Patient Advocacy for Health Care Quality Book

Patient Advocacy for Health Care Quality

  • Author : Jo Anne L. Earp
  • Publisher : Jones & Bartlett Publishers
  • File Size : 12,9 Mb
  • Release Date : 2007-07-23
  • Genre: Medical
  • Pages : 645
  • ISBN 10 : 9780763765255
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As a contribution to the emerging healthcare quality movement, Patient Advocacy for Healthcare Quality: Strategies for Achieving Patient-Centered Care is distinct from any others of its kind in its focus on the consumer’s perspective and in its emphasis on how advocacy can influence change at multiple social levels. This introductory volume synthesizes patient advocacy from a multi-level approach and is an ideal text for graduate and professional students in schools of public health, nursing and social work.Important Notice: The digital edition of this book is missing some of the images or content found in the physical edition.

Patient Advocacy for Health Care Quality Strategies for Achieving Patient Centered Care Book

Patient Advocacy for Health Care Quality Strategies for Achieving Patient Centered Care

  • Author : Jo Earp
  • Publisher : Jones & Bartlett Learning
  • File Size : 10,6 Mb
  • Release Date : 2008-05-02
  • Genre: Medical
  • Pages : 646
  • ISBN 10 : 9780763749613
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As a contribution to the emerging healthcare quality movement, Patient Advocacy for Healthcare Quality: Strategies for Achieving Patient-Centered Care is distinct from any others of its kind in its focus on the consumer’s perspective and in its emphasis on how advocacy can influence change at multiple social levels. This introductory volume synthesizes patient advocacy from a multi-level approach and is an ideal text for graduate and professional students in schools of public health, nursing and social work.

Improving Healthcare Through Advocacy Book
Score: 5
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Improving Healthcare Through Advocacy

  • Author : Bruce S. Jansson
  • Publisher : John Wiley & Sons
  • File Size : 5,8 Mb
  • Release Date : 2011-01-25
  • Genre: Political Science
  • Pages : 516
  • ISBN 10 : 9780470505298
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Praise for Improving Healthcare Through Advocacy A Guide for the Health and Helping Professions "Bruce Jansson's thoughtful and innovative book will appeal to students in social work, nursing, and public health as well as those working in the health field of practice. The case examples are extraordinary, and Jansson provides the ideas, context, and theoretical base for readers to acquire the skills of advocacy in healthcare. This is by far the best advocacy book I have seen." —Gary Rosenberg, PhD Director, Division of Social Work and Behavioral Science Mount Sinai School of Medicine "Improving Healthcare Through Advocacy is a terrific description of opportunities for advocacy intervention and provides the skill sets necessary for effective advocacy. A needed book." —Laura Weil, LCSW Director, Health Advocacy Program Sarah Lawrence College "Improving Healthcare Through Advocacy is an invaluable resource for practitioners working in the healthcare field as well as for students. It very thoroughly covers healthcare advocacy issues, contains real-world case examples, and provides a clear, step-by-step framework for practicing advocacy." —Kimberly Campbell, ACSW, LCSW Lecturer, Department of Social Work Ball State University An important resource for all who strive for the best in healthcare treatment for their patients, themselves, and the nation Bestselling author and award-winning researcher Bruce S. Jansson uses an intervention framework to illustrate how everyone in the healthcare system can advocate effectively, not just for better healthcare delivery to individual clients but for the necessary policy change that will deliver long- term solutions to our nation's healthcare crisis as well. Improving Healthcare Through Advocacy provides professionals with: Tools to move from traditional services to case advocacy and policy advocacy tasks Over 100 case studies from the perspective of patients, healthcare providers, and others who relate the experiences they have

Policy and Politics for Nurses and Other Health Professionals Book

Policy and Politics for Nurses and Other Health Professionals

  • Author : Donna M. Nickitas
  • Publisher : Jones & Bartlett Publishers
  • File Size : 18,6 Mb
  • Release Date : 2014-12
  • Genre: Medical
  • Pages : 352
  • ISBN 10 : 9781284053296
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Each new print copy includes Navigate 2 Advantage Access that unlocks a comprehensive and interactive eBook, student practice activities and assessments, a full suite of instructor resources, and learning analytics reporting tools. Policy and Politics for Nurses and Other Health Professionals, Second Edition focuses on the idea that all health care providers require a fundamental understanding of the health care system including but not limited to knowledge required to practice their discipline. The text discusses how health care professionals must also prepare themselves to engage in the economic, political and policy dimensions of health care. The Second Edition offers a nursing focus with an interdisciplinary approach intertwined to create an understanding of health care practice and policy. The text is enriched through the contributions from nurses and other health professionals including activists, politicians, and economists who comprehend the forces of healthcare in America how their impact on the everyday provider. The new edition features key updates on the current health care environment including the Affordable Care Act. Instructor Resources include: Test Bank Web Link Resources PowerPoint(TM) Slides

