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Ethics in psychiatry : European contributions

https://libcat.nshealth.ca/en/permalink/provcat40976
Hanfried Helmchen, Norman Sartorius, editors. --Dordrecht: Springer , c2010.
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Location
Online
Available Online
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Other Authors
Helmchen, H (Hanfried)
Sartorius, N
Responsibility
Hanfried Helmchen, Norman Sartorius, editors
Place of Publication
Dordrecht
Publisher
Springer
Date of Publication
c2010
Physical Description
1 online resource (xviii, 573 p.)
Series Vol.
45
Series Title
International library of ethics, law and the new medicine
ISBN
9789048187218
9789048187201 (print ed.)
Subjects (MeSH)
Bioethical Issues
Patient Rights
Psychiatry - ethics
Contents
Part I. The Context -- 1. Societal Framework of Psychiatry -- 2. Stigmatisation of People with Mental Illness and of Psychiatric Institutions -- 3. Economical Framework of Psychiatric Care -- 4. Conflicts of Interest -- 5. Between Legislation and Bioethics: The European Convention on Human Rights and Biomedicine -- 6. Ethics Committees for Clinical Research – The West-European Paradigm -- 7. Clinical Ethics Committees and Ethics Consultation in Psychiatry -- Part II. Principles of Ethics in Psychiatry -- 8. Ethical Principles in Psychiatry: The Declarations of Hawaii and Madrid -- 9. Informed Consent in Psychiatric Practice -- 10. Advance Directives: Balancing Patient’s Self-Determination with Professional Paternalism -- 11. Confidentiality -- 12. Justice in Access to and Distribution of Resources in Psychiatry and Mental Health Care -- Part III. The Applications of the Ethical Principles in Psychiatric Practice and Research -- 13. Ethics of Diagnosis and Classification in Psychiatry -- 14. Competence Assessment -- 15. General Overview of Ethical Issues in Psychiatric Treatment -- 16. Prevention and Early Treatment -- 17. Ethical Implications of Psychopharmacotherapy -- 18. Ethical Problems in Psychotherapy -- 19. Neuromodulation – ECT, rTMS, DBS -- 20. ‘Coercive’ Measures -- 21. Ethics of Deinstitutionalization -- 22. Ethical Issues in Forensic and Prison Psychiatry -- 23. Treatment of Substance Dependence -- 24. Dementia and End-of-Life Decisions: Ethical Issues – A Perspective from The Netherlands -- 25. Ethics of Research with Decisionally Impaired Patients -- 26. Ethical Concerns in Carrying Out Surveys of Psychiatric Morbidity -- 27. Genetics – Ethical Implications of Research, Diagnostics and Counseling -- Part IV. Non-medical Uses of Psychiatry -- 28. Political Abuse of Psychiatry -- 29. Abuse of Psychiatry for Political Purposes in the USSR: A Case-Study and Personal Account of the Efforts to Bring Them to an End -- 30. (Neuro-)Enhancement -- Part V. Teaching Ethics in Psychiatry -- 31. Teaching Ethics in Psychiatry -- Part VI. Conclusions and Summary -- 32. Summary and Conclusions.
Format
e-Book
Location
Online
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Healthcare research ethics and law : regulation, review and responsibility

https://libcat.nshealth.ca/en/permalink/provcat23813
Biggs, Hazel. --London, England: Routledge-Cavendish , 2010.
Call Number
W 20.55 .E7 B592h 2010
Location
Halifax Infirmary
Call Number
W 20.55 .E7 B592h 2010
Author
Biggs, Hazel
Place of Publication
London, England
Publisher
Routledge-Cavendish
Date of Publication
2010
Physical Description
188 p.
Series Title
Biomedical law and ethics library
ISBN
9780415429177
Subjects (MeSH)
Biomedical Research - ethics
Biomedical Research - legislation & jurisprudence
Ethics, Research
Ethics Committees, Research
Format
Book
Location
Halifax Infirmary
Loan Period
3 weeks
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Pediatric bioethics

https://libcat.nshealth.ca/en/permalink/provcat27748
edited by Geoffrey Miller. --Cambridge: Cambridge University Press , 2010.
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Location
Online
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Author
Miller, Geoffrey
Responsibility
edited by Geoffrey Miller
Place of Publication
Cambridge
Publisher
Cambridge University Press
Date of Publication
2010
Physical Description
1 online resource (289 p.)
ISBN
9780511642388 (ebook)
9780521517980 (hardback)
Subjects (MeSH)
Pediatrics - ethics
Bioethical Issues
Contents
Virtues and goals in pediatrics / G. Kevin Donovan and Edmund D. Pellegrino -- Contributions of ethical theory to pediatric ethics : parents as co-fiduciaries of pediatrics patients / Laurence B. McCullough -- Using the best interests standards in treatment decisions for young children / Loretta M. Kopelman -- Moral and legal status of children and parents / Sadath A. Sayeed -- The ethics of pediatric research / Jonathan D. Moreno and Alexandra Kravitt -- Truth telling in pediatrics : what they don't know might hurt them / Christine Harrison -- Pediatric ethics committees / Mark R. Mercurio -- Newborn screening / Lainie Friedman Ross -- Presymptomatic genetic testing in children / Kimberly A. Quaid -- Extreme prematurity : truth and justice / Geoffrey Miller -- Disorders of sex development / Alice D. Dreger and David Sandberg -- Rationality, personhood, and Peter Singer on the fate of severely impaired infants / Eva Feder Kittay -- The ethics of controlling reproduction in a population with mental disabilities / Paul A. Lombardo -- Pediatric innovative surgery / Angelique M. Reitsma -- Conjoined twins / Alice D. Dreger and Geoffrey Miller -- Ethics and immunization / Joel E. Frader and Erin Flanagan-Klygis -- Psychotropic drug use in children : the case of stimulants / Ilina Singh -- Brain death, minimal consciousness, and vegetative states in children / Geoffrey Miller and Stephen Ashwal -- The foregoing of life sustaining treatment for children / Sadath A. Sayeed and Geoffrey Miller.
Format
e-Book
Location
Online
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Institutional review board : member handbook

https://libcat.nshealth.ca/en/permalink/provcat40914
Robert Amdur, Elizabeth A. Bankert. (Third edition) --Sudbury, MA: Jones and Bartlett Publishers , c2011.
Call Number
W 20.5 A4971 2011
Location
Dickson Building
Designed to give Institutional Review Board (IRB) members the information they need to protect the rights and welfare of research subjects in a way that is both effective and efficient, the chapters of the Institutional Review Board Member Handbook are short and to the point. Topic-specific chapters list the criteria IRB members should use to determine how to vote on specific kinds of studies and offer practical advice on what IRB members should do before and during full-committee meetings. Thi…
Call Number
W 20.5 A4971 2011
Author
Amdur, Robert J
Other Authors
Bankert, Elizabeth A
Responsibility
Robert Amdur, Elizabeth A. Bankert
Edition
Third edition
Place of Publication
Sudbury, MA
Publisher
Jones and Bartlett Publishers
Date of Publication
c2011
Physical Description
xii, 215 pages
ISBN
9781449647445
9780763780005
Subjects (MeSH)
Biomedical Research - ethics
Ethical Review - standards
Ethics Committees, Research - organization & administration
Ethics, Medical
Human Experimentation - ethics
Abstract
Designed to give Institutional Review Board (IRB) members the information they need to protect the rights and welfare of research subjects in a way that is both effective and efficient, the chapters of the Institutional Review Board Member Handbook are short and to the point. Topic-specific chapters list the criteria IRB members should use to determine how to vote on specific kinds of studies and offer practical advice on what IRB members should do before and during full-committee meetings. This handbook is an excellent accompaniment to Institutional Review Board: Management and Function, Second Edition and the Study Guide that IRB members can access and refer to quickly and easily.
Format
Book
Publication Type
Handbook
Location
Dickson Building
Loan Period
3 weeks
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The art of applying to Canadian medical schools

