[Multidisciplinary Management of Non-cystic-fibrosis Bronchiectasis - State of the Art].

Interdisziplinäre Behandlung der Non-Cystic-Fibrosis-Bronchiektasie – State of the Art.

Journal

Zentralblatt fur Chirurgie
ISSN: 1438-9592
Titre abrégé: Zentralbl Chir
Pays: Germany
ID NLM: 0413645

Informations de publication

Date de publication:
Jun 2021
Historique:
entrez: 21 6 2021
pubmed: 22 6 2021
medline: 24 6 2021
Statut: ppublish

Résumé

Bronchiectasis is a mostly irreversible bronchial dilatation induced by a destruction of elastic and muscular fibers of the bronchial wall. Radiological criteria of bronchiectasis are met, when the inner diameter of the bronchial wall surpasses the outer diameter of the accompanying pulmonary artery. Its incidence increases with age, even though it often lacks true clinical signs of disease. Only when it is accompanied by cough, expectorations and recurring bronchopulmonary infections, it can be considered a true bronchiectatic disease. Cystic fibrosis (CF) is one of its preeminent triggers, but certainly plays a particular role in this entity, which is why the terminus of "non-CF-bronchiectasis" was coined in the first place.Multidisciplinary management consists in extensive diagnostic work-up, treatment of potential triggers of bronchiectasis and supportive care in form of vaccination programs, secretolysis and pulmonary rehabilitation, as well as antibiotic treatment of pulmonary exacerbations.Surgical treatment has to be considered a last resort in case of hemoptysis, recurring severe pneumonia or secondary aspergilloma with complete resection of all pathological findings, ideally by minimally-invasive approach. Bronchiektasien, die nicht durch eine Zystische Fibrose bedingt sind, sind eine ätiologisch äußerst heterogene Erkrankung. Dieser Beitrag gibt einen Überblick über die Ursachen, das diagnostische Vorgehen und die therapeutischen Optionen bei dieser nicht seltenen Lungenerkrankung.

Autres résumés

Type: Publisher (ger)
Bronchiektasien, die nicht durch eine Zystische Fibrose bedingt sind, sind eine ätiologisch äußerst heterogene Erkrankung. Dieser Beitrag gibt einen Überblick über die Ursachen, das diagnostische Vorgehen und die therapeutischen Optionen bei dieser nicht seltenen Lungenerkrankung.

Identifiants

pubmed: 34154019
doi: 10.1055/a-1361-2252
doi:

Types de publication

Journal Article

Langues

ger

Sous-ensembles de citation

IM

Pagination

346-358

Informations de copyright

Thieme. All rights reserved.

Auteurs

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Classifications MeSH