Koch Rachel, Inci Errol, Grubb Kendra, Leshnower Bradley, Paone Gaetano, Ueyama Hiroki, Devireddy Chandan, Gleason Patrick, Xie Joe, Wei Jane, Rainer Katharine, Ceretto-Clark Brendan, Byku Isida, Greenbaum Adam, Babaliaros Vasilis, Perdoncin Emily
Department of Internal Medicine, Emory University Hospital, Atlanta, GA, USA.
Division of Cardiology, Emory Structural Heart and Valve Center, Emory University Hospital Midtown, Atlanta, GA, USA.
Cardiovasc Revasc Med. 2023 Jan;46:85-89. doi: 10.1016/j.carrev.2022.08.010. Epub 2022 Aug 11.
We aim to compare in-hospital and 30-day outcomes of transcatheter aortic valve replacement (TAVR) versus surgical aortic valve replacement (SAVR) for native aortic insufficiency (AI).
TAVR is increasingly used off-label in patients with AI deemed high risk for SAVR. There is a paucity of data comparing TAVR and SAVR with current commercially available TAVR devices.
A single-center, retrospective cohort study of patients undergoing TAVR or SAVR for native AI between 2014 and 2020 was performed. Data were obtained from the Society of Thoracic Surgeons (STS) Adult Cardiac Surgery Database, Transcatheter Valve Therapy (TVT) registry, and chart review. In-hospital and 30-day outcomes are reported.
Of 125 total patients, 91 underwent SAVR and 34 underwent TAVR. The TAVR group had a higher STS predictive risk of mortality (PROM) (TAVR = 3.96 %, SAVR = 1.25 %, p < 0.0001). In the postoperative period, the SAVR group had higher rates of new-onset atrial fibrillation (20.9 % vs. 0 %, p < 0.001), while the TAVR group had higher rates of complete heart block requiring permanent pacemaker implantation (20.6 % vs. 2.2 %, p < 0.001). There was no difference in in-hospital or 30-day mortality, stroke, myocardial infarction, residual AI, or repeat valve intervention.
Despite higher STS PROM and more comorbidities, patients who underwent TAVR for AI had similar in-hospital and 30-day outcomes as patients who underwent SAVR for AI. These results support TAVR in selected high-risk patients with AI, with the knowledge that pacemaker needs may be higher than patients undergoing SAVR.
我们旨在比较经导管主动脉瓣置换术(TAVR)与外科主动脉瓣置换术(SAVR)治疗原发性主动脉瓣关闭不全(AI)的院内及30天结局。
TAVR越来越多地被用于那些被认为进行SAVR风险较高的AI患者,作为一种非标签治疗方法。目前比较TAVR和SAVR与现有市售TAVR装置的数据较少。
对2014年至2020年间因原发性AI接受TAVR或SAVR的患者进行了一项单中心回顾性队列研究。数据来自胸外科医师协会(STS)成人心脏手术数据库、经导管瓣膜治疗(TVT)注册库以及病历审查。报告了院内及30天结局。
在125例患者中,91例接受了SAVR,34例接受了TAVR。TAVR组的STS预测死亡风险(PROM)更高(TAVR = 3.96%,SAVR = 1.25%,p < 0.0001)。术后,SAVR组新发房颤的发生率更高(20.9%对0%,p < 0.001),而TAVR组需要植入永久性起搏器的完全性心脏传导阻滞发生率更高(20.6%对2.2%,p < 0.001)。在院内或30天死亡率、中风、心肌梗死、残余AI或再次瓣膜干预方面没有差异。
尽管TAVR组的STS PROM更高且合并症更多,但因AI接受TAVR的患者与因AI接受SAVR的患者的院内及30天结局相似。这些结果支持在选定的高风险AI患者中使用TAVR,同时要知道起搏器需求可能高于接受SAVR的患者。