Abstract | CONTEXT: OBJECTIVE: DESIGN: Three telephone surveys were conducted; Survey 1 prior to initiating therapy with FSC 250/50, and Surveys 2 and 3 at 2 weeks and 30 days after initiating therapy with FSC 250/50, respectively. SETTING: One thousand primary care physicians recruited outpatients into the trial. PATIENTS: INTERVENTIONS: Patients initiated FSC 250/50 and received a 1-month supply of FSC 250/50 with an albuterol inhaler for rescue use. MAIN OUTCOME MEASURES: Outcome measures were patient perceptions of satisfaction, compliance, and convenience and changes in breathing on 1 (negative) to 9 (positive) point scales. RESULTS: Five hundred sixteen patients completed all 3 surveys. The mean age was 61 years, 63% were female, and 62% had been diagnosed with COPD associated with chronic bronchitis for 3 years or less (Table 1). CONCLUSION: Patients reported high satisfaction, compliance, and convenience with FSC 250/50 within 2 weeks of initiating therapy, all maintained over the trial period. Additionally, patients had positive changes in breathing, including improvements in the ability to breathe upon awakening in the morning.
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Authors | Stuart Stoloff, Steven Samuels, Donna Kerney, Christy P Brown |
Journal | MedGenMed : Medscape general medicine
(MedGenMed)
Vol. 8
Issue 1
Pg. 86
(Mar 29 2006)
ISSN: 1531-0132 [Electronic] United States |
PMID | 16915216
(Publication Type: Clinical Trial, Journal Article)
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Chemical References |
- Androstadienes
- Drug Combinations
- Fluticasone-Salmeterol Drug Combination
- Albuterol
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Topics |
- Administration, Inhalation
- Albuterol
(administration & dosage, analogs & derivatives)
- Androstadienes
(administration & dosage)
- Bronchitis, Chronic
(complications)
- Drug Combinations
- Female
- Fluticasone-Salmeterol Drug Combination
- Humans
- Male
- Middle Aged
- Patient Satisfaction
- Pulmonary Disease, Chronic Obstructive
(complications, drug therapy)
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