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Melissa M. Brown

Researcher at Emory University

Publications -  9
Citations -  86

Melissa M. Brown is an academic researcher from Emory University. The author has contributed to research in topics: Ranibizumab & Macular degeneration. The author has an hindex of 3, co-authored 9 publications receiving 36 citations. Previous affiliations of Melissa M. Brown include Thomas Jefferson University & Wills Eye Institute.

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Cost-Utility Analysis of VEGF Inhibitors for Treating Neovascular Age-Related Macular Degeneration.

TL;DR: 11-year and 2-year, healthcare sector (ophthalmic) and societal cost perspective reference case, cost-utility analyses comparing bevacizumab, ranibizumAB and aflibercept monotherapies for neovascular age-related macular degeneration (NVAMD) revealed early treatment was 138%-149% more cost-effective than late treatment.
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Cost-utility analysis of cataract surgery in the United States for the year 2018.

TL;DR: Cataract surgery in both the first eye and second eye, when analyzed by standard health economic methodologies, is highly cost-effective.
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A Cost-Benefit Analysis of VEGF-Inhibitor Therapy for Neovascular Age-Related Macular Degeneration in the United States.

TL;DR: Intravitreal NVAMD bevacIZumab, ranibizumab and aflibercept monotherapies accrue considerable financial, returns-on-investment to patients and insurers as they increase national wealth.
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The comparative effectiveness and cost-effectiveness of ranibizumab for neovascular macular degeneration revisited.

TL;DR: Ranibizumab therapy for neovascular AMD in 2015, considering treatment of both eyes, conferred greater patient value gain and improved cost-effectiveness than in 2006, as well as a large monetary return-on-investment to the Gross Domestic Product and nation’s wealth.
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Opportunities to Reduce Potential Bias in Ophthalmic Cost-Utility Analysis.

TL;DR: In this paper, a comparative effectiveness and cost-utility analysis for cataract surgery and intravitreal ranibizumab therapy for neovascular age-related macular degeneration (NVAMD) using vision utilities acquired from patients with ophthalmic disease and from surrogate individuals (nonophthalmic patient vision utilities) with and without integrating systemic comorbidity utility limits on vision utility gain was performed.