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Comparing Budesonide and Fluticasone Propionate in Children with Moderate to Severe Asthma: A Pilot Randomized
Mansour Sadeghzadeh1, Parisa Khoshnevisasl2, Akefeh Ahmadiafshar3
1Department of Pediatrics, Zanjan University of Medical Sciences, Zanjan, Iran. sadeghzadeh@zums.ac.ir.
Insights
Fluticasone propionate (FP) significantly improved asthma control test scores and reduced rescue medication use in children with moderate to severe asthma compared to budesonide (Bud). FP demonstrated superior efficacy in managing pediatric asthma symptoms.
Area of Science:
- Pediatric Pulmonology
- Respiratory Medicine
- Clinical Pharmacology
Background:
- Asthma management in children requires effective anti-inflammatory strategies.
- Inhaled corticosteroids (ICS) are foundational therapies for persistent asthma.
- Comparing the efficacy of different ICS is crucial for optimizing treatment.
Purpose of the Study:
- To compare the efficacy of fluticasone propionate (FP) and budesonide (Bud) in children with moderate to severe asthma.
- To evaluate the impact of FP versus Bud on asthma control, clinical symptoms, and rescue medication use.
- To assess treatment outcomes over a 3-month period in pediatric asthma patients.
Main Methods:
- An open-label study involving 50 children (ages 4-7) with moderate to severe asthma.
- Randomized assignment to receive either FP 250 mcg or Bud 400 mcg daily for 3 months.
- Monthly assessment of Asthma Control Test (ACT) scores, clinical symptoms, drug adherence, and rescue inhaler use.
Main Results:
- Both FP and Bud groups showed significant improvements in ACT scores, nocturnal symptoms, and cough rates.
- The fluticasone propionate group achieved higher average ACT scores (24.84±2.67 by month 3) compared to the budesonide group (22.48±4.12).
- Fluticasone propionate significantly reduced the need for salbutamol (rescue medication) compared to budesonide throughout the study period.
Conclusions:
- Fluticasone propionate (250 mcg) is more effective than budesonide (400 mcg) in improving asthma control and reducing rescue medication needs in children with moderate to severe asthma.
- FP demonstrated superior efficacy in enhancing asthma control test scores and decreasing salbutamol use.
- These findings suggest FP may be a preferred treatment option for optimizing asthma management in this pediatric population.
Abstract:
The aim of asthma treatment is to reduce airway inflammation by avoiding environmental triggers and using daily anti-inflammatory medications. This study aimed to compare the effects of fluticasone propionate (FP) and budesonide (Bud) on the clinical symptoms and control of asthma in children with moderate to severe asthma. In this open-label study, children with moderate to severe asthma were randomly selected to receive either FP 250 mcg or Bud 400 mcg for 3 months. Asthma control test scores were measured in both groups monthly. The clinical symptoms, drug adherence, and rescue medication were also evaluated. A total of 50 patients with ages between 4 and 7 years old were included in the study (25 cases received Bud and 25 cases received FP). Asthma control test scores, daily and nocturnal symptoms, and cough rates were significantly improved in both groups. The average asthma control scores for the fluticasone group were 21.68±3.32 in the second month and 24.84±2.67 in the third month, whereas the budesonide group had scores of 18.52±3.32 and 22.48±4.12 during the same periods. These variances were statistically significant. Additionally, the requirement for salbutamol use was notably reduced in the fluticasone group compared to the budesonide group throughout all three months. The efficacy of fluticasone propionate in decreasing the need for rescue medication and enhancing asthma control test scores was markedly superior to that of budesonide.
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