A Physician's Guide to Life Care Planning


Book Description

This book is intended to provide physicians a strong theoretical and conceptual framework upon which to rely when life care planning, as well as a common language to help physician life care planners articulate, compartmentalize, and contextualize key life care planning concepts.In addition, the book is intended to serve as an ongoing, subject-specific resource to aid physicians in producing comprehensive, well-formulated life care plans.




Life Care Planning and Case Management Handbook


Book Description

Life Care Planning and Case Management Handbook, Second Edition brings together the many concepts, beliefs, and procedures regarding life care plans into one state-of-the-art publication. This second edition of a bestseller is focused on prioritizing and managing the spectrum of services for people with serious medical problems and their families.




Pediatric Life Care Planning and Case Management, Second Edition


Book Description

Pediatric Life Care Planning and Case Management provides a comprehensive and unique reference that goes beyond the clinical discussion to include legal and financial aspects, life expectancy data, and assistive technology. It also includes case samples of actual plans related to specific conditions. The book is divided into five parts: Normal Growth and Development of Children describes the normal growth and development and the cognitive and psychosocial development of children. The Roles of the Life Care Plan Team details the roles of members of a life care plan team, from the pediatric care manager and life care planner to the vocational rehabilitation consultant, among others. Chronic Conditions and Disability States offers guidelines for life care planning for children with a wide range of chronic health conditions and disabilities, including traumatic injuries and organ transplants. Forensic Considerations examines life care planning in legal cases, life expectancy issues, and life care plan foundation strategies and requirements. Special Issues discusses assistive technology, medical homes, funding sources, and ethical issues in caring for children with special needs—including a mother’s perspective on caring for her son. With contributions from highly respected professionals, this text provides a guide for life care planners, health-care professionals, education specialists, insurance decision makers, attorneys, and families who work with children with special health-care needs.




Dying in America


Book Description

For patients and their loved ones, no care decisions are more profound than those made near the end of life. Unfortunately, the experience of dying in the United States is often characterized by fragmented care, inadequate treatment of distressing symptoms, frequent transitions among care settings, and enormous care responsibilities for families. According to this report, the current health care system of rendering more intensive services than are necessary and desired by patients, and the lack of coordination among programs increases risks to patients and creates avoidable burdens on them and their families. Dying in America is a study of the current state of health care for persons of all ages who are nearing the end of life. Death is not a strictly medical event. Ideally, health care for those nearing the end of life harmonizes with social, psychological, and spiritual support. All people with advanced illnesses who may be approaching the end of life are entitled to access to high-quality, compassionate, evidence-based care, consistent with their wishes. Dying in America evaluates strategies to integrate care into a person- and family-centered, team-based framework, and makes recommendations to create a system that coordinates care and supports and respects the choices of patients and their families. The findings and recommendations of this report will address the needs of patients and their families and assist policy makers, clinicians and their educational and credentialing bodies, leaders of health care delivery and financing organizations, researchers, public and private funders, religious and community leaders, advocates of better care, journalists, and the public to provide the best care possible for people nearing the end of life.




Dying Well


Book Description

From Ira Byock, prominent palliative care physician and expert in end of life decisions, a lesson in Dying Well. Nobody should have to die in pain. Nobody should have to die alone. This is Ira Byock's dream, and he is dedicating his life to making it come true. Dying Well brings us to the homes and bedsides of families with whom Dr. Byock has worked, telling stories of love and reconciliation in the face of tragedy, pain, medical drama, and conflict. Through the true stories of patients, he shows us that a lot of important emotional work can be accomplished in the final months, weeks, and even days of life. It is a companion for families, showing them how to deal with doctors, how to talk to loved ones—and how to make the end of life as meaningful and enriching as the beginning. Ira Byock is also the author of The Best Care Possible: A Physician's Quest to Transform Care Through the End of Life.







