| Papers [1-15] of 100 :: [Page 1 of 7] | | Go to page : 1 2 3 4 5 6 7 —> | Search results on "HEALTH CARE HIV AIDS PATIENTS": |
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Health Care for HIV/AIDS Patients, 2002.
A review of the literature relevant to access to care, quality of care and funding for HIV and AIDS patients.
9,674 words (approx. 38.7 pages), 51 sources, MLA, $ 197.95
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Abstract
The difficulty of HIV/AIDS patients in acquiring adequate and equitable health care coverage is examined. The specific problem that is investigated concerns variations between HIV/AIDS patients and non HIV/AIDS patients in relation to denial of coverage, premium levels and experimental drug approval. A thorough review of published literature from different fields is conducted in support of this study. This literature is categorized, analyzed and collected as a unified body. Conclusions about the meaning of the various reviewed studies are presented. The primary conclusions of this study are the needs for portability and true universality in health care for all, as well as guarantees that expensive and experimental treatments will be covered. The writer explains that such changes would benefit not only HIV/AIDS patients, but all Americans as well.
Abstract
The Problem
Introduction
Statement of the Problem
Purpose to the Study
Importance of the Study
Scope of the Study
Review of the Literature
Access to Care for HIV/AIDS Patients
Bioethical Issues
Social Psychological Influences
Effects of Managed Care on Health Care Access for HIV/AIDS Patients
Quality of Care Received by HIV/AIDS Patients
HIV/AIDS Funding
Conclusion
References
From the Paper
"A critical factor affecting access to necessary health care for HIV/AIDS patients is health care insurance coverage. Approximately 60-percent of the American population is covered by private health care insurance programs (Congressional Budget Office, 1999). Most of these programs?the very great majority?are either fully or partly funded by employers, while the remainder of such programs is funded fully by the covered individuals and families. For the remaining 40 percent of the population, the delivery of health care services is dealt with in a variety of ways, as follows: (1) for approximately 25 percent of the population, health care services are funded by the federal government, primarily through the Medicaid and Medicare programs; (2) approximately five-percent of the population, both individuals and families, who for whatever reason do not choose to contract for health care insurance, are in the financial position to pay for health care services at the time of delivery; and (3) approximately 10 percent of the population defer health care services to the point where they can non longer be deferred, at which time they typically enter the health care system as emergency patients (Congressional Budget Office, 1999). As emergency patients, their care is more expensive than it would have been if treated earlier, and the care is either (1) paid by government or charity or (2) results in charges to the patients and their families that they seldom have any hope of ever paying. In the latter case, caregivers, typically public hospitals, must absorb the losses. "
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HIV-AIDS Patients and the Health Care System, 2002.
An assessment of minority access to the American health
care system focusing on the HIV-AIDS community.
5,926 words (approx. 23.7 pages), 36 sources, APA, $ 141.95
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Abstract
Approximately 12 percent of the American population is without any formal health care insurance coverage. The research problem investigated in this paper concerns minority access to health care. The central issue is the determination of the best approach to improve such access, especially in relation to HIV-AIDS patients.
Outline:
Introduction
Problem
Minorities and HIV-AIDS
Interaction with Health Care System
Racial and Ethnic Orientation
Structure and Method of Investigation
Structure
Method [Focus on Outcomes]
Minorities: Health Care Delivery Problems in the Community and Health Care System
Bioethical Issues
Failure to Address Racial Differences
Failure to Address Insurance Status Differences
Health Care Delivery and Accessibility
Delivery
Accessibility
HMOs and Fee-for-Service Providers
Social Psychological Influences
Distrust of the Health Care System
Health Beliefs of Minorities
Social Identity Influences
Minority Status and HIV-AIDS
HIV-AIDS and Minority Population Groups
Origins
Ethical Issues
HIV-AIDS Health Care for Minorities
Initiatives to Improve Minority Access to Health Care
Proposed Initiative
Conclusions and Recommendations
Restatement of Problem
Summary of Findings
Conclusions
Potential Solutions
Assessment
Recommendations
References
From the Paper
"Decisions made by health care professionals in the conduct of practice typically are reached within the context of an ethical framework (Marty, 1992). Clinical ethics is defined as the systematic identification, analysis, and resolution of ethical problems associated with the care of particular patients (Zuckerman, 1994). The goals of clinical ethics include protecting the rights and interests of patients, assisting clinicians in ethical decision-making, and encouraging cooperative relationships among patients and those close to patients, clinicians, and health care institutions. Important in the definition of clinical ethics is an emphasis on clinicians, not only physicians, thus underscoring the fact that clinical ethics needs to be a multi-disciplinary endeavor that encompasses the range of clinician expertise involved in patient care."
