Melissa L.D. Christopher
University of Montana
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Publication
Featured researches published by Melissa L.D. Christopher.
Journal of Evaluation in Clinical Practice | 2012
Jignesh J. Patel; Margaret A.S. Mendes; Mark Bounthavong; Melissa L.D. Christopher; Daniel T. Boggie; Anthony P. Morreale
OBJECTIVE To evaluate the cost-effectiveness of intravitreal bevacizumab to ranibizumab in patients with neovascular age-related macular degeneration (AMD). METHODS A cost-utility analysis using a Markov model was performed to evaluate incremental cost-effectiveness ratio [ICER,
PharmacoEconomics | 2012
Christine M. Nguyen; Mark Bounthavong; Margaret A.S. Mendes; Melissa L.D. Christopher; Josephine N. Tran; Rashid Kazerooni; Anthony P. Morreale
US per quality-adjusted life year (QALY) gained] between bevacizumab and ranibizumab from a US payer perspective. Transition probabilities for ranibizumab and bevacizumab were extrapolated from published studies and local institutional data. Utility values, likewise, were obtained from another published study. Mortality rates were determined from the Centers for Disease Control 2003 Life Tables. Resource utilization and total direct costs were estimated using the Centers for Medicare and Medicaid Services and the Veterans Affairs Decision Support System. A hypothetical cohort of 1000 patients was simulated through the model for 20 years. Sensitivity analyses were performed using univariate and probabilistic sensitivity analysis (PSA) on all costs, transition probabilities and utility values. An acceptability curve was generated to illustrate the cost-effectiveness probability of bevacizumab to ranibizumab with increasing willingness-to-pay (WTP). RESULTS The cost-effectiveness ratios (CER) for bevacizumab and ranibizumab were
PharmacoEconomics | 2012
Christine M. Nguyen; Mark Bounthavong; Margaret A.S. Mendes; Melissa L.D. Christopher; Josephine N. Tran; Rashid Kazerooni; Anthony P. Morreale
1405 per QALY and
International Journal of Pharmacy Practice | 2010
Mark Bounthavong; Melissa L.D. Christopher; Margaret A.S. Mendes; Emerald B. Foster; Scott T. Johns; Lesley Lim; Lisa M. Rubin; Jignesh J. Patel; Anthony G. Stewart
12,177 per QALY, respectively. The ICER for bevacizumab was dominant compared to ranibizumab. The base-case CER was sensitive to drug costs of the study medications with a breakeven point of
PharmacoEconomics | 2012
Mark Bounthavong; Christine M. Nguyen; Margaret A.S. Mendes; Melissa L.D. Christopher; Josephine N. Tran; Rashid Kazerooni; Anthony P. Morreale
44 for ranibizumab and
Journal of The American Pharmacists Association | 2017
Mark Bounthavong; Michael Harvey; Daina Wells; Sarah J. Popish; Julianne Himstreet; Elizabeth M. Oliva; Chad L. Kay; Marcos K. Lau; Priyanka P. Randeria-Noor; Andrea G. Phillips; Melissa L.D. Christopher
2666 for bevacizumab. PSA revealed a 95% probability of bevacizumab being more cost-effective than ranibizumab at a WTP of
Journal of The American Pharmacists Association | 2017
Elizabeth M. Oliva; Melissa L.D. Christopher; Daina Wells; Mark Bounthavong; Michael Harvey; Julianne Himstreet; Thomas Emmendorfer; Michael Valentino; Mariano Franchi; Francine Goodman; Jodie A. Trafton
50,000 per QALY gained. CONCLUSION Based on a WTP defined at
Substance Abuse | 2018
Helen Valenstein-Mah; Hildi Hagedorn; Chad L. Kay; Melissa L.D. Christopher; Adam J. Gordon
50,000 per QALY gained, bevacizumab was cost-effective versus ranibizumab 95% of the time because of lower acquisition costs and increased efficacy.
Pain Medicine | 2018
Amanda M. Midboe; Justina Wu; Taryn Erhardt; Jannet M Carmichael; Mark Bounthavong; Melissa L.D. Christopher; Randall Gale
BackgroundRheumatoid arthritis (RA) is a chronic autoimmune disease that affects approximately 1.5 million people in the US. Tumour necrosis factor (TNF)-α inhibitors have been shown to effectively treat and maintain remission in patients with moderately to severely active RA compared with conventional agents. The high acquisition cost of TNF-α inhibitors prohibits access, which mandates economic investigations into their affordability. The lack of head-to-head comparisons between these agents makes it difficult to determine which agent is the most cost effective.ObjectiveThis study aimed to determine which TNF-α inhibitor was the most cost-effective agent for the treatment of moderately to severely active RA from the US healthcare payer’s perspective.MethodsA Markov model was constructed to analyse the cost utility of five TNF-α inhibitors (in combination with methotrexate [+MTX]) versus MTX monotherapy using Bayesian methods for evidence synthesis. The model had a cycle length of 3 months and an overall time horizon of 5 years. Transition probabilities and utility scores were based on published studies. Total direct costs were adjusted to year 2009
/data/revues/07356757/unassign/S073567571830679X/ | 2018
Comilla Sasson; Jason Smith; Chad Kessler; Jason S. Haukoos; Julianne Himstreet; Melissa L.D. Christopher; Thomas Emmendorfer
US using the medical component of the Consumer Price Index. All costs and QALYs were discounted at a rate of 3% per year. Patient response to the different strategies was determined by the American College of Rheumatology (ACR)50 criteria. One-way and probabilistic sensitivity analyses (PSAs) were performed to test the robustness of the base-case scenario. The base-case scenario was changed to ACR20 criteria (scenario 1) and ACR70 criteria (scenario 2) to determine the model’s robustness. Cost-effectiveness acceptability curves and cost-effectiveness frontiers were used to estimate the cost-effectiveness probability of each treatment strategy. A willingness-to-pay (WTP) threshold was defined as three times the US GDP per capita (