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Types of laryngomalacia in children: interrelationship between clinical course and comorbid conditions
The aim of this study was to: (1) find out whether laryngomalacia (LM) types are related to clinical course; (2) which patients with LM are at higher risk of other airway malacia [tracheomalacia (TM) and/or bronchomalacia (BM)]; and (3) evaluate the prevalence of LM in our region. Patients with esta...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309268/ https://www.ncbi.nlm.nih.gov/pubmed/27722899 http://dx.doi.org/10.1007/s00405-016-4334-5 |
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author | Kusak, Beata Cichocka-Jarosz, Ewa Jedynak-Wasowicz, Urszula Lis, Grzegorz |
author_facet | Kusak, Beata Cichocka-Jarosz, Ewa Jedynak-Wasowicz, Urszula Lis, Grzegorz |
author_sort | Kusak, Beata |
collection | PubMed |
description | The aim of this study was to: (1) find out whether laryngomalacia (LM) types are related to clinical course; (2) which patients with LM are at higher risk of other airway malacia [tracheomalacia (TM) and/or bronchomalacia (BM)]; and (3) evaluate the prevalence of LM in our region. Patients with established LM diagnosis and complete clinical and endoscopy records were enrolled. They were classified into different LM types according to classification based on the side of supraglottic obstruction. One hundred ten children were included. The most common LM appearance was type I—58 children, followed by combine types (I + II and I + III)—38. The other airway malacia were found in 47 patients: TM in 31, BM in 10, and TM with BM in 6. Other comorbidities (cardiac, neurological, and genetic disorders) were identified in 30 children. Patients with combine types of LM differ from those with single type of LM in terms of prematurity (13 vs 31 %, p = 0.04) and higher weight on the examination day (p = 0.006). Patients with other airway malacia differ from children with isolated LM in terms of prematurity (40 vs 13 %, p = 0.008), comorbidities (38 vs 19 %, p = 0.024), and lower weight on the examination day (p = 0.014). The prevalence of clinically relevant LM was one in 2600–3100 newborns. Clinical course of LM cannot be anticipated on the basis of solely endoscopic evaluation of the larynx. Comorbidities and prematurity increase the risk of other airway malacia. The prevalence of LM is relatively high in the middle-south part of Poland. |
format | Online Article Text |
id | pubmed-5309268 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-53092682017-02-28 Types of laryngomalacia in children: interrelationship between clinical course and comorbid conditions Kusak, Beata Cichocka-Jarosz, Ewa Jedynak-Wasowicz, Urszula Lis, Grzegorz Eur Arch Otorhinolaryngol Laryngology The aim of this study was to: (1) find out whether laryngomalacia (LM) types are related to clinical course; (2) which patients with LM are at higher risk of other airway malacia [tracheomalacia (TM) and/or bronchomalacia (BM)]; and (3) evaluate the prevalence of LM in our region. Patients with established LM diagnosis and complete clinical and endoscopy records were enrolled. They were classified into different LM types according to classification based on the side of supraglottic obstruction. One hundred ten children were included. The most common LM appearance was type I—58 children, followed by combine types (I + II and I + III)—38. The other airway malacia were found in 47 patients: TM in 31, BM in 10, and TM with BM in 6. Other comorbidities (cardiac, neurological, and genetic disorders) were identified in 30 children. Patients with combine types of LM differ from those with single type of LM in terms of prematurity (13 vs 31 %, p = 0.04) and higher weight on the examination day (p = 0.006). Patients with other airway malacia differ from children with isolated LM in terms of prematurity (40 vs 13 %, p = 0.008), comorbidities (38 vs 19 %, p = 0.024), and lower weight on the examination day (p = 0.014). The prevalence of clinically relevant LM was one in 2600–3100 newborns. Clinical course of LM cannot be anticipated on the basis of solely endoscopic evaluation of the larynx. Comorbidities and prematurity increase the risk of other airway malacia. The prevalence of LM is relatively high in the middle-south part of Poland. Springer Berlin Heidelberg 2016-10-08 2017 /pmc/articles/PMC5309268/ /pubmed/27722899 http://dx.doi.org/10.1007/s00405-016-4334-5 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Laryngology Kusak, Beata Cichocka-Jarosz, Ewa Jedynak-Wasowicz, Urszula Lis, Grzegorz Types of laryngomalacia in children: interrelationship between clinical course and comorbid conditions |
title | Types of laryngomalacia in children: interrelationship between clinical course and comorbid conditions |
title_full | Types of laryngomalacia in children: interrelationship between clinical course and comorbid conditions |
title_fullStr | Types of laryngomalacia in children: interrelationship between clinical course and comorbid conditions |
title_full_unstemmed | Types of laryngomalacia in children: interrelationship between clinical course and comorbid conditions |
title_short | Types of laryngomalacia in children: interrelationship between clinical course and comorbid conditions |
title_sort | types of laryngomalacia in children: interrelationship between clinical course and comorbid conditions |
topic | Laryngology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5309268/ https://www.ncbi.nlm.nih.gov/pubmed/27722899 http://dx.doi.org/10.1007/s00405-016-4334-5 |
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