Clinical characteristics and outcome of non-cystic fibrosis bronchiectasis in children: A tertiary care perspective.

IF 2.3 Q2 MEDICINE, GENERAL & INTERNAL
SAGE Open Medicine Pub Date : 2025-02-19 eCollection Date: 2025-01-01 DOI:10.1177/20503121251320849
Phanthila Sitthikarnkha, Apichaya Anekvorakul, Sirapoom Niamsanit, Leelawadee Techasatian, Suchaorn Saengnipanthkul, Rattapon Uppala
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Abstract

Introduction: Bronchiectasis is a chronic respiratory disease caused by various respiratory and systemic conditions. It is now considered a potentially reversible disease, particularly when diagnosed early and managed with appropriate respiratory care strategies. Although rare in children, it typically develops in patients with recurrent lower respiratory tract infections. The etiology of bronchiectasis in children differs from that in adults. This study aims to identify the clinical features, causes, and outcomes of non-cystic fibrosis bronchiectasis in children at a tertiary center.

Methods: A retrospective review was conducted among children with non-cystic fibrosis bronchiectasis who attended a university-affiliated hospital between January 2007 and December 2021. Clinical outcomes were assessed based on pulmonary function tests, exacerbation, and mortality.

Results: The study included 35 children with non-cystic fibrosis bronchiectasis. The median age at diagnosis was 36 months (IQR: 24-170 months). Bronchiectasis was linked to underlying conditions in 22 cases (62.9%), such as primary immunodeficiency, chronic aspiration, and primary ciliary dyskinesia. Thirteen children had infectious-associated bronchiectasis (37.1%), with four cases related to pulmonary tuberculosis. At diagnosis, cystic bronchiectasis was most common (n = 17, 48.6%), followed by varicose (n = 13, 37.1%) and cylindrical bronchiectasis (n = 5, 14.3%). Pulmonary exacerbation occurred in 28 (80%) children, with a higher rate in noninfectious bronchiectasis than postinfectious bronchiectasis (90.9% vs 61.5%, p = 0.036). Hospitalization was required for 26 (77.1%) children, with a higher rate of noninfectious bronchiectasis than postinfectious bronchiectasis (86.3% vs 53.8%, p = 0.033).

Conclusions: Primary immune deficiency and chronic aspiration are the most common non-infective causes of non-cystic fibrosis bronchiectasis. Noninfectious bronchiectasis leads to higher exacerbation and hospitalization rates.

儿童非囊性纤维化支气管扩张的临床特点和结局:三级护理的观点。
简介:支气管扩张是一种由多种呼吸系统疾病引起的慢性呼吸系统疾病。它现在被认为是一种潜在的可逆性疾病,特别是在早期诊断并采用适当的呼吸保健策略进行管理时。虽然在儿童中很少见,但它通常发生在下呼吸道感染复发的患者中。儿童支气管扩张的病因不同于成人。本研究旨在确定三级中心儿童非囊性纤维化支气管扩张的临床特征、原因和结局。方法:回顾性分析2007年1月至2021年12月在某大学附属医院就诊的非囊性纤维化支气管扩张儿童。临床结果根据肺功能测试、恶化和死亡率进行评估。结果:本研究纳入35例非囊性纤维化支气管扩张症患儿。诊断时中位年龄为36个月(IQR: 24-170个月)。22例(62.9%)支气管扩张与基础疾病有关,如原发性免疫缺陷、慢性误吸和原发性纤毛运动障碍。13例儿童发生感染性支气管扩张(37.1%),其中4例与肺结核有关。诊断时,囊性支气管扩张最为常见(n = 17, 48.6%),其次是静脉曲张(n = 13, 37.1%)和柱状支气管扩张(n = 5, 14.3%)。28例(80%)儿童发生肺加重,非感染性支气管扩张的发生率高于感染性支气管扩张(90.9% vs 61.5%, p = 0.036)。26例(77.1%)患儿需要住院治疗,非感染性支气管扩张率高于感染性支气管扩张率(86.3%比53.8%,p = 0.033)。结论:原发性免疫缺陷和慢性误吸是非囊性纤维化支气管扩张最常见的非感染性原因。非感染性支气管扩张导致更高的加重率和住院率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
SAGE Open Medicine
SAGE Open Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
3.50
自引率
4.30%
发文量
289
审稿时长
12 weeks
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