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MEDICATION — INHALED (NEBULIZED/DRY POWDER)

Inhaled antibiotics

Antibiotics breathed directly into the lungs to control chronic airway infection — especially Pseudomonas aeruginosa — a major driver of lung damage in cystic fibrosis.
Treatments & procedures › Inhaled antibiotics

What it is

Many people with CF develop chronic airway infection, most importantly with Pseudomonas aeruginosa. Inhaled antibiotics deliver high drug levels straight to the lungs while limiting whole-body side effects. The two mainstays are inhaled tobramycin (TOBI and others) and aztreonam lysine (Cayston). They are often used in repeating on/off cycles (commonly 28 days on, 28 days off), sometimes alternating between the two, to suppress infection and reduce flare-ups.

How it’s taken

Inhaled by nebulizer or dry-powder inhaler, usually in 28-day-on/28-day-off cycles, and timed after airway clearance and other inhaled medicines. The CF team selects and rotates agents based on sputum cultures and how the airways respond.

What to expect

This is ongoing, cyclic maintenance therapy to suppress (not eradicate) chronic infection. Regular sputum cultures guide which antibiotic is used and when. Acute flare-ups may still need oral or IV antibiotics.

Risks & side effects

  • Cough, throat irritation, and (with some) a temporary drop in lung function right after dosing
  • Bronchospasm — a bronchodilator is often given first
  • Antibiotic resistance over time
  • Rarely, hearing or kidney effects with aminoglycosides (less than with IV use)
  • Nebulizer hygiene is important

Alternatives

Oral / IV antibiotics
For acute exacerbations or eradication of new infection
Airway clearance & mucus-thinners
Reduce the mucus that harbors bacteria
CFTR modulators
Lower infection burden for eligible patients