https://libcat.nshealth.ca/en/permalink/provcat26343
Rosemary Marchant. --Toronto, ON: Worksafe Incorporated , c2012.
Call Number
WB 290 M315 2012
Location
Halifax Infirmary
This is a book on how to apply to Canadian medical schools. The approach coaches the student through the process of choosing the most appropriate schools to apply to. It also helps the applicant to present themselves effectively.
Call Number
WB 290 M315 2012
Author
Marchant, Rosemary
Responsibility
Rosemary Marchant
Alternate Title
Applying to Canadian medical schools
Place of Publication
Toronto, ON
Publisher
Worksafe Incorporated
Date of Publication
c2012
Physical Description
234 p.
Subjects (MeSH)
Medical colleges - Canada
Schools, Medical - Canada
Interviews as Topic - Canada
Job Application - Canada
Abstract
This is a book on how to apply to Canadian medical schools. The approach coaches the student through the process of choosing the most appropriate schools to apply to. It also helps the applicant to present themselves effectively.
Contents
Introduction -- Who are Medical Schools Seeking? -- What particular abilities are the admission committees seeking? Cognitive abilities: Non-cognitive abilities; Physical abilities; Selection process -- What is the success rate? -- When to apply? -- What if I was rejected last year, should I reapply? -- How to apply -- Considerations in the choice of medical schools -- Essays and long answers: Essay application requirements; General rules for writing essays; Constructing a paragraph; General approach to the long essay -- McMaster University’s CASPer -- The interview: Traditional interview: Multiple mini interviews; Interview preparation; At the interview; Sound advice -- Referees and verifiers -- Peak Performance: Using our thoughts to create success -- Will I get in? -- Integrity -- Appendices -- Biography.
Format
Book
Location
Halifax Infirmary
Copies
1
Loan Period
3 weeks
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Shoulder concepts 2013 : consensus and concerns : proceedings of the ISAKOS Upper Extremity Committees 2009-2013

https://libcat.nshealth.ca/en/permalink/provcat40807
Guillermo Arce [and 9 others], editors. --Berlin, Heidelberg: Springer , c2013.
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Location
Online
The ISAKOS Upper Extremity Committee (UEC) meets on a biannual basis for Closed Consensus Meetings. Each summit, a worldwide expert panel of surgeons and researchers convene for an in-depth discussion about a controversial topic. The purpose of this endeavor is to combine expertise and reach international consensus for the most appropriate management of various shoulder disorders. This booklet constitutes an integral part of the agreement encountered during these meetings. Section A provides a …
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Other Authors
Arce, Guillermo
Other Authors
International Society of Arthroscopy Knee Surgery and Orthopaedic Sports Medicine
Responsibility
Guillermo Arce [and 9 others], editors
Place of Publication
Berlin, Heidelberg
Publisher
Springer
Date of Publication
c2013
Physical Description
1 online resource (x, 98 p. : 29 illus., 21 illus. in color)
ISBN
9783642380976
9783642380969 (print ed.)
Subjects (MeSH)
Shoulder Injuries
Shoulder - surgery
Abstract
The ISAKOS Upper Extremity Committee (UEC) meets on a biannual basis for Closed Consensus Meetings. Each summit, a worldwide expert panel of surgeons and researchers convene for an in-depth discussion about a controversial topic. The purpose of this endeavor is to combine expertise and reach international consensus for the most appropriate management of various shoulder disorders. This booklet constitutes an integral part of the agreement encountered during these meetings. Section A provides a comprehensive review of the currently available Classifications and Outcome Scores for shoulder disorders, illustrating their potential pitfalls and limitations. Section B presents a summary of the Acromio-Clavicular Joint (ACJ) Consensus Summit, describing pioneering techniques to re-establish shoulder function after dislocation. Section C describes the current state of evidence of Rotator Cuff Disorders, providing novel theories regarding its underlying biomechanics and reconstruction techniques. The 2009-2013 ISAKOS UEC members hope the readers find this compendium an insightful update for daily shoulder management.
Contents
Part I. ISAKOS Shoulder Terminology Project; Preliminary Report; Classifications and Scoring Systems -- 1. Introduction -- 2. A Review of Rotator Cuff Classifications in Current Use -- 3. ISAKOS Classification System for Rotator Cuff Tears -- 4. Review of Current Classifications of Shoulder Instability -- 5. ISAKOS Consensus Shoulder Instability Classification System -- 6. Outcomes Scores for Shoulder Instability and Rotator Cuff Disease -- Part II. Copenhagen Consensus on Acromio-Clavicular Disorders -- 7. Copenhagen Consensus on Acromio-Clavicular Disorders -- Part III. Buenos Aires Consensus on Rotator Cuff Disease: Known Facts and Unresolved Issues -- 8. Anatomy (Bone, Tendon, Bursa and Neurovascular Anatomy) -- 9. Biomechanics -- 10. Tendinosis, Impingement and Ruptures -- 11. Arthroscopy and Repair -- 12. Augments and Prosthesis.
Format
e-Book
Location
Online
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The academic medicine handbook : a guide to achievement and fulfillment for academic faculty

https://libcat.nshealth.ca/en/permalink/provcat32568
Laura Weiss Roberts, editor. --New York, NY: Springer , c2013.
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Location
Online
Attaining professional success and finding personal happiness in academic medicine is not an easy path, yet both are critical if the future is to be brighter through better science, better clinical care, better training, better responsiveness to communities, and better stewardship and leadership in the health professions. This concise, easy to read title consists of 'mini' chapters intended as a resource to assist early- and middle-career physicians, clinicians, and scientists in understanding …
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Other Authors
Roberts, Laura Weiss
Responsibility
Laura Weiss Roberts, editor
Place of Publication
New York, NY
Publisher
Springer
Date of Publication
c2013
Physical Description
1 online resource (xxi, 486 p. : 19 ill., 11 ill. in color)
ISBN
9781461456933
Subjects (MeSH)
Clinical Medicine
Education, Medical
Subjects (LCSH)
Medicine
Internal medicine
Neurology
Psychiatry
Abstract
Attaining professional success and finding personal happiness in academic medicine is not an easy path, yet both are critical if the future is to be brighter through better science, better clinical care, better training, better responsiveness to communities, and better stewardship and leadership in the health professions. This concise, easy to read title consists of 'mini' chapters intended as a resource to assist early- and middle-career physicians, clinicians, and scientists in understanding the unique mission of academic medicine and building creative, effective, and inspiring careers in academic health organizations. Organized in eight sections, the Guide covers such areas as finding your path in academic medicine, getting established at an institution, approaching work with colleagues, writing and reviewing manuscripts, conducting empirical research, developing administrative skills, advancing your academic career, and balancing your professional and personal life. Each chapter includes pointers and valuable career and 'best practices' strategies in relation to the topic area. An exciting addition to the professional development literature, Achievement and Fulfillment in Academic Medicine: A Comprehensive Guide is an indispensable resource for anyone seeking to achieve a fulfilling career in academic medicine.
Contents
Approaching the Profession of Academic Medicine -- How To Find Your Path in Academic Medicine -- How to Build the Foundation for a Successful Career in Academia -- How to Be Organized and Manage Time -- How to Align Individual Goals with Institutional Goals -- How to Prepare the Best Possible Curriculum Vitae -- How to Interview -- EVALUATING A LETTER OF OFFER OR CONTRACT -- How to Give a Lecture -- How to Build Assessments -- How to Supervise Trainees in Clinical Settings -- HOW TO EVALUATE AND GIVE FEEDBACK -- How to Teach in Clinical Settings -- WRITING EFFECTIVE LETTERS OF RECOMMENDATION -- Creative Teaching -- Educational Innovation Using Technology -- Maintaining Excellent Clinical Documentation -- How to avoid medicolegal problems -- How to Network and Be a Good Colleague -- Best practices in interprofessional collaboration in academic settings -- FROM LESSONS LEARNED: MENTEE PERSPECTIVE ON MENTORSHIP -- How to Be a Good Mentor -- How to Participate in Institutional Review Board Activities -- How to Participate in Ethics Committees -- 24 Intervening With Unethical and Unprofessional Colleagues -- How to Write and Publish an Empirical Report -- How to Write a Case Report -- How to Review a Manuscript -- How to Evaluate Biomedical Research Publications Rigorously -- How to Understand Flaws in Clinical Research -- How to conceptualize a research project -- How to Conduct a First Small Project -- How to Prepare an IRB Application -- HOW TO ENGAGE COMMUNITIES IN RESEARCH -- How to Approach a First Grant Application -- Funding Your Research While Maintaining Your Curiosity -- How to Review Grant Applications -- How to Prepare a Poster -- How to Prepare and Give a Scholarly Oral Presentation -- How to Be an Effective Team Leader and Committee Member of Chair -- The Art of Principled Negotiation in Academic Medicine -- How to think about money in academic settings -- Departmental Strategic Planning -- How to Read a Basic Budget -- How to Strengthen Your Own and Others' Morale -- HOW TO CREATE YOUR PACKAGE FOR PROMOTION -- How to understand promotion criteria for 'traditional' & 'research' tracks -- How to Understand Promotion Criteria for 'Clinician Educator' and 'Teaching' Tracks -- How to Develop an Educator's Portfolio -- How to Build a National Reputation for Academic Medicine Promotion -- How to Recognize and Address Unconscious Bias -- IMGs in Academic Medicine: Challenges and Opportunities -- How to 'Pitch' a Non-traditional Career Path -- How to Approach a Healthy Life Balance -- How to Care for the Basics – Sleep, Nutrition, Exercise, Health -- How to Manage Personal Finances -- PROFESSIONAL RELATIONSHIPS AND FIVE KEY ELEMENTS ESSENTIAL FOR OPTIMAL CAREER SUCCESS -- How to Recognize and Avoid Burnout -- How to Manage Personal Finances -- How to Develop Professional Reationships -- Index.
Format
e-Book
Location
Online
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The FDA for Doctors