Addressing Sickle Cell Disease Book

Addressing Sickle Cell Disease

  • Author : National Academies of Sciences, Engineering, and Medicine
  • Publisher : National Academies Press
  • File Size : 12,6 Mb
  • Release Date : 2020-12-22
  • Genre: Medical
  • Pages : 522
  • ISBN 10 : 9780309669634
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Sickle cell disease (SCD) is a genetic condition that affects approximately 100,000 people in the United States and millions more globally. Individuals with SCD endure the psychological and physiological toll of repetitive pain as well as side effects from the pain treatments they undergo. Some adults with SCD report reluctance to use health care services, unless as a last resort, due to the racism and discrimination they face in the health care system. Additionally, many aspects of SCD are inadequately studied, understood, and addressed. Addressing Sickle Cell Disease examines the epidemiology, health outcomes, genetic implications, and societal factors associated with SCD and sickle cell trait (SCT). This report explores the current guidelines and best practices for the care of patients with SCD and recommends priorities for programs, policies, and research. It also discusses limitations and opportunities for developing national SCD patient registries and surveillance systems, barriers in the healthcare sector associated with SCD and SCT, and the role of patient advocacy and community engagement groups.

Health Professions Education Book

Health Professions Education

  • Author : Institute of Medicine
  • Publisher : National Academies Press
  • File Size : 10,7 Mb
  • Release Date : 2003-07-01
  • Genre: Medical
  • Pages : 191
  • ISBN 10 : 030913319X
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The Institute of Medicine study Crossing the Quality Chasm (2001) recommended that an interdisciplinary summit be held to further reform of health professions education in order to enhance quality and patient safety. Health Professions Education: A Bridge to Quality is the follow up to that summit, held in June 2002, where 150 participants across disciplines and occupations developed ideas about how to integrate a core set of competencies into health professions education. These core competencies include patient-centered care, interdisciplinary teams, evidence-based practice, quality improvement, and informatics. This book recommends a mix of approaches to health education improvement, including those related to oversight processes, the training environment, research, public reporting, and leadership. Educators, administrators, and health professionals can use this book to help achieve an approach to education that better prepares clinicians to meet both the needs of patients and the requirements of a changing health care system.

The Future of Nursing Book

The Future of Nursing

  • Author : Institute of Medicine
  • Publisher : National Academies Press
  • File Size : 18,9 Mb
  • Release Date : 2011-02-08
  • Genre: Medical
  • Pages : 700
  • ISBN 10 : 9780309208956
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The Future of Nursing explores how nurses' roles, responsibilities, and education should change significantly to meet the increased demand for care that will be created by health care reform and to advance improvements in America's increasingly complex health system. At more than 3 million in number, nurses make up the single largest segment of the health care work force. They also spend the greatest amount of time in delivering patient care as a profession. Nurses therefore have valuable insights and unique abilities to contribute as partners with other health care professionals in improving the quality and safety of care as envisioned in the Affordable Care Act (ACA) enacted this year. Nurses should be fully engaged with other health professionals and assume leadership roles in redesigning care in the United States. To ensure its members are well-prepared, the profession should institute residency training for nurses, increase the percentage of nurses who attain a bachelor's degree to 80 percent by 2020, and double the number who pursue doctorates. Furthermore, regulatory and institutional obstacles -- including limits on nurses' scope of practice -- should be removed so that the health system can reap the full benefit of nurses' training, skills, and knowledge in patient care. In this book, the Institute of Medicine makes recommendations for an action-oriented blueprint for the future of nursing.

A Theory for Patient Advocacy an Islamic Nursing Model Book

A Theory for Patient Advocacy an Islamic Nursing Model

  • Author : Manfred Mortell
  • Publisher : Unknown
  • File Size : 19,7 Mb
  • Release Date : 2020-06-24
  • Genre: Uncategoriezed
  • Pages : 344
  • ISBN 10 : 153618005X
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Patient advocacy for all human beings is a fundamental ideal as it assures the patient their rights and their safety when admitted to a healthcare facility. Nursing as a healthcare profession is complicated by the fact that it is concerned with vulnerable human beings, and ethical principles which need to be considered when providing treatment, or care for the patient. The logic for this book is twofold, the first justification for authoring this text was to enlighten nurses and other healthcare professionals to reflect on a dilemma which affects patient care and safety. A quandary in the literature which has been named a "Theory-Practice-Ethics gap" (Mortell et al, 2013). Patient safety and high quality of care are fundamental facets related to all healthcare practices. When people are admitted to hospital, they just presume that they will receive safe, quality treatment from healthcare professionals who have a duty of care. Society does not expect to be put at risk or be harmed, since the principal goal of healthcare is to augment care, safety and wellbeing, and so optimize the quality of people's lives (Leape, 2015; Wilson et al, 2009). The second justification for authoring this book, was to present an important new theory and model for patient advocacy to the professional healthcare community. The generated theory, states that, if healthcare professionals incorporate their religious, cultural and family values into their humanitarian ideals, they will be effective as patient advocates. The advocacy model which was generated the following components of advocacy, "Vulnerable-acy", which was advocacy for the vulnerable, "Familial-acy", which was advocacy that a family member would provide to a loved one, "Cultural-acy" was linked to culture, such as ethnic awareness and sensitivity, "Religion-acy" was coupled with a Muslim's Islamic holy obligations, however, this concept can be adapted for any religion and religious beliefs and "Human-acy", which identified a per

