Nishida Hidefumi, Jeevanandam Valluvan, Salerno Christopher, Nemoto Atsushi, Song Tae, Onsager David, Nguyen Ann, Grinstein Jonathan, Chung Bow, Sarswat Nitasha, Kim Gene, Ota Takeyoshi
Department of Surgery, University of Chicago Medicine, Chicago, Illinois, USA.
Department of Medicine, University of Chicago Medicine, Chicago, Illinois, USA.
Cardiology. 2025;150(4):381-388. doi: 10.1159/000542871. Epub 2024 Nov 29.
The intravascular ventricular assist device is a newly developed ambulatory and portable counter pulsation heart assist system. The purpose of this study was to compare the early and late outcomes of counter pulsation devices between intravascular ventricular assist system (iVAS) and axillary intra-aortic balloon pump (IABP) as a bridge to heart transplantation.
This is a single-center, retrospective study. Between April 2016 and March 2020, 24 patients underwent iVAS implantation (Group A), and 73 patients underwent axillary IABP (Group B) as a bridge to heart transplantation. We reviewed and compared perioperative data, as well as late survival outcomes.
There were no significant differences in baseline characteristics. All patients in Group A and 97.3% of patients in Group B were able to ambulate and participate in physical therapy (p = 0.28). There were no in-hospital deaths in the two groups. The median duration of device support in Group A was significantly longer than in Group B (A: 37.0 days vs. B: 15.0 days, p < 0.01). After the US Food and Drug Administration approved the discharge of patients with an iVAS, 4 patients (4/14, 28.6%) were discharged home with the device. The success rate of bridge to transplantation was not significantly different between the groups (A: 21/24, 87.5% vs. B: 68/73, 93.2%, p = 0.40). Late survival after heart transplantation also did not differ between the groups (A: 85.7% at 3-year vs. B: 94.0% at 3-year, log rank = 0.22).
Both iVAS and axillary IABP showed comparable success rates of bridge to transplantation and late survival after transplantation. The mobile design of iVAS facilitated excellent ambulatory capability and enabled patients to be discharged home.
血管内心室辅助装置是一种新开发的可移动便携式反搏心脏辅助系统。本研究的目的是比较血管内心室辅助系统(iVAS)和腋动脉主动脉内球囊泵(IABP)作为心脏移植桥梁的反搏装置的早期和晚期结果。
这是一项单中心回顾性研究。2016年4月至2020年3月期间,24例患者接受了iVAS植入(A组),73例患者接受了腋动脉IABP(B组)作为心脏移植的桥梁。我们回顾并比较了围手术期数据以及晚期生存结果。
基线特征无显著差异。A组所有患者和B组97.3%的患者能够行走并参与物理治疗(p = 0.28)。两组均无院内死亡。A组装置支持的中位持续时间显著长于B组(A组:37.0天 vs. B组:15.0天,p < 0.01)。在美国食品药品监督管理局批准iVAS患者出院后,4例患者(4/14,28.6%)携带该装置出院回家。两组间移植桥梁成功率无显著差异(A组:21/24,87.5% vs. B组:68/73,93.2%,p = 0.40)。心脏移植后的晚期生存率在两组间也无差异(A组3年时为85.7% vs. B组3年时为94.0%,对数秩检验 = 0.22)。
iVAS和腋动脉IABP在移植桥梁成功率和移植后晚期生存率方面表现相当。iVAS的可移动设计促进了出色的行走能力,并使患者能够出院回家。