RETROSPECTIVE, CLAIMS-BASED ANALYSIS DEMONSTRATES LIMITED PERSISTENCE AND ADHERENCE, AND LOW DAILY DOSES OF AMANTADINE IMMEDIATE RELEASE (AMT-IR) IN PATIENTS WITH PARKINSON'S DISEASE (PD)
Author(s)
Navarro RP1, Pahwa R2, Tanner CM3, Hauser RA4, Isaacson SH5, Patni R6
1University of Florida, Gainesville, FL, USA, 2University of Kansas Medical Center, Kansas City, KS, USA, 3UCSF School of Medicine, San Francisco, CA, USA, 4University of South Florida, Tampa, FL, USA, 5Parkinson’s Disease and Movement Disorders Center of Boca Raton, Boca Raton, FL, USA, 6Adamas Pharmaceuticals, Emeryville, CA, USA
OBJECTIVES: Five decades after introduction, levodopa remains the treatment of choice for PD. Chronic levodopa treatment with progressing PD contributes to levodopa-induced dyskinesia (LID), defined as involuntary, non-rhythmic, purposeless, unpredictable movements during waking hours occurring in approximately 30% of patients. LID can compromise optimal levodopa treatment. No FDA-approved drug for LID exists. AMT-IR was originally approved for influenza and later indicated in parkinsonism. It has also been evaluated in small studies for the treatment of dyskinesia. Conflicting guidelines for the use of AMT-IR in dyskinesia exist. While higher doses of AMT-IR have been shown to produce greater reductions in dyskinesia, they are associated with increased frequency of central nervous system adverse events. Real-world use, persistence, and adherence for AMT-IR has not been extensively analyzed or reported. METHODS: A retrospective claims-based analysis was conducted utilizing Symphony Health data to evaluate current AMT-IR utilization patterns in PD patients persistent on levodopa for at least 4 years (indicating presence of LID (Suh, 2012). Persistence was defined as continuous therapy without refill gaps > 90 days. Adherence was defined as ≤ 5 days between expected and actual refill dates. RESULTS: Among 22,000 patients persistent on levodopa for 4 years, approximately 1,500 (6.8%) had taken AMT-IR. At 1 year, 39% were persistent and 7% were adherent. The average starting dose was approximately 200 mg/day amantadine HCl (equivalent to 162 mg amantadine). Only 15% of patients started at 300mg/day amantadine HCl (equivalent to 243 mg amantadine) or greater. At one year, among those initiated on ≥300mg/day (243 mg amantadine), 38% were persistent while only 4% were adherent. CONCLUSIONS: This claims analysis demonstrates limited persistence and adherence at daily doses of 200-300 mg AMT-IR in PD patients. Higher dosage forms and improved delivery systems for amantadine in the treatment of LID may increase efficacy, persistence, and adherence.
Conference/Value in Health Info
2017-05, ISPOR 2017, Boston, MA, USA
Value in Health, Vol. 20, No. 5 (May 2017)
Code
PND46
Topic
Patient-Centered Research
Topic Subcategory
Adherence, Persistence, & Compliance
Disease
Neurological Disorders