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Published on: February 11, 2017
Alternate-day prednisone reduces morbidity and improves pulmonary function in cystic fibrosis
Insights
Alternate-day prednisone therapy significantly improved lung function and reduced hospitalizations in children with cystic fibrosis (CF) over four years without adverse effects.
Area of Science:
- Pediatrics
- Pulmonology
- Pharmacology
Background:
- Cystic Fibrosis (CF) is a genetic disorder affecting multiple organs, primarily the lungs.
- Lung disease progression and associated morbidity are significant concerns in pediatric CF patients.
- Optimizing treatment strategies to slow disease progression is crucial.
Purpose of the Study:
- To evaluate the efficacy of alternate-day prednisone therapy in managing lung disease progression in children with CF.
- To assess the impact of prednisone on various clinical and physiological parameters in CF patients.
- To determine the safety profile of long-term alternate-day prednisone use in this population.
Main Methods:
- A randomized, double-blind, placebo-controlled trial was conducted.
- Participants were pediatric patients (aged 1-12 years) with mild to moderate lung disease at baseline.
- Patients received either alternate-day prednisone or a placebo for four years.
Main Results:
- Prednisone-treated patients showed significant improvements in height, weight, vital capacity, FEV1, peak flow rate, ESR, and serum IgG compared to placebo.
- Hospital admissions for CF-related pulmonary disease were substantially lower in the prednisone group (9 admissions) versus the placebo group (35 admissions).
- No significant steroid-induced side effects were observed during the study period.
Conclusions:
- Alternate-day prednisone therapy is an effective treatment for improving clinical outcomes and reducing pulmonary exacerbations in pediatric CF patients.
- The treatment demonstrates a favorable safety profile with no discernible adverse effects over four years.
- This therapeutic approach offers a promising strategy for managing lung disease progression in cystic fibrosis.
Abstract:
A randomised, double-blind, placebo-controlled study examined the effects of alternate-day prednisone therapy on morbidity and progression of lung disease in cystic fibrosis (CF). At baseline the patients (aged 1-12 years) had mild to moderate lung disease, and the prednisone group did not differ significantly from the placebo group for any values measured. After 4 years, the prednisone-treated group had significant advantages over the placebo group for height, weight, vital capacity, forced expiratory volume in 1 s, peak flow rate, erythrocyte sedimentation rate, and serum IgG. The prednisone-treated group required 9 admissions to hospital for CF-related pulmonary disease compared with 35 for the placebo group. There were no steroid-induced side-effects. To rule out bias in case selection, 69 CF clinic patients comparable in age and clinical status but not included in the study were compared with the placebo group at 4 years; no significant differences between the groups were found.
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