Author

Kleespies, Phillip M

Place of Publication

Washington, DC

Publisher

American Psychological Association

Publication Date

2004

Subjects

Terminal Care - ethics

Terminal Care - psychology

Terminal Care - legislation & jurisprudence

Right to Die

Euthanasia

Suicide, Assisted

Advance Care Planning

Attitude to Death

ISBN

1591470676

Language

English

Material Type

Book

Audience

Professional

Location

Vancouver Library

Call Number

WB310 K63 2004

Copies

Corporate Author

Association of Registered Nurses of British Columbia

Place of Publication

[Vancouver, BC?]

Publisher

Association of Registered Nurses of British Columbia

Publication Date

2016

Subjects

Nurse's Role

Nurses - standards

Nurse Practitioners - standards

Patient Care - nursing

Patient care - ethics

Right to Die

Suicide, Assisted

Euthanasia, Active, Voluntary

Terminal Care - ethics

Terminal Care - legislation & jurisprudence

Legislation, Medical

Ethics, Nursing

Canada

Language

English

Material Type

Online

Report

Audience

Professional

Location

Internet

Website Notes

NNPBC membership is required to access position statements and policy discussion content.

Editor

Thornton, James E

Winkler, Earl R

Stuart-Stubbs, Megan

Place of Publication

[Vancouver, BC?]

Publisher

University of British Columbia Press

Publication Date

1988

Physical Description

xiii, 256 p. ; 23 cm.

Subjects

Social Conditions

Aged

Ethics

Delivery of Health Care

Aging - ethics

Geriatrics - ethics

Right to Die

ISBN

9780774803106

077480310X

Language

English

Material Type

Book

Audience

Professional

Location

Kelowna Library

Call Number

HQ1061 E83 1988

Copies

Author

Somerville, Margaret

Place of Publication

Montreal

Publisher

McGill-Queen's University Press

Publication Date

2001

Subjects

Euthanasia

Suicide, Assisted

Ethics, Medical

ISBN

077352245X

Language

English

Material Type

Book

Audience

Professional

Location

Vancouver Library

Call Number

W50 S696 2001

Copies

Author

Sessions, Roy B

Place of Publication

Lanham, MD

Publisher

Rowman & Littlefield Publishers, Inc.

Publication Date

2012

Series

Proquest Ebook Central

Ebrary books

Subjects

Ethics, Medical

Neoplasms - psychology

Patient care - ethics

Medical Oncology - ethics

Physician-Patient Relations

Health Knowledge, Attitudes, Practice

Suicide, Assisted

ISBN

9781442216235

9781626564275

Language

English

Material Type

Ebook

Audience

Professional

Location

Internet

Website Notes

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Editor

Kotalik, Jaro

Shannon, David W.

Edition

1st ed.

Place of Publication

Cham, Switzerland

Publisher

Springer International Publishing AG

Publication Date

c2023

Series

Proquest Ebook Central

Subjects

Suicide, Assisted

Euthanasia

Abstract

"This book, written both for a Canadian and an international readership, provides a multidisciplinary review of the framework and performance of the Canadian Medical Assistance in Dying (MAID) program. In the first five years (2015-2021) of operation, this program delivered voluntary euthanasia and assistance in suicide to over 30,000 Canadian residents, presently representing a 30% annual growth. Looking back on these first five years, the 30 Canadian scholars and clinicians contributing to this volume raise important issues and attempt to answer key questions that have arisen in regards to its operation and its stated objectives. This volume strikes the most appropriate balance between the autonomy of persons who seek medical assistance, versus the interests and protection of vulnerable persons. Finally, the book makes suggestions on how the program can presently be improved. It identifies gaps in knowledge about MAID's operational program and its impact on individuals, families and society in order to stimulate the necessary research that is essential to the evolution of a healthy and well-balanced program. As a first, comprehensive examination of medically assisted deaths in Canada, this publication will be of great value to lay, professional, academic, political audiences both domestically and internationally, especially in jurisdictions that are examining their options of permitting assisted deaths." --publisher

ISBN

9783031300011

Language

English

Material Type

Ebook

Audience

Professional

Location

Internet

Website Notes

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Editor

Bobbert, Monika

Herrmann, Beate

Eckart, Wolfgang Uwe

Place of Publication

Germany

Publisher

Verlag Karl Alber

Publication Date

2017

Series

Proquest Ebook Central

Angewandte Ethik ; Band 19

Subjects

Medical Oncology - ethics

Bioethical Issues

Neoplasms - therapy

Oncologists - ethics

Patient care - ethics

Europe

Congress

Notes

Conference proceedings: Ethics and Oncology (Conference) (2012 : Heidelberg, Germany)

ISBN

9783495485866

9783495813430

Language

English

Material Type

Ebook

Audience

Professional

Location

Internet

Website Notes

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Editor

Thomas, Keri

Lobo, Ben

Detering, Karen

Edition

2nd ed.