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AIDS/HIV Patients and Health Care, 2002.
A thorough examination of health care for HIV and AIDS patients and a review of the literature relevant to access to care, quality of care and funding.
9,785 words (approx. 39.1 pages), 46 sources, MLA, $ 199.95
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Abstract
A research study is proposed that investigates the experiences of HIV/AIDS patients with health insurance. The specific problem that is investigated concerns variations between HIV/AIDS patients and non HIV/AIDS patients in relation to denial of coverage, premium levels and experimental drug approval. Literature is reviewed is support of the proposed research study. The major bodies of literature reviewed are those related to access to care for HIV/AIDS patients, the quality of care received by HIV/AIDS patients and health care funding, especially as such funding applies to HIV/AIDS care and research and with a further emphasis on future funding prospects.
Introduction
Access to Care for HIV/AIDS Patients
Bioethical Issues
Social Psychological Influences
Effects of Managed Care on Health Care Access for HIV/AIDS Patients
Quality of Care Received by HIV/AIDS Patients
HIV/AIDS Funding
The Welfare State
Summary of the Literature Review
References
From the Paper
"A critical factor affecting access to necessary health care for HIV/AIDS patients is health care insurance coverage. Approximately 60-percent of the American population is covered by private health care insurance programs (Congressional Budget Office, 1999). Most of these programs?the very great majority?are either fully or partly funded by employers, while the remainder of such programs is funded fully by the covered individuals and families. For the remaining 40 percent of the population, the delivery of health care services is dealt with in a variety of ways, as follows: (1) for approximately 25 percent of the population, health care services are funded by the federal government, primarily through the Medicaid and Medicare programs; (2) approximately five-percent of the population, both individuals and families, who for whatever reason do not choose to contract for health care insurance, are in the financial position to pay for health care services at the time of delivery; and (3) approximately 10 percent of the population defer health care services to the point where they can non longer be deferred, at which time they typically enter the health care system as emergency patients (Congressional Budget Office, 1999). As emergency patients, their care is more expensive than it would have been if treated earlier, and the care is either (1) paid by government or charity or (2) results in charges to the patients and their families that they seldom have any hope of ever paying. In the latter case, caregivers, typically public hospitals, must absorb the losses.
When all is said and done, approximately 12 percent of the country?s population is without any formal health care insurance coverage (Minahan, 1999; Rosen, Fanshel, & Lutz, 1999), although some estimates of this proportion are higher. Further, in most cases, such individuals are not in a financial position to fund such services as required. With the size of the American population established at approximately 273 million by the 1999 census estimate (Population Reference Bureau, 2000), the 12 percent without formal health care insurance translates into approximately 33 million people."
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Emergency Room Treatment Of The HIV/Aid Patients., 2002.
An overview of emergency room treatment of HIV/Aid patients at the end of their illness.
650 words (approx. 2.6 pages), 5 sources, $ 26.95
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Abstract
This paper is on the topic of Emergency Care of the HIV/AIDS patient. Patients with HIV/Aids must often face emergency room treatment during the last stage of their illness. The question has been asked in the medical field, "Do doctors and nurses have to treat these patients?" What can the medical staff do to minimize their chances of getting the illness?
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Communication problems for HIV/AIDs Patients, 2002.
Doctor - patient communication and guidelines for those suffering from AID/HIV.
3,400 words (approx. 13.6 pages), 13 sources, $ 124.95
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Abstract
This paper looks at the communication problems between patients suffering from HIV/AIDs or for those who have an insecurity about discussing such problems with their general practitioners. Following on from this discussion is a brief case study and how to help the patient with his communication with his general practitioner.
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Minority Groups and the American Health Care System, 2002.
An assessment of minority access to the American Health
Care system, focusing on HIV-AIDS patients.
