Oscillometry Phenotypes in Children With Down Syndrome.

IF 2.7 3区 医学 Q1 PEDIATRICS
Katharine L Hamlington, Emily H Cooper, Kristine Wolter-Warmerdam, Monica L Vielkind, John T Brinton, Allison Keck, Rawan J Bresselsmith, Jennifer Maybee, Arwen Jackson, Francis Hickey, Emily M DeBoer
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Abstract

Objective: To evaluate lung function patterns measured by oscillometry in children with Down syndrome and determine associations with pulmonary diagnoses that may co-occur with Down syndrome, including evidence of dysphagia, obstructive sleep apnea, tracheomalacia, and congenital heart disease.

Study design and patients: Cross-sectional study of children with Down syndrome who were enrolled during 2019-2022 at ages 4-18 years old.

Measurements: Children performed oscillometry before and after albuterol administration to obtain respiratory impedance measures of resistance (R) and reactance (X). Aspiration from swallow study, obstructive sleep apnea from polysomnogram, tracheomalacia from flexible bronchoscopy, and congenital heart disease diagnoses were obtained from the electronic medical record.

Results: In 50 children with Down syndrome, more negative X (median X5 z-score -0.93 [IQR - 2.15, 0.17]) was observed compared to a z-score of zero representing the mean in a pediatric reference population, but R was not increased at any frequency. Neither R nor X were related to tested pulmonary co-occurring diagnoses. Frequency dependence of resistance (R5-19) was elevated (median z-score 0.50 [IQR - 0.01, 1.14]), which, in combination with the more negative X, could indicate heterogeneity in peripheral and/or central airway sizes. After bronchodilator, R5 and AX decreased -26% [IQR -32%, -12%] and -43% [IQR -58%, -28%], respectively, and X5 increased 31% [IQR 12%, 45%], indicating physiological improvement.

Conclusions: In our population, a phenotype of lower lung compliance in 50% of children with Down syndrome was not associated with the presence of co-occurring pulmonary diagnoses. More work is needed to understand if this may be related to their diagnosis of DS.

唐氏综合症儿童的振荡测定表型。
目的:评估唐氏综合征儿童的肺功能模式,并确定与可能与唐氏综合征共同发生的肺部诊断的关系,包括吞咽困难、阻塞性睡眠呼吸暂停、气管软化和先天性心脏病的证据。研究设计和患者:对2019-2022年期间入组的4-18岁唐氏综合征儿童进行横断面研究。测量方法:儿童在沙丁醇给药前后进行振荡测量,以获得呼吸阻抗的阻力(R)和电抗(X)。通过吞咽研究获得误吸,通过多导睡眠图获得阻塞性睡眠呼吸暂停,通过柔性支气管镜检查获得气管软化,通过电子病历获得先天性心脏病诊断。结果:在50名唐氏综合症儿童中,与代表儿童参考人群平均值的z-score为零相比,观察到更多的负X(中位X5 z-score -0.93 [IQR - 2.15, 0.17]),但R并未以任何频率增加。R和X均与肺部合并诊断无关。阻力的频率依赖性(R5-19)升高(中位数z得分0.50 [IQR - 0.01, 1.14]),结合更负的X,可能表明外周和/或中央气道大小的异质性。使用支气管扩张剂后,R5和AX分别下降-26% [IQR -32%, -12%]和-43% [IQR -58%, -28%], X5升高31% [IQR -12%, - 45%],表明生理改善。结论:在我们的人群中,50%的唐氏综合征儿童的低肺顺应性表型与合并肺部诊断的存在无关。需要更多的工作来了解这是否与他们的退行性椎体滑移的诊断有关。
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来源期刊
Pediatric Pulmonology
Pediatric Pulmonology 医学-呼吸系统
CiteScore
6.00
自引率
12.90%
发文量
468
审稿时长
3-8 weeks
期刊介绍: Pediatric Pulmonology (PPUL) is the foremost global journal studying the respiratory system in disease and in health as it develops from intrauterine life though adolescence to adulthood. Combining explicit and informative analysis of clinical as well as basic scientific research, PPUL provides a look at the many facets of respiratory system disorders in infants and children, ranging from pathological anatomy, developmental issues, and pathophysiology to infectious disease, asthma, cystic fibrosis, and airborne toxins. Focused attention is given to the reporting of diagnostic and therapeutic methods for neonates, preschool children, and adolescents, the enduring effects of childhood respiratory diseases, and newly described infectious diseases. PPUL concentrates on subject matters of crucial interest to specialists preparing for the Pediatric Subspecialty Examinations in the United States and other countries. With its attentive coverage and extensive clinical data, this journal is a principle source for pediatricians in practice and in training and a must have for all pediatric pulmonologists.
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