Cabrera Antonio G, Sundareswaran Kartik S, Samayoa Andres X, Jeewa Aamir, McKenzie E Dean, Rossano Joseph W, Farrar David J, Frazier O Howard, Morales David L
Texas Children's Hospital, Baylor College of Medicine, Houston, Texas.
J Heart Lung Transplant. 2013 Nov;32(11):1107-13. doi: 10.1016/j.healun.2013.07.012. Epub 2013 Aug 31.
The HeartMate II (HMII; Thoratec, Pleasanton, CA) continuous-flow left ventricular assist device (LVAD) is an established treatment modality for advanced heart failure in adults. The objective of this study was to evaluate outcomes of pediatric patients supported by the HMII LVAD.
This was a retrospective review of the Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS) of patients supported with a HMII from April 2008 to September 2011. The primary cohort comprised pediatric patients aged 11 to 18 years. Outcomes were compared with a group of young adults aged 19 to 39 years who underwent HMII implant during the same period. Ischemic etiologies for heart failure were excluded.
There were 28 pediatric patients, of whom 19 (68%) were males, 14 (46%) were African American, and 7 (25%) underwent device placement in a pediatric hospital. Competing outcomes analysis showed that at 6 months of follow-up, the composite of survival to transplantation, ongoing support, or recovery was 96% for the pediatric group, which was not significantly different from the young adult group (96%, p = 0.330). The 2 groups had similar INTERMACS profiles but differed in diagnosis, weight, and morbidities. Bleeding complications requiring surgical intervention were more common in the pediatric group.
Pediatric outcomes with a HMII LVAD are comparable to that of young adults. As we continue to monitor this growing group, more sophisticated characterization and comparisons will be possible. Also, as technology progress and second- and third-generation devices are introduced, the number of children who will benefit from mechanical support will continue to grow.
HeartMate II(HMII;Thoratec公司,加利福尼亚州普莱森顿)连续流左心室辅助装置(LVAD)是治疗成人晚期心力衰竭的一种既定治疗方式。本研究的目的是评估接受HMII LVAD支持的儿科患者的治疗结果。
这是一项对2008年4月至2011年9月接受HMII支持的患者的机构间机械辅助循环支持注册研究(INTERMACS)的回顾性分析。主要队列包括11至18岁的儿科患者。将结果与同期接受HMII植入的19至39岁的年轻成人组进行比较。排除心力衰竭的缺血性病因。
有28名儿科患者,其中19名(68%)为男性,14名(46%)为非裔美国人,7名(25%)在儿科医院接受了装置植入。竞争结果分析显示,在随访6个月时,儿科组移植、持续支持或恢复生存的综合率为96%,与年轻成人组(96%,p = 0.330)无显著差异。两组的INTERMACS特征相似,但在诊断、体重和发病率方面有所不同。需要手术干预的出血并发症在儿科组更为常见。
HMII LVAD在儿科患者中的治疗结果与年轻成人相当。随着我们继续监测这个不断增长的群体,将有可能进行更精细的特征描述和比较。此外,随着技术的进步以及第二代和第三代装置的推出,将受益于机械支持的儿童数量将继续增加。