Clinical Practice Guidelines We Can Trust Book

Clinical Practice Guidelines We Can Trust

  • Author : Institute of Medicine
  • Publisher : National Academies Press
  • File Size : 12,8 Mb
  • Release Date : 2011-06-16
  • Genre: Medical
  • Pages : 290
  • ISBN 10 : 9780309216463
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Advances in medical, biomedical and health services research have reduced the level of uncertainty in clinical practice. Clinical practice guidelines (CPGs) complement this progress by establishing standards of care backed by strong scientific evidence. CPGs are statements that include recommendations intended to optimize patient care. These statements are informed by a systematic review of evidence and an assessment of the benefits and costs of alternative care options. Clinical Practice Guidelines We Can Trust examines the current state of clinical practice guidelines and how they can be improved to enhance healthcare quality and patient outcomes. Clinical practice guidelines now are ubiquitous in our healthcare system. The Guidelines International Network (GIN) database currently lists more than 3,700 guidelines from 39 countries. Developing guidelines presents a number of challenges including lack of transparent methodological practices, difficulty reconciling conflicting guidelines, and conflicts of interest. Clinical Practice Guidelines We Can Trust explores questions surrounding the quality of CPG development processes and the establishment of standards. It proposes eight standards for developing trustworthy clinical practice guidelines emphasizing transparency; management of conflict of interest ; systematic review--guideline development intersection; establishing evidence foundations for and rating strength of guideline recommendations; articulation of recommendations; external review; and updating. Clinical Practice Guidelines We Can Trust shows how clinical practice guidelines can enhance clinician and patient decision-making by translating complex scientific research findings into recommendations for clinical practice that are relevant to the individual patient encounter, instead of implementing a one size fits all approach to patient care. This book contains information directly related to the work of the Agency for Healthcare Research and Quality (AHRQ

A Psychiatrist s Guide to Advocacy Book

A Psychiatrist s Guide to Advocacy

  • Author : Mary C. Vance, M.D.
  • Publisher : American Psychiatric Pub
  • File Size : 6,8 Mb
  • Release Date : 2020-03-31
  • Genre: Medical
  • Pages : 460
  • ISBN 10 : 9781615372331
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The book explores the diverse definitions of advocacy and helps to identify methods and opportunities for advocacy by mental health practitioners. The editors argue for a greater culture of advocacy among psychiatrists in order to effect broad and lasting systemic and structural change. Legislative advocacy is just one of the many types explored in the book; advocacy takes many forms, including patient-level advocacy, organizational advocacy, education and research as advocacy, and media-targeted advocacy.

Health IT and Patient Safety Book

Health IT and Patient Safety

  • Author : Institute of Medicine
  • Publisher : National Academies Press
  • File Size : 8,5 Mb
  • Release Date : 2012-03-15
  • Genre: Computers
  • Pages : 234
  • ISBN 10 : 9780309221153
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IOM's 1999 landmark study To Err is Human estimated that between 44,000 and 98,000 lives are lost every year due to medical errors. This call to action has led to a number of efforts to reduce errors and provide safe and effective health care. Information technology (IT) has been identified as a way to enhance the safety and effectiveness of care. In an effort to catalyze its implementation, the U.S. government has invested billions of dollars toward the development and meaningful use of effective health IT. Designed and properly applied, health IT can be a positive transformative force for delivering safe health care, particularly with computerized prescribing and medication safety. However, if it is designed and applied inappropriately, health IT can add an additional layer of complexity to the already complex delivery of health care. Poorly designed IT can introduce risks that may lead to unsafe conditions, serious injury, or even death. Poor human-computer interactions could result in wrong dosing decisions and wrong diagnoses. Safe implementation of health IT is a complex, dynamic process that requires a shared responsibility between vendors and health care organizations. Health IT and Patient Safety makes recommendations for developing a framework for patient safety and health IT. This book focuses on finding ways to mitigate the risks of health IT-assisted care and identifies areas of concern so that the nation is in a better position to realize the potential benefits of health IT. Health IT and Patient Safety is both comprehensive and specific in terms of recommended options and opportunities for public and private interventions that may improve the safety of care that incorporates the use of health IT. This book will be of interest to the health IT industry, the federal government, healthcare providers and other users of health IT, and patient advocacy groups.

