Does Cost-effectiveness Analysis Have a Role in US Managed Care Drug Formularies? : an Empirical Study of Utilization, Costs, Outcomes, and Elasticity of Demand of a Value-based Formulary

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ISBN 13 :
Total Pages : 51 pages
Book Rating : 4.:/5 (945 download)

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Book Synopsis Does Cost-effectiveness Analysis Have a Role in US Managed Care Drug Formularies? : an Empirical Study of Utilization, Costs, Outcomes, and Elasticity of Demand of a Value-based Formulary by : Kai Yeung

Download or read book Does Cost-effectiveness Analysis Have a Role in US Managed Care Drug Formularies? : an Empirical Study of Utilization, Costs, Outcomes, and Elasticity of Demand of a Value-based Formulary written by Kai Yeung and published by . This book was released on 2015 with total page 51 pages. Available in PDF, EPUB and Kindle. Book excerpt: The standard economic model for health insurance posits that in order to account for moral hazard in a population for which there is varying marginal benefit of treatment that is unknown to the insurer, cost-sharing should be proportional to the price elasticity of demand. Yet, many have observed that when faced with cost-sharing, consumers may reduce utilization to suboptimal levels due to underestimation of the marginal benefit of treatment. Hence, optimal health insurance design requires consideration of both insurer and consumer information asymmetries regarding the marginal benefits of treatment. This dissertation investigates whether cost-effectiveness analysis (CEA) may be useful for optimizing insurance in the face of insurer and consumer information asymmetries. In 2010, Premera Blue Cross, a large non-profit health plan in the Pacific Northwest implemented a value based formulary (VBF) benefit among their own employees and dependents that explicitly uses CEA to inform medication placement within copayment tiers. We exploit this natural experiment to empirically assess the impact of the VBF on medication utilization and other health services utilization and the impact of the VBF on medication costs and non-medication costs from the member, health plan, and overall perspectives. We also estimate price elasticities of demand for pharmaceuticals overall, by therapeutic class, by brand-generic status, and finally by the copayment tiers informed by CEA. In the first paper, we use individual-level data from July 2006 to June 2013 drawn from the employees of Premera and their dependents as well as data from employees and dependents of 5 employer sponsored plans administrated by Premera and chosen based on similarity to the intervention group in industry classification. After controlling for member demographics and plan characteristics and secular trends using an interrupted time series design with concurrent control, we find that the VBF shifted member medication utilization towards drugs placed in lower copayment tiers. The VBF also was associated with increased member medication costs and decreased health plan medication costs, leading to a net medication savings of $8 per member per month (PMPM) (95% confidence interval [CI], -$15, -$2). Over the 3 year period of the study, the medication cost savings totaled over $1.1 million USD. The findings regarding non-medication costs were comparatively small and not statistically significant. Total costs decreased by $9 PMPM (95% CI, -$49, $30) but was not statistically significant. We did not detect any changes in the probability or the number of emergency department visits, hospitalizations, or office visits. This evaluation suggests that the VBF may have reduced overall medication costs without negatively impacting utilization of other health services – a proxy for adverse outcomes. In the second paper, we use data from July 2009 to June 2011 drawn from the employees of Premera and their dependents to construct a medication level dataset of 284 unique medications. These medications accounted for 79.3% of the prescription medication volume over the period of observation. After controlling for member demographics and using a pre-post design, we find that our elasticity estimates of -0.14 for the probability of filling a medication were similar to the overall elasticity estimates of -0.17 from the RAND Health Insurance Experiment. We also find that the estimates by therapeutic class and brand-generic status also were generally similar to published studies. Finally, we estimate of price elasticity of demand by copayment tiers informed by CEA. We found that elasticity estimates for the probability of fill and days’ supply of medication respectively were -0.07 and -0.06 for the preventive tier, -0.09 and 0.08 for tier 1, -0.26 and -0.26 for tier 2, -0.27 and -0.32 for tier 3, and -0.45 and -0.55 for tier 4. Thus we observed a general trend of increasing elasticity with increasing copayment tiers. These results suggest that a cost sharing strategy based on elasticity estimates may be similar to a cost sharing strategy informed by CEA. Furthermore, since in the first paper we observed that the VBF was associated with decreased medication costs without negatively impacting health services utilization, we suggest that the use of CEA to inform medication copayment tiers may have a role in optimizing insurance benefit design. Contemporaneous with the implementation of the VBF on July 2010, the US health insurance market has experienced many changes. The passage of the Patient Protection and Affordable Care Act (PPACA) in March 2010 and the progressive implementation of many provisions in that law have fundamentally altered the insurance and provider markets. One provision in PPACA explicitly supports the development of value-based insurance design. This provision has led to the promulgation of federal regulations that have focused on eliminating cost-sharing for certain preventive services. The PPACA also has mandated coverage of preventive services recommended by Advisory Committee on Immunization Practices and the US Preventive Services Task Force. Due to the direct influence these national advisory bodies now have on the coverage of preventive services, others have advocated use of CEA by these bodies to inform the relative costs and benefits of their decisions. Our research suggests that the application of CEA to explicitly inform cost-sharing may allow the expansion of value-based principles beyond waivers of cost-sharing for specific “high value” services. Another important provision of PPACA is the formation of Accountable Care Organizations (ACOs) by health care providers that are accountable for the quality, cost, and overall care of Medicare beneficiaries. Under this provision, the ACOs enter into payment contracts that share both financial risk and savings for the care of beneficiaries. This shift in financial risk may cause ACOs to become more aware of the cost of health care. Further, since providers can greatly influence medications utilization behavior, ACOs may become an important lever for the introduction of value-based principles in integrated delivery system models. Finally, PPACA and the Health Information Technology for Economic and Clinical Health Act of 2009 have financially incentivized the use of electronic health records (EHR). It is possible that future iterations of VBFs could utilize patient-level information from EHRs to more accurately triangulate levels of cost-sharing with better estimates of treatment benefit. Further, the adoption of electronic health records may allow for future evaluations of VBFs that are able to assess true health outcomes. In sum, changes in the health insurance market present many opportunities and challenges for the adoption and evaluation of value-based principles in health insurance design. Policymakers and researchers should carefully assess such dynamics when considering the role of value-based insurance in health insurance markets in the future. Footnote: A joint regulation issued by the Department of Health and Human Services, the Internal Revenue Service and the Department of Labor, regarding the elimination copayments for certain preventive services states “The Departments recognize the important role that value-based insurance design can play in promoting the use of appropriate preventive services.”

