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2.
Kennedy Inst Ethics J ; 29(1): 1-31, 2019.
Article in English | MEDLINE | ID: mdl-31080175

ABSTRACT

Physicians' advocacy obligations are best understood as going beyond advocacy on behalf of individual patients, which I call the "individualistic view," to include advocacy for intelligent research-based allocation schemes that promote good outcomes and cost-effective care for all patients, which I call the "systemic view." This systemic view includes moving beyond self-interest to promote less-wasteful and more cost-conscious allocation decisions and the setting of priorities at all levels to expand health care access. It includes physician involvement in discussions with patients in the context of clinical care, involvement in the formulation and administration of benefit structures and other allocation policies, and, finally, involvement in promoting public dialogue about health care priorities. This involvement is based on a concept of a deliberative process that can result in "just enough" decisions within systems for the preservation and promotion of health care and other societal goods.


Subject(s)
Health Care Rationing/ethics , Health Services Accessibility/ethics , Patient Advocacy/ethics , Physician's Role , Resource Allocation/ethics , Social Justice/ethics , Cost Allocation/ethics , Decision Making , Health Care Costs/ethics , Health Care Rationing/economics , Health Priorities/economics , Health Priorities/ethics , Health Promotion/economics , Health Promotion/ethics , Health Services Accessibility/economics , Humans , Informed Consent/ethics , Insurance Benefits/economics , Insurance Benefits/ethics , Insurance, Health, Reimbursement/ethics , Patient Advocacy/economics , Resource Allocation/economics
4.
Biosci Trends ; 12(2): 109-115, 2018 May 13.
Article in English | MEDLINE | ID: mdl-29657242

ABSTRACT

Fee for services (FFS) is the prevailing method of payment in most Chinese public hospitals. Under this retrospective payment system, medical care providers are paid based on medical services and tend to over-treat to maximize their income, thereby contributing to rising medical costs and uncontrollable health expenditures to a large extent. Payment reform needs to be promptly implemented to move to a prospective payment plan. The diagnosis-related group (DRG)-based case-mix payment system, with its superior efficiency and containment of costs, has garnered increased attention and it represents a promising alternative. This article briefly describes the DRG-based case-mix payment system, it comparatively analyzes differences between FFS and case-mix funding systems, and it describes the implementation of DRGs in China. China's social and economic conditions differ across regions, so establishment of a national payment standard will take time and involve difficulties. No single method of provider payment is perfect. Measures to monitor and minimize the negative ethical implications and unintended effects of a DRG-based case-mix payment system are essential to ensuring the lasting social benefits of payment reform in Chinese public hospitals.


Subject(s)
Decision Support Systems, Management/economics , Diagnosis-Related Groups/economics , Fee-for-Service Plans/economics , Health Care Reform/economics , Hospitals, Public/economics , China , Decision Support Systems, Management/ethics , Diagnosis-Related Groups/ethics , Fee-for-Service Plans/ethics , Financing, Government/economics , Health Care Reform/ethics , Health Expenditures/ethics , Insurance Benefits/economics , Insurance Benefits/ethics , Length of Stay
5.
Z Evid Fortbild Qual Gesundhwes ; 108(2-3): 157-65, 2014.
Article in German | MEDLINE | ID: mdl-24780715

ABSTRACT

The economic pressure on German hospitals has increased considerably over the last years, mainly because of the introduction of a flat-rate payment system, and it will most likely further increase under the current demographic and political conditions. The growing dominance of economics in the inpatient sector increases the pressure on hospital staff and results in an increased volume of care (with sometimes inappropriate overtreatment) and uncontrolled rationing and a continuous struggle to maintain the quality of patient care. This development is not only alarming from an ethical perspective, but also impairs the hospital's economic performance. To counter the increasing economic pressure with "more ethics" does--according to the line of reasoning adopted in this article--not appear to be very successful. Rather, central ethical values in inpatient care have to become an integral part of hospital management. This value management first requires a clear definition of the normative standards, e.g. within a mission statement. Second, the realisation of the normative standards in routine inpatient care has to be systematically assessed, evaluated and managed. Since normative standards are difficult to measure objectively and on a quantitative scale, (repeated) surveys among hospital staff are the central instrument to secure the "internal quality" of the hospital. It appears very likely that more ethics in the hospital will pay off by improving its economic performance. The empirical proof for this conceptually extremely plausible hypothesis has yet to be provided.


