Highlights
- •Reducing treatment burden is a high priority for people living with CF.
- •Standard of care involves the use of multiple nebulized therapies which are time consuming.
- •Prescription refills for nebulized dornase alfa and hypertonic saline decreased in the first year post-ETI.
- •Several ongoing studies are evaluating the safety of withdrawing nebulized therapies post-ETI.
Keywords
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References
- High treatment burden in adults with cystic fibrosis: challenges to disease self-management.J Cyst Fibros. 2009; 8 (Mar): 91-96
- Efficacy and safety of the elexacaftor plus tezacaftor plus ivacaftor combination regimen in people with cystic fibrosis homozygous for the F508del mutation: a double-blind, randomised, phase 3 trial.Lancet. 2019; 394 (Nov 23): 1940-1948
- Elexacaftor-tezacaftor-ivacaftor for cystic fibrosis with a single phe508del allele.N Engl J Med. 2019; 381 (Nov 7): 1809-1819
- Persistent recovery of pancreatic function in patients with cystic fibrosis after ivacaftor.Pediatr Pulmonol. 2020; 55: 3381-3383
- Pulmonary medication adherence and health-care use in cystic fibrosis.Chest. 2014 Jan 30; 146: 142-151
Article info
Publication history
Published online: May 15, 2022
Accepted:
May 9,
2022
Received in revised form:
May 6,
2022
Received:
January 12,
2022
Identification
Copyright
© 2022 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.