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In children with cystic fibrosis (CF), pulmonary deterioration may be delayed by aggressive treatment with antibiotics (oral, inhaled, or both) early after Pseudomonas aeruginosa (Pa) infection is first detected. In a recent multicenter, controlled trial, investigators assessed the efficacy and safety of four such regimens.
The study involved 304 children with CF, aged 1 to 12 years, who were recruited from 55 U.S. clinical centers; all had Pa newly isolated from the respiratory tract within the preceding 6 months. The children were randomized to receive one of four treatments for 18 months:
Scheduled tobramycin inhalation plus oral ciprofloxacin, every 3 months
Scheduled tobramycin inhalation plus oral placebo, every 3 months
Tobramycin inhala…