Place of Publication

Oxford, UK

Publisher

Oxford University Press

Publication Date

2018

Series

EBSCOhost eBook

Subjects

Advance Care Planning

Advance Care Planning - organization & administration

Decision Making

Terminal Care

Right to Die

Abstract

Table of Contents :

Introduction to advance care planning -- Overview and introduction to advance care planning -- What are the benefits of advance care planning and how do we know? -- An introduction to advance care planning: practice at the frontline -- Person-centred care: how does advance care planning support this and what are the economic benefits? -- Advance care planning for an ageing population -- Spiritual and ethical aspects of advance care planning -- Advance care planning: a personal view and stories from the frontline -- Context and experience of advance care planning in the UK -- Advance care planning in the UK: update on policy and practice -- Advance decisions to refuse treatment and the impact of wider legislation -- Discussions and decisions about cardiopulmonary resuscitation -- The implications of the Mental Capacity Act (MCA) 2005 for advance care planning and decision making -- Experience of use of advance care planning in care homes -- Advance care planning in the community -- Advance care planning in hospices and palliative care -- Advance care planning in hospitals -- Advance care planning: thinking ahead for parents, carers, children, and young people -- Advance care planning and people with dementia -- Experience of advance care planning internationally -- Advance care planning in Australia -- Advance care planning in Canada -- Advance directives and advance care planning: the US experience -- Advance care planning in New Zealand: our Voice--to tatou reo -- Advance care planning in Germany: on track for nationwide implementation -- Advance care planning in an Asian country -- Practicalities and areas of common ground -- Communication skills and advance care planning -- Advance care planning in chronic disease: finding the known in the midst of the unknown -- Planning ahead in all areas -- A population-based approach to end-of-life care and advance care planning.

ISBN

9780198802136

9780192542359

9780192542366

Language

English

Material Type

Ebook

Audience

Professional

Location

Internet

Website Notes

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Author

Jonsen, Albert R

Siegler, Mark

Winslade, William J

Edition

4th ed.

Place of Publication

New York, NY

Publisher

McGraw-Hill, Inc.

Publication Date

1998

Subjects

Ethics, Clinical

Bioethical Issues

Patient Participation

Quality of Life

ISBN

0070331200

Language

English

Material Type

Book

Audience

Professional

Location

Victoria Library

Call Number

W50 J81c 1998

Copies

Corporate Author

Institute of Medicine (U.S.). Committee on Palliative and End-of-Life Care for Children and Their Families

Editor

Field, Marilyn Jane

Behrman, Richard E

Place of Publication

Washington, DC

Publisher

Institute of Medicine, National Academies Press

Publication Date

2003

Physical Description

xx, 690 p. : ill. ; 24 cm.

Subjects

Terminal Care

Child

Health Policy

Patient Participation

Professional-Family Relations

Terminal Care - economics

Terminal Care - legislation & jurisprudence

United States

ISBN

9780309084376

0309084377

Language

English

Material Type

Book

Online

Audience

Professional

Location

Vancouver Library

Internet

Call Number

WS200 W567 2003

Copies

Author

Jonsen, Albert R

Siegler, Mark

Winslade, William J

Edition

6th ed.

Place of Publication

New York, NY

Publisher

McGraw-Hill, Inc.

Publication Date

2006

Series

R2 Library

Subjects

Ethics, Clinical

Bioethical Issues

Patient Participation

Decision Making

Ethical Analysis - methods

Quality of Life

ISBN

0071441999

Language

English

Material Type

Book

Ebook

Audience

Professional

Location

Internet

Kelowna Library

Call Number

WB 60 J81 2006

Website Notes

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Copies

Corporate Author

American College of Physicians

Editor

Snyder, Lois

Edition

6th ed.

