Rheumatoid Arthritis
Conditions
Brief summary
The purpose of this study is to assess the impact of patient cost sharing on treatment discontinuation of biologic agents in patients with Rheumatoid Arthritis (RA)
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
Patients diagnosed with Rheumatoid Arthritis (RA) who newly initiated a biologic DMARD (bDMARD) during a study timeframe of 1/01/06 to 3/31/09. Inclusion Criteria: * 18 to 64 years of age at index date * Diagnosis of RA during the study period (ICD-9CM 714.xx) * Evidence of at least one biologic DMARD of interest during the study timeframe * Continuous enrollment during the study timeframe * Both medical and pharmacy benefits * No evidence of a claim for a bDMARD in the 6-month pre-period
Exclusion criteria
* Patients are excluded if they have a diagnosis of psoriasis, psoriatic arthritis, ankylosing spondylitis, Crohn's disease, or ulcerative colitis at any time during the study timeframe; have a claim for Rituxan, IV etanercept, or IV adalimumab; or have Medicare or Medicaid during the study timeframe
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Effect of patient cost share on discontinuation | Assessed from first prescription date and followed for 1-year |
Secondary
| Measure | Time frame |
|---|---|
| RA-related healthcare utilization and costs | Pre-index: 6-month period prior to the index drug date |
| All-cause healthcare utilization and costs | Pre-index: 6-month period prior to the index drug date |