Bouzas-Cruz Noelia, Gonzalez-Fernandez Oscar, Ferrera-Durán Carlos, Woods Andrew, Robinson-Smith Nicola, Tovey Sian, Jungschleger Jérôme, Booth Karen, Shah Asif, Parry Gareth, MacGowan Guy A, Schueler Stephan
Department of Cardiology, Freeman Hospital, Newcastle Upon Tyne, UK.
University of Santiago de Compostela, Santiago, Spain.
Int J Artif Organs. 2020 Jul;43(7):444-451. doi: 10.1177/0391398819896585. Epub 2019 Dec 30.
Pump thrombosis is a serious left ventricular assist device complication, though there are no guidelines regarding its treatment. The main aim of this study was to describe a strategy of intravenous anticoagulation as the initial treatment in these patients and then to compare intravenous heparin with bivalirudin.
All consecutive patients who received a HeartWare left ventricular assist device from July 2009 to March 2019 were retrospectively analysed. Patients developing a pump thrombosis were selected, and treatment, outcomes and complications were recorded.
During this period of time (116 months), 220 patients underwent HeartWare left ventricular assist device implantation and 57 developed pump thrombosis, with an incidence rate of first pump thrombosis of 0.17 events per patient-year of support (incidence rate of all episodes of pump thrombosis: 0.30 events per patient-year of support). All the patients were initially treated medically, predominantly with either intravenous heparin (n = 26) or bivalirudin (n = 16). Patients treated with bivalirudin during the first pump thrombosis episode had less subsequent re-thrombosis episodes (18.7% vs 57.7%, p < 0.05). In addition, percentage time in therapeutic range was greater for bivalirudin compared with heparin (68.5% ± 16.9% vs 37.4% ± 31.0%, p < 0.01). During the first pump thrombosis episode, 26.3% of the patients needed surgery (left ventricular assist device exchange (n = 8), transplant (n = 6) or decommissioning (n = 1)). The overall survival at 1 year was 61.4%, and there was no significant difference in survival.
Left ventricular assist device thrombosis is a serious life-threatening complication; hence, we propose an initial conservative management of pump thrombosis with enhanced intravenous anticoagulation with either intravenous heparin or bivalirudin, with surgery reserved for refractory cases.
泵血栓形成是左心室辅助装置的一种严重并发症,然而目前尚无关于其治疗的指南。本研究的主要目的是描述一种将静脉抗凝作为这些患者初始治疗的策略,然后比较静脉使用肝素与比伐芦定的效果。
对2009年7月至2019年3月期间所有连续接受HeartWare左心室辅助装置的患者进行回顾性分析。选取发生泵血栓形成的患者,记录其治疗情况、结局和并发症。
在此期间(116个月),220例患者接受了HeartWare左心室辅助装置植入,57例发生泵血栓形成,首次泵血栓形成的发生率为每患者支持年0.17次事件(所有泵血栓形成发作的发生率:每患者支持年0.30次事件)。所有患者最初均接受药物治疗,主要使用静脉肝素(n = 26)或比伐芦定(n = 16)。在首次泵血栓形成发作期间接受比伐芦定治疗的患者后续再血栓形成发作较少(18.7% 对57.7%,p < 0.05)。此外,与肝素相比,比伐芦定处于治疗范围内的时间百分比更高(68.5% ± 16.9% 对37.4% ± 31.0%,p < 0.01)。在首次泵血栓形成发作期间,26.3%的患者需要手术(更换左心室辅助装置(n = 8)、移植(n = 6)或停用(n = 1))。1年时的总体生存率为61.4%,生存率无显著差异。
左心室辅助装置血栓形成是一种严重的危及生命的并发症;因此,我们建议对泵血栓形成进行初始保守治疗,采用强化静脉抗凝,可使用静脉肝素或比伐芦定,难治性病例则考虑手术治疗。