Abstract
Reducing treatment burden in cystic fibrosis (CF) is the top research priority for patients and clinicians. Difficulty accessing medication is one aspect of treatment burden. We investigated this with an online survey available globally for patients with CF and healthcare professionals. Almost three quarters of patients with CF in our survey report difficulty getting repeat prescriptions on time, and most community pharmacists experience interrupted supplies of CF-specific medications. These barriers affect emotional and physical health of people with CF. Two-thirds of people with CF would like to get all their CF medication from one place, their CF centre.
Original language | English |
---|---|
Pages (from-to) | 295-297 |
Number of pages | 3 |
Journal | Thorax |
Volume | 77 |
Issue number | 3 |
Early online date | 23 Sept 2021 |
DOIs | |
Publication status | Published - 01 Mar 2022 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.
Keywords
- cystic fibrosis
- psychology
- respiratory infection
ASJC Scopus subject areas
- Pulmonary and Respiratory Medicine