Modeling the Impacts of Restrictive Formularies on Patients With HIV
Constraining access to HIV regimens can have significant implications for patients. This study examined the economic and health impacts of restrictive HIV formulary designs.
Treatment Patterns Among Adults With ADHD Receiving Long-Acting Therapy
Adults with attention-deficit/hyperactivity disorder (ADHD) who received long-acting combination therapy had significantly lower adherence and persistence compared with those who received long-acting monotherapy.
Two-Year Adherence and Costs for Biologic Therapy for Rheumatoid Arthritis
Adherence to newly initiated biologic therapy for rheumatoid arthritis is important for long-term adherence.
Direct Oral Anticoagulant Prescription Trends, Switching Patterns, and Adherence in Texas Medicaid
July 12th 2018Direct oral anticoagulants (DOACs) are associated with increased prescription costs. Actual practice data show a high switch rate and poor adherence among DOAC initiators that need to be addressed.
5-ASA to Sulfasalazine Drug Switch Program in Patients With Ulcerative Colitis
A 5-aminosalicylic acid (5-ASA) drug switch program switching from 5-ASA to sulfasalazine was instituted for insured patients with ulcerative colitis. Unanticipated barriers limited the number of patients who switched, but significant cost savings were still obtained.
Costs Associated With Long-Acting Insulin Analogues in Patients With Diabetes
Findings from a literature review indicate that overall costs of long-acting insulin analogues are not significantly different from those of intermediate-acting human insulin and oral antidiabetic agents.
Cost Per Response Analysis of Strategies for Chronic Immune Thrombocytopenia
This decision tree model estimates the cost per response and incremental cost per additional responder for romiplostim, eltrombopag, and “watch and rescue” for immune thrombocytopenia.
A Gray Area for Reimbursement: Medical Foods for Non–Inborn Errors of Metabolism
July 10th 2018Most non–inborn errors of metabolism (non-IEM) medical foods (MFs) do not meet the regulatory MF definition and lack scientific evidence for safety and efficacy. Non-IEM MFs are not yet ready for reimbursement by public insurers.