2009-10-01
Recombinant human DNase in children with airway malacia and lower respiratory tract infection
Publication
Publication
Pediatric Pulmonology , Volume 44 - Issue 10 p. 962- 969
Background: Children with airway malacia often have protracted courses of airway infections, because dynamic airway collapse during coughing results in impaired mucociliary clearance. The aim of this study was to determine the effect of the mucolytic drug recombinant human deoxyribonuclease (rhDNase) on the recovery of respiratory symptoms in children with airway malacia and lower respiratory tract infection (LRTI). Methods: In a randomized double-blind controlled clinical trial, 40 children with airway malacia andLRTIwere randomlyassigned to receive either 2.5mg nebulized rhDNase or placebo twice daily for 2 weeks. The primary endpoint was the change in the cough diary score (CDS) (scale 0-5) from baseline to the second week of treatment. Secondary endpoints were VAS symptom scores for cough, dyspnea, and difficulty in expectorating sputum, need for an antibiotic course, and lung function data (FVC, FEV1, FEF75, Rinte ). Results: There was no significant difference in the mean change in CDSs from baseline between the rhDNase group and the placebo group (mean difference for daytime 0.19 (95% CI -0.53 to 0.90); for nighttime 0.38 (95% CI -0.30 to 1.05). Proportions of patients requiring antibiotics, and the mean changes in symptom scores and lung function from baseline did not significantly differ between both groups. Conclusion:Treatment with 2weeks of nebulized rhDNase does not enhance recovery or reduce the need for antibiotics in children with airway malacia and LRTI. (Controlled-trials.com number, ISRCTN85366144).
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doi.org/10.1002/ppul.21073, hdl.handle.net/1765/24122 | |
Pediatric Pulmonology | |
Organisation | Erasmus MC: University Medical Center Rotterdam |
Boogaard, R., de Jongste, J., Vaessen-Verberne, A., Hop, W., & Merkus, P. (2009). Recombinant human DNase in children with airway malacia and lower respiratory tract infection. Pediatric Pulmonology, 44(10), 962–969. doi:10.1002/ppul.21073 |