Making Medicines Affordable

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Publisher : National Academies Press
ISBN 13 : 0309468086
Total Pages : 235 pages
Book Rating : 4.3/5 (94 download)

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Book Synopsis Making Medicines Affordable by : National Academies of Sciences, Engineering, and Medicine

Download or read book Making Medicines Affordable written by National Academies of Sciences, Engineering, and Medicine and published by National Academies Press. This book was released on 2018-03-01 with total page 235 pages. Available in PDF, EPUB and Kindle. Book excerpt: Thanks to remarkable advances in modern health care attributable to science, engineering, and medicine, it is now possible to cure or manage illnesses that were long deemed untreatable. At the same time, however, the United States is facing the vexing challenge of a seemingly uncontrolled rise in the cost of health care. Total medical expenditures are rapidly approaching 20 percent of the gross domestic product and are crowding out other priorities of national importance. The use of increasingly expensive prescription drugs is a significant part of this problem, making the cost of biopharmaceuticals a serious national concern with broad political implications. Especially with the highly visible and very large price increases for prescription drugs that have occurred in recent years, finding a way to make prescription medicinesâ€"and health care at largeâ€"more affordable for everyone has become a socioeconomic imperative. Affordability is a complex function of factors, including not just the prices of the drugs themselves, but also the details of an individual's insurance coverage and the number of medical conditions that an individual or family confronts. Therefore, any solution to the affordability issue will require considering all of these factors together. The current high and increasing costs of prescription drugsâ€"coupled with the broader trends in overall health care costsâ€"is unsustainable to society as a whole. Making Medicines Affordable examines patient access to affordable and effective therapies, with emphasis on drug pricing, inflation in the cost of drugs, and insurance design. This report explores structural and policy factors influencing drug pricing, drug access programs, the emerging role of comparative effectiveness assessments in payment policies, changing finances of medical practice with regard to drug costs and reimbursement, and measures to prevent drug shortages and foster continued innovation in drug development. It makes recommendations for policy actions that could address drug price trends, improve patient access to affordable and effective treatments, and encourage innovations that address significant needs in health care.

