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单心室生理患儿气管切开术的临床转归:来自儿科心脏重症监护学会多中心队列的协作研究,2010-2021 年。

Clinical Outcomes After Tracheostomy in Children With Single Ventricle Physiology: Collaborative Research From the Pediatric Cardiac Intensive Care Society Multicenter Cohort, 2010-2021.

机构信息

Department of Pediatrics, Division of Critical Care Indiana University School of Medicine, Riley Hospital for Children, Indianapolis, IN.

Department of Cardiac Surgery, C.S. Mott Children's Hospital, Ann Arbor, MI.

出版信息

Pediatr Crit Care Med. 2024 Aug 1;25(8):728-739. doi: 10.1097/PCC.0000000000003523. Epub 2024 Apr 29.

Abstract

OBJECTIVES

Multicenter studies reporting outcomes following tracheostomy in children with congenital heart disease are limited, particularly in patients with single ventricle physiology. We aimed to describe clinical characteristics and outcomes in a multicenter cohort of patients with single ventricle physiology who underwent tracheostomy before Fontan operation.

DESIGN

Multicenter retrospective cohort study.

SETTING

Twenty-one tertiary care pediatric institutions participating in the Collaborative Research from the Pediatric Cardiac Intensive Care Society.

PATIENTS

We reviewed 99 children with single ventricle physiology who underwent tracheostomy before the Fontan operation at 21 institutions participating in Collaborative Research from the Pediatric Cardiac Intensive Care Society between January 2010 and December 2020, with follow-up through December 31, 2021.

INTERVENTIONS

None.

MEASUREMENTS AND MAIN RESULTS

Death occurred in 51 of 99 patients (52%). Cox proportional hazard analysis was performed to determine factors associated with death after tracheostomy. Results are presented as hazard ratio (HR) with 95% CIs. Nonrespiratory indication(s) for tracheostomy (HR, 2.21; 95% CI, 1.14-4.32) and number of weeks receiving mechanical ventilation before tracheostomy (HR, 1.06; 95% CI, 1.02-1.11) were independently associated with greater hazard of death. In contrast, diagnosis of tricuspid atresia or Ebstein's anomaly was associated with less hazard of death (HR, 0.16; 95% CI, 0.04-0.69). Favorable outcome, defined as survival to Fontan operation or decannulation while awaiting Fontan operation with viable cardiopulmonary physiology, occurred in 29 of 99 patients (29%). Median duration of mechanical ventilation before tracheostomy was shorter in patients who survived to favorable outcome (6.1 vs. 12.1 wk; p < 0.001), and only one of 16 patients with neurologic indications for tracheostomy and 0 of ten patients with cardiac indications for tracheostomy survived to favorable outcome.

CONCLUSIONS

For children with single ventricle physiology who undergo tracheostomy, mortality risk is high and should be carefully considered when discussing tracheostomy as an option for these children. Favorable outcomes are possible, although thoughtful attention to patient selection and tracheostomy timing are likely necessary to achieve this goal.

摘要

目的

先天性心脏病患儿行气管切开术的多中心研究报告结果有限,尤其是单心室生理患儿。本研究旨在描述接受 Fontan 手术前行气管切开术的单心室生理患儿多中心队列的临床特征和结局。

设计

多中心回顾性队列研究。

地点

参与儿科心脏重症监护学会协作研究的 21 家三级护理儿科机构。

患者

我们回顾了 2010 年 1 月至 2020 年 12 月期间,21 家参与儿科心脏重症监护学会协作研究的机构中 99 例单心室生理患儿在接受 Fontan 手术前进行气管切开术的病例,随访至 2021 年 12 月 31 日。

干预措施

无。

测量和主要结果

99 例患者中有 51 例(52%)死亡。进行 Cox 比例风险分析以确定气管切开术后死亡的相关因素。结果以风险比(HR)及其 95%置信区间(CI)表示。气管切开术的非呼吸指征(HR,2.21;95%CI,1.14-4.32)和气管切开术前接受机械通气的周数(HR,1.06;95%CI,1.02-1.11)与死亡风险增加独立相关。相比之下,三尖瓣闭锁或 Ebstein 畸形的诊断与死亡风险降低相关(HR,0.16;95%CI,0.04-0.69)。定义为Fontan 手术存活或等待Fontan 手术时脱机且心肺生理状态良好的有利结局,在 99 例患者中发生 29 例(29%)。气管切开术前机械通气的中位持续时间在存活至有利结局的患者中更短(6.1 周比 12.1 周;p<0.001),16 例因神经学指征而行气管切开术的患者中仅有 1 例,10 例因心脏指征而行气管切开术的患者中无一例存活至有利结局。

结论

对于接受气管切开术的单心室生理患儿,死亡率较高,在讨论该类患儿行气管切开术的选择时应谨慎考虑。尽管可能需要仔细考虑患者选择和气管切开术时机,但有可能获得良好的结局。

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