发并不罕见。本研究未证实EVEREST II随机对照试验中先前报道的观察结果,即如果MitraClip治疗最初成功,4年时结果得以维持。与外科EE联合瓣环成形术相比,MitraClip治疗在4年时疗效较低。