Respiratory Medicine Case Reports (Jan 2015)

Hyperpharmacotherapy in ageing cystic fibrosis patients: The first report of an atypical hip fracture

  • W.A.K. Al-Azzani,
  • L. Evans,
  • L. Speight,
  • M. Lea-Davies,
  • M.D. Stone,
  • D. Lau,
  • R.I. Ketchell,
  • J. Duckers

DOI
https://doi.org/10.1016/j.rmcr.2015.09.013
Journal volume & issue
Vol. 16, no. C
pp. 148 – 150

Abstract

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Cystic fibrosis (CF) is a common autosomal recessive disorder in Caucasian populations with respiratory, gastrointestinal and endocrine manifestations. Thanks to recent advances in medical therapies and infection control, life expectancy of a patient with CF has significantly increased from less than 5 years in the mid-1900s to almost 50 years nowadays. However, as CF patients are living longer, multimorbidity and Hyperpharmacotherapy are becoming more common. This case illustrates a cascade of problems that ensued from medication side-effects, highlighting the increasing challenge of managing an ageing CF population.

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