| Papers [1-15] of 100 :: [Page 1 of 7] | | Go to page : 1 2 3 4 5 6 7 —> | Search results on "PATIENT": |
|
|
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
»
Click here to show/hide summary
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."
| |
|
Praying With Patients, 2005.
This paper looks at the ethical dilemma of praying with patients from a nursing perspective.
4,859 words (approx. 19.4 pages), 10 sources, APA, $ 123.95
»
Click here to show/hide summary
Abstract
The current controversy regarding the ethical considerations of nurses praying with patients has not always been an issue. In the past, prayer was an acceptable treatment method for the sick. This paper shows that while nurses do pray with patients, it is still controversial for some professionals. Supporters of Holistic nursing practices believe that nurses should not only pray with patients but also receive training on the subject, while many people believe that prayer is an aspect of religion and to pray with a patient would be to impose religious values on the patient. This paper examines the many aspects of this controversy.
Table of Contents:
Abstract
History of Praying with Patients
The Current Practice of Prayer with Patients
Ethical Values Affecting Prayer with Patients
Ethical Theory of Divine Command
Ethical Principles
Nursing Perspective of Praying with Patients
Conclusion
Bibliography
From the Paper
"If a nurse was a divine-theory believer, she could be inclined to pray for a patient due to Biblical knowledge or a personal request from God. The problem with only using divine-theory to justify praying with patients is that, "Divine-command theory rightly indicates that our sense of obligation ultimately flows from our relationship with God" (Vacek 1996 633). At this point the nurse would not be using personal motivation and a nurse must be motivated internally to become as independent as possible. Nurses are obligated to solve this dilemma of whether or not to pray with patients by using Divine Theory because it is part of the training they receive while being educated to nurse. The field of nursing lays part of it's foundation on Divine Theory so it should therefore be utilized by nurses in all situations possible."
| |
|
Aquatic Therapy for Multiple Sclerosis Patients, 2002.
Reviews literature on Aquatic Therapy and its general effects on patients with Multiple Sclerosis (MS) in order to evaluate the effectiveness of this form of rehabilitation for MS patients.
6,747 words (approx. 27.0 pages), 29 sources, APA, $ 153.95
»
Click here to show/hide summary
Abstract
This paper examines the nature of Multiple Sclerosis. It discusses its symptoms, probable causes, diagnosis and treatment. The paper then evaluates the effectiveness of a rehabilitative technique said to be useful to a variety of patients with chronic illnesses including those patients with multiple sclerosis. In particular, the study evaluates the effects of Aquatic Therapy for improving the functionality of MS patients. The primary method used to develop this evaluation is that of a literature search on the subject.
From the Paper
"Because MS is a neurological disorder, other pertinent literature regarding the benefits of aquatic therapy consists of studies indicating that the rehabilitation strategy has worked for patients with general neurologic disorders. In this regard, Morris (1997) discusses several benefits that have been for Aquatic Therapy with patients with neurologic disorders. The benefits listed by Morris include: profound relaxation, greater stretching of muscles resulting in increased flexibility, increased muscular strength, increased ability of the patient to stabilize multiple segments of the body, improved skill in specific patterns of movement, and increases in postural stability during functional activities."
| |
|
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
»
Click here to show/hide summary
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. "
| |
|
The Patients' Bill of Rights, 2007.
This paper discusses the the history and future of The Patients' Bill of Rights.
5,770 words (approx. 23.1 pages), 16 sources, MLA, $ 138.95
»
Click here to show/hide summary
Abstract
This paper addresses the present state of the Patients' Bill of Rights, as well as its history and future possibilities. Also explored are the issues of political support, arguments for and against, and major pitfalls in getting this legislation passed into law. The paper attempts to further explain general intentions of the Patients' Bill of Rights. The most pertinent bills specific to the Patients' Bill of Rights are presented and analyzed.
