过敏和特应性表型与早期妊娠和支气管肺发育不良呼吸道症状的严重程度有关。

IF 3.1 3区 医学 Q1 PEDIATRICS
Brianna C Aoyama, Joseph M Collaco, Amit Agarwal, Gangaram Akangire, Eric D Austin, Manvi Bansal, Anita Bhandari, A Ioana Cristea, Lystra P Hayden, Jonathan C Levin, Winston M Manimtim, Audrey N Miller, Paul E Moore, Antonia P Popova, Lawrence M Rhein, Catherine A Sheils, Steven H Abman, Christopher D Baker, Sara K Dawson, Mehtap Haktanir Abul, Jennifer K Henningfeld, Joanne M Lagatta, Roopa Siddaiah, Nicole Stephenson, Demet Toprak, Sharon A McGrath-Morrow
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引用次数: 0

摘要

背景:特应性病史与足月新生儿呼吸系统疾病有关;然而,对于过敏/特应性反应如何影响支气管肺发育不良(BPD)儿童的呼吸预后,我们知之甚少。本研究旨在描述报告的过敏/特应性反应在BPD幼儿中的流行程度,并评估过敏/特应性反应是否与门诊结果相关。方法:对门诊BPD门诊0 - 36月龄儿童进行回顾性纵向队列研究,使用常规临床就诊时发放的问卷数据。过敏/特应性反应的存在通过护理人员问卷来确定。使用广义估计方程来调整过敏/特应性与呼吸结果之间的关联。结果:在一组患有BPD的婴儿和儿童中报告的过敏/特应性反应率(21.6%)与先前公布的健康儿童的比率相似。与非特应性儿童相比,患有特应性/过敏的儿童更有可能出生在更早的胎龄,患有肺动脉高压,非白人和非西班牙裔,并且在生命的前三年出现呼吸困难,夜间症状,活动限制和抢救药物使用。结论:在患有BPD的儿童中,过敏/特应性反应在胎龄较早出生的儿童中更为常见,并且在生命的前3年与呼吸道症状的增加显著相关。需要进一步的研究来评估过敏/特应性与呼吸道发病率增加之间的关联是否在整个儿童时期持续存在并影响后来的肺功能,以及包括吸入类固醇在内的潜在干预措施是否可以改变这种风险。影响:关于支气管肺发育不良(BPD)儿童的特应性/过敏患病率以及该人群中过敏/特应性与呼吸结局之间的关系的数据有限。我们的研究结果表明,在BPD儿童中,过敏/特应性反应在胎龄较早出生的儿童中更为常见,并且在生命的前3年与呼吸道症状的增加和抢救药物的使用有关。需要进一步的研究来确定这种关联是否在整个儿童时期持续存在并影响后来的肺功能,以及潜在的干预措施是否可以改变这种风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Allergy and atopic phenotype are associated with earlier gestation and severity of respiratory symptoms in bronchopulmonary dysplasia.

Background: A history of atopy is associated with respiratory morbidities in term-born children; however, little is known about how allergies/atopy affect respiratory outcomes in children with bronchopulmonary dysplasia (BPD). This study aims to describe the prevalence of reported allergies/atopy in young children with BPD and assess whether allergies/atopy are associated with outpatient outcomes.

Methods: A retrospective longitudinal cohort study of children between 0 and 36 months of age followed at outpatient BPD clinics was performed using data from questionnaires administered during routine clinical encounters. The presence of allergy/atopy was defined by caregiver questionnaires. Generalized estimating equations were used to adjust associations between allergy/atopy and respiratory outcomes.

Results: Rates of reported allergy/atopy in a cohort of infants and children with BPD (21.6%) were similar to previously published rates in healthy children. Children with atopy/allergy were more likely to be born at earlier gestational ages, have pulmonary hypertension, and be non-white and non-Hispanic compared to their non-atopic peers and to experience trouble breathing, nighttime symptoms, activity limitations, and rescue medication use during the first three years of life.

Conclusions: In children with BPD, allergy/atopy was more common among those born at earlier gestational ages and was significantly associated with increased respiratory symptoms during the first 3 years of life. Further studies are needed to assess whether the association between allergy/atopy and increased respiratory morbidity persists throughout childhood and affects later lung function and whether potential interventions, including inhaled steroids, may modify this risk.

Impact: There is limited data on the prevalence of atopy/allergy in children with bronchopulmonary dysplasia (BPD) and the association between allergy/atopy and respiratory outcomes in this population. Our findings demonstrate that in children with BPD, allergy/atopy was more common among those born at earlier gestational ages and was associated with increased respiratory symptoms and rescue medication use during the first 3 years of life. Further studies are needed to determine whether this association persists throughout childhood and affects later lung function and whether potential interventions may modify this risk.

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来源期刊
Pediatric Research
Pediatric Research 医学-小儿科
CiteScore
6.80
自引率
5.60%
发文量
473
审稿时长
3-8 weeks
期刊介绍: Pediatric Research publishes original papers, invited reviews, and commentaries on the etiologies of children''s diseases and disorders of development, extending from molecular biology to epidemiology. Use of model organisms and in vitro techniques relevant to developmental biology and medicine are acceptable, as are translational human studies
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