Cystic fibrosis is the most common life-threatening inherited
disease in the UK and Europe. It affects around 1 in 2500 live
births in the UK. There have been enormous advances in the
treatment of CF over the last 40 years, with life expectancy
increasing from just 5 years in 1964 to mid 30s today, and it now
affects as many adults as children. The burden of care for CF
patients is, however, considerable, and with the increase in life
expectancy the impact of CF on respiratory medicine has increased
considerably.
Part of the Oxford Respiratory Medicine Library series, this
pocketbook aims to be a concise companion for all health care
professionals who manage, or come across, patients with CF. The
book covers all aspects of care, including both paediatric and
adult-specific issues. The book will appeal to a wide variety of
health professionals in respiratory medicine, paediatrics, and
primary care.
General
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