https://libcat.nshealth.ca/en/permalink/provcat39622
William H. Eaglstein. --Cham: Springer , c2014.
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Location
Online
This book explains the Food and Drug Administration (FDA) as an institution and provides understanding of its nomenclature, societal role, policies, goals and challenges. While many readers will have some knowledge of the FDA, few have an appreciation of the many specific areas of FDA authority. For example, how many realize that the US is one of only two countries which allow direct-to-consumer drug advertising, which is regulated by FDA? Or that FDA itself advertises to try to prevent young p…
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Author
Eaglstein, William H
Responsibility
William H. Eaglstein
Place of Publication
Cham
Publisher
Springer
Date of Publication
c2014
Physical Description
1 online resource (xi, 97 p. : 1 illus. in color)
ISBN
9783319083629
9783319083612 (print ed.)
Subjects (MeSH)
Biological Products - standards
Device Approval
Drug Approval
Government Regulation
United States Government Agencies
Other Subjects
United States. Food and Drug Administration
Other Subjects
United States
Abstract
This book explains the Food and Drug Administration (FDA) as an institution and provides understanding of its nomenclature, societal role, policies, goals and challenges. While many readers will have some knowledge of the FDA, few have an appreciation of the many specific areas of FDA authority. For example, how many realize that the US is one of only two countries which allow direct-to-consumer drug advertising, which is regulated by FDA? Or that FDA itself advertises to try to prevent young people from smoking cigarettes, and that all proprietary drug names must be approved by FDA? How many doctors or other readers are familiar with the formal definition distinguishing drugs from devices and the importance this has for development costs and for our knowledge about the ultimate products? How many know how much nutritional supplements are regulated by FDA? The FDA for Doctors is not for those looking for detailed instruction on dealing with the FDA or its operations. Rather, it is written by a doctor with doctors in mind, with the hope that the information in this book will make physicians, and other readers, more thoughtful and insightful, especially with regards to therapeutics and the many broad societal issues underlying FDA's activities. With over 40 years of experience as a clinical investigator in many trials done for FDA registration, the author has been a member of and chaired an FDA advisory committee, and has been a consultant to several divisions of the FDA. He has also had the opportunity to serve on the U.S. Senate Labor Committee, helping with its FDA oversight activities. In addition to a long academic medical career the author has been a consultant to and a full time employee of drug and device companies.
Contents
1. Doctors and the FDA -- 2. What Are Drugs? -- 3. What Are Devices? -- 4. What Are Biologics, Biological Products and Biological Drugs? -- 5. What Are Combination Products -- 6. What Are Dietary Supplements and Nutraceuticals? -- 7. What Are Cosmetics and Cosmeceuticals? -- 8. What Is the FDA and What Does It Do? -- 9. Foods, Doctors and the FDA -- 10. The FDA Approval Process and Drug Development -- 11. The New Drug Application (NDA), the Investigative New Drug Exemption (IND) and the General Drug Approval Pathway -- 12. FDA and Tobacco Products -- 13. FDA Advisory Committees -- 14. FDA, Labels and Labeling for Medical Products -- 15. FDA and Product Names -- 16. FDA and Promotion and Advertising -- 17. Off-Label Use -- 18. Additional Drug Approval Pathways and Expanded Access (Treatment INDs); and Personal Importation of Unapproved Drugs -- 1.9 FDA Exclusivity and Patents -- 20. Adverse Event Reporting, Pharmacovigilance and FDA -- 21. FDA Rule Making and Guidances -- 22. Enforcement and Warning Letters -- 23. The FDA, Politics and Criticism -- 24. Brief History of the FDA.
Format
e-Book
Location
Online
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Learning to Lead in the Academic Medical Center : A Practical Guide

