About
About us
Our methods
Updated report
Multilinguality
Help
How to use
Key concepts
FAQ
Contact
Sign up
Login
العربية
Deutsch
English
Español
Français
Italiano
Nederlands
Português
中文
×
Email:
Password:
Forgot Password
×
Edit Thread Title
Thread name
Thread full name
Thread alternative names
Thread phase
×
Delete Thread
Are you sure you want to delete the thread
? This operation cannot be undone.
Amirav, I, Amirav I
ID:
56e9226c18d84e184cd77d6b
3 Documents
Export all
Document ID
Add to Thread
Thread ID
Merge thread
Close
3 References
( articles)
Revert
Studify
Primary study
Unclassified
Double blind placebo controlled randomized trial of montelukast in acute RSV bronchiolitis [Abstract]
Authors
»
Amirav, I
,
Kruger, N
,
Borovitch, Y
,
Babai, I
,
Miron, D
,
Zuker, M
,
Luder, A
,
Mandelberg, A
Journal
»
European respiratory journal
Year
»
2007
Links
»
pesquisa.bvsalud
Loading references information
No abstract
Show abstract
Hide abstract
Primary study
Unclassified
A double-blind, placebo-controlled, randomized trial of montelukast for acute bronchiolitis
Authors
»
Amirav I
,
Luder AS
,
Kruger N
,
Borovitch Y
,
Babai I
,
Miron D
,
Zuker M
,
Tal G
,
Mandelberg A
Journal
»
Pediatrics
Year
»
2008
Links
»
Pubmed
DOI
Loading references information
No abstract
Show abstract
BACKGROUND. Cysteinyl leukotrienes are implicated in the inflammation of bronchiolitis. Recently, a specific cysteinyl leukotriene receptor antagonist, montelukast (Sin-gulair [MSD, Haarlem, Netherlands]), has been approved for infants in granule sachets. OBJECTIVE. Our goal was to evaluate the effect of montelukast on clinical progress and on cytokines in acute bronchiolitis. METHODS. This was a randomized, placebo-controlled, double-blind, parallel-group study in 2 medical centers. Fifty-three infants (mean age: 3.8 ± 3.5 months) with a first episode of acute bronchiolitis were randomly assigned to receive either 4-mg montelukast sachets or placebo, every day, from hospital admission until discharge. The primary outcome was length of stay, and secondary outcomes included clinical severity score (maximum of 12) and changes in type 1 and 2 cytokine levels (including interleukin4/IFN-y ratio as a surrogate for the T-helper 2/T-helper 1 ratio) in nasal lavage. RESULTS. Both groups were comparable at baseline, and cytokine levels correlated positively with disease severity. There were neither differences in length of stay (4.63 ± 1.88 [placebo group] vs 4.65 ± 1.97 days [montelukast group]) nor in clinical severity score and cytokine levels between the 2 groups. No differences in interleukin 4/IFN-y ratio between the 2 groups were seen. There was a slight tendency for infants in the montelukast group to recover more slowly than those in the placebo group (clinical severity score at discharge: 6.1 ± 2.4 vs 4.8 ± 2.2, respectively). CONCLUSIONS. Montelukast did not improve the clinical course in acute bronchiolitis. No significant effect of montelukast on the T-helper 2/T-helper 1 cytokine ratio when given in the early acute phase could be demonstrated. Copyright © 2008 by the American Academy of Pediatrics.
Hide abstract
Primary study
Unclassified
A double-blind, placebo-controlled, randomized trial of montelukast for acute bronchiolitis
Authors
»
Amirav, I
,
Luder, AS
,
Kruger, N
,
Borovitch, Y
,
I, Babai
,
Miron, D
Journal
»
Pediatrics
Year
»
2009
Loading references information
No abstract
Show abstract
Hide abstract
Abstract
About this article
Related evidence
Study Design
»
Randomized controlled trial (RCT)