Literature DB >> 24115706

Coming of age in cystic fibrosis - transition from paediatric to adult care.

Dilip Nazareth1, Martin Walshaw.   

Abstract

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.

Entities:  

Keywords:  CF survival; Cystic fibrosis; transition

Mesh:

Year:  2013        PMID: 24115706      PMCID: PMC4953800          DOI: 10.7861/clinmedicine.13-5-482

Source DB:  PubMed          Journal:  Clin Med (Lond)        ISSN: 1470-2118            Impact factor:   2.659


  3 in total

1.  Transition from paediatric surgery: how many patients do we need to plan for?

Authors:  A R Jones; M John; S J Singh; A R Williams
Journal:  Ann R Coll Surg Engl       Date:  2016-09-22       Impact factor: 1.891

2.  Changes in Clinical Markers During A Short-Term Transfer Program of Adult Cystic Fibrosis Patients from Pediatric to Adult Care.

Authors:  Matthias Welsner; Sivagurunathan Sutharsan; Christian Taube; Margarete Olivier; Uwe Mellies; Florian Stehling
Journal:  Open Respir Med J       Date:  2019-06-30

3.  Transition of children with life-limiting conditions to adult care and healthcare use: a systematic review.

Authors:  Stuart W Jarvis; Daniel Roberts; Kate Flemming; Gerry Richardson; Lorna K Fraser
Journal:  Pediatr Res       Date:  2021-03-02       Impact factor: 3.756

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.