Serum tobramycin levels following delivery of tobramycin (Tobi®) via eFlow® advanced nebuliser in children with cystic fibrosis☆
Abstract
Background
Safety and toxicity data for nebulised tobramycin are mainly derived from use of the Pari LC® Plus nebuliser, yet many centres are now using advanced nebulisers, such as the eFlow®.
Methods
Ten children (ages 2–16
years) receiving 300
mg TOBI® via eFlow® for clinical reasons participated. Serum tobramycin levels were obtained 1
h post nebulisation. Nine provided samples for urinary NAG, and 10 underwent audiology.
Results
Tobramycin levels were >
1
mg/L in 3 children (maximum 3.8, 2 children aged 2
years). Urine NAG/creatinine levels were raised (>
0.94
μmol/min/mmol) in 5 children, 1 of these had a tobramycin level of >
1
mg/L. One patient had high frequency hearing loss.
Conclusion
Serum tobramycin levels over 1
mg/L can occur 1
h post 300
mg TOBI® delivered by eFlow®. Raised urinary NAG levels suggest that some children may have some associated early renal toxicity.
Keywords: Cystic fibrosis, Paediatric, TOBI, eFlow, Pseudomonas aeruginosa
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☆ The title has been presented as a poster at the 32nd European Cystic Fibrosis Conference, 10–13th June 2009, Brest, France.
PII: S1569-1993(10)00034-2
doi:10.1016/j.jcf.2010.03.007
© 2010 European Cystic Fibrosis Society. Published by Elsevier Inc All rights reserved.