Unequal Treatment Book
Score: 4
From 1 Ratings

Unequal Treatment

  • Author : Institute of Medicine
  • Publisher : National Academies Press
  • File Size : 20,7 Mb
  • Release Date : 2009-02-06
  • Genre: Medical
  • Pages : 781
  • ISBN 10 : 9780309082655
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Racial and ethnic disparities in health care are known to reflect access to care and other issues that arise from differing socioeconomic conditions. There is, however, increasing evidence that even after such differences are accounted for, race and ethnicity remain significant predictors of the quality of health care received. In Unequal Treatment, a panel of experts documents this evidence and explores how persons of color experience the health care environment. The book examines how disparities in treatment may arise in health care systems and looks at aspects of the clinical encounter that may contribute to such disparities. Patients' and providers' attitudes, expectations, and behavior are analyzed. How to intervene? Unequal Treatment offers recommendations for improvements in medical care financing, allocation of care, availability of language translation, community-based care, and other arenas. The committee highlights the potential of cross-cultural education to improve provider-patient communication and offers a detailed look at how to integrate cross-cultural learning within the health professions. The book concludes with recommendations for data collection and research initiatives. Unequal Treatment will be vitally important to health care policymakers, administrators, providers, educators, and students as well as advocates for people of color.

Registries for Evaluating Patient Outcomes Book

Registries for Evaluating Patient Outcomes

  • Author : Agency for Healthcare Research and Quality/AHRQ
  • Publisher : Government Printing Office
  • File Size : 20,8 Mb
  • Release Date : 2014-04-01
  • Genre: Medical
  • Pages : 356
  • ISBN 10 : 9781587634338
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This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.

Patient Advocacy Matters Book

Patient Advocacy Matters

  • Author : Teri Dreher
  • Publisher : NShore Publishing
  • File Size : 20,7 Mb
  • Release Date : 2016-11-02
  • Genre: Uncategoriezed
  • Pages : null
  • ISBN 10 : 0692791779
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Who do you trust to make what could be life-altering decisions on your behalf? Who do you trust to handle your finances, if you're no longer able? Do you have any idea where to start in order to protect yourself?In today's era of modern healthcare, there is a very real possibility that, at some point, you will be admitted to a hospital, whether it is a life-threatening crisis or you simply need routine tests performed.Patient Advocacy Matters, the Ultimate "How-To" Guide is a resource, a vital tool to equip, empower and educate consumers who wish to protect their life, their health, their rights and/or that of their loved ones as it pertains to healthcare and finances. Use this resource to guide you along the path to: *Know your medical rights for different situations*The reason you need a medical power of attorney and a financial proxy*When it's time to ask for help*The difference between a private patient advocate vs other "patient" advocates and why it's important to know the difference*How nurse advocates can be there at a critical stage to advocate on your behalf No one intends to be unprepared in these situations, we simply never imagine them happening before we have time to put our affairs in order. Patient Advocacy Matters delivers all you need to help you plan for the unforeseen should you become incapacitated.As you read through Patient Advocacy Matters, you will quickly understand why this guide must be your primary resource for the answers you need to ensure your preparedness for whatever lies ahead. No stone is left unturned in this guide and you will be glad to have this vital tool to help you organize your affairs in the event that you suffer a medical catastrophe and are unable to advocate for yourself.

Advocacy in Health Care Book

Advocacy in Health Care

  • Author : Joan H. Marks
  • Publisher : Springer Science & Business Media
  • File Size : 19,8 Mb
  • Release Date : 2012-12-06
  • Genre: Medical
  • Pages : 140
  • ISBN 10 : 9781461250043
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The roles of both the consumer and the health advocate professional have become increasingly significant in to day's climate of "rationed" health care. It seems clear that the timely exchange of ideas among seasoned health care advocates is necessary if we are to deal with the complex problems of a technologically advanced so ciety seeking to ration its heath care in a truly humane way. Toward such a timely exchange, the first Confer ence on Advocacy in Health Care was organized by the Health Advocacy Program of Sarah Lawrence College and recently held. Advocacy in Health Care: The Power of a Silent Constituency is the proceedings of the conference and will, we believe, greatly extend our efforts to share both the problems and solutions that effective patient advocacy entails. Never before has the issue of advocating for special population groups by combining the resources of consumers and professionals been the exclusive focus of one volume. This book discusses the power of such an alignment and describes specific organizational techniques that have been effective in bringing about changes in the delivery system. The final section of the book, "Questions, Com ments and Answers," presents a selection of topics of special interest that surfaced during the open disc- vii viii Preface sion at the last conference session. The comments were forthright in their criticism of public policy, and the vigor of the argument underscored the vitality of the co alition between professionals and consumers.