Exploring the Uptake of Value-based Formulary Strategies and Their Application to Specialty Drugs

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Publisher :
ISBN 13 :
Total Pages : 79 pages
Book Rating : 4.:/5 (119 download)

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Book Synopsis Exploring the Uptake of Value-based Formulary Strategies and Their Application to Specialty Drugs by : Elizabeth D Brouwer

Download or read book Exploring the Uptake of Value-based Formulary Strategies and Their Application to Specialty Drugs written by Elizabeth D Brouwer and published by . This book was released on 2020 with total page 79 pages. Available in PDF, EPUB and Kindle. Book excerpt: Background: Value-based formularies (VBF) are a way to implement the overarching idea of value-based insurance design (VBID) by tying pharmacy cost-sharing to value based on cost-effectiveness evidence. Empirical evidence over the last decade has shown that this strategy can reduce patient costs, increase drug adherence, and be cost neutral for payers when applied to many traditional drugs, such as antihypertensive and antihyperlipidemic therapies. It is unclear whether these same outcomes could be achieved if VBF strategies were applied to other drugs, such as specialty drugs. Specialty drugs are broadly defined as expensive, complex, and requiring special handling. Their high costs make them an attractive candidate for cost-containment policies such as VBF, however the potential lack of therapy alternatives to some specialty drugs along with the ubiquitous practice of manufacturer patient assistance programs may undermine the influence of payers' cost-sharing strategies. Objective: This dissertation seeks to evaluate the potential of value-based formulary strategies to effectively improve access and affordability of specialty medications. Aims: The first aim seeks to estimate the implicit adoption of cost-effectiveness driven value-based formularies in private health insurance (2010-2013) by using a random effects model of the effect of value tier on out-of-pocket costs over time. The second aim seeks to estimate the price elasticity of demand for multiple sclerosis (MS) specialty medications in the Kaiser Permanente Washington system accounting for copay assistance using a two-part model with patient assistance programs as a source of price variation. Study Implications: This dissertation will provide evidence to stakeholders (particularly payers) regarding 1) the potential utility of value-based formularies in the face of diminishing marginal gains from increased generic drug use, and 2) the impact of patient assistance programs on patient demand for specialty drug therapies and the subsequent implications for applying VBID strategies to specialty medications.

How Increased Competition from Generic Drugs Has Affected Prices and Returns in the Pharmaceutical Industry

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Publisher : U.S. Government Printing Office
ISBN 13 :
Total Pages : 94 pages
Book Rating : 4.:/5 (327 download)

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Book Synopsis How Increased Competition from Generic Drugs Has Affected Prices and Returns in the Pharmaceutical Industry by :

Download or read book How Increased Competition from Generic Drugs Has Affected Prices and Returns in the Pharmaceutical Industry written by and published by U.S. Government Printing Office. This book was released on 1998 with total page 94 pages. Available in PDF, EPUB and Kindle. Book excerpt:

China's Healthcare System and Reform

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Publisher : Cambridge University Press
ISBN 13 : 1316738396
Total Pages : 744 pages
Book Rating : 4.3/5 (167 download)

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Book Synopsis China's Healthcare System and Reform by : Lawton Robert Burns

Download or read book China's Healthcare System and Reform written by Lawton Robert Burns and published by Cambridge University Press. This book was released on 2017-01-26 with total page 744 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume provides a comprehensive review of China's healthcare system and policy reforms in the context of the global economy. Following a value-chain framework, the 16 chapters cover the payers, the providers, and the producers (manufacturers) in China's system. It also provides a detailed analysis of the historical development of China's healthcare system, the current state of its broad reforms, and the uneasy balance between China's market-driven approach and governmental regulation. Most importantly, it devotes considerable attention to the major problems confronting China, including chronic illness, public health, and long-term care and economic security for the elderly. Burns and Liu have assembled the latest research from leading health economists and political scientists, as well as senior public health officials and corporate executives, making this book an essential read for industry professionals, policymakers, researchers, and students studying comparative health systems across the world.