Outline:
Introduction
Arguments For and Against Patients' Bill of Rights
History of the Patients' Bill of Rights
Why the Patients' Bill of Rights has Failed
Summary and Conclusion
From the Paper
"Before exploring the more complex issues involved, it is necessary to understand the general intentions of the Patients' Bill of Rights. Numerous bills involving patients' rights have been presented to the House of Representatives and the U.S. Senate. Discussed in this paper are the most pertinent bills specific to the Patients' Bill of Rights: the 1998 Patients' Bill of Rights, H.R. 3605 and S. 1890; the Bipartisan Patient Protection Act of 2001, S. 1052, S. 872, and H.R. 526; and the 2005 Patients' Bill of Rights, H.R. 2259, H.R. 2650, and S. 1012. In general, federal legislation that safeguards patients' rights is supported by both major political parties and the President, and also has considerable public appeal (Chavez, 2001, 606; Chaddock, 2001, 1)."
| |
|
Nurses and the Treatment of HIV + Patients, 2002.
How nurses treat patients with HIV.
1,150 words (approx. 4.6 pages), 5 sources, $ 44.95
»
Click here to show/hide summary
Abstract
This paper discusses the treatment of HIV + patients in the hospital setting from a nurse's point of view. A discussion of nurses' emerging attitudes about treating patients and their vigilance with every patient due to this deadly disease is focused on. This paper also stresses the social responsibilities necessary in caring for these patients.
| |
|
Dialogues with Nursing Patients, 2008.
This paper analyzes three nursing dialogues with very different patients.
1,345 words (approx. 5.4 pages), 5 sources, APA, $ 45.95
»
Click here to show/hide summary
Abstract
This paper explains that the only way that nurses will learn about patients' needs and concerns is to really listen and to communicate well. The author points out that the purpose of the dialogues described in the paper was to identify or express the concerns of a patient with tachycardia, a breast cancer patient and a person with chronic abdominal pain. The paper stresses that the better the nurse's communication skills, the higher will be the quality of care that she or he provides. The author underscores that the most important point learned from these dialogues is the importance of the patient's perspective. The paper suggest that open-ended questions, going with the flow, patients' use of certain words or sentences and attentive listening are essential to a successful patient-nurse dialogue.
From the Paper
"I made other errors with Mrs. K, but they became a learning experience for the next two dialogues. For instance, I interrupted Mrs. K at times to respond to her. The most valuable lesson from Dialogue 1 was that we can remain true to the original intent by asking open-ended questions. The whole direction of the communication can be guided with open-ended questions. At the same time, there were blocks to effective communication because I began with a closed question. When Mrs. K stated that she felt she was becoming paralyzed, that statement needs to be explored with a great deal of empathy."
| |
|
Mentally Ill Patients, 2005.
A look at the reasons that mentally ill patients do not receive adequate care.
1,620 words (approx. 6.5 pages), 7 sources, MLA, $ 52.95
»
Click here to show/hide summary
Abstract
This paper examines the causes of inadequate care with regard to patients with mental illnesses, irrespective of the type of mental illness the patient has. Some of the causes cited and discussed by the paper include: (1) a lack of adequate healthcare coverage, (2) lack of access to sufficient and qualified healthcare professionals/providers and (3) social stigma that might prevent patients from seeking out care when needed.
Introduction
Barriers to Effective Care for Mentally Ill Patients
Conclusions
From the Paper
"Mentally ill patients have historically faced many obstacles when seeking out health care. For those that do have health insurance, many policies limit coverage. In some instances for example, patients are limited to 90 day in patient stays, even in the event that they are diagnosed with symptoms that indicate they may pose a danger to themselves or others (SAMHSA, 1999). The Surgeon General recently discussed the issue of parity with regard to mental health care. Specifically parity deals with the notion that mental health treatment should be financed in the same manner that general heath care services are (SAMHSA, 1999). "
| |
|
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
»
Click here to show/hide summary
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?
| |
|
Caring for Alzheimer's Patients, 2003.
An evaluation of the Calista Roy nursing model for caring for patients with Alzheimers.
690 words (approx. 2.8 pages), 3 sources, APA, $ 23.95
»
Click here to show/hide summary
Abstract
This paper paper applies the Calista Roy nursing practice model to the care of elderly Alzheimer's patients. The paper begins by discussing the five major concepts of nursing, according to the model. Next the paper evaluates the impact of both internal and external environments on patient care. Finally, the paper discusses how the burden of care for Alzheimer's patients most often falls on family members and asks whether the Calista Roy model might alleviate this burden.
| |
|
Depression in Hispanic Epileptic Patients, 2006.
