Jaquiss Robert D B, Woods Ronald K
Department of Thoracic and Cardiovascular Surgery, University of Texas Southwestern Medical Center, Children's Health System of Texas, Dallas, TX, USA.
Division of Pediatric Cardiothoracic Surgery, Department of Surgery, Medical College of Wisconsin, Herma Heart Institute, Children's Hospital of Wisconsin, Milwaukee, WI, USA.
Ann Cardiothorac Surg. 2020 Mar;9(2):134-140. doi: 10.21037/acs.2020.03.11.
Though the Fontan circulation provides long-term palliation for patients with univentricular hearts, failure of the circulation may ensue, leaving heart transplantation as the only definitive treatment. For Fontan patients awaiting transplant, both "right-sided" and "left-sided" symptoms may be present and severe, hence, biventricular mechanical circulatory support may be indicated. This can be provided by implantation of the total artificial heart (TAH), a procedure which is performed slightly differently than in patients with biventricular hearts. In this article, the unique aspects of implantation of this device in a patient with a Fontan operation are reviewed, with specific attention to the most commonly encountered anatomic variants of importance to the implanting surgeon.
尽管Fontan循环为单心室心脏患者提供了长期姑息治疗,但循环功能仍可能衰竭,最终心脏移植成为唯一的确定性治疗方法。对于等待移植的Fontan患者,可能会出现严重的“右侧”和“左侧”症状,因此,可能需要双心室机械循环支持。这可以通过植入全人工心脏(TAH)来实现,该手术的操作与双心室心脏患者略有不同。本文回顾了在接受Fontan手术的患者中植入该装置的独特方面,并特别关注植入外科医生最常遇到的重要解剖变异。