1988
DOI: 10.1136/bmj.297.6642.163
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Controlled trial of budesonide given by the nebuhaler in preschool children with asthma.

Abstract: Objective-To determine whether the inhaled corticosteroid budesonide, given by a Nebuhaler spacing device, was effective in prophylaxis of asthma in preschool children.Design-Double blind, placebo controlled, random order crossover trial with two week practice run in period.Setting

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Cited by 74 publications
(27 citation statements)
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“…To allow for the modulating effect of treatment on symptom severity (attack severity, attack number, total severity score and interval score) the modelling was repeated after multiplying each severity score by 2 in those on inhaled steroids; this was performed with and without the three children on cromoglycate. A factor of 2 was chosen, as approximately a halving of symptoms following inhaled steroid therapy has been demonstrated in children of this age [13,14].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…To allow for the modulating effect of treatment on symptom severity (attack severity, attack number, total severity score and interval score) the modelling was repeated after multiplying each severity score by 2 in those on inhaled steroids; this was performed with and without the three children on cromoglycate. A factor of 2 was chosen, as approximately a halving of symptoms following inhaled steroid therapy has been demonstrated in children of this age [13,14].…”
Section: Discussionmentioning
confidence: 99%
“…Multiplying the severity score by 2.0 in those receiving inhaled steroids, to allow for a possible beneficial effect, however, made no material difference to the results. Since, in carefully supervised placebo-controlled trials in this age group, the mean improvement in symptoms on inhaled steroids is approximately 30-60% [13,14], this adjustment is probably reasonable.…”
Section: Discussionmentioning
confidence: 99%
“…7, 20-22, 24-26, 28-32, 35-37 All were double-blind RCTs. Thirteen studies had a parallel design, and 2 had crossover designs: Gleeson and Price 28 and Webb et al 36 (3-week washout period and no washout, respectively). The studies used several different delivery systems and types of ICS, with most studies using medium daily doses (budesonide 0.4 mg/day, fluticasone 0.2 mg/day, beclomethasone 0.15 mg/day, ciclesonide 0.16 mg/day, flucinolide 40 μg/kg/day).…”
Section: Included Studiesmentioning
confidence: 99%
“…Two experienced exacerbations on placebo. Eleven of 18 parents whose children completed the maximum treatment preferred budesonide to placebo and one preferred placebo. Mean symptom scores on budesonide were better than on placebo for the 15 15 In this paper, we report the results of a double blind, crossover study investigating the effects of inhaled budesonide in wheezy infants who were less than 18 months of age.…”
Section: Introductionmentioning
confidence: 99%