Subject(s)
Ethics, Institutional , Insurance Benefits/ethics , National Health Programs/ethics , Quality of Life , Chronic Disease/economics , Chronic Disease/therapy , Cost-Benefit Analysis , Drug Costs , Germany , Health Care Rationing/economics , Health Care Rationing/ethics , Humans , Insurance Benefits/economics , National Health Programs/economics , Neoplasms/economics , Neoplasms/therapy
6.
Health Econ Policy Law ; 8(4): 529-35, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23962575

ABSTRACT

There has been an explosion of interest in the concept of 'universal health coverage', fuelled by publication of the World Health Report 2010. This paper argues that the system of user charges for health services is a fundamental determinant of levels of coverage. A charge can lead to a loss of utility in two ways. Citizens who are deterred from using services by the charge will suffer an adverse health impact. And citizens who use the service will suffer a loss of wealth. The role of social health insurance is threefold: to reduce households' financial risk associated with sickness; to promote enhanced access to needed health services; and to contribute to societal equity objectives, through an implicit financial transfer from rich to poor and healthy to sick. In principle, an optimal user charge policy can ensure that the social health insurance funds are used to best effect in pursuit of these objectives. This paper calls for a fundamental rethink of attitudes and policy towards user charges.


Subject(s)
Fees and Charges/ethics , Health Care Reform/economics , Health Services Accessibility/economics , Insurance Benefits/economics , Insurance, Health/economics , Universal Health Insurance/economics , Health Care Reform/ethics , Health Services Accessibility/ethics , Humans , Insurance Benefits/ethics , Insurance, Health/ethics , Universal Health Insurance/ethics
9.
PLoS One ; 7(11): e50395, 2012.
Article in English | MEDLINE | ID: mdl-23185616

ABSTRACT

BACKGROUND: Poverty due to illness has become a substantial social problem in rural China since the collapse of the rural Cooperative Medical System in the early 1980s. Although the Chinese government introduced the New Rural Cooperative Medical Schemes (NRCMS) in 2003, the associations between different health insurance benefit package designs and healthcare utilization remain largely unknown. Accordingly, we sought to examine the impact of health insurance benefit design on health care utilization. METHODS AND FINDINGS: We conducted a cross-sectional study using data from a household survey of 15,698 members of 4,209 randomly-selected households in 7 provinces, which were representative of the provinces along the north side of the Yellow River. Interviews were conducted face-to-face and in Mandarin. Our analytic sample included 9,762 respondents from 2,642 households. In each household, respondents indicated the type of health insurance benefit that the household had (coverage for inpatient care only or coverage for both inpatient and outpatient care) and the number of outpatient visits in the 30 days preceding the interview and the number of hospitalizations in the 365 days preceding the household interview. People who had both outpatient and inpatient coverage compared with inpatient coverage only had significantly more village-level outpatient visits, township-level outpatient visits, and total outpatient visits. Furthermore, the increased utilization of township and village-level outpatient care was experienced disproportionately by people who were poorer, whereas the increased inpatient utilization overall and at the county level was experienced disproportionately by people who were richer. CONCLUSION: The evidence from this study indicates that the design of health insurance benefits is an important policy tool that can affect the health services utilization and socioeconomic equity in service use at different levels. Without careful design, health insurance may not benefit those who are most in need of financial protection from health services expenses.


Subject(s)
Health Services Needs and Demand/economics , Insurance Benefits/economics , Insurance, Health/economics , Rural Health Services/organization & administration , Adolescent , Adult , China , Cross-Sectional Studies , Female , Health Services Needs and Demand/ethics , Health Services Needs and Demand/statistics & numerical data , Humans , Insurance Benefits/ethics , Insurance, Health/ethics , Insurance, Health/statistics & numerical data , Male , Middle Aged , Poverty , Rural Health Services/statistics & numerical data , Rural Population
10.
J Prim Prev ; 32(1): 3-15, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21274748

ABSTRACT

In recent decades, prevention policies--i.e., insurance policies constructed to give incentives to investments in prevention and thereby reduce reliance on insurance--have been much discussed both with regard to different kinds of market insurance and, albeit primarily within a European context and in relation to an ongoing discussion about the need for a shift towards an "active" welfare state, with regard to social insurance. The present contribution identifies normative issues that deserve attention in relation to a general introduction of prevention policies in market insurance and social insurance. It is argued that the importance of these normative issues suggests that arguments and distinctions drawn from moral and political philosophy should play a more prominent role both in the debate on the shift towards an active welfare state and the use of prevention policies in market insurance.