https://libcat.nshealth.ca/en/permalink/provcat39374
Jeffrey L. Houpt, Roderick W Gilkey, Susan H. Ehringhaus. (1st ed.) --Cham: Springer , c2015.
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Location
Online
This compelling title is a comprehensive, practical guide for current and aspiring leaders in academic medical centers (AMC). Offering both a broad overview of the dynamics of the AMC and a detailed "how-to" set of instructions for the wide-ranging situations that demand skilled leadership, this expertly designed volume is filled with meaningful examples and insights. Learning to Lead in the Academic Medical Center: A Practical Guide consists of five parts. The first three sections are narrativ…
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Author
Houpt, Jeffrey L
Other Authors
Gilkey, Roderick W
Ehringhaus, Susan H
Responsibility
Jeffrey L. Houpt, Roderick W Gilkey, Susan H. Ehringhaus
Edition
1st ed.
Place of Publication
Cham
Publisher
Springer
Date of Publication
c2015
Physical Description
1 online resource (xxi, 219 p. : 1 illus. in color)
ISBN
9783319212609
9783319212593 (print ed.)
Subjects (MeSH)
Academic Medical Centers - organization & administration
Leadership
Abstract
This compelling title is a comprehensive, practical guide for current and aspiring leaders in academic medical centers (AMC). Offering both a broad overview of the dynamics of the AMC and a detailed "how-to" set of instructions for the wide-ranging situations that demand skilled leadership, this expertly designed volume is filled with meaningful examples and insights. Learning to Lead in the Academic Medical Center: A Practical Guide consists of five parts. The first three sections are narrative and intended to help the reader become a better leader. The first section looks at the AMC as a social system and emphasizes an understanding of group dynamics. The second section discusses the critical role of personality, while the third covers all the necessary leadership skill sets such as negotiation, persuasion, conflict resolution, running a meeting, and so on. The fourth section is a fascinating series of case vignettes to solve based on the material that preceded it. The final section provides a set of highly instructional solutions to those cases. An indispensable reference authored by three highly accomplished leaders in the field, Learning to Lead in the Academic Medical Center: A Practical Guide will be of great interest to all physicians and trainees who seek a comprehensive yet handy resource on the need-to-know basics of success in the AMC environment.
Contents
Part I. The Academic Medical Center (AMC): How It Really Works -- 1. The AMC: the Formal and Informal Organization -- 2. Culture Is King -- 3. Authority is Earned, not Bestowed -- Part II. The Role of Personality -- 4. Personality Traits and Leadership -- 5.Managing Personality Disorders in the Workplace -- 6.The Importance of Emotional Intelligence -- Part III. Essential Skills -- 7. Getting Started the Right Way -- 8. Negotiation -- 9. Recruitment: Negotiation in Action -- 10. Conflict Resolution: Making Friends with Conflict -- 11. Mastering the Art of Persuasion -- 12. Running a Meeting -- 13. Making Good Decisions -- 14. Stimulating Change without Enduring a Coup -- 15. A Final Word to Applicants and Search Committees: Picking the Right People for Leadership Roles the First Time -- Part IV. Cases For Discussion -- 16. Strategic Planning/Outside Consultants: Power and Authority, Vertical Hierarchies, and the Informal Organization -- 17. Dr. Newby: Change, Getting Started, and Your Baby Is Ugly -- 18. Dr. Worksalot: Personality and Getting Started -- 19. Negotiating for a Center Director -- 20. Dr. Un Settled: Negotiation and Middle Age Dysphoria -- 21. Dr. Green, Conflict Resolution, and Managing Up and Down -- 22. Drs. Rich and Pure: Conflict of Interest and Creating School Wide Policies -- 23. Budget Cuts and Managing Bad News and Incentivizing Faculty -- 24. A "No Brainer": Dr. Virtue Comes to State University Medical Center -- Part V. Teaching Materials -- 25. Strategic Planning/Outside Consultants: Power and Authority, Vertical Hierarchies, and the Informal Organization -- 26. Dr. Newby: Change, Getting Started, and Your Baby Is Ugly -- 27. Dr. Worksalot: Personality and Getting Started -- 28. Negotiating for a Center Director -- 29. Dr. Unsettled: Negotiation and Middle Age Dysphoria -- 30. Dr. Green, Conflict Resolution, and Managing Up and Down -- 31. Drs. Rich and Pure: Conflict of Interest and Creating School Wide Policies -- 32. Budget Cuts and Managing Bad News and Incentivizing Faculty -- 33. A "No Brainer": Dr. Virtue Comes to State University Medical Center -- Appendix A: Developmental Steps -- Appendix B: Questions on Interpersonal and Management Skills -- Appendix C: Annotated Bibliography.
Format
e-Book
Location
Online
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Ethics, Law and Governance of Biobanking : National, European and International Approaches

https://libcat.nshealth.ca/en/permalink/provcat39547
Deborah Mascalzoni, editor. --Dordrecht: Springer Netherlands , c2015.
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Location
Online
Biobank research and genomic information are changing the way we look at health and medicine. Genomics challenges our values and has always been controversial and difficult to regulate. In the future lies the promise of tailored medical treatments and pharmacogenomics but the borders between medical research and clinical practice are becoming blurred. We see sequencing platforms for research that can have diagnostic value for patients. Clinical applications and research have been kept separate,…
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Other Authors
Mascalzoni, Deborah
Responsibility
Deborah Mascalzoni, editor
Place of Publication
Dordrecht
Publisher
Springer Netherlands
Date of Publication
c2015
Physical Description
1 online resource (viii, 277 p.)
Series Vol.
14
Series Title
The International Library of Ethics, Law and Technology
ISBN
9789401795739
9789401795722 (print ed.)
ISSN
1875-0044
Subjects (MeSH)
Biological Specimen Banks - ethics
Biological Specimen Banks - legislation & jurisprudence
Genetic Privacy - standards
Genetic Research - ethics
Health Policy
Internationality
Abstract
Biobank research and genomic information are changing the way we look at health and medicine. Genomics challenges our values and has always been controversial and difficult to regulate. In the future lies the promise of tailored medical treatments and pharmacogenomics but the borders between medical research and clinical practice are becoming blurred. We see sequencing platforms for research that can have diagnostic value for patients. Clinical applications and research have been kept separate, but the blurring lines challenges existing regulations and ethical frameworks.Then how do we regulate it? This book contains an overview of the existing regulatory landscape for biobank research in the Western world and some critical chapters to show how regulations and ethical frameworks are developed and work. How should international sharing work? How design an ethical informed consent? An underlying critique: the regulatory systems are becoming increasingly complex and opaque. The international community is building systems that should respond to that. According to the authors in fact, it is time to turn the ship around. Biobank researchers have a moral responsibility to look at and assess their work in relation to the bigger picture: the shared norms and values of current society. Research ethics shouldn't only be a matter of bioethicists writing guidelines that professionals have to follow. Ethics should be practiced through discourse and regulatory frameworks need to be part of that public discourse. Ethics review should be then not merely application of bureaucracy and a burden for researchers but an arena where researchers discuss their projects, receive advice and practice their ethics skills.
Contents
Ethics Law and Governance of Biobanking: A Very Complex Normative Puzzle -- Biobanks: A Definition -- A Participatory Space Beyond the “Autonomy Versus Property” Dichotomy -- Intellectual Property and Biobanks -- Consent, Privacy and Property in the Italian Biobanks Regulation: A Hybrid Model Within EU? -- Data Protection Principles and Research in the Biobanks Age -- The New General Data Protection Regulation—Where Are We and Where Might We Be Heading? -- The Tension Between Data Sharing and the Protection of Privacy in Genomics Research -- Incidental Findings: The Time Is not yet Ripe for a Policy for Biobanks -- Biobanking Across Borders: The Challenges of Harmonisation -- Governing Biobanks Through a European Infrastructure -- EU Governance for Research and Ethics in Biobanks -- A Bold Experiment: Iceland’s Genomic Venture -- The Estonian Genome Center, University of Tartu -- Management of the Ethical Aspects of a Local Mental Diseases Biobank for Research Purposes: The Italian Experience -- Biobank Governance in Spain: From the Autonomy of Research Ethics Committees to the Autonomy of Lay People -- Public Deliberation and the Role of Stakeholders as a New Frontier in the Governance of Science: The British Columbia Biobank Deliberation and the DePGx Project -- Making Researchers Moral.
Format
e-Book
Location
Online
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Clinical trials : study design, endpoints and biomarkers, drug safety, and FDA and ICH guidelines

https://libcat.nshealth.ca/en/permalink/provcat31841
by Tom Brody. (2nd ed.) --Amsterdam, Netherlands: Elsevier , c2016.
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Location
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Clinical Trials, Second Edition, offers those engaged in clinical trial design a valuable and practical guide. This book takes an integrated approach to incorporate biomedical science, laboratory data of human study, endpoint specification, legal and regulatory aspects and much more with the fundamentals of clinical trial design. It provides an overview of the design options along with the specific details of trial design and offers guidance on how to make appropriate choices. Full of numerous…
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Author
Brody, Tom
Responsibility
by Tom Brody
Edition
2nd ed.
Place of Publication
Amsterdam, Netherlands
Publisher
Elsevier
Date of Publication
c2016
Physical Description
1 online resource,
ISBN
9780128042175
Subjects (MeSH)
Clinical Trials as Topic
Clinical Trials Data Monitoring Committees
Drug Approval
Research Design
Abstract
Clinical Trials, Second Edition, offers those engaged in clinical trial design a valuable and practical guide. This book takes an integrated approach to incorporate biomedical science, laboratory data of human study, endpoint specification, legal and regulatory aspects and much more with the fundamentals of clinical trial design. It provides an overview of the design options along with the specific details of trial design and offers guidance on how to make appropriate choices. Full of numerous examples and now containing actual decisions from FDA reviewers to better inform trial design, the 2nd edition of Clinical Trials is a must-have resource for early and mid-career researchers and clinicians who design and conduct clinical trials.
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Registration required for PDF access.
Format
e-Book
Location
Online
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Biomedical Research : An Insider's Guide

