Walczewski Michał, Gąsecka Aleksandra, Witkowski Adam, Dabrowski Maciej, Huczek Zenon, Wilimski Radosław, Ochała Andrzej, Parma Radosław, Rymuza Bartosz, Grygier Marek, Jemielity Marek, Olasińska-Wiśniewska Anna, Jagielak Dariusz, Targoński Radosław, Pastuszak Krzysztof, Grešner Peter, Grabowski Marcin, Kochman Janusz
1 Chair and Department of Cardiology, Medical University of Warsaw, Warsaw, Poland.
Department of Interventional Cardiology and Angiology, National Institute of Cardiology, Warsaw, Poland.
Postepy Kardiol Interwencyjnej. 2023 Sep;19(3):251-256. doi: 10.5114/aic.2023.131478. Epub 2023 Sep 27.
Data regarding patients with a previous medical record of immunosuppression treatment who have undergone transcatheter aortic valve implantation (TAVI) are limited and extremely inconclusive. Available studies are mostly short term observations; thus there is a lack of evidence on efficacy and safety of TAVI in this specific group of patients.
To compare the in-hospital and long-term outcomes between patients with or without a medical history of immunosuppressive treatment undergoing TAVI for aortic valve stenosis (AS).
We conducted a retrospective registry-based analysis including patients undergoing TAVI for AS at 5 centres between January 2009 and August 2017. The primary endpoint was long-term all-cause mortality. Secondary endpoints comprised major vascular complications, life-threatening or disabling bleeding, stroke and new pacemaker implantation.
Of 1451 consecutive patients who underwent TAVI, two propensity-matched groups including 25 patients with a history of immunosuppression and 75 patients without it were analysed. No differences between groups in all-cause mortality were found in a median follow-up time of 2.7 years following TAVI ( = 0.465; HR = 0.73; 95% CI: 0.30-1.77). The rate of major vascular complications (4.0% vs. 5.3%) was similar in the two groups ( = 1.000). There were no statistically significant differences in the composite endpoint combining life-threatening or disabling bleeding, major vascular complications, stroke and new pacemaker implantation (40.0% vs. 20.0%, = 0.218).
Patients who had undergone TAVI for AS had similar long-term mortality regardless of whether they had a previous medical record of immunosuppression. Procedural complication rates were comparable between the groups.
关于既往有免疫抑制治疗病史且接受经导管主动脉瓣植入术(TAVI)患者的数据有限且极不确定。现有研究大多为短期观察;因此,缺乏关于TAVI在这一特定患者群体中的疗效和安全性的证据。
比较有或无免疫抑制治疗病史的主动脉瓣狭窄(AS)患者接受TAVI后的住院和长期结局。
我们进行了一项基于注册登记的回顾性分析,纳入了2009年1月至2017年8月期间在5个中心接受TAVI治疗AS的患者。主要终点是长期全因死亡率。次要终点包括主要血管并发症、危及生命或致残性出血、中风和新起搏器植入。
在1451例连续接受TAVI的患者中,分析了两个倾向匹配组,其中25例有免疫抑制病史,75例无免疫抑制病史。在TAVI后中位随访时间2.7年时,两组全因死亡率无差异(P = 0.465;HR = 0.73;95%CI:0.30 - 1.77)。两组主要血管并发症发生率相似(4.0%对5.3%,P = 1.000)。在将危及生命或致残性出血、主要血管并发症、中风和新起搏器植入合并的复合终点方面,无统计学显著差异(40.0%对20.0%,P = 0.218)。
接受TAVI治疗AS的患者,无论既往有无免疫抑制治疗病史,长期死亡率相似。两组的手术并发症发生率相当。