The Pharmaceutical Industry

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Publisher : DIANE Publishing
ISBN 13 : 1428953639
Total Pages : 226 pages
Book Rating : 4.4/5 (289 download)

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Book Synopsis The Pharmaceutical Industry by : Roy Levy

Download or read book The Pharmaceutical Industry written by Roy Levy and published by DIANE Publishing. This book was released on 1999 with total page 226 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Medical Care Output and Productivity

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Publisher :
ISBN 13 :
Total Pages : 630 pages
Book Rating : 4.X/5 (4 download)

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Book Synopsis Medical Care Output and Productivity by : David M. Cutler

Download or read book Medical Care Output and Productivity written by David M. Cutler and published by . This book was released on 2001 with total page 630 pages. Available in PDF, EPUB and Kindle. Book excerpt: With the United States and other developed nations spending as much as 14 percent of their GDP on medical care, economists and policy analysts are asking what these countries are getting in return. Yet it remains frustrating and difficult to measure the productivity of the medical care service industries. This volume takes aim at that problem, while taking stock of where we are in our attempts to solve it.

Promoting Access to Medical Technologies and Innovation - Intersections between Public Health, Intellectual Property and Trade

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Publisher : WIPO
ISBN 13 : 9280523082
Total Pages : 259 pages
Book Rating : 4.2/5 (85 download)

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Book Synopsis Promoting Access to Medical Technologies and Innovation - Intersections between Public Health, Intellectual Property and Trade by : World Intellectual Property Organization

Download or read book Promoting Access to Medical Technologies and Innovation - Intersections between Public Health, Intellectual Property and Trade written by World Intellectual Property Organization and published by WIPO. This book was released on 2013 with total page 259 pages. Available in PDF, EPUB and Kindle. Book excerpt: This study has emerged from an ongoing program of trilateral cooperation between WHO, WTO and WIPO. It responds to an increasing demand, particularly in developing countries, for strengthened capacity for informed policy-making in areas of intersection between health, trade and IP, focusing on access to and innovation of medicines and other medical technologies.

Handbook of Health Economics

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Publisher : Elsevier
ISBN 13 : 0080544177
Total Pages : 1000 pages
Book Rating : 4.0/5 (85 download)

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Book Synopsis Handbook of Health Economics by : A J. Culyer

Download or read book Handbook of Health Economics written by A J. Culyer and published by Elsevier. This book was released on 2000-07-19 with total page 1000 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Handbook of Health Economics provide an up-to-date survey of the burgeoning literature in health economics. As a relatively recent subdiscipline of economics, health economics has been remarkably successful. It has made or stimulated numerous contributions to various areas of the main discipline: the theory of human capital; the economics of insurance; principal-agent theory; asymmetric information; econometrics; the theory of incomplete markets; and the foundations of welfare economics, among others. Perhaps it has had an even greater effect outside the field of economics, introducing terms such as opportunity cost, elasticity, the margin, and the production function into medical parlance. Indeed, health economists are likely to be as heavily cited in the clinical as in the economics literature. Partly because of the large share of public resources that health care commands in almost every developed country, health policy is often a contentious and visible issue; elections have sometimes turned on issues of health policy. Showing the versatility of economic theory, health economics and health economists have usually been part of policy debates, despite the vast differences in medical care institutions across countries. The publication of the first Handbook of Health Economics marks another step in the evolution of health economics.

Extending the Cure

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Publisher : Routledge
ISBN 13 : 1136527605
Total Pages : 193 pages
Book Rating : 4.1/5 (365 download)

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Book Synopsis Extending the Cure by : Ramanan Laxminarayan

Download or read book Extending the Cure written by Ramanan Laxminarayan and published by Routledge. This book was released on 2010-09-30 with total page 193 pages. Available in PDF, EPUB and Kindle. Book excerpt: Our ability to treat common bacterial infections with antibiotics goes back only 65 years. However, the authors of this report make it clear that sustaining a supply of effective and affordable antibiotics cannot be without changes to the incentives facing patients, physicians, hospitals, insurers, and pharmaceutical manufacturers. In fact, increasing resistance to these drugs is already exacting a terrible price. Every day in the United States, approximately 172 men, women, and children die from infections caused by antibiotic-resistant bacteria in hospitals alone. Beyond those deaths, antibiotic resistance is costing billions of dollars through prolonged hospital stays and the need for doctors to resort to ever more costly drugs to use as substitute treatments. Extending the Cure presents the problem of antibiotic resistance as a conflict between individual decision makers and their short-term interest and the interest of society as a whole, in both present and future: The effort that doctors make to please each patient by prescribing a drug when it might not be properly indicated, poor monitoring of discharged patients to ensure that they do not transmit drug-resistant pathogens to other persons, excesses in the marketing of new antibiotics, and the broad overuse of antibiotics all contribute to the development and spread of antibiotic-resistant bacteria. The book explores a range of policy options that would encourage patients, health care providers, and managed care organizations to serve as more responsible stewards of existing antibiotics as well as proposals that would give pharmaceutical firms greater incentives to develop new antibiotics and avoid overselling. If the problem continues unaddressed, antibiotic resistance has the potential to derail the health care system and return us to a world where people of all ages routinely die from simple infections. As a basis for future research and a spur to a critically important dialogue, Extending the Cure is a fundamental first step in addressing this public health crisis. The Extending the Cure project is funded in part by the Robert Wood Johnson Foundation through its Pioneer Portfolio.