7,229 words (approx. 28.9 pages), 39 sources, APA, $ 160.95
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Abstract
Approximately 12 percent of America's population is without any formal health care insurance coverage, although some estimates of this proportion are higher. The research problem investigated in this study concerns minority access to health care. The central issue in the study is the determination of the best approach to improve such access, especially in relation to HIV-AIDS patients. The paper begins with a review of health care delivery problems for minority population groups, which is followed by a consideration of the HIV-AIDS issue among minority population groups. The primary focus of this assessment is on health care outcomes.
Paper Outline:
Introduction
Minorities and HIV-AIDS
Interaction with Health Care System
Racial and Ethnic Orientation
Structure and Method of Investigation
Minorities: Health Care Delivery Problems in the Community and Health Care System
Bioethical Issues
Failure to Address Racial Differences
Failure to Address Insurance Status Differences
Health Care Delivery and Accessibility
HMOs and Fee-for-Service Providers
Social Psychological Influences
Distrust of the Health Care System
Health Beliefs of Minorities
Social Identity Influences
Minority Status and HIV-AIDS
HIV-AIDS and Minority Population Groups
Origins
Ethical Issues
HIV-AIDS Health Care for Minorities
Initiatives to Improve Minority Access to Health Care
Proposed Initiative
Conclusions and Recommendations
Restatement of Problem
Summary of Findings
Conclusions
Potential Solutions
Assessment
Recommendations
From the Paper
"In the 1990s, one initiative designed to broaden access to health care services needs for the nation?s indigent involved the development of nurse-managed clinics targeting low-income persons. A nurse practitioner is a specially educated and trained nurse who provides some level of health care directly to patients without supervision by a physician.
Nurse managed clinics for the indigent are prominent in the nation?s inner cities. Nurse managed clinics such as those associated with the Kellogg Homeless Project in Washington, the Pine Street Inn in Boston, and the Los Angeles School of Nursing Health Center are delivering health care services to indigent persons at cost savings (compared to more traditional delivery venues) and in areas that would not otherwise be served by health care professionals (Sharp, 1992; Lutz, 1991)."
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AIDS and the Health Care Delivery System, 2005.
A look at the effects of AIDS and HIV on the health care delivery system.
1,413 words (approx. 5.7 pages), 7 sources, APA, $ 47.95
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Abstract
This paper begins with a description of the AIDS virus and how it effects the human body and an explanation of how the virus is transmitted. The paper then examines the costs of HIV infection to the health care system and how these additional costs affect the health care delivery system in general.
From the Paper
"In 1982, a disease known as Acquired Immune Deficiency Syndrome, or AIDS, was officially recognized in the United States (Shi & Singh, 2004). Since that time, the disease has become a world-wide epidemic, with more than 830,000 cases reported in the U.S. (National Institute of Health (NIH), 2003). The disease, caused by the Human Immunodeficiency Virus (HIV), has infected scores of people as well, with over 38 million people living with the virus worldwide in 2003. Since the first diagnosis of AIDS in 1982, over 20 million people have died worldwide (UNAIDS, 2004)."
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HIV/AIDS Ethics, 2007.
This paper discusses how health care professionals who encounter HIV/AIDS must rely on personal ethical principles.
818 words (approx. 3.3 pages), 3 sources, MLA, $ 29.95
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Abstract
The paper notes that caring for persons with HIV/AIDS has become a fundamental feature of all health care professions, due to the staggering rates of infection worldwide. The paper explains that becoming aware of the numerous nuances in ethical reasoning can help guide a health care professional's decisions in providing optimal care for patients diagnosed with HIV/AIDS. The paper discusses how preserving patient confidentiality and minimizing medical paternalism have become keys to providing ethical treatment for all patients. Yet, the paper points out that health care workers may have to break the patient's confidentiality in order to preserve public health, one of the key responsibilities of the health care professional.
From the Paper
"Patient autonomy is a central issue in health care in general. Preserving patient confidentiality and minimizing medical paternalism have become keys to providing ethical treatment for all patients. Patients with HIV/AIDS deserve similar ethical treatment and are entitled by law and by hospital regulations to a reasonable assumption of both autonomy and confidentiality. Decisions regarding courses of treatment, for example, should be made by the patient except in extreme cases in which patient consciousness has been compromised. Similarly, patients with HIV/AIDS assume the preservation of confidentiality. Ethical dilemmas regarding confidentiality and patient autonomy can easily arise when health care professionals suspect that a patient with HIV/AIDS is not taking adequate precautions to prevent the transmission of the illness."
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Impediments to Health Care Access for Low Income Visible Minorities, 2002.
