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使用短期连续血流装置支持儿科患者。

Supporting pediatric patients with short-term continuous-flow devices.

作者信息

Conway Jennifer, Al-Aklabi Mohammed, Granoski Don, Islam Sunjidatul, Ryerson Lyndsey, Anand Vijay, Guerra Gonzalo, Mackie Andrew S, Rebeyka Ivan, Buchholz Holger

机构信息

Division of Cardiology, Division of Pediatric Cardiology, University of Alberta, Edmonton, Alberta, Canada.

Division of Pediatric Cardiac Surgery, Stollery Children's Hospital, Edmonton, Alberta, Canada.

出版信息

J Heart Lung Transplant. 2016 May;35(5):603-9. doi: 10.1016/j.healun.2016.01.1224. Epub 2016 Feb 8.

Abstract

BACKGROUND

Short-term continuous-flow ventricular assist devices (STCF-VADs) are increasingly being used in the pediatric population. However, little is known about the outcomes in patients supported with these devices.

METHODS

All pediatric patients supported with a STCF-VAD, including the Thoratec PediMag or CentriMag, or the Maquet RotaFlow, between January 2005 and May 2014, were included in this retrospective single-center study.

RESULTS

Twenty-seven patients (15 girls [56%]) underwent 33 STCF-VAD runs in 28 separate hospital admissions. The STCF-VAD was implanted 1 time in 23 patients (85%), 2 times in 2 patients (7%), and 3 times in 2 patients (7%). Implantation occurred most commonly in the context of congenital heart disease in 14 runs (42.2%), cardiomyopathy in 11 (33%), and after transplant in 6 (18%). The median age at implantation was 1.7 (interquartile range [IQR] 0.1, 4.1) years, and median weight was 8.9 kg (IQR 3.7, 18 kg). Patients were supported for a median duration of 12 days (IQR 6, 23 days) per run; the longest duration was 75 days. Before implantation, 15 runs (45%) were supported by extracorporeal membrane oxygenation (ECMO). After implantation, an oxygenator was required in 20 runs (61%) and continuous renal replacement therapy in 21 (64%). Overall, 7 runs (21%) resulted in weaning for recovery, 14 (42%) converted to a long-term VAD, 4 (12%) resulted in direct transplantation, 3 (9%) were converted to ECMO, and 5 (15%) runs resulted in death on the device or within 1 month after decannulation. The most common complication was bleeding requiring reoperation in 24% of runs. In addition, 18% of runs were associated with neurologic events and 15% with a culture-positive infection. Hospital discharge occurred in 19 of 28 STCF-VAD admissions (67%). In follow-up, with a median duration of 9.2 months (IQR 2.3, 38.3 months), 17 patients (63%) survived.

CONCLUSIONS

STCF-VADs can successfully bridge most pediatric patients to recovery, long-term device, or transplant, with an acceptable complication profile. Although these devices are designed for short-term support, longer support is possible and may serve as an alternative approach to patients not suitable for the current long-term devices.

摘要

背景

短期连续流心室辅助装置(STCF-VADs)在儿科患者中的应用越来越广泛。然而,对于接受这些装置支持的患者的预后情况知之甚少。

方法

本回顾性单中心研究纳入了2005年1月至2014年5月期间接受STCF-VAD支持的所有儿科患者,包括Thoratec PediMag或CentriMag,或Maquet RotaFlow。

结果

27例患者(15例女孩[56%])在28次单独的住院治疗中进行了33次STCF-VAD运行。23例患者(85%)植入STCF-VAD 1次,2例患者(7%)植入2次,2例患者(7%)植入3次。植入最常见于先天性心脏病患者,共14次运行(42.2%),心肌病患者11次(33%),移植后患者6次(18%)。植入时的中位年龄为1.7岁(四分位间距[IQR]0.1,4.1),中位体重为8.9 kg(IQR 3.7,18 kg)。每次运行患者接受支持的中位持续时间为12天(IQR 6,23天);最长持续时间为75天。植入前,15次运行(45%)由体外膜肺氧合(ECMO)支持。植入后,20次运行(61%)需要使用氧合器,21次运行(64%)需要进行持续肾脏替代治疗。总体而言,7次运行(21%)成功撤机恢复,14次(42%)转为长期VAD,4次(12%)直接进行移植,3次(9%)转为ECMO,5次(15%)运行在装置上或拔管后1个月内死亡。最常见的并发症是出血,24%的运行需要再次手术。此外,18%的运行与神经系统事件相关,15%与培养阳性感染相关。28次STCF-VAD住院治疗中有19次(67%)出院。随访期间,中位持续时间为9.2个月(IQR 2.3,38.3个月),17例患者(63%)存活。

结论

STCF-VADs能够成功地将大多数儿科患者过渡到恢复、长期装置支持或移植,并发症情况可接受。尽管这些装置设计用于短期支持,但更长时间的支持也是可能的,并且可以作为不适用于当前长期装置的患者的替代方法。

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