Clinical impact of levofloxacin inhalation solution in cystic fibrosis patients in a real-world setting.


Journal

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society
ISSN: 1873-5010
Titre abrégé: J Cyst Fibros
Pays: Netherlands
ID NLM: 101128966

Informations de publication

Date de publication:
11 2021
Historique:
received: 17 11 2020
revised: 04 03 2021
accepted: 06 03 2021
pubmed: 9 6 2021
medline: 10 2 2022
entrez: 8 6 2021
Statut: ppublish

Résumé

Levofloxacin inhalation solution is the most recently approved inhaled antibiotic in Europe and Canada for adult cystic fibrosis patients. Its efficacy and safety have been assessed in randomized controlled trials. Our aim was to evaluate real life experience and outcomes in our treatment centre. We evaluated the efficacy of inhaled levofloxacin solution in 86 patients with cystic fibrosis in terms of the following outcome parameters: changes in %-predicted forced expiratory volume in one second (FEV Change in FEV In patients with cystic fibrosis, inhaled levofloxacin solution has the potential to improve FEV

Sections du résumé

BACKGROUND
Levofloxacin inhalation solution is the most recently approved inhaled antibiotic in Europe and Canada for adult cystic fibrosis patients. Its efficacy and safety have been assessed in randomized controlled trials. Our aim was to evaluate real life experience and outcomes in our treatment centre.
METHODS
We evaluated the efficacy of inhaled levofloxacin solution in 86 patients with cystic fibrosis in terms of the following outcome parameters: changes in %-predicted forced expiratory volume in one second (FEV
RESULTS
Change in FEV
CONCLUSIONS
In patients with cystic fibrosis, inhaled levofloxacin solution has the potential to improve FEV

Identifiants

pubmed: 34099405
pii: S1569-1993(21)00051-5
doi: 10.1016/j.jcf.2021.03.002
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Levofloxacin 6GNT3Y5LMF

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1035-1039

Informations de copyright

Copyright © 2021 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest Carsten Schwarz received a research grant from Chiesi and he has given lectures during scientific conferences and advisory boards and received financial support by Chiesi for these activities. Claudia Grehn, Svenja Temming, Frederik Holz, Patience Ndidi Eschenhagen have no conflict of interest.

Auteurs

Carsten Schwarz (C)

Department of Pediatric Pulmonology, Immunology and Intensive Care Medicine, Division of Cystic Fibrosis, Charité - Universitätsmedizin, Augustenburger Platz 1, 13353 Berlin, Germany. Electronic address: carsten.schwarz@gmail.com.

Claudia Grehn (C)

Department of Pediatric Pulmonology, Immunology and Intensive Care Medicine, Division of Cystic Fibrosis, Charité - Universitätsmedizin, Augustenburger Platz 1, 13353 Berlin, Germany. Electronic address: claudia.grehn@charite.de.

Svenja Temming (S)

Department of Pediatric Pulmonology, Immunology and Intensive Care Medicine, Division of Cystic Fibrosis, Charité - Universitätsmedizin, Augustenburger Platz 1, 13353 Berlin, Germany. Electronic address: svenja.temming@charite.de.

Frederik Holz (F)

Department of Pediatric Pulmonology, Immunology and Intensive Care Medicine, Division of Cystic Fibrosis, Charité - Universitätsmedizin, Augustenburger Platz 1, 13353 Berlin, Germany. Electronic address: frederik.holz@charite.de.

Patience Ndidi Eschenhagen (PN)

Department of Pediatric Pulmonology, Immunology and Intensive Care Medicine, Division of Cystic Fibrosis, Charité - Universitätsmedizin, Augustenburger Platz 1, 13353 Berlin, Germany. Electronic address: patience.eschenhagen@charite.de.

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Classifications MeSH