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Coming of age in cystic fibrosis – transition from paediatric to adult care
Cystic fibrosis (CF) is the most common multi-system inherited disorder, with a UK population exceeding 9,000. There have been significant improvements in CF survival over the decades, attributed to improvements in therapies available, our understanding of the disease and better organisation of care...
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Published in: | Clinical medicine (London, England) England), 2013-10, Vol.13 (5), p.482-486 |
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container_title | Clinical medicine (London, England) |
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creator | Nazareth, Dilip Walshaw, Martin |
description | Cystic fibrosis (CF) is the most common multi-system inherited disorder, with a UK population exceeding 9,000. There have been significant improvements in CF survival over the decades, attributed to improvements in therapies available, our understanding of the disease and better organisation of care. CF care providers have been early advocates for successful healthcare transition from the paediatric to adult sector and CF can be considered a model process where a paediatric disease has now become an adult one. This article looks at the transition process in CF and the future challenges CF physicians will face. |
doi_str_mv | 10.7861/clinmedicine.13-5-482 |
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ispartof | Clinical medicine (London, England), 2013-10, Vol.13 (5), p.482-486 |
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source | Open Access: PubMed Central; ScienceDirect Journals |
subjects | Adolescent Adult Biological and medical sciences CF survival Child Cystic fibrosis Cystic Fibrosis - complications Cystic Fibrosis - epidemiology Cystic Fibrosis - therapy Errors of metabolism Female General aspects Humans Male Medical sciences Metabolic diseases Miscellaneous hereditary metabolic disorders Survival Analysis transition Transition to Adult Care Transitional Care United Kingdom - epidemiology |
title | Coming of age in cystic fibrosis – transition from paediatric to adult care |
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