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Use of inhaled antibiotics among Danish patients with cystic fibrosis

BACKGROUND: Inhaled antibiotics are an important part of cystic fibrosis (CF) airway disease management and should be individualized to fit the microorganism and match patient needs. To investigate the implementation of personalized treatment, this study mapped the use of different types of inhaled...

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Detalles Bibliográficos
Autores principales: Møller, Rikke, Nielsen, Bibi Uhre, Faurholt‐Jepsen, Daniel, Katzenstein, Terese Lea, Skov, Marianne, Philipsen, Lue Katrine Drasbæk, Pressler, Tacjana, Johansen, Helle Krogh, Qvist, Tavs
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324817/
https://www.ncbi.nlm.nih.gov/pubmed/35478387
http://dx.doi.org/10.1002/ppul.25942
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author Møller, Rikke
Nielsen, Bibi Uhre
Faurholt‐Jepsen, Daniel
Katzenstein, Terese Lea
Skov, Marianne
Philipsen, Lue Katrine Drasbæk
Pressler, Tacjana
Johansen, Helle Krogh
Qvist, Tavs
author_facet Møller, Rikke
Nielsen, Bibi Uhre
Faurholt‐Jepsen, Daniel
Katzenstein, Terese Lea
Skov, Marianne
Philipsen, Lue Katrine Drasbæk
Pressler, Tacjana
Johansen, Helle Krogh
Qvist, Tavs
author_sort Møller, Rikke
collection PubMed
description BACKGROUND: Inhaled antibiotics are an important part of cystic fibrosis (CF) airway disease management and should be individualized to fit the microorganism and match patient needs. To investigate the implementation of personalized treatment, this study mapped the use of different types of inhaled antibiotics and adherence patterns. METHODS: We performed individual structured interviews in a cross‐sectional study at the CF Centre in Copenhagen, Denmark. Patients with CF older than 15 years attending clinical consultations were included. Clinical data were obtained from centralized databases. RESULTS: Among 149 participants, 107 (72%) had indication for treatment with inhaled antibiotics. In this group, 97 (91%) reported the use of inhaled antibiotics within the last 12 months. Change from one inhaled antibiotic to another during that period was reported by 31 (29%), and 17 (25%) with Pseudomonas aeruginosa had used off‐label antibiotics. Adherence to a minimum of one daily dose of antibiotic was reported by 78%, while adherence to all daily doses was 28 percentage points lower. Skipping inhalations was due to side effects and doubt about the effect in less than 5% of cases. CONCLUSION: Change of inhaled antibiotics and use of off‐label antibiotics for inhalation were common and side effects were a rare cause of nonadherence. This suggests satisfactory implementation of the principle of tailored antibiotic inhalation prescription in the Copenhagen CF population. Adherence to at least one daily inhalation dose was markedly higher than adherence to multiple daily inhalations.
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spelling pubmed-93248172022-07-30 Use of inhaled antibiotics among Danish patients with cystic fibrosis Møller, Rikke Nielsen, Bibi Uhre Faurholt‐Jepsen, Daniel Katzenstein, Terese Lea Skov, Marianne Philipsen, Lue Katrine Drasbæk Pressler, Tacjana Johansen, Helle Krogh Qvist, Tavs Pediatr Pulmonol ORIGINAL ARTICLES BACKGROUND: Inhaled antibiotics are an important part of cystic fibrosis (CF) airway disease management and should be individualized to fit the microorganism and match patient needs. To investigate the implementation of personalized treatment, this study mapped the use of different types of inhaled antibiotics and adherence patterns. METHODS: We performed individual structured interviews in a cross‐sectional study at the CF Centre in Copenhagen, Denmark. Patients with CF older than 15 years attending clinical consultations were included. Clinical data were obtained from centralized databases. RESULTS: Among 149 participants, 107 (72%) had indication for treatment with inhaled antibiotics. In this group, 97 (91%) reported the use of inhaled antibiotics within the last 12 months. Change from one inhaled antibiotic to another during that period was reported by 31 (29%), and 17 (25%) with Pseudomonas aeruginosa had used off‐label antibiotics. Adherence to a minimum of one daily dose of antibiotic was reported by 78%, while adherence to all daily doses was 28 percentage points lower. Skipping inhalations was due to side effects and doubt about the effect in less than 5% of cases. CONCLUSION: Change of inhaled antibiotics and use of off‐label antibiotics for inhalation were common and side effects were a rare cause of nonadherence. This suggests satisfactory implementation of the principle of tailored antibiotic inhalation prescription in the Copenhagen CF population. Adherence to at least one daily inhalation dose was markedly higher than adherence to multiple daily inhalations. John Wiley and Sons Inc. 2022-05-14 2022-07 /pmc/articles/PMC9324817/ /pubmed/35478387 http://dx.doi.org/10.1002/ppul.25942 Text en © 2022 The Authors. Pediatric Pulmonology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle ORIGINAL ARTICLES
Møller, Rikke
Nielsen, Bibi Uhre
Faurholt‐Jepsen, Daniel
Katzenstein, Terese Lea
Skov, Marianne
Philipsen, Lue Katrine Drasbæk
Pressler, Tacjana
Johansen, Helle Krogh
Qvist, Tavs
Use of inhaled antibiotics among Danish patients with cystic fibrosis
title Use of inhaled antibiotics among Danish patients with cystic fibrosis
title_full Use of inhaled antibiotics among Danish patients with cystic fibrosis
title_fullStr Use of inhaled antibiotics among Danish patients with cystic fibrosis
title_full_unstemmed Use of inhaled antibiotics among Danish patients with cystic fibrosis
title_short Use of inhaled antibiotics among Danish patients with cystic fibrosis
title_sort use of inhaled antibiotics among danish patients with cystic fibrosis
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324817/
https://www.ncbi.nlm.nih.gov/pubmed/35478387
http://dx.doi.org/10.1002/ppul.25942
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