Aggressive approach for spontaneous pneumothorax treatment in children with Marfan syndrome?

Background and objectivesMarfan syndrome (MS) is a systemic disease of connective tissues consisting of a variable combination of anomalies. These patients have an increased risk of spontaneous pneumothorax (SP). However, there is a scarcity of pediatric literature on management, and no specific gui...

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Main Authors: Angelo Zarfati, Simone Frediani, Valerio Pardi, Ivan Pietro Aloi, Silvia Madafferi, Antonella Accinni, Arianna Bertocchini, Alessandro Inserra
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-12-01
Series:Frontiers in Pediatrics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2023.1301902/full
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author Angelo Zarfati
Simone Frediani
Valerio Pardi
Ivan Pietro Aloi
Silvia Madafferi
Antonella Accinni
Arianna Bertocchini
Alessandro Inserra
author_facet Angelo Zarfati
Simone Frediani
Valerio Pardi
Ivan Pietro Aloi
Silvia Madafferi
Antonella Accinni
Arianna Bertocchini
Alessandro Inserra
author_sort Angelo Zarfati
collection DOAJ
description Background and objectivesMarfan syndrome (MS) is a systemic disease of connective tissues consisting of a variable combination of anomalies. These patients have an increased risk of spontaneous pneumothorax (SP). However, there is a scarcity of pediatric literature on management, and no specific guidelines exist. Our aim was to analyze the management of spontaneous pneumothorax in children and adolescents with Marfan syndrome, comparing syndromic and non-syndromic patients.MethodsRetrospective analysis of pediatric patients (18 years) with SP diagnosed at our tertiary pediatric hospital (January 10–June 22), with special emphasis on diagnosis, treatment, and follow-up (FU).ResultsSixty-six patients with SP were identified, with nine (13%) having MS. In terms of baseline, there were no significant differences between the groups (age, sex, asthma, symptoms, and side, first-line treatment and hospitalization length). Overall, Marfan patients had significantly more first-line treatment failures requiring additional surgery, as well as more contralateral occurrences and the need for surgery/chest drain during the follow-up. Instead, conservative management resulted in significantly more ipsilateral recurrences and the need for surgery/chest drain in Marfan patients than controls during the follow-up.ConclusionsTreatment failure, contralateral occurrence, ipsilateral recurrence, and the need for surgery/chest drain during follow-up make management of patients with Marfan syndrome and spontaneous pneumothorax more difficult. In patients with a diagnosed MS a more aggressive first-line management should be considered, bearing in mind the higher risks of this population.
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spelling doaj.art-72cb0fffef334d9cb5324e274b628b832023-12-18T07:17:55ZengFrontiers Media S.A.Frontiers in Pediatrics2296-23602023-12-011110.3389/fped.2023.13019021301902Aggressive approach for spontaneous pneumothorax treatment in children with Marfan syndrome?Angelo ZarfatiSimone FredianiValerio PardiIvan Pietro AloiSilvia MadafferiAntonella AccinniArianna BertocchiniAlessandro InserraBackground and objectivesMarfan syndrome (MS) is a systemic disease of connective tissues consisting of a variable combination of anomalies. These patients have an increased risk of spontaneous pneumothorax (SP). However, there is a scarcity of pediatric literature on management, and no specific guidelines exist. Our aim was to analyze the management of spontaneous pneumothorax in children and adolescents with Marfan syndrome, comparing syndromic and non-syndromic patients.MethodsRetrospective analysis of pediatric patients (18 years) with SP diagnosed at our tertiary pediatric hospital (January 10–June 22), with special emphasis on diagnosis, treatment, and follow-up (FU).ResultsSixty-six patients with SP were identified, with nine (13%) having MS. In terms of baseline, there were no significant differences between the groups (age, sex, asthma, symptoms, and side, first-line treatment and hospitalization length). Overall, Marfan patients had significantly more first-line treatment failures requiring additional surgery, as well as more contralateral occurrences and the need for surgery/chest drain during the follow-up. Instead, conservative management resulted in significantly more ipsilateral recurrences and the need for surgery/chest drain in Marfan patients than controls during the follow-up.ConclusionsTreatment failure, contralateral occurrence, ipsilateral recurrence, and the need for surgery/chest drain during follow-up make management of patients with Marfan syndrome and spontaneous pneumothorax more difficult. In patients with a diagnosed MS a more aggressive first-line management should be considered, bearing in mind the higher risks of this population.https://www.frontiersin.org/articles/10.3389/fped.2023.1301902/fullMarfan syndromechildrenpneumothoraxthoracic drainagethorax
spellingShingle Angelo Zarfati
Simone Frediani
Valerio Pardi
Ivan Pietro Aloi
Silvia Madafferi
Antonella Accinni
Arianna Bertocchini
Alessandro Inserra
Aggressive approach for spontaneous pneumothorax treatment in children with Marfan syndrome?
Frontiers in Pediatrics
Marfan syndrome
children
pneumothorax
thoracic drainage
thorax
title Aggressive approach for spontaneous pneumothorax treatment in children with Marfan syndrome?
title_full Aggressive approach for spontaneous pneumothorax treatment in children with Marfan syndrome?
title_fullStr Aggressive approach for spontaneous pneumothorax treatment in children with Marfan syndrome?
title_full_unstemmed Aggressive approach for spontaneous pneumothorax treatment in children with Marfan syndrome?
title_short Aggressive approach for spontaneous pneumothorax treatment in children with Marfan syndrome?
title_sort aggressive approach for spontaneous pneumothorax treatment in children with marfan syndrome
topic Marfan syndrome
children
pneumothorax
thoracic drainage
thorax
url https://www.frontiersin.org/articles/10.3389/fped.2023.1301902/full
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