This is a one-of-a-kind, all-inclusive reference guide for new Clinical Nurse Specialists entering the field as well as seasoned practitioners looking to update their knowledge. Disseminating a wealth of current professional practice guidance and practical information on reimbursement and certification, the second edition has been fully updated to reflect changes resulting from the Affordable Care Act and the APRN Consensus Model. Four new chapters address changes and emerging trends, expanding focus on independent practice, increasing demands on health care due to the growing population of older adults, and updated reimbursement/economic issues. This authoritative toolkit is organized in an easy-to-use, bullet-point format and includes numerous clinical examples, case scenarios, and personal anecdotes culled from the contributors' own professional experiences. New to the Second Edition: Fully revised and updated. Addresses CNS practice within Affordable Care Organizations. Describes CNS leadership role in system-level evidence-based practice initiatives. Covers documentation and communication of CNS activities aligning with strategic initiatives and CNS practice priorities. Discusses facilitating transitions of care to assure safety and quality. Addresses the CNS role in interprofessional education in clinical settings. Key Features: Presents crucial information on negotiating and securing a job. Provides advice on establishing credibility, prioritising, and finding a mentor. Contains guidelines on mentoring staff, leading groups, and precepting students. Addresses documenting and measuring clinical outcomes. Describes how to network with professional organisations and community agencies. Offers practical guidance on applying for reimbursement and pursuing certification and licensure.

Biomedical research today has a high public profile, largely because of patient advocacy. Following in the footsteps of HIV/AIDS activists, advocates representing an array of patient groups are now vocal partners in the research enterprise. This book shows how advocates have transformed health research, often - but not always - for the better. Dresser is the first to examine patient advocacy through the lens of research ethics. She exposes the bright and dark sides of patients' expanded opportunities to enroll in clinical trials and join researchers in planning and evaluating studies. She considers the virtues and drawbacks of giving patients more influence over how the government invests its research dollars. She argues that advocates should do more to promote ethical human studies and responsible media reporting about research. Patient advocates can help make research more ethical, but advocacy raises ethical issues of its own. This book clearly and vividly recounts the advocacy contribution to research and explores the thorny ethical issues facing research advocates.