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儿童先天性心脏病合并气道异常的管理策略

Management Strategies for Congenital Heart Disease Comorbid with Airway Anomalies in Children.

作者信息

Liu Yuze, He Qiyu, Dou Zheng, Ma Kai, Chen Weinan, Li Shoujun

机构信息

Pediatric Cardiac Surgery Centre, Fuwai Hospital, National Centre for Cardiovascular Diseases, State Key Laboratory of Cardiovascular Disease, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China.

Information Center, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

J Pediatr. 2024 Jan;264:113741. doi: 10.1016/j.jpeds.2023.113741. Epub 2023 Sep 17.

Abstract

OBJECTIVE

To assess management strategies for pediatric patients with the challenging combination of congenital heart diseases (CHDs) and airway anomalies.

STUDY DESIGN

Patients diagnosed with CHD and airway anomalies in the Pediatric Cardiac Surgery Centre of Fuwai Hospital from January 2016 to December 2020 were included in this retrospective study. Patients were divided into three groups based on different management, including the conservative group, the slide group (slide tracheoplasty), and the suspension group (suspension with external stenting). Patients' data and computed tomography measurements from medical records were reviewed.

RESULTS

A total of 139 patients were included in the cohort; 107 had conservative airway treatment (conservative group), 15 had slide tracheoplasty (slide group), and 17 had tracheal suspension operation (suspension group). The top three associated intracardiac anomalies were ventricular septal defect (n = 34, 24%), pulmonary artery sling (n = 22, 16%), and tetralogy of Fallot (n = 15, 11%). Compared with patients with conservative airway management (100 minutes [median], 62-152 [IQR]), the extra airway procedure prolonged cardiopulmonary bypass duration, with 202 minutes (IQR, 119-220) for the slide group and 150 minutes (IQR, 125-161) for the suspension group. Patients who underwent slide tracheoplasty required prolonged mechanical ventilation (129 minutes [median], 56-328 [IQR]). Of the total cohort, 6 in-hospital deaths, all in the conservative group, and 8 mid-to long-term deaths, with 6 in the conservative group, occurred.

CONCLUSIONS

Both conservative and surgical management of CHD patients with airway anomalies have promising outcomes. Extra tracheobronchial procedures, especially the slide tracheoplasty, significantly prolonged cardiopulmonary bypass duration. Based on multidisciplinary team assessment, individualized management strategies should be developed for these patients.

摘要

目的

评估患有先天性心脏病(CHD)和气道异常这一具有挑战性组合的儿科患者的管理策略。

研究设计

本回顾性研究纳入了2016年1月至2020年12月在阜外医院小儿心脏外科中心诊断为CHD和气道异常的患者。根据不同的管理方式将患者分为三组,包括保守组、滑动组(滑动气管成形术)和悬吊组(外部支架悬吊)。回顾了病历中的患者数据和计算机断层扫描测量结果。

结果

该队列共纳入139例患者;107例接受了气道保守治疗(保守组),15例接受了滑动气管成形术(滑动组),17例接受了气管悬吊手术(悬吊组)。最常见的三种相关心脏内异常为室间隔缺损(n = 34,24%)、肺动脉吊带(n = 22,16%)和法洛四联症(n = 15,11%)。与气道保守管理的患者(100分钟[中位数],62 - 152[四分位间距])相比,额外的气道手术延长了体外循环时间,滑动组为202分钟(四分位间距,119 - 220),悬吊组为150分钟(四分位间距,125 - 161)。接受滑动气管成形术的患者需要延长机械通气时间(129分钟[中位数],56 - 328[四分位间距])。在整个队列中,发生了6例院内死亡,均在保守组,以及8例中至长期死亡,其中保守组有6例。

结论

CHD合并气道异常患者的保守治疗和手术治疗均有良好预后。额外的气管支气管手术,尤其是滑动气管成形术,显著延长了体外循环时间。应基于多学科团队评估为这些患者制定个体化管理策略。

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