Spinal Cord Injury Desk Reference


Book Description

"This text provides a quick, easy-to-understand, comprehensive, evidence-based reference for health care practitioners who formulate life care plans for persons with SCI. Features that will facilitate use by practitioners includes a variety of reference materials for health care professionals who provide life care planning/case management for SCI. Life care planning/case management practitioners would best be served by utilizing this text as a source of information and a guide from which to incorporate their professional knowledge, judgment, and ethical responsibilities when working with individuals with SCI to meet the challenge of addressing their unique long-term care needs. It is our hope this text will provide readers with tools and insights for competently addressing the long-term consequences of SCI. This text arose out of a perceived need to have a single reference that would both contain information and serve as a reminder of areas central to the life care planning process for persons with SCI. It offers practitioners a single, easy-to-use resource that summarizes - in a clear, understandable way with easily accessible references - a body of studies and research on SCI that have important implications for life care planning and case management. This text is an introduction to the basic aspects related to understanding SCI, including epidemiology, functional classification, and complications related to aging a with disability. In addition, it covers functional outcomes, potential associated costs, long-term management and care considerations, model LCP guidelines, and legislative, organizational, and agency resources. This need for a continuum of care presents great challenges to health care professionals as well as to individuals with SCI and their families. Life care planning, which entered into the rehabilitation scene in the late 1970s and early 1980s, has proven to be one way of meeting this challenge by providing an organized framework of services, recommendations, and requirements for long-term care management. By using a consistent methodology in assessing the individual needs of the person with SCI, the life care plan (LCP) helps the health care professionals as well as the person with SCI acquire a comprehensive understanding of the immediate and long-term care requirements necessary to maximize productivity and independence. Although the text was written primarily for life care planning and case management practitioners, it can also be useful to other professionals who may be involved with the long-term care and management needs of people with SCI. Included in this group are primary care and speciality care physicians, nurses, rehabilitation counselors, therapists, insurers/HMOs, attorneys, governmental agencies, disability organizations, and educators, as well as people with SCI and their families. "




Life Care Planning and Case Management Handbook


Book Description

Life care planning is an advanced collaborative case management specialty practice focused on assessing, evaluating, coordinating, consulting, planning for, and monitoring necessary services for individuals with complex medical care needs over their lifetime. This handbook provides a comprehensive resource for all people involved with catastrophic impairments and chronic medical care case management. The Life Care Planning and Case Management Handbook, Fourth Edition, begins by defining the roles played by each of the key team members working with the life care planner. It provides planners with insights critical to successful interactions with medical and health care–related professionals as well as the team members they are most likely to encounter as they work to build an accurate and reliable life care plan. Next, the text offers up-to-date information on the medical conditions most frequently encountered by the life care planner. The contributors, who are recognized experts in their disciplines, also address issues in forensic settings, ethics, standards, research, and credentials. The fourth edition includes numerous chapters on general issues, as well as updated standards of practice from the International Academy of Life Care Planners (IALCP), Life Care Planning Consensus Statements, and valuable step-by-step charts and checklists. Completely updated and expanded, this revised handbook now includes new chapters on multicultural considerations in life care planning, admissibility of life care plans in U.S. courts, and Canadian life care planning practice. Additionally, infused in other chapters, is new information on medical coding and costing for life care planners, life care planning in non-litigated contexts, as well as research and education within life care planning.




A Core Curriculum for Nurse Life Care Planning


Book Description

A Core Curriculum for Nurse Life Care Planning helps registered nurse life care planners prepare to take the CNLCP credentialing exam and serves as a foundation for a successful nurse life care planning practice. This textbook is based on the nursing process of assessment, critical thinking, and nursing diagnoses, and it also covers applying nursing research, evidenced-based practice, case management skills, and legal nursing practices. Written by practicing nurse life care planners and peer-reviewed by AANLCP member nurse life care planners, this core curriculum includes basic nurse life care planning knowledge on - The history of nurse life care planning - The use of critical thinking in the life care planning process - How to critique a life care plan - How to address spinal cord injuries, traumatic brain injuries, chronic pain, amputations, burns, cerebral palsy, and considerations with aging - How to understand disability rights laws - The legal aspects of nurse life care planning - Litigation processes Providing a foundation to encourage nurse life care planners to research and learn, A Core Curriculum for Nurse Life Care Planning offers a valuable resource for nurses practicing in this field.




A Guide to Psychosocial and Spiritual Care at the End of Life


Book Description

Psychological, social, and spiritual care is as important as physical care at the end of life. Yet caregivers often feel ill-equipped to give that nonphysical care. This book shows how to do it. The book addresses all caregivers who attend dying patients: doctors, nurses, chaplains, clergy in the pastorate, social workers, clinical psychologists, family caregivers, and others. It covers such topics as the functional and emotional trajectories of dying; the varied approaches of patients and caregivers to end-of-life decisions; culturally based beliefs about dying; the differences between depression and grief; and people’s views about the right time to die, the death experience itself, and the afterlife. For each topic the book introduces core concepts and summarizes recent research about them. The book presents much of its material in readable tables for easy reference; applies the material to real-life cases; lists the main “take home” points for each chapter; and gives references for additional reading. The book helps caregivers anticipate the reactions of patients and survivors to end-of-life traumas and suggests how caregivers can respond insightfully and compassionately. At the same time the book challenges caregivers to think through their own views about death and dying. This book, therefore, is a must-read for all caregivers―professional and nonprofessional alike―who strive to give their patients comprehensive, high-quality end-of-life care.