Subject(s)
Environmental Health/ethics , Health Behavior , Health Policy , Insurance, Health/ethics , Preventive Health Services/ethics , Cross-Cultural Comparison , Environmental Health/economics , Environmental Health/methods , Europe , Humans , Insurance Benefits/economics , Insurance Benefits/ethics , Insurance Benefits/standards , Insurance, Health/standards , Motivation , Preventive Health Services/economics , Preventive Health Services/methods , Social Security/ethics , Social Security/standards , United States
11.
Health Econ ; 19(5): 596-607, 2010 May.
Article in English | MEDLINE | ID: mdl-19459186

ABSTRACT

In societal priority setting between health programs for different patient groups, many people are reluctant to discriminate too strongly between those who can benefit much from treatment and those who can benefit moderately. We suggest that this view of distributive fairness has a counterpart in personal valuations of gains in health. Such valuations may be influenced by psychological reference points and diminishing marginal utility such that the individual utility of care in patient groups with different potentials may be more similar than what conventional QALY estimates suggest. In interviews in three convenience samples, there is some support for the hypothesis. Most respondents do not think that desire for treatment is significantly less in those who stand to gain only moderately compared with those who stand to gain much - even when the treatment is associated with a mortality risk. When stating insurance preferences, a majority of subjects express a greater concern for avoiding the worst states in question than for maximising expected value for money in terms of treatment effects. The tendency applies to outcomes in terms of both quality and quantity of life. Choices between prefixed response options fit well with oral explanations of these choices.


Subject(s)
Health Care Rationing/economics , Health Priorities/economics , Insurance, Health/economics , Quality-Adjusted Life Years , Cost-Benefit Analysis , Health Care Rationing/ethics , Health Priorities/ethics , Health Services Needs and Demand/economics , Health Services Needs and Demand/ethics , Humans , Insurance Benefits/economics , Insurance Benefits/ethics , Insurance, Health/ethics , Norway , Patient Preference/economics , Patient Preference/statistics & numerical data , Severity of Illness Index , State Medicine/economics , State Medicine/standards
12.
AJS ; 114(3): 738-80, 2008 Nov.
Article in English | MEDLINE | ID: mdl-19569397

ABSTRACT

This article adopts an institutional approach to describe the changing secondary market for life insurance in the United States. Since the 1990s, this market, in which investors buy strangers' life insurance policies, has grown in the face of considerable moral ambivalence. The author uses news reports and interviews to identify and describe three conceptions of this market: sacred revulsion, consumerist consolation, and rationalized reconciliation. Differences among the conceptions are considered in view of the institutional legacy of life insurance and its success in organizing practices, perceptions, and understandings about markets and death. From this case, the author draws implications for analyses of morals in markets, an important and emergent topic within economic sociology.


Subject(s)
Attitude to Death , Commerce/ethics , Insurance, Life/ethics , Morals , Ethics, Institutional , Humans , Insurance Benefits/ethics , Insurance, Life/economics , United States
13.
Health Aff (Millwood) ; 26(4): 1129-34, 2007.
Article in English | MEDLINE | ID: mdl-17630456

ABSTRACT

Patients, providers, and policy leaders need a new moral compass to guide them in the turbulent U.S. health care system. Task forces have proposed excellent ethical codes, but these have been seen as too abstract to provide guidance at the front lines. Harvard Pilgrim Health Care's ten-year experience with an organizational ethics program suggests ways in which health care organizations can strengthen transparency, consumer focus, and overall ethical performance and contribute to the national health policy dialogue.


Subject(s)
Health Care Rationing/ethics , Health Maintenance Organizations/ethics , Independent Practice Associations/ethics , Community Participation , Decision Making, Organizational , Ethics, Institutional , Financial Management/ethics , Gatekeeping/economics , Gatekeeping/ethics , Health Care Rationing/economics , Health Maintenance Organizations/economics , Humans , Independent Practice Associations/economics , Insurance Benefits/economics , Insurance Benefits/ethics , Maine , Massachusetts , New Hampshire , Organizational Case Studies , Piperazines/economics , Piperazines/supply & distribution , Purines/economics , Purines/supply & distribution , Quality of Health Care/economics , Quality of Health Care/ethics , Sildenafil Citrate , Sulfones/economics , Sulfones/supply & distribution
15.
Am J Bioeth ; 4(3): 87-100, 2004.
Article in English | MEDLINE | ID: mdl-16192158

ABSTRACT

Patients and physicians often perceive the current health care system to be unfair, in part because of the ways in which coverage decisions appear to be made. To address this problem the Ethical Force Program, a collaborative effort to create quality improvement tools for ethics in health care, has developed five content areas specifying ethical criteria for fair health care benefits design and administration. Each content area includes concrete recommendations and measurable expectations for performance improvement, which can be used by those organizations involved in the design and administration of health benefits packages, such as purchasers, health plans, benefits consultants, and practitioner groups.


Subject(s)
Bioethics , Insurance Benefits/ethics , Insurance Coverage/ethics , Insurance, Health/ethics , Quality Assurance, Health Care , Advisory Committees , Cost-Benefit Analysis , Empathy , Health Services Research , Humans , Insurance Benefits/economics , Insurance Coverage/economics , Insurance, Health/economics , Research Design , Social Justice , Total Quality Management , United States
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