Place of Publication

Philadelphia, PA

Publisher

American College of Physicians

Publication Date

2012

Series

R2 Library

Subjects

Ethics, Medical

Ethics, Clinical

Human Experimentation - ethics

Interprofessional Relations - ethics

Physician-Patient Relations - ethics

Physicians - ethics

Social Responsibility

Terminal Care - ethics

Handbooks

ISBN

9781934465981

1934465984

Language

English

Material Type

Ebook

Audience

Professional

Location

Internet

Website Notes

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Editor

Snyder, Lois

Place of Publication

Totowa, NJ

Publisher

Humana Press

Publication Date

2007

Series

Biomedical ethics reviews 2007

Subjects

Complementary Therapies - ethics

Physician-Patient Relations - ethics

Ethics, Clinical

ISBN

1588295842 (alk. paper)

Language

English

Material Type

Book

Audience

Professional

Location

Vancouver Library

Call Number

WB100 C737 2007

Copies

Author

Bernhagen, Michael

Kaldhusdal, Terry

Place of Publication

Shorewood, WI

Publisher

Burning Hay Wagon Production

Publication Date

2011

Physical Description

60 minutes + 1 guide

Subjects

Terminally Ill

Attitude to Death

Terminal Care

Hospice Care

Advance Care Planning

Right to Die

Social Support

Communication

Decision Making

Professional-Patient Relations

Interpersonal Relations

Documentaries and Factual Films

Abstract

Wishes

History

What's next?

Hope

Magic

Conflict

100 things

Conversation

Why?

Credits

Language

English

Material Type

Video

DVD

Audience

Professional

Location

Vancouver Library AV Room

Call Number

WB310 C755 2011

Website Notes

URL links to the discussion guide.

Copies

Author

Cundiff, David

Place of Publication

Totowa, NJ

Publisher

Humana Press

Publication Date

1992

Subjects

Euthanasia

Suicide

Patient Compliance

Hospices

ISBN

089603237X

Language

English

Material Type

Book

Audience

Professional

Location

Vancouver Library

Call Number

BF789 C972 1992

Copies

Author

Seguin, Marilynne

Place of Publication

[Toronto, ON]

Publisher

Key Porter Books

Publication Date

1994

Subjects

Euthanasia

Death

Physician-Patient Relations

Terminal Care

Ethics, Medical

ISBN

1550135538

Language

English

Material Type

Book

Audience

Professional

Location

Vancouver Library

Call Number

W50 S456 1994

Copies

Editor

Gallagher, Colleen

Ewer, Michael

Place of Publication

San Diego, CA

Publisher

Academic Press

Publication Date

2017

Physical Description

xiv, 333 p. : ill. ; 24 cm.

Series

Proquest Ebook Central

Subjects

Medical Oncology - ethics

Ethics, Medical

Abstract

Contents:

1 Ethics and Organizational Identity in a Cancer Care Setting; Introduction; What Makes Cancer Care Ethically Distinct?; Organizational Identity and Ethics; Mission Statements; Codes of Ethics; Institutional Decision-Making Process; The Consequentialist Standard; The Deontological Standard; The Justice Standard; The Common Good Standard; The Character Standard; The Reactive Attitudes Standard; Leadership Structure Putting an Organization?s Ethical Vision into Practice: Some ChallengesConclusion; References; 2 Experience Matters: A Partnership Between Patient and Physician; Introduction; Patient Experience; Leadership in the Face of Clinical Uncertainty; Clinical Scenario; The Predicament: Informed Decision Making in the Face of Clinical Uncertainty; Recommended Action: Be Transparent, Admit Uncertainty; Models of Decision Making; Recommended Action: Educate One Another; Recommended Action: Establish the Roles of the Patient and Physician; Discussion; The Battle of Autonomies in this New Partnership Clinical ScenarioThe Story Continues; Physician Autonomy Comes With Responsibility; Limits to Appropriate and Beneficial Therapies; Communication; Conclusion; References; 3 Patient Experience and End-of-Life Care: A Discussion and Analysis of Four Patients; Introduction; Person-Centered, Family-Oriented Care, and the Patient Experience; Bioethical Principles and End-of-Life Care; Some Challenging Clinical Situations in End-of-Life Care; When Disclosure and Decision-Making Preferences Differ Among Clinicians, Patient and Family; When Patients and Families Demand Care Outside the Usual System When the Value Driving Patient or Family Requests for Care is Not RecognizedWhen Support of Patient Autonomy Is Counterintuitive to Beneficence and Nonmaleficence; Ethical Challenges Inherent in End-of-Life care and Strategies to Facilitate Optimal Outcomes; Conclusions; List of Acronyms and Abbreviations; References; 4 Ethical Issues for Children With Cancer; The Ethical Treatment of Children in Research Studies; Direct Benefit to Minor Patients; Proportionality of Risks and Benefits; Parental Permission; Child Assent; Refusal of Care; Religious Objections; Legal Remedies Physician?s Responsibility and RoleParents? Responsibility and Role; Patient?s Responsibility and Role; Ethical Issues at the End of Life for Children With Cancer; Prognostic Disclosure; Advance Care Planning; Euthanasia, Physician-Assisted Suicide, and Palliative Sedation; Withholding Nutrition and Hydration; Conclusion; References; 5 Ethical Issues in Cancer Survivorship; Introduction; Vignette 1: I Can Beat This Cancer; Who is a Survivor and What is Survivorship?; Survivors and Providers Worldviews Toward Ethics and Survivorship; Ethical Considerations in Survivorship Care