Identifies causal factors for the gap in health care access for lower-income Americans and visible minorities and the more affluent members of America's majority.
29,350 words (approx. 117.4 pages), 135 sources, APA, $ 249.95
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Abstract
As the American population continues to become more diverse racially, members of visible minority groups within the population become more prominent. Simultaneously, with the increase in diversity, income distribution in the American economy has become more distorted. While economic growth in the United States has surged over the past decade, the income gap has widened; not only between the richest and poorest Americans, but also between moderate-income and low-income Americans. Members of visible minorities in the population tend to be represented disproportionately in the low-income and poverty classifications in the United States. While there is an abundance of implications of this state of affairs, one of the more crucial ones is access to health care. Individual and household financial capacity, the scarcity of employer-paid health insurance among small businesses, cultural differences based in social psychology and other factors frequently act as impediments to health care access for low-income individuals and households among visible minority population groups in the contemporary United States. This problem and these issues are investigated in this study. The study identifies causal factors for the gap in health care access between lower-income Americans and members of visible minorities in the United States, on the one hand, and more affluent Americans and members of the majority segment of the population, on the other hand. The initial chapter of this study delineates the problem investigated. Specific research questions are formulated and stated to provide greater focus for the investigation.
Social psychological theory and applied social psychology literature are reviewed in the second chapter. Literature relevant to the functioning of low-income and visible minority population groups in the United States within a social psychological context are reviewed in the third chapter. The fourth chapter is devoted to a review of literature relevant to both the health care system in the United States and the experiences of low-income and visible minority population groups in relation to health care access and health care delivery in the United States. An assessment of the problem investigated, performed within the structure of the research questions, is presented in the final (fifth) chapter. Conclusions drawn from the study findings are stated and recommendations for further research are made. The summary conclusions reached through the conduct of this study relate both to health care access and health care utilization by low-income persons and members of visible minorities. With respect to health care access, the summary conclusion reached is that a universal system of health care entitlement is required in the United States. In relation to health care utilization by low-income persons and members of visible minorities, the summary conclusion reached is that extensive education is required for both low-income persons and members of visible minorities, on the one hand, and health care providers, on the other hand. Low-income persons and members of visible minorities require education on the benefits and function of health care services, while health care providers require education in the social mores of the diverse populations they must serve.
Table of Contents:
Introduction
Problem Delineation
Background on the Problem
Statement of the Problem
Research Questions
Review of Relevant Social Psychology Theory and Literature
Introduction
Sociological Theory and Health Care
The Welfare State
Accessing Contemporary Health Care
Role of Ethics in Accessing Health Care
Alternative Health Care Delivery Systems
Chapter Conclusions
Social Functioning of Low-Income and Visible Minority Population Groups
Introduction
HIV/AIDS Related Behavior
Initiatives to Improve Health Care
Access and Behaviors
The American Health Care System and the Experiences of Low-Income and Visible Minority Groups
Introduction
The American Health Care System
Analysis of Health Care Delivery Systems
Care Quality
Alternative Approaches to Health Care
Bioethical Issues
Problems of Accessibility
Initiatives to Improve Minority Access
Chapter Conclusions
Assessment of the Problem Discussion, Recommendations for Further Research
Appendices
Annotated Bibliography
From the Paper
"Social Cognitive Theory [self-efficacy] emphasizes the role of expectancies, self-efficacy, peer normative influences, and social competency skills as key components affecting adolescents? behaviors (DiClemente, Lodico, Grinstead, Harper, Rickman, Evans, & Coates, 1996). The applicability of models based on social psychological principles for understanding African-Americans? decision-making and sexual behavior has been questioned because most such models tend to be individually-focused and do not take into account the social context in which the behavior is embedded (Cochran & Mays, 1993). Social cognitive theory, however, explicitly integrates behavioral, cognitive, and environmental factors as reciprocally interactive. Thus, given the hypothesized multi-factorial nature of sexual decision making and the potential impact of the high-risk social environment of the study population, approaches based on social cognitive theory are thought to be particularly relevant for understanding the myriad factors that may affect African-Americans? sexual behavior."
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HIV/AIDS, the Internet and Community Health, 2002.
How the internet is helping the HIV community obtain more information.
