Use-Value Assessment Legislation in the United States

1973 ◽  
Vol 49 (2) ◽  
pp. 206 ◽  
Author(s):  
Raleigh Barlowe ◽  
James G. Ahl ◽  
Gordon Bachman
2018 ◽  
Vol 3 (1) ◽  
pp. 1-3 ◽  
Author(s):  
Vakaramoko Diaby ◽  
Askal A. Ali ◽  
Alberto J. Montero

Author(s):  
Peter J. Neumann ◽  
Joshua T. Cohen ◽  
Daniel A. Ollendorf

New medications can provide substantial benefits, but high prescription drug prices have led to calls to contain costs. Even after accounting for discounts and rebates, average prices of leading brand-name drugs in the United States are two to four times higher than in other wealthy countries, raising questions about what these higher prices are buying us. With the advent of ever more targeted and powerful treatments, including cell- and gene-based therapies with multimillion dollar price tags, the need for sensible drug pricing policies will intensify. Price controls, common in other countries, seem appealing, but these measures can discourage innovation. Moreover, on what basis should policymakers develop such controls? This book argues that pricing prescription drugs to reflect the value they bring to patients, families, and society achieves the right balance. The book reviews the distinguishing features of the prescription drug market and explains why simple solutions like price controls and importing drugs from countries with lower drug prices are problematic without explicit assessments of value. It then describes how economists measure value, how value assessment for drugs is now being used in the United States, and what must happen going forward to overcome challenges.


2021 ◽  
pp. 95-111
Author(s):  
Neumann Peter J. ◽  
Cohen Joshua T. ◽  
Ollendorf Daniel A

As healthcare costs increased around the world in recent decades, countries incorporated health technology assessment (HTA) into their decisions about which new technologies to pay for and how much they should pay. This chapter describes approaches for drug value assessment that are part of the HTA procedures in these countries, highlighting England and Wales’ National Institute for Health and Care Excellence, perhaps the world’s most visible HTA body. We then describe efforts since the 1980s to introduce HTA in the United States, including Oregon’s Medicaid experiment and the federally funded Office of Technology Assessment. The chapter explores the roots of resistance to these efforts, including the notion of American exceptionalism—the belief that personal and economic freedom is paramount and deep resistance to the idea of healthcare rationing. The resistance, explained at least partly by these factors, ultimately led to a scaling back of HTA in the United States.


2021 ◽  
pp. 009539972110231
Author(s):  
Staci M. Zavattaro ◽  
Rebecca Entress ◽  
Jenna Tyler ◽  
Abdul-Akeem Sadiq

The COVID-19 pandemic, which is still gripping the world, brought death front and center into many people’s lives. In the United States, however, some of the deaths were treated as “more tragic” than others given someone’s economic use value coupled with dehumanizing language. Using Debord’s Society of the Spectacle, this is understood as a public values failure when economic productivity eclipses public health and humanity. Introducing a conceptual framework, this article explores this death narrative and implores public administrators to think about death management in a humane framing.


EDIS ◽  
2011 ◽  
Vol 2011 (8) ◽  
Author(s):  
Edward A. Evans ◽  
Mauricio Mosquera ◽  
Rodney L. Clouser ◽  
Jonathan Crane

Use-value assessment is the most widely used technique in the United States today for maintaining land in agricultural production. Although general guidelines are provided to Florida counties on the application of the state’s use-value assessment law, counties may vary slightly in the application and determination of the agricultural land’s value. Therefore, it is important for agricultural landowners to understand the guidelines used to determine value in the county where the land is assessed and taxed. This 6-page factsheet applies specifically to Miami-Dade County, Florida. Written by Edward A. Evans, Mauricio Mosquera, Rodney L. Clouser, and Jonathan Crane, and published by the UF Department of Food and Resource Economics, August 2011.


2021 ◽  
pp. 175-212
Author(s):  
Neumann Peter J. ◽  
Cohen Joshua T. ◽  
Ollendorf Daniel A

Value assessment is becoming more prominent in the United States, but challenges remain. First, should assessments include only impacts pertinent to payers or take a broader, “societal” perspective? Second, should quality adjusted life years (QALYs) be used to measure benefits? Critics complain that QALYs discriminate against people with health conditions and fail to capture aspects of health. Third, should assessments account for drug price reductions anticipated to accompany patent expirations? Prices do not always follow the expected pattern, but assuming they will not can lead to an overstatement of a drug’s true long-term cost. Fourth, how should data gaps be addressed? Outcome-based risk sharing agreements let payers and drug companies amend pricing decisions as additional data become available. Finally, who should conduct value assessments? Government agencies do so in many other countries, but that seems unlikely in the United States. For now, the Institute for Clinical and Economic Review, a private organization, has stepped into this role.


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