Respiratory Disease in Practice

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Home therapies in cystic fibrosis – the way forward
RDIP, Volume 15, Number 4.

With the average life expectancy of cystic fibrosis (CF) patients in the UK approaching 31 years,1 CF has long ceased to be a disease of childhood. The nature of the disease demands that the treatments required to maintain optimum health, such as physiotherapy, nebulised therapies, antibiotics and nutritional supplementation are time-consuming, relentless and expensive.2 The effect of this on the quality of life may be significant. This article discusses the potential benefits of home vs hospital treatments.

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