2,650 words (approx. 10.6 pages), 4 sources, $ 97.95
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Abstract
This paper examines information available on the Internet concerning HIV/AIDS. It gives a detailed analysis of four specific websites. It concludes with a summary of the uses of the Internet for public health nurses involved with youth testing HIV positive.
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HIV/AIDS Mitigation, 2008.
This paper examines good governance in the prevention and mitigation of HIV/AIDS, specifically as evidenced in the HIV/AIDS program of Zamboanga City, a highly-urbanized city in the Philippines.
6,910 words (approx. 27.6 pages), 9 sources, APA, $ 156.95
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Abstract
This paper stresses that stopping the spread of HIV/AIDS has to be made integral to any development endeavor aimed at improving the lives and well-being of citizens of the world. The author points out that the United Nations acknowledges that good governance has to be integrated into the creation and management of institutions, processes and programs aimed at beating the targets set forth in the "Millennium Declaration of 2000". The paper reviews and analyzes the present and future scenario of HIV/AIDS prevention and mitigation in the Philippines and identifies some elements of intervention needed to operationalize a strategy for good governance. The author underscores that the HIV/AIDS program of Zamboanga city is built around improved capacities for public administration and civil service, decentralization in delivery of services, transparency and accountability, expanded role of civil-society, and the centrality of participation grounded on the rule of law and human rights.
Table of Contents:
Abstract
Introduction
Conceptual Framework
Related Literature
Pro-Poor Policy Framework
Public Administration and Civil Services
Decentralization and Delivery of Services
Accountability and Transparency Situations and Context of HIV/AIDS in the Philippines
Sexually Transmitted Infections (STIs)
Socio-Economic Impact of HIV Aids
Participatory Approach
Cultural and Moral Dimensions
Grounding Development
Mobilizing the Cultural Resources
Key Lessons in Good Governance from the United Nations
Case in Point: Zamboanga City HIV/AIDS Program
Public-Civil Society Partnership
Organization and Management
Community-Oriented/ Community Based
Innovative Optimized Use of Infrastructure Support
Livelihood Assistance
Financial Resources
Lessons from HIV/Program Implementation
Conclusion
From the Paper
"According to the United Nations, a critical requisite for achieving the MDG's is a conducive and coherent policy framework. This involves first, the contextualization of the goals by each country, and down to identifying sectoral concerns and on to effective local responses. Responses and interventions to HIVAIDS entails a national policy framework that provides for effective decentralization of action and one that effectively coordinate implementation and resource mobilization as well as achieve a critical mass of support from the public in a much cost effective way. The policy framework to be pro-poor means, that it recognizes the social and economic implications of HIV/AIDS and seeks to integrate social and economic interventions to mitigate the spread of the infection and disease."
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HIV/AIDS, 2002.
An examination of the laws against discrimination to HIV/AIDS patients.
1,220 words (approx. 4.9 pages), 5 sources, MLA, $ 41.95
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Abstract
This paper gives a short description of the history and demographics of HIV/AIDS over the past few years and examines the development of laws in different countries to protect HIV/AIDS patients from prejudice. Criminals and vandals who target HIV/AIDS positive men and women are subject to harsher penalties because it is considered a hate crime to target someone based on a disability. In the Western World, disability is a special status, and it is treated as such with respect to the law.
From the Paper
"These laws were put in place to protect a class of people that were subject to discrimination. Discrimination in all forms begs certain philosophical, ethical questions. For example, there are only 36.1 million people with AIDS across the globe. This is less than 1% of the world?s population. Many more people die of hunger everyday. Instead of making medication widely available, why don?t we spend that money developing under-developed, hungry countries? Furthermore, AIDS/HIV can be infectious. One someone is sick, they stay away from people, so that they don?t get others sick."
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HIV/AIDS, 2004.
This paper discusses the costs of treating and not treating HIV/AIDS patients in the U.S. and globally.
1,430 words (approx. 5.7 pages), 4 sources, APA, $ 47.95
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Abstract
This paper stresses that government must take financial responsibility to control the rising cost of health care to HIV/AIDS patients. The issue isn't whether the United States can afford to treat, but whether the world can afford not to treat those affected by AIDS. The paper points out that, in the U.S., the cost of treating somebody who already has the disease costs between $20,000-$60,000 a year, depending on the available outpatient services. Pre-AIDS treatment now costs as little as $5,500 a year; but the cost of not treating a person with AIDS includes loss of income of patient and care givers, cost of treatment in homes, clinics, and hospital, funeral costs, deaths, survivor benefits, and the cost of orphans' care and support. The paper concludes that now there is no real solution to keeping costs manageable or to making sure that everyone, globally, who needs the drug treatments gets what they need.
