Airway Characteristics of Patients With 22q11 Deletion Undergoing Pulmonary Artery Reconstruction Surgery: Retrospective Cohort Study.

Danielle Sganga, Kara Meister, Douglas R Sidell, Lisa Wise-Faberowski, Jennifer Shek, Michael Ma, Elisabeth Martin, Frank L Hanley, Doff McElhinney, Ritu Asija
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引用次数: 3

Abstract

Objectives: We have previously shown that patients with a chromosome 22q11 microdeletion are at risk for prolonged respiratory failure after pulmonary artery reconstruction surgery compared with those with normal genotype. We sought to describe preexisting airway abnormalities in this patient population and examine relationships between airway abnormalities and outcomes.

Design: Single-center retrospective chart review from Society of Thoracic Surgery and Pediatric Cardiac Critical Care Consortium databases and the electronic medical record.

Setting: Lucile Packard Children's Hospital at Stanford from September 2017 to February 2019.

Patients: All patients undergoing pulmonary artery reconstruction surgery were considered for inclusion.

Interventions: We identified 127 patients meeting study inclusion criteria. Thirty-nine patients met specific criteria and underwent screening preoperative bronchoscopy including microdirect laryngoscopy and lower airway examination. Postoperative bronchoscopy was performed at the discretion of the intensive care team.

Measurements and main results: Airway abnormalities were detected in 25/26 of children (96%) with a chromosome 22q11 deletion who underwent preoperative bronchoscopy. Upper and lower airway pathologies were found in 19/25 (73%) and 21/25 (81%) patients, respectively, and it was common for patients to have more than one abnormality. Presence of 22q11 deletion was associated with longer duration of mechanical ventilation (9.1 vs 4.3 d; p = 0.001), use of noninvasive positive pressure support (13 vs 6 d; p = 0.001), and longer hospital stays (30 vs 14 d; p = 0.002). These outcomes were worse when compared with patients with known airway abnormalities who did not have 22q11 deletion.

Conclusions: Preexisting upper and lower airway pathologies are common in patients with a chromosome 22q11 deletion who undergo pulmonary artery reconstruction surgery. Despite similar postoperative hemodynamics and outcomes as their counterparts without 22q11 deletion, 22q11 deletion is associated with more postoperative respiratory complications not entirely explained by preexisting airway abnormalities.

22q11缺失患者接受肺动脉重建手术的气道特征:回顾性队列研究
目的:我们之前已经表明,与基因型正常的患者相比,染色体22q11微缺失的患者在肺动脉重建手术后存在延长呼吸衰竭的风险。我们试图描述该患者人群中先前存在的气道异常,并检查气道异常与预后之间的关系。设计:从胸外科学会和小儿心脏危重症护理协会数据库和电子病历中选取单中心回顾性图表。环境:Lucile Packard Children's Hospital at Stanford(2017年9月至2019年2月)。患者:所有接受肺动脉重建手术的患者均被纳入研究。干预措施:我们确定了127例符合研究纳入标准的患者。39例患者符合特定标准,术前行支气管镜筛查,包括微直接喉镜检查和下气道检查。术后支气管镜检查由重症监护小组决定。测量结果和主要结果:术前行支气管镜检查的22q11染色体缺失患儿中有25/26(96%)检测到气道异常。上呼吸道病变占19/25(73%),下呼吸道病变占21/25(81%),多处异常较为常见。22q11缺失的存在与机械通气持续时间较长相关(9.1 vs 4.3 d;P = 0.001),使用无创正压支持(13 vs 6 d;P = 0.001),住院时间更长(30天vs 14天;P = 0.002)。与没有22q11缺失的已知气道异常患者相比,这些结果更差。结论:22q11染色体缺失患者在接受肺动脉重建手术时,既往存在上、下气道病变是常见的。尽管与未缺失22q11的患者的术后血流动力学和结果相似,但22q11缺失与更多的术后呼吸并发症相关,这并不能完全用先前存在的气道异常来解释。
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