https://libcat.nshealth.ca/en/permalink/provcat39724
Seward B. Rutkove. --New York, NY: Springer , c2016.
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This comprehensive yet concise book introduces people at all levels of training--undergraduate, graduate, and medical students, residents, fellows, and junior faculty--to the basic joys and challenges of biomedical research. By discussing many key research issues, would-be and early-stage academics will not only be better informed about the world of biomedical research, but will learn a basic set of instructions to help jumpstart their careers. Biomedical Research: An Insider's Guide is divided…
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Author
Rutkove, Seward B
Responsibility
Seward B. Rutkove
Place of Publication
New York, NY
Publisher
Springer
Date of Publication
c2016
Physical Description
1 online resource (xvii, 299 p.)
ISBN
9781493936557
9781493936533 (print ed.)
Subjects (MeSH)
Biomedical Research - methods
Research Design
Abstract
This comprehensive yet concise book introduces people at all levels of training--undergraduate, graduate, and medical students, residents, fellows, and junior faculty--to the basic joys and challenges of biomedical research. By discussing many key research issues, would-be and early-stage academics will not only be better informed about the world of biomedical research, but will learn a basic set of instructions to help jumpstart their careers. Biomedical Research: An Insider's Guide is divided into five sections. The first focuses on decision points regarding whether or not to enter research and if so what type: basic, clinical, or translational. The second section focuses on the practicalities of pursuing medical research, including institutional review boards and animal care committees as well general suggestions regarding idea generation and collaboration. The third section covers a core aspect of research: writing--detailing the evolution of both grants and papers. The fourth section addresses a range of issues, including conferencing to patents to working with industry to obtaining philanthropic support. The final section deals with all-important broader life issues from job choices to being a mentor to thoughts on how to keep the big picture front and center. An invaluable resource that offers insightful, practical advice, Biomedical Research: An Insider's Guide reveals how biomedical research can be both challenging and truly rewarding.
Contents
Part 1: Basic considerations -- 1. So do you really want to pursue research? -- 2. What's in store: The brighter side of medical research -- 3. What's in store: The darker side of medical research -- 4. One degree of separation -- 5. Choosing and working with a mentor -- 6. Identifying a research niche you can call your own -- 7. Useful Definitions -- Part 2: Research Foundations and Structures -- 8. The Institutional Review Board: Do's, Don'ts, and Nevers -- 9. Animal Care and Use Committees -- 10. Research beyond humans and vertebrates -- 11. Hiring Research Staff -- 12. Strategy and Tactics: Running a Successful Laboratory -- 13. Everything you ever wanted to know about collaboration -- Part 3: Successful Paper and Grant Writing -- 14. Writing a successful research paper. I. Up to the point of submission -- 15. Writing a successful research paper. II Revising, resubmitting, and post-acceptance tasks -- 16. Funding: An overview -- 17. Where to apply for funding: making the right choices -- 18. Writing a winning grant application -- 19. Grant budgeting -- 20. Grant writing: Pearls and lumps of coal -- 21. Research Training, Fellowship, and Career grants -- 22. Grant review from the inside -- 23. Interpreting your reviews -- 24. To resubmit or not resubmit and how to do it -- Part 4: Good presentations, conferencing, networking, and other useful tools -- 25. The art of good presentation -- 26. Effective conferencing -- 27. Networking in the 21st century -- 28. Conflicts of interest -- 29. Scientific conduct and misconduct: what is right and proper, what is not, and what is somewhere in the middle -- 30. Article review and reading: being efficient and as thorough as you need to be -- 31. Patents -- 32. Working with industry -- Part 5: Career choices and life lessons -- 33. Jobs in biomedical science: seeking, landing, and changing -- 34. Academic Promotion and Titles -- 35. On being a mentor -- 36. Yardsticks of success -- 37. Research Life Lesson #1: Everything takes longer than you think, so plan for it -- 38. Research life lesson #2: A person's research is endlessly important to them -- 39. Research Life lesson #3: Balance, timing, cycles and seeing the big picture -- 40. Research Life Lesson #4: Your career is an ultramarathon, not a sprint -- 41. Conclusion: Nothing satisfies like meaningful work.
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Cancer of the Oral Cavity, Pharynx and Larynx : Evidence-Based Decision Making

https://libcat.nshealth.ca/en/permalink/provcat39795
Jesus E. Medina, Nilesh R. Vasan, editors. --Cham: Springer , c2016.
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Written for residents and practitioners of otolaryngology, medical oncology, radiation oncology, and maxiollofacial surgery, this book provides the reader with a comprehensive, concise discussion of the best evidence available on which to base clinical decisions needed when managing patients with squamous cell carcinomas of the oral cavity, pharynx and larynx. Because of its accessible and practical format, this book is considerably different than other related titles on the market. Formatted w…
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Other Authors
Medina, Jesus E
Vasan, Nilesh R
Responsibility
Jesus E. Medina, Nilesh R. Vasan, editors
Place of Publication
Cham
Publisher
Springer
Date of Publication
c2016
Physical Description
1 online resource (ix, 116 p. : 22 illus., 14 illus. in color)
ISBN
9783319186306
9783319186290 (print ed.)
Subjects (MeSH)
Evidence-Based Medicine
Laryngeal Neoplasms
Mouth Neoplasms
Pharyngeal Neoplasms
Abstract
Written for residents and practitioners of otolaryngology, medical oncology, radiation oncology, and maxiollofacial surgery, this book provides the reader with a comprehensive, concise discussion of the best evidence available on which to base clinical decisions needed when managing patients with squamous cell carcinomas of the oral cavity, pharynx and larynx. Because of its accessible and practical format, this book is considerably different than other related titles on the market. Formatted with questions at the beginning of each chapter that are then answered with evidence and best practices available for each case, each chapter addresses situations the clinician is likely to face in the diagnostic evaluation and treatment of a patient with cancer of the head and neck. Most clinical decisions in the management of cancers of the head and neck region are based on the results of a few controlled, randomized clinical trial trials (Evidence Level I). However, most decision-making is based on the results of case-control studies (Evidence Level II), descriptive studies, reports of expert committees, or opinions of respected authorities (Evidence Level III). This information is scattered throughout the literature and often comingled with information about other topics. Therefore, there is a need for a publication in which the evidence pertinent to making decisions regarding a particular clinical problem is distilled from the literature and presented in a single concise, clinical, situation-driven source. Cancer of the Oral Cavity, Pharynx and Larynx: Evidence-Based Decision Making is just such a resource.
Contents
Preface -- 1. Evidence-Based Medicine -- 2. Oral Cavity Cancer -- 3. Oropharynx Cancer -- 4. Cancer of the Nasopharynx -- 5. Cancer of the Hypopharynx -- 6. Larynx Cancer.
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e-Book
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Equitable Access to Human Biological Resources in Developing Countries : Benefit Sharing Without Undue Inducement

https://libcat.nshealth.ca/en/permalink/provcat39811
Roger Scarlin Chennells. --Cham: Springer , c2016.
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The main question explored by the book is: How can cross-border access to human genetic resources, such as blood or DNA samples, be governed in such a way as to achieve equity for vulnerable populations in developing countries? The book situates the field of genomic and genetic research within global health and research frameworks, describing the concerns that have been raised about the potential unfairness in exchanges during recent decades. Access to and sharing in the benefits of human biolo…
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Author
Chennells, Roger Scarlin
Responsibility
Roger Scarlin Chennells
Place of Publication
Cham
Publisher
Springer
Date of Publication
c2016
Physical Description
1 online resource (xix, 197 p.)
ISBN
9783319197258
9783319197241 (print ed.)
Subjects (MeSH)
Bioethics
Developing Countries
Genetic Research - ethics
Global Health - ethics
Health Equity
Healthcare Disparities
Abstract
The main question explored by the book is: How can cross-border access to human genetic resources, such as blood or DNA samples, be governed in such a way as to achieve equity for vulnerable populations in developing countries? The book situates the field of genomic and genetic research within global health and research frameworks, describing the concerns that have been raised about the potential unfairness in exchanges during recent decades. Access to and sharing in the benefits of human biological resources are aspects not regulated by any international legal framework such as the Convention on Biological Diversity, which applies only to the exchange of plants, animals and microorganisms, as well as to associated traditional knowledge. Examples of genetic research perceived as exploitative are provided in order to illustrate the legal vacuum concerning the global governance of human genetic resources. The main conclusions drawn from the legal and ethical analysis are: Benefit sharing is crucial in order to avoid the exploitation of developing countries in human genetic research; With functioning research ethics committees, undue inducement is less of a concern in genetic research than in other areas of medical research (e.g. clinical trials); Concerns remain over research involving indigenous populations; accordingly, recommendations are provided. In drawing these conclusions, the book addresses in detail a highly pressing topic in global bioethics and international law. In this regard, it combines bioethical arguments with jurisprudence, in particular with reference to the law of equity and the legal concepts of duress (coercion), unconscionable dealing, and undue inducement.
Contents
Introduction -- Exploitation -- Common Heritage of Humankind -- The Altruism Argument -- The "No Value Added" Argument -- Justice and Exploitation in Bilateral Exchanges -- Undue Inducement and Coercion -- Risks to Indigenous Peoples as Vulnerable Population -- Closing Chapter -- List of Legal Cases.
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e-Book
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Clinical trials : study design, endpoints and biomarkers, drug safety, and FDA and ICH guidelines

