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Respiratory infections require intensive antibiotic therapy and together with lung damage are the commonest causes of death in people with cystic fibrosis. Viscous secretion is treated with vigorous physiotherapy and the use of mucolytics. Infections in cystic fibrosis are often due to Staphylococcus aureus, Haemophilus influenzae or Pseudomonas aeruginosa. Infecting organisms need to be identified so that the most appropriate antibiotics can be used. Antibiotics used to treat respiratory infections in cystic fibrosis commonly include ciprofloxacin, erythromycin, flucloxacillin and amoxicillin.

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For the safety of patients, it is essential that the independent prescriber and the supplementary prescriber use and share access to the same common patient record and jointly keep it up to date. The key to safe and effective supplementary prescribing is the relationship between the individual independent prescriber and the individual supplementary prescriber. There are likely to be many nurses, pharmacists and other health care professionals who meet the criteria for training to become supplementary prescribers.

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