Frontiers in Health Policy Research

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Publisher : MIT Press
ISBN 13 : 9780262532662
Total Pages : 196 pages
Book Rating : 4.5/5 (326 download)

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Book Synopsis Frontiers in Health Policy Research by : David M. Cutler

Download or read book Frontiers in Health Policy Research written by David M. Cutler and published by MIT Press. This book was released on 2004 with total page 196 pages. Available in PDF, EPUB and Kindle. Book excerpt: Leading economists discuss current health policy challenges, including prescription drugs benefits as a component of Medicare and conversion to for-profit health plans.

OECD Health Policy Studies Pharmaceutical Pricing Policies in a Global Market

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Publisher : OECD Publishing
ISBN 13 : 9264044159
Total Pages : 219 pages
Book Rating : 4.2/5 (64 download)

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Book Synopsis OECD Health Policy Studies Pharmaceutical Pricing Policies in a Global Market by : OECD

Download or read book OECD Health Policy Studies Pharmaceutical Pricing Policies in a Global Market written by OECD and published by OECD Publishing. This book was released on 2008-09-24 with total page 219 pages. Available in PDF, EPUB and Kindle. Book excerpt: This report assesses how pharmaceutical pricing and reimbursement policies have contributed to the achievement of certain health policy objectives, and it examines the national and transnational effects of these policies.

The Oxford Handbook of the Economics of the Biopharmaceutical Industry

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Publisher : Oxford University Press
ISBN 13 : 0199909261
Total Pages : 618 pages
Book Rating : 4.1/5 (999 download)

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Book Synopsis The Oxford Handbook of the Economics of the Biopharmaceutical Industry by : Patricia M. Danzon

Download or read book The Oxford Handbook of the Economics of the Biopharmaceutical Industry written by Patricia M. Danzon and published by Oxford University Press. This book was released on 2012-04-12 with total page 618 pages. Available in PDF, EPUB and Kindle. Book excerpt: The biopharmaceutical industry has been a major driver of technological change in health care, producing unprecedented benefits for patients, cost challenges for payers, and profits for shareholders. As consumers and companies benefit from access to new drugs, policymakers around the globe seek mechanisms to control prices and expenditures commensurate with value. More recently the 1990s productivity boom of new products has turned into a productivity bust, with fewer and more modest innovations, and flat or declining revenues for innovative firms as generics replace their former blockbuster products. This timely volume examines the economics of the biopharmaceutical industry, with eighteen chapters by leading academic health economists. Part one examines the economics of biopharmaceutical innovation including determinants of the costs and returns to new drug development; how capital markets finance R&D and how costs of financing the biopharmaceutical industry compare to financing costs for other industries; the effects of safety and efficacy regulation by the Food and Drug Administration (FDA) and of price and reimbursement regulation on incentives for innovation; and the role of patents and regulatory exclusivities. Part two examines the market for biopharmaceuticals with chapters on prices and reimbursement in the US, the EU, and other industrialized countries, and in developing countries. It looks at the optimal design of insurance for drugs and the effects of cost sharing on spending and on health outcomes; how to measure the value of pharmaceuticals using pharmacoeconomics, including theory, practical challenges, and policy issues; how to measure pharmaceutical price growth over time and recent evidence; empirical evidence on the value of pharmaceuticals in terms of health outcomes; promotion of pharmaceuticals to physicians and consumers; the economics of vaccines; and a review of the evidence on effects of mergers, acquisitions and alliances. Each chapter summarizes the latest insights from theory and recent empirical evidence, and outlines important unanswered questions and areas for future research. Based on solid economics, it is nevertheless written in terms accessible to the general reader. The book is thus recommended reading for academic economists and non-economists, and for those in industry and policy who wish to understand the economics of this fascinating industry.