ISBN

9780128038314

9780128039014

Language

English

Material Type

Book

Ebook

Audience

Professional

Location

Kelowna Library

Internet

Call Number

W50 E84 2017

Website Notes

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Copies

Editor

Emanuel, Ezekiel J

Place of Publication

New York, NY

Publisher

Oxford University Press

Publication Date

2008

Physical Description

xx, 827 p. : ill. ; 29 cm.

Subjects

Human Experimentation - ethics

Ethics, Research

Ethics Committees, Research

Research Subjects - legislation & jurisprudence

Abstract

I: Selected history of research with humans

Walter Reed and the yellow fever experiments by Susan E. Lederer

Nazi medical experiments by Paul J. Weindling

Imperial Japanese experiments in China by Takashi Tsuchiya

Randomized controlled trial of streptomycin by Alan Yoshioka

Salk polio vaccine field trial of 1954 by Marcia L. Meldrum

Jewish chronic disease hospital case by John D. Arras

Hepatitis experiments at the Willowbrook State School by Walter M. Robinson and Brandon T. Unruh

Tuskegee syphilis experiment by James H. Jones

HIV research by John Y. Killen Jr.

Gelsinger case by Robert Steinbrook II: Codes, declarations, and other ethical guidance for research with humans

Ethical framework for biomedical research by Ezekiel J. Emanuel, David Wendler and Christine Grady

Nuremberg code by George J. Annas and Michael A. Grodin

Declaration of Helsinki by Richard E. Ashcroft

Belmont report by Tom L. Beauchamp

Regulations for the protection of humans in research in the United States: The common rule by Joan P. Porter and Greg Koski

International ethical guidance rrom the Council for International Organizations of Medical Sciences by Juhana E. ldanpaan-Heikkila and Sev S. Fluss

Council of Europe by Peteris Zilgalvis

European Community directives on data protection and clinical trials by Deryck Beyleveld and Sebastian Sethe

National bioethics commissions and research ethics by Eric M. Meslin and Summer Johnson III. Context, purpose, and value of clinical research

Exploitation in clinical research by Alan Wertheimer

Nature, scope, and justification of Clinical Research : what Is research? Who Is a subject? by Robert J. Levine

Four paradigms of clinical research and research oversight by Ezekiel J. Emanuel and Christine Grady

Role of patient advocates and public representatives in research by Rebecca Dresser IV. Scientific design

Equipoise and randomization by Steven Joffe and Robert D. Truog

Ethics of placebo-controlled trials by Franklin G. Miller

Challenge experiments by Franklin G. Miller and Donald L. Rosenstein

Emergency research by Jason H. T. Karlawish

Research with biological samples by David Wendler

Genetic diagnostic, pedigree, and screening research by Eric T. Juengst and Aaron Goldenberg

Deception in clinical research by David Wendler and Franklin G. Miller

Epidemiology : observational studies on human populations by Douglas L. Weed and Robert E. McKeown

Behavioral and social science research by Felice J. Levine and Paula R. Skedsvold

Phase I Oncology research by Manish Agrawal and Ezekiel J. Emanuel

Surgical innovation and research by Grant R. Gillett V. Participant selection Sect. A. Fair Participant selection