An in-depth analysis of the relationship between epilepsy and depression in Hispanic patients.
19,050 words (approx. 76.2 pages), 100 sources, MLA, $ 249.95
»
Click here to show/hide summary
Abstract
This research study examines the rates of depression in Hispanic patients suffering from epilepsy. According to this paper, recent research suggests that the prevalence of epilepsy is higher in the Hispanic community. The paper further discusses how the Epilepsy Foundation reported that the substantial future growth in the number of Hispanics with epilepsy is of particular concern and that patients with epilepsy have a high rate of co-morbidity with depression.
Table of Contents:
Chapter 1
Introduction
Statement of the Problem and Relevance
Purpose of the Study
Theoretical Framework: Biopsychosocial
Previous Research Studies
Epilepsy
Comorbidity of Depression and Epilepsy
Hispanic Community
Hispanics and Depression
Depression and Hispanics with Epilepsy
Delimitation of the Problem
Definition of Terms
Hypothesis
Chapter two
Methods
Type of Research Design
Participants--Sample Characteristics
Instruments/Measures
Procedures
Data Analysis Procedure
Anticipated Ethical Issues
Chapter Three
Results
Chapter Four
Discussion
Chapter Five
Significance of the Study and Future Implications
References
From the Paper
"Differences are important to consider on the part of the patient, for their comfort with the doctor, but they are also important from the doctor's point of view. The reason behind this is that a doctor who is extremely uncomfortable with a patient will likely not be able to treat that patient in the same way they would treat another patient whom they liked better or felt that they could communicate well with. How the doctor feels about a patient is just as important to the relationship and the conversation as how the patient feels about the doctor (Lambert & Ogles, 2004).
Similarities and differences between patients and their doctors can have a very definite effect on whether or not the two get along well, and a strong language barrier can make both doctors and clients very uncomfortable. It is really not part of the healing process, but it does relate to the alliance that these individuals could form, in that it influences the development of some of the more critical therapeutic processes. Some psychotherapists consider this matching up between patient and doctor to be less distinct from other therapeutic ideas such as alliance, transference, and countertransference, for example (Lambert & Ogles, 2004).
The boundaries between these concepts as they relate to a therapist-client or doctor-patient match when it comes to Hispanics are often unclear. The better the match between patient and therapist, both in culture and in language, the more therapeutic benefits the patient will get from the therapy, and the easier the depression can be treated. Studies of this nature often show that ethnicity is not much of an issue if the patient and therapist like each other, but the language barrier for Hispanic patients can be very difficult to work through, and there are not that many therapists that are Hispanic or that are fluent in Spanish and understand the Hispanic culture well enough to put their patients at ease. Patients who were given the option to choose between therapists often chose the one that they felt was the most understanding and competent in their work, and the one that they felt they could communicate the most easily with. "
| |
|
Flavor Aversion and Chemotherapy Patients, 2004.
A look at flavor aversion and its relevance to chemotherapy patients.
2,475 words (approx. 9.9 pages), 6 sources, APA, $ 87.95
»
Click here to show/hide summary
Abstract
This paper discusses flavor aversion and its relevance to patients undergoing chemotherapy treatment. It looks at the role of classical Pavlovian conditioning in establishing food and flavor aversions, and ways to counteract them. The paper also points out the importance of this phenomenon in cancer patients undergoing chemotherapy.
From the Paper
"This paper concerns the topic of flavor aversion which develops in cancer patients undergoing chemotherapy. It is an interesting subject to me because I have known people undergoing such treatment and many of my friends have had family members or friends who have had to undergo chemotherapy treatment for cancer. The one thing that all these people notice is that they can no longer enjoy their favorite foods. One reason is because chemotherapy is very non-specific and is aimed at killing dividing cells.
| |
|
Brain Trauma Patients and Their Families, 2008.
