Fluticasone Propionate-salmeterol Combination Adherence in Patients With Chronic Obstructive Pulmonary Disease (COPD)
- Conditions
- Pulmonary Disease, Chronic Obstructive
- Interventions
- Registration Number
- NCT01381471
- Lead Sponsor
- GlaxoSmithKline
- Brief Summary
The specific aim of this study is to describe 1 year Advair dispensing rates for patients with COPD, and to measure the association between Advair adherence and healthcare utilization (e.g. emergency room visits and inpatient admissions, etc.). To compare the risk of a COPD exacerbation (moderate or severe) during a 3-month follow-up period between patients thqat are adherent versus those that are not.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 11060
Not provided
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description COPD fluticasone propionate/salmeterol xinafoate combination Patients with a diagnosis code of COPD
- Primary Outcome Measures
Name Time Method Mean Number of Pharmacy Claims by Participants During the Post-Index Period One Year The mean number of pharmacy claims incurred by participants during the one-year post-index period was measured.
Mean Number of Healthcare Encounters Incurred by Participants During the Post-Index Period One Year The mean number of outpatient office visits, inpatient visits, and emergency department visits incurred by participants during the one-year post-index period was measured.
- Secondary Outcome Measures
Name Time Method