RT Journal Article
SR Electronic
T1 Full, shared and hybrid paediatric care for cystic fibrosis in South and Mid Wales
JF Archives of Disease in Childhood
JO Arch Dis Child
FD BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health
SP 17
OP 20
DO 10.1136/adc.2010.199380
VO 97
IS 1
A1 Doull, Iolo
A1 Evans, Hazel
A1 ,
YR 2012
UL http://adc.bmj.com/content/97/1/17.abstract
AB Background Although care for children with cystic fibrosis (CF) is increasingly shared between CF centres and local CF clinics, the optimal model is unclear. Objectives The authors compared three models of care within a well established CF network: full centre care; local clinic based care with annual review by the CF centre; and hybrid care, where the child is usually reviewed at least three times a year by the specialist CF centre. Results Of 199 children and young people with CF in South and Mid Wales, 77 were receiving full care, 102 shared care and 20 hybrid care. There were no significant differences in baseline characteristics, nutritional outcomes or use of chronic therapies. There was however a statistically significant difference between full, shared and hybrid care in mean forced expiratory volume in 1 s (FEV1) per cent predicted (89.2% vs 74.5% vs 88.9%; p=0.001). Conclusions These differences in pulmonary function are likely to reflect the model of care received, and may affect long term outcomes.