Transition from paediatric to adult care in cystic fibrosis

Daniel Office*, Inge Heeres

*Corresponding author for this work

Research output: Contribution to journalReview articleAcademicpeer-review

3 Citations (Scopus)
19 Downloads (Pure)

Abstract

In the decades since cystic fibrosis (CF) was first clinically defined in the 1930s, there have been many advancements in the treatment and management of this disease. Initially it was considered a disease of childhood where the majority of those affected died before reaching adolescence. Now, through advancements in management and treatment, the vast majority of those affected will live into adulthood. Therefore, paediatric and adult CF services must collaborate to ensure that young people and their families experience a positive and supportive transition into adult services. Key aspects of transition will be discussed, including when to begin the transition process, who should coordinate this and how the transition process should be structured. Challenges of the transition process and potential pitfalls when transition does not run smoothly will also be discussed, as well as tools that may be used to support a positive transition for young people and their families.

Original languageEnglish
Article number210157
JournalBreathe
Volume18
Issue number3
DOIs
Publication statusPublished - 1 Sept 2022

Bibliographical note

Funding Information:
Manuscript received July 26, 2010; revised December 1, 2010; accepted December 1, 2010. Date of publication December 10, 2010; date of current version March 9, 2011. This work was supported by the High School Educational and Scientific Research Ministry of Algeria under the National Funding of Research.

Publisher Copyright:
© ERS 2022.

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