https://libcat.nshealth.ca/en/permalink/provcat50526
Brody, Tom. (2nd ed.) --Philadelphia, PA: Elsevier , 2016.
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Author
Brody, Tom
Edition
2nd ed.
Place of Publication
Philadelphia, PA
Publisher
Elsevier
Date of Publication
2016
ISBN
9780128042175
Subjects (MeSH)
Clinical Trials as Topic
Clinical Trials Data Monitoring Committees
Drug Approval
Research Design
Notes
Access to this online resource is restricted to IWK Health Centre employees working from inside the hospital network.
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e-Book
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Quick Guide to Good Clinical Practice : How to Meet International Quality Standard in Clinical Research

https://libcat.nshealth.ca/en/permalink/provcat41519
Cemal Cingi, Nuray Bayar Muluk. --Cham: Springer , 2017.
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This brand-new book offers a reference guide to understanding and applying the rules for properly conducting clinical trials to meet the international quality standard, Good Clinical Practice, provided by the International Conference on Harmonization (ICH). The work offers an updated perspective on the clinical research landscape within the context of the clinical trial regulatory frameworks in Europe and the USA. In addition to providing a historical review and a detailed definition of GPC reg…
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Author
Cingi, Cemal
Other Authors
Bayar Muluk, Nuray
Responsibility
Cemal Cingi, Nuray Bayar Muluk
Place of Publication
Cham
Publisher
Springer
Date of Publication
2017
Physical Description
1 online resource (xviii, 237 pages)
ISBN
9783319443447
9783319443430 (print ed.)
Subjects (MeSH)
Biomedical Research - standards
Clinical Trials as Topic - standards
Data Accuracy
Ethics, Research
Internationality
Total Quality Management - standards
Specialty
Research
Abstract
This brand-new book offers a reference guide to understanding and applying the rules for properly conducting clinical trials to meet the international quality standard, Good Clinical Practice, provided by the International Conference on Harmonization (ICH). The work offers an updated perspective on the clinical research landscape within the context of the clinical trial regulatory frameworks in Europe and the USA. In addition to providing a historical review and a detailed definition of GPC regulations, it includes step-by-step explanations of all the requirements that researchers should bear in mind when designing and performing new trials. Further topics covered include: ethics of clinical research; the drug development process and evolution of regulations; investigator and sponsor responsibilities; and clinical trial protocols. Written by clinicians for clinicians, the book represents a valuable read also for researchers, pharmacists and all professionals involved in applications to the ethic committees, whose approval is required for new clinical studies.
Contents
1. Clinical Trials: Historical Aspects and Importance and New Drug Developments -- 2. The Definition of GCP -- 3. The Principles of GCP -- 4. The Drug Development Process and Evolution of Regulations -- 5. Planning Clinical Research -- 6. Preparation of Ethics Committee (IRB) Proposal -- 7. Preparation of Informed Consent -- 8. Preparation of Findings Tables -- 9. Setting the Ideal Statistical Methods -- 10. The Duties of a Clinical Research Coordinator -- 11. The Duties of Clinical Researchers -- 12. The Phases of Clinical Studies -- 13. Safety in Clinical Trials -- 14. Setting the Size -- 15. Setting the Ideal Method -- 16. Ethics of Clinical Research -- 17. Recruitment and Enrolment -- 18. Why we need Clinical Consent and Other Documentation -- 19. Monitoring the Trial -- 20. Inspection -- 21. Ethics: Institutional Review Board/Independent Ethics Committee(IRB/IEC) -- 22. Responsibilities of the Investigator -- 23. Responsibilities of the Sponsor -- 24. Clinical Trial Protocols.
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e-Book
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Online
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Clinical Medical Ethics : Landmark Works of Mark Siegler, MD