This paper provides an analysis of a qualitative research report: "Needs of Family Members of Patients with Severe Traumatic Brain Injury" by
A. E. Bond, C. R. L. Draeger, B. Mandleco, and M. Donnelly.
2,499 words (approx. 10.0 pages), 3 sources, APA, $ 75.95
»
Click here to show/hide summary
Abstract
The paper analyzes the study "Needs of Family Members of Patients with Severe Traumatic Brain Injury," which attempts to determine the needs of brain trauma patients and their families who enter neurological ICU in need of more specific care. The paper outlines the study design, the data collection and analysis methods and evaluates the study's strengths and weaknesses. The paper points out that, although the findings from this study are limited, the study does successfully outline the principles needed to formulate a more effective and comprehensive health care experience.
Outline:
Problem
Purpose
Research Question
Study Design
Subjects and Setting
Data Collection Methods
Data Analysis Procedures
Strengths and Limitations
From the Paper
"The study, "Needs of Family Members of Patients with Severe Traumatic Brain Injury," addresses to determine the needs of brain trauma patients who enter neurological ICU in need of more specific care. Traumatic brain surgery occurs in 500,000 persons each year in the United States; approximately 50,000 of these die before reaching the hospital (Bond, Draeger, Mandelco & Donnelly, 2003, p. 63)."
"According to the study, brain trauma patients normally are admitted to ICU for observation. However, 10% of those patients admitted, require immediate care, usually involving surgery or relieving pressure on the brain."
"Due to the nature of severe brain trauma, the ability for families to cope with the concept of this ailment becomes significantly more difficult. As unpredictable brain trauma injuries can be, it is even more important for medical staff to be aware of all the needs for the families and patients."
| |
|
Psychotherapy with Elder Patients, 2002.
Examining the effectiveness of psychotherapy in elderly patients.
1,951 words (approx. 7.8 pages), 8 sources, MLA, $ 62.95
»
Click here to show/hide summary
Abstract
This paper presents an examination of psychotherapy with elderly patients in nursing homes. The writer explores the issues of confidentiality, cognitive understanding and the benefits of therapy for the elderly. It asks whether this form of treatment is necessary and effective and if the age of the patients presents a barrier.
From the Paper
"Advances in medical science now allow people to live longer than ever before. With the longevity however, comes a higher incidence of several things including the need for nursing home care, the need for mental health services and the need for a combination of them both. Nationwide, nursing homes are filled to and beyond capacity, which often translates to understaffing of employees. The elderly population of the United States, particularly those in nursing homes is often overlooked when it comes to mental health issues. Many times symptoms are attributed to the aging process, if they are noticed at all by a harried staff member who takes a cursory sweep through the patient?s inpatient records and compares them to the patient?s present state of mind. The need for psychotherapy in the elderly population has historically been ignored or overlooked. However, recent studies had attention have place a focus on the need for mental health care in the elderly, including those who reside in nursing homes."
| |
|
Nursing Patients in Labor, 2005.
This paper discusses alternative therapeutic support by nurses for patients in labor to increase their comfort level and to provide a positive childbirth outcome.
1,505 words (approx. 6.0 pages), 9 sources, APA, $ 49.95
»
Click here to show/hide summary
Abstract
This paper explains that, as more and more patients turn to alternative or non-pharmacological therapies for support during labor, it is important that nurses educate themselves regarding these measures so they can inform patients of the effective options for mitigating pain, which are available to them. The author points out that the literature review suggests that alternative therapeutic methods, such as acupuncture, intra-dermal water blocks, position changes and in some cases hypnosis, can be utilized successfully during the childbirth process to improve maternal satisfaction and facilitate a positive outcome. The paper relates that more research is needed to evaluate the efficacy of other therapies including massage, aromatherapy and other potential alternatives.
Table of Contents
Introduction
Purpose
Problem Statement
Hypothesis
Literature Review
Conceptual Framework
Conclusions
From the Paper
"Women's experience of pain during labor and delivery vary; Lundgren & Dahlberg's (1998) model of care provide a framework for understanding women's experience and perceptions of pain management and outcome during childbirth. Their assumption suggest that four themes help identify the meanings women assign their childbirth experience. These include a woman's ability to trust in oneself and one's body, trust in the caregiver and partner, the manner in which a mother transitions into motherhood and the acceptance that pain is difficult to describe completely and often contradictory."
|
|
|