From the Paper
"The cause of so many people being infected with this deadly disease is due to irresponsibility. Drug and alcohol abuse, sexual promiscuity, ignorance, unsafe sex and unfaithfulness within the sanction of holy matrimony all contribute to the infection rate skyrocketing worldwide. In looking at the preset condition of the HIV/AIDS virus current status, we have come a long way from the individual outbreak of the 1980's but we still have a lot further to go in totally understanding what we're dealing with concerning this disease."
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The Impact of Depression on HIV/AIDS Progression, 2006.
A look at the correlation between depression and the progression of HIV/AIDS in patients suffering from the disease.
2,504 words (approx. 10.0 pages), 10 sources, MLA, $ 76.95
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Abstract
This paper takes a look at depression in patients suffering with HIV/AIDS. According to the paper, depression is not caused by HIV directly, but it has been found that those who have HIV/AIDS often also suffer from depression. The paper goes on to say that it is important to understand how depression impacts HIV/AIDS with regard to the disease progression so that depression treatment can be effectively handled to reduce the advance of the disease in those who suffer from it.
Outline:
Background of the Problem
Conclusion
From the Paper
" One of the weaknesses that this study had, was the instrument used to determine depression. While it is a marker for depressive illness it does not determine the rate or severity of the depression in the individual patient, which may have been helpful in separating the results into more definable categories(McDermott, 1999)."
"The study concluded that depression does not speed the progress of HIV but admits because of some of the inconsistent issues, such as the failure to divide the degrees of depression within the participants that the study should be repeated using different instruments to determine its validity(McDermott, 1999)."
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Health Care Access for Low-Income Minorities, 2002.
This paper is a qualitative thesis, which assesses the impediments to health care access for low-income visible minorities in the United States.
30,578 words (approx. 122.3 pages), 135 sources, APA, $ 249.95
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Abstract
This paper, based in sociological and social psychology concepts, identifies the causal factors for the gap between lower-income Americans and members of visible minorities in the United States and more affluent Americans and members of the majority segment of the population with respect to health care access. The author concludes, after an extensive review of the literature, that a universal system of health care entitlement is required in the United States. The author suggests that an extensive education is required for low-income persons and members of visible minorities to know the benefits and function of health care services, and health care providers require education in the social mores of the diverse populations they must serve.
Table of Contents
Problem Delineation
Background on the Problem
Statement of the Problem
Research Questions
Review of Relevant Social Psychology Theory and Literature
Introduction
Sociological Theory and Health Care
The Welfare State
Accessing Contemporary Health Care
Role of Ethics in Accessing Health Care
Alternative Health Care Delivery Systems
Chapter Conclusions
Social Functioning of Low-Income and Visible Minority Population Groups
Introduction
HIV/AIDS Related Behavior
Initiatives to Improve Health Care Access and Behaviors
The American Health Care System and The Health Care Experiences of Low-Income and Visible Minority Population Groups
Introduction
The American Health Care System
Delivery of Health Care to the Poor
Care Quality
Alternative Approaches to Delivery
Bioethical Issues
Problems of Accessibility
Initiatives to Improve Access
Chapter Conclusions
Assessment of the Problem
Discussion
Recommendations for Further Research
Annotated Bibliography
From the Paper
"One of the major impediments to the attainment of universal access to healthcare in the United States is the functioning of for-profit Health Maintenance Organizations (HMOs) and managed care organizations (MCOs). These organizations are investor-owned organizations that are in business to make a profit on healthcare delivery. Non-for-profit healthcare organizations also must earn a profit on their operations in order to be able to compensate and train staff, acquire new technology, and generally improve the quality of their services. Unlike investor-owned healthcare companies, however, non-for-profit organizations are not driven by share prices and the bottom-line mentality of for-profit companies. Thus, patient-centered care in not-for-profit healthcare organizations may be contrasted with the investor orientation of the for-profit healthcare companies. Recent decisions by for-profit healthcare companies to drop their Medicare healthcare groups because of substandard profit growth illustrates as no amount of rhetoric can the precedent of investor concerns over patient concerns in the for-profit healthcare companies."
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