Table of Contents
Table of Contents
Preface
Chapter 1. Distinctive Features of Public Health Ethics in the Domain of Expanded Genetic Screening and Population Biobanking
Stephen M. Modell, Toby Citrin, Jodyn E. Platt and Sharon L. R. Kardia (Department of Health Management and Policy, Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, MI, USA)
Chapter 2. An Ethical Framework for the Routine Randomization of Medical Therapies
Ahmed Elsayyad (Public Health Studies, Johns Hopkins University, Baltimore, MD, USA)
Chapter 3. Effective Medical Informed Consent: A Challenge to Bioethicists
David Trafimow, Jordan H. Trafimow, and A. Jonathan Trafimow (New Mexico State University, NM, USA, and others)
Chapter 4. Informed Consent and other Ethical and Regulatory Considerations in Emergency Research
Daniel P. Nussbaum (Paul J. Speicher, Duke University Medical Center Durham, North Carolina, USA)
Chapter 5. Right to Health and Dental Care
Francesca Zangari (Dental Service – Local Health Service of Romagna, Italy)
Chapter 6. The Ethics of HIV Screening Targeted to the Seriously Mentally Ill
Mary V. Seeman (Department of Psychiatry; University of Toronto, Canada)
Chapter 7. Truth-Telling, Best Interests, and Autonomy
Kam-Yuen Cheng (Centennial College, Pokfulam, Hong Kong)
Chapter 8. Problem in Ethics for Medical Publications: Brief Review and Cases from Thailand
Somsri Wiwanitkit and Viroj Wiwanitkit (Wiwanitkit House, Bangkhae, Bangkok, Thailand, and others)
Chapter 9. Patients’ Rights in India: Do they Assure Empowerment?
Ravindra B. Ghooi and Shailesh R. Deshpande (Diector, Scientia Clinical Services, Pune, India, and others)
Index
