Fugar S, Okoh A K, Eshun D, Yirerong J, Appiah L T, Mbachi C, Legge T, Camacho M, Russo M J
Department of Medicine, John H. Stroger Hospital of Cook County, Chicago, Illinois, USA.
Department of Cardiothoracic Surgery, RWJ Barnabas Health, Newark Beth Israel Medical Center, Newark, New Jersey.
Transplant Proc. 2019 Apr;51(3):852-858. doi: 10.1016/j.transproceed.2019.01.036. Epub 2019 Jan 9.
Continuous flow left ventricular assist devices (CF-LVAD) are widely used as a bridge to transplantation (BTT) among patients with advanced heart failure. The primary outcome of the current study was to study the incidence of waitlist mortality and morbidity of CF-LVAD patients bridged to heart transplantation in the current BTT era and to determine the factors that increased their risk of delisting.
Patients who were bridged to heart transplant with a CF-LVAD between April 2008 and September 2015 were identified from the United Network for Organ Sharing heart transplant registry. They were then categorized based on the development of complications. Cox proportional hazards and Kaplan-Meier survival curves were used for time-to-event analysis for the primary outcome.
Out of 7070 patients who were bridged to heart transplant, 2510 (36%) developed device-related complications. The primary outcome was present in 1631 of 7070 patients (23%). Independent predictors of primary outcome were age, ABO blood group, etiology of cardiomyopathy, and history of diabetes mellitus. Developing one device-related complication was associated with a hazard ratio (HR) of 2.59 of having the primary outcome. The HR increased to 3.45 when ≥2 of the defined complications occurred. In patients who developed the primary outcome, they most likely had a device infection (odds ratio 2.51).
Findings from the current study add to the existing literature about the incidence of morbidity and mortality in the current BTT era. Development of one device-related complication increases the risk of death or delisting among patients on the heart transplant waitlist; however, this risk almost doubles when 2 or more complications occur.
连续流左心室辅助装置(CF-LVAD)在晚期心力衰竭患者中被广泛用作移植桥梁(BTT)。本研究的主要结局是研究在当前BTT时代接受心脏移植的CF-LVAD患者等待名单上的死亡率和发病率,并确定增加其被除名风险的因素。
从器官共享联合网络心脏移植登记处识别出2008年4月至2015年9月期间使用CF-LVAD过渡到心脏移植的患者。然后根据并发症的发生情况对他们进行分类。Cox比例风险模型和Kaplan-Meier生存曲线用于对主要结局进行事件发生时间分析。
在7070例过渡到心脏移植的患者中,2510例(36%)出现了与装置相关的并发症。7070例患者中有1631例(23%)出现了主要结局。主要结局的独立预测因素是年龄、ABO血型、心肌病病因和糖尿病史。发生一种与装置相关的并发症与出现主要结局的风险比(HR)为2.59相关。当发生≥2种定义的并发症时,HR增加到3.45。在出现主要结局的患者中,他们最有可能发生装置感染(优势比2.51)。
本研究结果补充了现有关于当前BTT时代发病率和死亡率的文献。发生一种与装置相关的并发症会增加心脏移植等待名单上患者死亡或被除名的风险;然而,当发生2种或更多并发症时,这种风险几乎会加倍。