https://libcat.nshealth.ca/en/permalink/provcat41735
Laura Weiss Roberts, Mark Siegler, editors. --Cham: Springer , 2017.
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This instant gold standard title is a major contribution to the field of clinical medical ethics and will be used widely for reference and teaching purposes for years to come. Throughout his career, Mark Siegler, MD, has written on topics ranging from the teaching of clinical medical ethics to end-of-life decision-making and the ethics of advances in technology. With more than 200 journal publications and 60 book chapters published in this area over the course of his illustrious career, Dr. Sie…
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Other Authors
Roberts, Laura Weiss
Siegler, Mark
Responsibility
Laura Weiss Roberts, Mark Siegler, editors
Place of Publication
Cham
Publisher
Springer
Date of Publication
2017
Physical Description
1 online resource (xvii, 419 pages) : 17 illus., 8 illus. in color
ISBN
9783319538754
9783319538730 (print ed.)
Subjects (MeSH)
Ethics, Medical
Ethics, Clinical
Abstract
This instant gold standard title is a major contribution to the field of clinical medical ethics and will be used widely for reference and teaching purposes for years to come. Throughout his career, Mark Siegler, MD, has written on topics ranging from the teaching of clinical medical ethics to end-of-life decision-making and the ethics of advances in technology. With more than 200 journal publications and 60 book chapters published in this area over the course of his illustrious career, Dr. Siegler has become the pre-eminent scholar and teacher in the field. Indeed his work has had a profound impact on a range of therapeutic areas, especially internal medicine, pediatrics, surgery, oncology, and medical education. Having grown steadily in importance the last 30 years, clinical ethics examines the practical, everyday ethical issues that arise in encounters among patients, doctors, nurses, allied health workers, and health care institutions. The goal of clinical ethics is to improve patient care and patient outcomes, and almost every large hospital now has an ethics committee or ethics consultation service to help resolve clinical ethical problems; and almost every medical organization now has an ethics committee and code of ethics. Most significantly, clinical ethics discussions have become a part of the routine clinical discourse that occurs in outpatient and inpatient clinical settings across the country. This seminal collection of 46 landmark works written by Dr. Siegler with colleagues throughout his career was edited by Dr. Laura Weiss Roberts and by Dr. Siegler. Dr. Roberts is a prominent psychiatric ethicist and physician-scientist as well as a mentee and longtime collaborator of Dr. Siegler. The text is organized around five themes of foundational scholarship: restoring and transforming the ethical basis of modern clinical medicine, the doctor-patient relationship, education and professionalism, end-of-life care, and clinical innovation.With introductory perspectives by a group of renowned scholars in medicine, Clinical Medical Ethics: Landmark Works of Mark Siegler, MD explains the field authoritatively and comprehensively and will be of invaluable assistance to all clinicians and scholars concerned with clinical ethics. .
Contents
Part I -- Restoring and Transforming the Ethical Basis of Modern Clinical Medicine -- 1. An Introduction from Laura Weiss Roberts, M.D., M.A. -- 2. A Perspective from Mark Siegler, M.D. -- 3. A Perspective from Daniel P. Sulmasy, M.D., Ph.D. -- 4. A Perspective from Dana Levinson, M.P.H., Holly J. Humphrey, M.D., and Kenneth S. Polonsky, M.D. -- 5. A Perspective from Jordan J. Cohen, M.D. -- 6. A Perspective from Peter A. Singer, M.D. -- Part II Landmark Works on Clinical Medical Ethics by Mark Siegler, M.D. -- 7. Foundational Scholarship -- 7.1 Clinical ethics and clinical medicine (1979) -- 7.2 Decision-making strategy for clinical ethical problems in medicine (1982) -- 7.3 An ethics consultation service in a teaching hospital. Utilization and evaluation (1988) -- 7.4 Clinical medical ethics (1990) -- 7.5 Ethics committees and consultants (1990) -- 7.6 Future directions in clinical ethics (1991) -- 7.7 Clinical ethics (1991) -- 7.8 Clinical ethics in the practice of medicine (1996) -- 7.9 Five major themes in bioethics (1997) -- 7.10 The contributions of clinical ethics to patient care (1997) -- 8. The Doctor-Patient Relationship -- 8.1 Searching for moral certainty in medicine: a proposal for a new model of the doctor-patient encounter 1981) -- 8.2 Clinical intuition: a procedure for balancing the rights of patients and the responsibilities of physicians (1981) -- 8.3 The doctor-patient encounter and its relationship to theories of health and disease (1981) -- 8.4 The physician-patient accommodation: a central event in clinical medicine (1982) -- 8.5 Confidentiality in medicine: a decrepit concept (1982) -- 8.6 Medical consultations in the context of the physician-patient relationship (1982) -- 8.7 Metaphors and models of doctor-patient relationships: their implications for autonomy (1984) -- 8.8 The progression of medicine: from physician paternalism to patient autonomy to bureaucratic parsimony (1985) -- 8.9 Learning from our patients: one participants impact on clinical trial research and informed consent (1997) -- 8.10 The physician-surrogate relationship (2007) -- 9. Education and Professionalism -- 9.1 A legacy of Osler: teaching clinical ethics at the bedside (1978) -- 9.2 Basic curricular goals in medical ethics: the DeCamp conference on the teaching of medical ethics (1985) -- 9.3 Fellowship training programs in clinical ethics (1988) -- 9.4 Development of a teaching program in clinical medical ethics at the University of Chicago (1989) -- 9.5 Internal medicine residents' preferences regarding medical ethics education (1989) -- 9.6 Caring for medical students as patients (1990) -- 9.7 Teaching clinical ethics (1990) -- 9.8 Medical students as patients: a pilot study of their health care needs, practices, and concerns (1996) -- 9.9 What and how psychiatry residents at ten training programs wish to learn about ethics (1996) -- 9.10 Clinical ethics teaching in psychiatric supervision (1996) -- 9.11 Training doctors for professionalism: some lessons from teaching clinical medical ethics (2002) -- 10. End-of-Life Care -- 10.1 Pascal's wager and the hanging of crepe (1975) -- 10.2 Critical illness: the limits of autonomy (1977) -- 10.3 Brain death and live birth (1982) -- 10.4 Against the emerging stream: should fluids and nutritional support be discontinued? (1985) -- 10.5 Euthanasia: a critique (1990) -- 10.6 Elective use of life-sustaining treatments in internal medicine (1991) -- 10.7 Intimacy and caring: the legacy of Karen Ann Quinlan (1993) -- 10.8 The rise and fall of the futility movement (2000) -- 11. Clinical Innovation 11.1 Ethical issues in growth hormone therapy (1989) -- 11.2 Orthopedic surgeons' attitudes and practices concerning the treatment of patients with human immunosuppressive virus infection (1989) -- 11.3 Ethics of liver transplantation with living donors (1989) -- 11.4 Bone marrow transplantation for sickle cell disease; a study of parentsÇÖ decisions (1991) -- 11.5 Ethical justification for living liver donation (1992) -- 11.6 Transplantation of liver grafts from living donors into adults: too much, too soon (2001) -- 11.7 Elective surgical patients as living organ donors: a clinical and ethical innovation (2009) -- Appendix.
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Peer Review, Peer Education, and Modeling in the Practice of Clinical Ethics Consultation : The Zadeh Project

https://libcat.nshealth.ca/en/permalink/provcat43969
Stuart G. Finder, Mark J. Bliton, editors. --Cham: SpringerOpen , c2018.
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This open access book about the Zadeh Project demonstrates and explores a core question in clinical ethics: how can ethics consultants be accountable in the face of a robust plurality of ethical standpoints, especially those that underwrite practices and methods for doing ethics consultation as well as those viewpoints and values encountered in daily clinical ethics practice? Underscoring this question is the recognition that the field of clinical ethics consultation has arrived at a crucial po…
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Other Authors
Finder, Stuart G.
Bliton, Mark J.
Responsibility
Stuart G. Finder, Mark J. Bliton, editors
Place of Publication
Cham
Publisher
SpringerOpen
Date of Publication
c2018
Physical Description
1 online resource (xi, 228 p.) : 2 illus.
ISBN
9783319909554
9783319909530 (Print ed.)
9783319909547 (Print ed.)
9783030081409 (Print ed.)
Subjects (MeSH)
Ethics, Clinical
Ethics Consultation
Ethics Committees, Clinical
Peer Review, Health Care
Specialty
Ethics
Abstract
This open access book about the Zadeh Project demonstrates and explores a core question in clinical ethics: how can ethics consultants be accountable in the face of a robust plurality of ethical standpoints, especially those that underwrite practices and methods for doing ethics consultation as well as those viewpoints and values encountered in daily clinical ethics practice? Underscoring this question is the recognition that the field of clinical ethics consultation has arrived at a crucial point in its maturation. Many efforts are underway to more formally “professionalize” the field, with most aimed toward stabilizing a specific set of institutional considerations. Stretched between these institutional and practical initiatives resides a crucial set of of ethical considerations, chief among them the meaning and scope of responsibility for clinical ethics consultants. Developed around a long-form case scenario, the Zadeh Project provides a multi-layered series of “peer-reviews”: critique of the actions of the case scenario’s ethics consultant; reflection on clinical ethics method; examination of the many ways that commitments to method and practice can, and do, intersect, overlap, and alter one another. The design and format of this book thus models a key element for clinical ethics practice: the need and ability to provide careful and thoughtful explanation of core moral considerations that emerge among diverse standpoints. Specifically designed for those studying to become and those who are ethics consultants, this book, with its innovative and multi-layered approach, allows readers to share a peer-review-like experience that shows accountability to be what it is, an ethical, not merely procedural or administrative, undertaking.
Contents
INTRODUCTION -- The Zadeh Project – A Frame for Understanding the Generative Ideas, Formation, and Design -- PART ONE. A CLINICAL ETHICS CONSULTATION NARRATIVE -- The Zadeh Scenario -- PART TWO. CRITICAL RESPONSE TO THE ZADEH SCENARIO -- Brief Summary of the Essays in Part Two -- Critical Self-Reflection as Moral Practice: A Collaborative Meditation on Peer Review in Ethics Consultation -- Telling About Engagement Is Not Enough: Seeking the “Ethics” of Ethics Consultation in Clinical Ethics Case Reports -- Ethics Consultation for Mrs. Hamadani – A Focus on Process -- Ethics Consultation, Professional Praxis, and What it Means to Be a “Consultant" -- This May, or May Not, Be an Ethics Consultation -- PART THREE. REFLECTIONS ON METHOD IN RESPONSE TO THE ZADEH SCENARIO AND PART TWO -- Brief Summary of the Essays in Part Three -- Not Principlism nor Casuistry, Not Narrative Ethics nor Clinical Pragmatism: A Case for Proceduralism -- (Meta-) Methodological Lessons for Ethics Consultation -- Narrative and Method in Ethics Consultation -- Standardizing the Case Narrative -- PART FOUR. CRITICAL INQUIRY INTO PARTS ONE, TWO, AND THREE (ON THE WAY TOWARDS PEER REVIEW) -- Brief Summary of the Essays in Part Four -- Evaluating Clinical Ethics Support: On What Grounds Do We Make Judgments About Reports of Ethics Consultation? -- Doing Well or Doing Good in Ethics Consultation -- Peer Review and Beyond: Towards a Dialogical Approach of Quality in Ethics Support -- PART FIVE. REFLECTIVE SUMMARY AND RESPONSE -- Peer Review and Responsibility in/as/for/to Practice.
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Care in Healthcare : Reflections on Theory and Practice

