Kocabeyoglu Sinan Sabit, Kervan Umit, Sert Dogan Emre, Unal Ertekin Utku, Demirkan Burcu, Guray Yesim, Aygun Emre, Beyazal Osman Fehmi, Karahan Mehmet, Pac Mustafa
Department of Cardiovascular Surgery, Turkiye Yuksek Ihtisas Hospital, Ankara, Turkey.
Department of Cardiology, Turkiye Yuksek Ihtisas Hospital, Ankara, Turkey.
Artif Organs. 2018 Dec;42(12):1132-1138. doi: 10.1111/aor.13289. Epub 2018 Nov 4.
HeartMate 3 (HM3) left ventricular assist device (LVAD) is a compact, intrapericardial, centrifugal flow pump with a fully magnetically levitated rotor and a wide range of operation (2-10 L/min) to accommodate a broad range of clinical needs. We analyzed our experience with Heartware VAD (HVAD) and HM3 implantation through minimally invasive left thoracotomy (MILT) and upper minimal J sternotomy. Between March 2015 and October 2016, 31 patients who underwent LVAD implantation through MILT were included in this study. Twenty-three patients had HVAD (Group A) implantation, whereas 8 patients had HM3 (Group B). To compare outcomes of these pumps, measures were; mortality, cardiopulmonary bypass (CPB) time, duration of mechanical ventilatory support, blood loss and transfusion, intensive care unit (ICU) stay, right ventricular failure (RVF) and requirement of support with temporary devices, stroke, pump thrombosis, gastrointestinal bleeding and driveline infection rates. Interagency Registry for Mechanically Assisted Circulatory Support profiles, Pennsylvania and Michigan Risk Scores, right ventricular stroke work index and central venous pressure/pulmonary capillary wedge pressure ratio did not differ between these two groups. There was no difference in the length of ICU stay (P = 0.056), post-operative blood product administration (P = 0.701), total time on mechanical ventilation (P = 0.386), RVF (P = 1) or duration of CPB (P = 0.836). In-hospital cerebrovascular event rate was 13% in Group A and 0% in Group B, respectively. The HM3 assist system can be successfully implanted with minimally invasive techniques. This technique has proved to be safe and reproducible, with good clinical outcomes. Further, large collaborative studies are needed to identify the advantages of this approach.
HeartMate 3(HM3)左心室辅助装置(LVAD)是一种紧凑型的心包内离心式血泵,其转子完全磁悬浮,运行范围广(2 - 10升/分钟),可满足广泛的临床需求。我们分析了通过微创左胸切开术(MILT)和上半部分微创胸骨切开术植入Heartware VAD(HVAD)和HM3的经验。在2015年3月至2016年10月期间,本研究纳入了31例通过MILT进行LVAD植入的患者。23例患者植入了HVAD(A组),而8例患者植入了HM3(B组)。为比较这些血泵的结果,测量指标包括:死亡率、体外循环(CPB)时间、机械通气支持时间、失血量及输血情况、重症监护病房(ICU)住院时间、右心室衰竭(RVF)以及临时装置支持需求、中风、泵血栓形成、胃肠道出血和驱动线感染率。这两组之间的机构间机械辅助循环支持概况登记、宾夕法尼亚州和密歇根州风险评分、右心室卒中做功指数以及中心静脉压/肺毛细血管楔压比值并无差异。ICU住院时间(P = 0.056)、术后血液制品输注(P = 0.701)、机械通气总时间(P = 0.386)、RVF(P = 1)或CPB持续时间(P = 0.836)均无差异。A组和B组的院内脑血管事件发生率分别为13%和0%。HM3辅助系统可通过微创技术成功植入。该技术已被证明是安全且可重复的,临床效果良好。此外,还需要开展大型协作研究以确定这种方法的优势。