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* From the Department of Pediatric Pulmonary Medicine, Stanford University Medical Center, Palo Alto, CA.
Correspondence to: Richard B. Moss, MD, FCCP, Pediatric Pulmonary Medicine, Stanford University Medical Center, 701 Welch Rd, Room 3328, Palo Alto, CA, CA 94304-5786; e-mail: rmoss{at}stanford.edu
High rates of colonization and the challenge of managing
Pseudomonas aeruginosa infections in patients with
cystic fibrosis (CF) have necessitated a search for safe and effective
antibiotics. Currently, therapy with an aminoglycoside in combination
with a ß-lactam or a quinolone antibiotic is the standard.
Unfortunately, it is difficult to deliver high doses of these
antibiotics via the IV route without significant systemic adverse
events (AEs) (eg, ototoxicity and nephrotoxicity).
Recently, a reformulation of the aminoglycoside antibiotic tobramycin
has become available in a preservative-free, pH-adjusted solution for
inhalation by jet nebulizer. A 96-week series of clinical studies
including 520 patients, aged
6 years, with moderate-to-severe CF
has evaluated the long-term safety and effectiveness of this
formulation. Patients received tobramycin solution for inhalation (TSI)
or placebo, which was administered in alternating cycles of 28-days-on
and 28-days-off therapy, plus their usual CF care for 6 months with
open-label follow-up extended to 2 years. Most AEs declined in
frequency with increasing TSI exposure. Patients receiving TSI spent 25
to 33% fewer days in the hospital. Following the initiation of TSI
treatment, patients experienced significant increases in
FEV1. FEV1 values were maintained above
baseline for the duration of the study series. Antibiotic
susceptibility of the bacterial isolates did not predict clinical
response. TSI was safe, well-tolerated, and effective for long-term
treatment (96 weeks) of P aeruginosa colonization and
infection in CF patients.
Key Words: aerosolized antibiotics cystic fibrosis Pseudomonas aeruginosa tobramycin solution for inhalation
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