https://libcat.nshealth.ca/en/permalink/provcat43976
Franziska Krause, Joachim Boldt, editors. --Cham: Palgrave Macmillan , 2018.
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This book is open access under a CC BY 4.0 license. ; This book examines the concept of care and care practices in healthcare from the interdisciplinary perspectives of continental philosophy, care ethics, the social sciences, and anthropology. Areas addressed include dementia care, midwifery, diabetes care, psychiatry, and reproductive medicine. Special attention is paid to ambivalences and tensions within both the concept of care and care practices. Contributions in the first section of the b…
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Krause, Franziska
Boldt, Joachim
Responsibility
Franziska Krause, Joachim Boldt, editors
Place of Publication
Cham
Publisher
Palgrave Macmillan
Date of Publication
2018
Physical Description
1 online resource (xi, 298 p.)
ISBN
9783319612911
9783319612904 (Print ed.)
9783319612928 (Print ed.)
9783319870434 (Print ed.)
Subjects (MeSH)
Ethics, Clinical - history
Patient Care - ethics
Philosophy, Medical
Specialty
Ethics
Health Services Research
Abstract
This book is open access under a CC BY 4.0 license.
This book examines the concept of care and care practices in healthcare from the interdisciplinary perspectives of continental philosophy, care ethics, the social sciences, and anthropology. Areas addressed include dementia care, midwifery, diabetes care, psychiatry, and reproductive medicine. Special attention is paid to ambivalences and tensions within both the concept of care and care practices. Contributions in the first section of the book explore phenomenological and hermeneutic approaches to care and reveal historical precursors to care ethics. Empirical case studies and reflections on care in institutionalised and standardised settings form the second section of the book. The concluding chapter, jointly written by many of the contributors, points at recurring challenges of understanding and practicing care that open up the field for further research and discussion. This collection will be of great value to scholars and practitioners of medicine, ethics, philosophy, social science and history.
Contents
Understanding Care: Introductory Remarks -- Framing Care -- Forgotten Approaches to Care: The Human Being as Neighbour in the German-Jewish Tradition of the Nineteenth Century -- Nursing as Accommodated Care: A Contribution to the Phenomenology of Care. Appeal, Concern, Volition, Practice -- Fundamentals of an Ethics of Care -- The Interdependence of Care and Autonomy Caring Relationships: Commercial Surrogacy and the Ethical Relevance of the Other -- Situated Care -- Sociomaterial Will-Work: Aligning Daily Wanting in Dutch Dementia Care -- The Dementia Village: Between Community and Society -- Regulation as an Obstacle to Care? A Care-Ethical Evaluation of the Regulation on the Use of Seclusion Cells in Psychiatric Care in Flanders (Belgium) -- Witnessing as an Embodied Practice in German Midwifery Care - Tensions in Diabetes Care Practice: Ethical Challenges with a Focus on Nurses in a Home-Based Care Team -- Caring About Care in the Hospital Arena and Nurses’ Voices in Hospital Ethics Committees: Three Decades of Experiences -- Towards a Three-Dimensional Perspective of Space for Humanizing Hospital Care -- Conclusion: Asking the Right Questions.
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The Sports Medicine Physician

https://libcat.nshealth.ca/en/permalink/provcat44086
Sérgio Rocha Piedade, Andreas B. Imhoff, Mark Clatworthy, Moises Cohen, João Espregueira-Mendes, editors. --Cham: Springer , 2019.
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This superbly illustrated book provides information of outstanding quality on the presentation and management of the entire range of sports injuries and conditions likely to be encountered by the sports medicine physician, as well as many other topics relating to sports activity, events, and outcomes. It is the product of close collaboration among members of several ISAKOS committees, and the chapter authors are clinicians and scientists from across the world who are acknowledged experts in spo…
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Other Authors
Rocha Piedade, Sérgio
Imhoff, Andreas B.
Clatworthy, Mark
Cohen, Moises
Espregueira-Mendes, João
Other Authors
International Society of Arthroscopy Knee Surgery and Orthopaedic Sports Medicine
Responsibility
Sérgio Rocha Piedade, Andreas B. Imhoff, Mark Clatworthy, Moises Cohen, João Espregueira-Mendes, editors
Place of Publication
Cham
Publisher
Springer
Date of Publication
2019
Physical Description
1 online resource (xi, 695 p.) : 273 illus., 233 illus. in color
ISBN
9783030104337
9783030104320 (Print ed.)
9783030104344 (Print ed.)
Subjects (MeSH)
Athletic Injuries
Physical Conditioning, Human
Sports Medicine
Specialty
Sports Medicine
Abstract
This superbly illustrated book provides information of outstanding quality on the presentation and management of the entire range of sports injuries and conditions likely to be encountered by the sports medicine physician, as well as many other topics relating to sports activity, events, and outcomes. It is the product of close collaboration among members of several ISAKOS committees, and the chapter authors are clinicians and scientists from across the world who are acknowledged experts in sports medicine and orthopedics. The book opens by discussing fundamental topics and principles, covering subjects such as the biomechanics of injuries, physiological demands in sports practice, sports activity at different ages, nutrition and hydration, strength and conditioning, injury prevention, recovery, rehabilitation, and return to play. Subsequent chapters focus in depth on overtraining injuries, neurological disorders, sports trauma to different parts of the body, and special clinical conditions. Further topics to be addressed are different scenarios in sports (e.g., indoor vs outdoor), sports equipment, biologic treatment of sports injuries, major sporting events, and patient-recorded outcome measures.
Contents
PART 1. Sports Practice Principles -- Multidisciplinary Sports Medicine Team -- Pre-participation Evaluation in Sports Practice -- Biomechanics of Musculoskeletal Injuries -- Physiological Demands in Sports Practice -- Sports Activity at Childhood and Adolescence -- Sports Activity at Adult Life and Old Age -- Oriented Warm-up -- Nutrition and Hydration -- Sports Rehabilitation -- Role of Strength and Conditioning Coach -- Sports Injuries Primary and Secondary Prevention -- Return to Play -- PART 2. Overtraining Injuries -- Achilles Tendinopathy -- Muscle Injuries -- Stress Fractures -- Shin Pain -- Groin Injuries -- PART 3. Neurological Disorders -- Seizures and Epilepsies -- Spine Injuries -- PART 4. Sports Trauma -- Face -- Thoracic -- Abdomen -- Shoulder -- Elbow -- Wrist and Hand -- Hip -- Knee -- Ankle and Foot -- PART 5. Special Conditions -- Female Athlete Triad and RED-S -- Sudden Cardiac Arrest -- Concussion -- Dopping -- Dermatological Injuries -- Oral Health -- Travelling Management -- Sports Management in Extreme Conditions -- Sports After Knee Arthroplasty -- Ringside physician -- PART 6. Different Scenarios in Sports -- Indoor Sports -- Outdoor Sports: Winter -- PART 7. Sports Equipment -- Sports Footwear: Problems and Advances -- PART 8. Biologics in Sports Injuries -- Biologic Treatment in Tendon and Muscle Injuries -- Biologic Treatment in Ligament Injuries -- Biologic Treatment in Meniscus Injuries -- PART 9. Major Events in Sports -- Olympic Games -- Paralympic Games -- FIFA World Cup -- Extreme Sports -- JUDO, Brazilian jiu-jistsu, and Mix Martial arts -- PART 10. PROMS -- Proms in Sports Medicine.
Format
e-Book
Location
Online
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