Discontinuation of supportive therapies in people with cystic fibrosis treated with elexacaftor/tezacaftor/ivacaftor – A patient-reported outcomes’ study

Many people with CF are reducing supportive therapies despite the absence of clear guidelines. Decision-making is influenced by factors such as the desire to lessen therapy burden, reduced symptom severity, and maximizing therapeutic effects. The study highlights the need for comprehensive recommendations and calls for further research to understand the factors involved in therapy adherence and reduction.

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Publication Details

Journal
Respiratory Medicine
Published
2025-10-29
DOI
https://doi.org/10.1016/j.rmed.2025.108464
Citations
1
Primary Topic
Cystic Fibrosis Research Advances
Type
article
Field-Weighted Citation Impact
1.52
Controls
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article

Discontinuation of supportive therapies in people with cystic fibrosis treated with elexacaftor/tezacaftor/ivacaftor – A patient-reported outcomes’ study

Constance Henn, B. Wollschläger, A.-L. Strehlow, Maike vom Hove et al.
1 citations
Respiratory Medicine
Cystic Fibrosis Research Advances
1.52
article

Discontinuation of supportive therapies in people with cystic fibrosis treated with elexacaftor/tezacaftor/ivacaftor – A patient-reported outcomes’ study

Constance Henn, B. Wollschläger, A.-L. Strehlow, Maike vom Hove, Freerk Prenzel, Mandy Vogel, Ulrike Issa, Simone Ahting, Julia Hentschel, C. Ludwig
article en
1 citations

Abstract

Many people with CF are reducing supportive therapies despite the absence of clear guidelines. Decision-making is influenced by factors such as the desire to lessen therapy burden, reduced symptom severity, and maximizing therapeutic effects. The study highlights the need for comprehensive recommendations and calls for further research to understand the factors involved in therapy adherence and reduction.

Respiratory MedicineVol. 249
The Cystic Fibrosis Institute (DE), University Hospital Leipzig (DE), Pulmonary Associates (US), University Hospital in Halle (DE), Leipzig University (DE)
Openalex Percentile: Top 13%
Cystic Fibrosis Research Advances
1.52
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