Elizur Arnon, Sweet Stuart C, Huddleston Charles B, Gandhi Sanjiv K, Boslaugh Sarah E, Kuklinski Cadence A, Faro Albert
Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, Missouri 63110, USA.
J Heart Lung Transplant. 2007 Feb;26(2):127-31. doi: 10.1016/j.healun.2006.11.597.
Patients with cystic fibrosis (CF) who are listed for lung transplantation may require mechanical ventilatory support before transplant. Although CF is a risk factor for poor outcomes in adults, no data currently exist pertaining to pre-transplant ventilatory support in children with CF.
In a retrospective cohort study, we reviewed the medical records of 18 consecutive CF patients transplanted at St. Louis Children's Hospital (SLCH) who required mechanical ventilation before lung transplantation. Controls included patients transplanted at SLCH who were not mechanically ventilated before transplant and were matched for underlying diagnosis, gender, age, type of transplant (cadaveric vs living donor) and year of transplant.
Ventilated and non-ventilated patients were similar in their pre-transplant characteristics (weight, height and body mass index) and ischemic and bypass times. However, patients ventilated before transplantation had significantly worse immediate post-transplant outcomes, including early graft dysfunction (p = 0.012), prolonged mechanical ventilation (34.1 vs 5 days, p = 0.009), prolonged stay in the pediatric intensive care unit (35.4 vs 8.1 days, p = 0.01), longer time to hospital discharge (38.4 vs 21.3 days, p = 0.033), and worse 1-year mortality after transplant (221.6 vs 335.2 days, p = 0.021). Among ventilated patients, length of pre-transplant ventilation did not affect post-transplant outcomes (length of ventilation, p = 0.92; length of stay in the pediatric intensive care unit, p = 0.68; time to hospital discharge, p = 0.46; and 1-year mortality rate, p = 0.25).
This is the first report in pediatric patients with CF demonstrating that mechanical ventilation before lung transplant is a predictor of poor short-term outcomes, including 1-year-survival, after transplant. Length of pre-transplant ventilatory support does not appear to impact outcomes.
列入肺移植名单的囊性纤维化(CF)患者在移植前可能需要机械通气支持。尽管CF是成人预后不良的一个风险因素,但目前尚无关于CF患儿移植前通气支持的数据。
在一项回顾性队列研究中,我们查阅了在圣路易斯儿童医院(SLCH)接受肺移植的18例连续CF患者的病历,这些患者在肺移植前需要机械通气。对照组包括在SLCH接受移植但移植前未进行机械通气的患者,这些患者在基础诊断、性别、年龄、移植类型(尸体供体与活体供体)和移植年份方面进行了匹配。
通气和未通气患者在移植前特征(体重、身高和体重指数)以及缺血和旁路时间方面相似。然而,移植前进行通气的患者移植后即刻预后明显更差,包括早期移植物功能障碍(p = 0.012)、机械通气时间延长(34.1天对5天,p = 0.009)、在儿科重症监护病房停留时间延长(35.4天对8.1天,p = 0.01)、出院时间延长(38.4天对21.3天,p = 0.033)以及移植后1年死亡率更高(221.6天对335.2天,p = 0.021)。在通气患者中,移植前通气时间长短不影响移植后预后(通气时间,p = 0.92;在儿科重症监护病房停留时间,p = 0.68;出院时间,p = 0.46;1年死亡率,p = 0.25)。
这是关于CF患儿的首份报告,表明肺移植前的机械通气是移植后包括1年生存率在内的短期不良预后的一个预测因素。移植前通气支持时间长短似乎不影响预后。