A Star in the East

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Publisher :
ISBN 13 : 9786161128203
Total Pages : 219 pages
Book Rating : 4.1/5 (282 download)

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Book Synopsis A Star in the East by : Anthony J. Culyer

Download or read book A Star in the East written by Anthony J. Culyer and published by . This book was released on 2016 with total page 219 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Countering the Problem of Falsified and Substandard Drugs

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Publisher : National Academies Press
ISBN 13 : 0309269393
Total Pages : 377 pages
Book Rating : 4.3/5 (92 download)

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Book Synopsis Countering the Problem of Falsified and Substandard Drugs by : Institute of Medicine

Download or read book Countering the Problem of Falsified and Substandard Drugs written by Institute of Medicine and published by National Academies Press. This book was released on 2013-06-20 with total page 377 pages. Available in PDF, EPUB and Kindle. Book excerpt: The adulteration and fraudulent manufacture of medicines is an old problem, vastly aggravated by modern manufacturing and trade. In the last decade, impotent antimicrobial drugs have compromised the treatment of many deadly diseases in poor countries. More recently, negligent production at a Massachusetts compounding pharmacy sickened hundreds of Americans. While the national drugs regulatory authority (hereafter, the regulatory authority) is responsible for the safety of a country's drug supply, no single country can entirely guarantee this today. The once common use of the term counterfeit to describe any drug that is not what it claims to be is at the heart of the argument. In a narrow, legal sense a counterfeit drug is one that infringes on a registered trademark. The lay meaning is much broader, including any drug made with intentional deceit. Some generic drug companies and civil society groups object to calling bad medicines counterfeit, seeing it as the deliberate conflation of public health and intellectual property concerns. Countering the Problem of Falsified and Substandard Drugs accepts the narrow meaning of counterfeit, and, because the nuances of trademark infringement must be dealt with by courts, case by case, the report does not discuss the problem of counterfeit medicines.

Valuing Health for Policy

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Publisher : University of Chicago Press
ISBN 13 : 9780226807133
Total Pages : 470 pages
Book Rating : 4.8/5 (71 download)

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Book Synopsis Valuing Health for Policy by : George Tolley

Download or read book Valuing Health for Policy written by George Tolley and published by University of Chicago Press. This book was released on 1994-11 with total page 470 pages. Available in PDF, EPUB and Kindle. Book excerpt: How stringent should environmental and occupational safety regulations be? How far should Medicaid support go? Should funding for research on Alzheimer's disease be increased? Should more money be spent on programs to discourage smoking? What are appropriate ways to determine damages in wrongful injury or death suits? Toward answering such questions, this volume examines various models of health valuation, including the cost-of-illness, preventive-expenditures, and quality-adjusted-life-year approaches. The authors favor a willingness-to-pay approach grounded in individual preferences.

The Pharmacist Guide to Implementing Pharmaceutical Care

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Publisher : Springer
ISBN 13 : 3319925768
Total Pages : 506 pages
Book Rating : 4.3/5 (199 download)

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Book Synopsis The Pharmacist Guide to Implementing Pharmaceutical Care by : Filipa Alves da Costa

Download or read book The Pharmacist Guide to Implementing Pharmaceutical Care written by Filipa Alves da Costa and published by Springer. This book was released on 2018-09-17 with total page 506 pages. Available in PDF, EPUB and Kindle. Book excerpt: Through the contributions of global experts, this book meets the growing need to understand the implementation and development of pharmaceutical care. Pharmaceutical Care Implementation details the clinical pharmacist's role in providing care to different kind of patients using clinical strategies that improve humanistic, economic and clinical outcomes. Written with a focus for students and pharmacists, this book offers multiple scenarios that serve to improve technical skills. These examples show step-by-step implementation processes from pharmacists who have worked for many years in these fields: drug-related problems, pharmaceutical care in different settings (community, hospital, home care), research outcomes, communication skills, indicators, advertising, remuneration of practice, standards, guidelines, protocols and teaching approaches for universities. Readers will use this book to:- Improve their skills to prevent, detect and solve drug-related problems - Understand the characteristics of care for patients in different settings- Consolidate knowledge from different global research outcomes- Develop and improve communication skills to establish relationships with patients and healthcare professionals.- Learn to use indicators, standards,guidelines,and protocols to guide and evaluate pharmaceutical care performance- Use different tools to advertise pharmaceutical care services- Document pharmaceutical care practices and create evidence for remuneration