Clinicians’ Perspectives on the Duty to Inform Patients About Medical Aid-in-Dying-Reference-Cited by-同舟云学术

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Clinicians’ Perspectives on the Duty to Inform Patients About Medical Aid-in-Dying

Published:2019-12-12 Issue:1 Volume:11 Page:53-62
ISSN:2329-4515
Container-title:AJOB Empirical Bioethics
language:en
Short-container-title:AJOB Empirical Bioethics

Author:

Brassfield Elizabeth R.¹,Buchbinder Mara²

Affiliation:

1. Department of Philosophy and School of Medicine, University of North Carolina at Chapel Hill, North Carolina, USA;

2. Center for Bioethics, Department of Social Medicine, School of Medicine, University of North Carolina at Chapel Hill, North Carolina, USA

Publisher

Informa UK Limited

Subject

Health Policy,Philosophy,Health (social science)

Link

https://www.tandfonline.com/doi/pdf/10.1080/23294515.2019.1695016

Reference40 articles.

1. ‘Talk to me’: a mixed methods study on preferred physician behaviours during end-of-life communication from the patient perspective

2. Clinician-Patient Interactions About Requests for Physician-Assisted Suicide

3. ‘I wish I knew more ...’ the end-of-life planning and information needs for end-stage fibrotic interstitial lung disease: views of patients, carers and health professionals: Table 1

4. Communication about euthanasia in general practice: Opinions and experiences of patients and their general practitioners

5. Aid-in-dying laws and the physician's duty to inform

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1. The Impact of Legalizing Medical Aid in Dying on Patient Trust: A Randomized Controlled Survey Study;Journal of Palliative Medicine;2024-08-21

2. Opening the Door: Rethinking “Difficult Conversations” about Living and Dying with Dementia;Hastings Center Report;2024-01

3. Revisão bioética sobre a legalidade da morte assistida no Equador;Revista Bioética;2024

4. Revisión bioética acerca de la legalidad de la muerte asistida en el Ecuador;Revista Bioética;2024

5. Bioethical review on the legality of assisted dying in Ecuador;Revista Bioética;2024

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