This revised and updated edition explores the law relating to patient confidentiality and reflects the recent legislation in the field. The text is written in a jargon free, non-legalistic way to allow the reader to understand the principles and how they apply to practice. The book is aimed at all health professionals who care for the patient, and for patient service managers, patient groups, relatives and anybody who is interested in understanding the law relating to patient confidentiality. The book includes case studies throughout.
This revised and updated edition explores the law relating to patient confidentiality and reflects the recent legislation in the field. The text is written in a jargon free, non-legalistic way to allow the reader to understand the principles and how they apply to practice. The book is aimed at all health professionals who care for the patient, and for patient service managers, patient groups, relatives and anybody who is interested in understanding the law relating to patient confidentiality. The book includes case studies throughout.
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.
Concise overview of the laws relating to the supply, administration and prescribing of medicines. User-friendly format for easy reference on the job, or a handy revision aid. Highly practical with case studies throughout to demonstrate application of theory into practice and revised and updated to reflect current law. This book is intended for all health professionals who are likely to be involved in the dispensing, administration, prescribing or supply of medication, whether in hospitals or in the community. It may also be of assistance to others, such as health service managers, patient groups and their representatives, lecturers and clinical supervisors. Each chapter uses a situation to illustrate the relevant laws so that the law can be explained in a practical jargon-free way. The book is intended to introduce readers to the basic principles which apply and the sources of law, so that they can, by following up the further reading and websites provided, add to their knowledge. This book will provide a baseline on which readers can develop their knowledge and understanding of the law relating to medicines.
This revised and updated edition explores the law relating to pain management in recent years.It considers the legal issues which have arisn in recent high-profile cases and discusses the implications of legisation extending prescribing powers. The text is written in a user-friendly, readable form for the non-lawyer. It aims to provide a succinct, useful basis from which practtioner and others can extend their knowledge of the law for the protection of their patients, their colleagues and themselves. Scope and contents Human rights law Criminal law and procedure Negligence Professional registration Consent in relation to adults, children and mentally disabled adults.
Presented in a clear and concise format that makes for easy reference and understanding, this revised and updated edition covers issues that are becoming increasingly important to health professionals, managers and educators, including proposed changes to the law since Lord Young's 2010 report Common Sense, Common Safety. Topics include cross infection and the spread of MRSA, greater regulation of health and safety standards, stress and bullying and the laws relating to notifiable diseases such as HIV/AIDS. Illustrated with case studies throughout, this book is designed to provide a clear introduction to the laws relating to health and safety, case law and statute law, so that the health professional has a sound understanding of the law.
This second edition has been revised and updated to reflect current changes in legislation on consent in the medical and healthcare setting. This book explores the law relating to consent, covering both the general principles where the patient is a mentally competent adult, and also the specialist areas of mental incapacity, children and parents. The text is written for all health professionals who care for the patient, and for patient service managers, patient groups, relatives, lecturers and others who are interested in understanding the law relating to consent.
Highly Commended in Health and social care in the 2017 BMA Medical Book Awards The Mental Capacity Act (2005) regulates decision making processes on behalf of adults who are unable to give informed consent, due to a loss in mental capacity (be that from birth, or due to an illness or injury at some point in their lives). Since the Act’s original conception the new Court of Protection is now firmly established, and there have been significant Supreme Court cases, as well as further guidance on the 2005 Act and major developments in the use and assessment for Deprivation of Liberty Safeguards. Thoroughly updated to take account of the many updates, developments and changes in legislation and guidance, the new edition of Dimond’s authoritative guide will be warmly welcome by practitioners and students who need to understand and work within the Mental Capacity Act, and how it applies to their professional responsibilities. A highly practical guide to the Mental Capacity Act and its provisions since its conception in 2005 Relevant for a wide range of practitioners and students within health and social care Highly readable and easily accessible, even for those with no legal background Includes a range of learning features, including scenarios, questions and answers, key summary points, and applications for practice. Legal Aspects of Mental Capacity is an essential resource for all healthcare and social services professionals, students patient services managers and carers working with those who lack the capacity to make their own decisions.
This is a short textbook of ethics and law aimed primarily at medical students. The book is in two sections. The first considers general aspects of ethics (in the context of medicine); the second section covers the topics identified in the 'consensus agreement'. The content of medical law is not intended to be comprehensive and relates very much to the ethical issues. The law will be updated throughout including: consent in light of Mental Capacity Act; mental health law in light of Mental Health Act; end of life (depending on outcome of Burke case and the passage of the Joffe Bill); assisted reproduction in light of expected changes in HFEA. New guidelines to be added: the guidelines and processes around medical research are under review and likely to develop and change; GMC guidelines are under continual revision (the Burke case in particular may have direct impact, but it is also likely that the confidentiality guidelines will undergo revision particularly in view of the increasing importance of genetic data). The new legal aspects outlined above will require some changes to the ethical analysis: the ethical issues of new technology will be included (cloning; transgenesis and chimera, i.e. forming organisms from more than one species) and stem-cells; resource allocation ethics is moving on to examining a wider range of issues than covered in the first edition and this will be discussed; the whole area of mental disorder and capacity to consent is an active area of ethical research and the second edition would cover some of this new work.