What Is fair participant selection? by Leslie A. Meltzer and James F. Childress

Incentives for research participants by Neal Dickert and Christine Grady

Recruiting research participants by Franklin G. Miller

Sect. B. Special populations

Research involving women by Christine Grady and Colleen Denny

Research with ethnic and minority populations by Bernard Lo and Nesrin Garan

Research involving economically disadvantaged participants by Carol Levine

Research involving those at risk for impaired decision-making capacity by Donald L. Rosenstein and Franklin G. Miller

Research with children by Alan R. Fleischman and Lauren K. Collogan

Research with captive populations :prisoners, students, and soldiers by Valerie H. Bonham and Jonathan D. Moreno

Research with identifiable and targeted communities by Morris W. Foster and Richard R. Sharp

Research with healthy volunteers by Albert R. Jensen and Franklin G. Miller

Research with fetuses, embryos, and stem cells by Ronald M. Green VI. Risk-benefit assessments

Risk-benefit analysis and the net risks test by David Wendler and Franklin G. Miller

Assessing and comparing potential benefits and risks of harm by Nancy M. P. King and Larry R. Churchill

Risk-benefit assessment in pediatric research by Sumeeta Varma and David Wendler VII. Independent review and oversight

Origins and policies that govern institutional review boards by Charles R. McCarthy

Models of institutional review board function by Angela J. Bowen

Evaluating the effectiveness of institutional review boards by Marjorie A. Speers

Data and safety monitoring boards by Lawrence M. Friedman and Eleanor B. Schron

Food and drug administration and drug development : historic, scientific, and ethical considerations by Robert Temple and Sara F. Goldkind VIII. Informed consent

History of informed consent in clinical research by Erika Blacksher and Jonathan D. Moreno

Philosophical justifications of informed consent in research by Dan W. Brock

Legal and regulatory standards of informed consent in research by Alexander M. Capron

Therapeutic misconception by Paul S. Appelbaum and Charles W. Lidz

Empirical issues in informed consent for research by James H. Flory, David Wendler and Ezekiel J. Emanuel

Assent requirement in pediatric research by David Wendler IX. Respect for human research participants

Confidentiality by James G. Hodge Jr. and Lawrence O. Gostin

Liability and compensation for injury of research subjects by Wendy K. Mariner

Obligation to ensure access to beneficial treatments for research participants at the conclusion of clinical trials by James V. Lavery X. Multinational research

Appropriate ethical standards by Ruth Macklin

Benefits to host countries by Ezekiel J. Emanuel

Standard of care in multinational research by Soren Holm and John Harris

Responsiveness to host community health needs by Alex John London XI. Clinical investigator behavior

Conflict of interest in medical research : historical developments by Trudo Lemmens

Concept of conflicts of interest by Ezekiel J. Emanuel and Dennis F. Thompson

Empirical data on donflicts of interest by Lindsay A. Hampson, Justin E. Bekelman and Cary P. Gross

Industrialization of academic science and threats to scientific integrity by Eric G. Campbell and David Blumenthal

Fraud, fabrication, and falsification by David B. Resnik

Obligation to publish and disseminate results by Drummond Rennie.

ISBN

9780195168655

0195168658

Language

English

Material Type

Book

Audience

Professional

Location

Vancouver Library

Kelowna Library

Surrey Library

Victoria Library

Abbotsford Library

Call Number

W20.55 H9 O98 2008

Copies

Editor

Friedman, Emily

Place of Publication

Chicago, Ill.

Publisher

American Hospital Publishing, Inc.

Publication Date

1992

Subjects

Ethics, Medical

Terminal Care

ISBN

1556480822

Language

English

Material Type

Book

Audience

Professional

Location

Vancouver Library

Call Number

W50 C545 1992

Copies

Editor

Angelos, Peter

Edition

2nd ed.

Place of Publication

New York, NY

Publisher

Springer

Publication Date

2008

Physical Description

xii, 258 p. ; 25 cm.

Series

Cancer treatment and research 140

Subjects

Ethics, Medical

Neoplasms - therapy

Physician-Patient Relations

Communication

Truth Disclosure

Palliative Care

ISBN

9780387736389

0387736387

Language

English

Material Type

Book

Audience

Professional

Location

Vancouver Library

Kelowna Library

Surrey Library

Victoria Library

Abbotsford Library

Call Number

QZ266 E84 2008

Copies