Research Handbook on Medical Consent

Research Handbook on Medical Consent portes grátis

Research Handbook on Medical Consent

Miola, Jose; Austin, Louise

Edward Elgar Publishing Ltd

04/2026

512

Dura

Inglês

9781803920528

Pré-lançamento - envio 15 a 20 dias após a sua edição

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Contents
List of contributors vii
1 Introduction: navigating the complexities of medical consent 1
Louise Austin and Jose Miola
PART I INFORMED CONSENT AND THE IMPACT OF MONTGOMERY
2 Mind the (ethico-legal) gap: the relationship between medical law and ethics in informed consent 7
Louise Austin and Jose Miola
3 Impact of Montgomery on clinical practice: the use of core information sets 25
Barry G. Main and Jane M. Blazeby
4 Rogers v Whitaker: much ado about nothing 63
Bernadette Richards
5 Medical negligence and the duty to advise: a Singapore story 76
Kumaralingam Amirthalingam
6 The Montgomery mistake 98
Craig Purshouse
7 Clinical practice guidelines for consent after Montgomery: uneasy bedfellows or a workable partnership? 112
Jo Samanta and Ash Samanta
PART II PERSPECTIVES ON INFORMED CONSENT
8 Healthcare harm and the safety of informed consent 143
Oliver Quick
9 Causation and consent to medical treatment: the risks and benefits of a consent-based approach to causation in negligence 163
Gemma Turton
10 Alternatives to autonomy 185
Charles Foster
11 Medical consent and the broader consent paradigm 200
Tsachi Keren-Paz
PART III NEW AND EXPERIMENTAL TREATMENTS AND PROCEDURES
12 Consent to innovative and experimental treatments from a Singaporean perspective 235
Sumytra Menon
13 Informed consent, English law and implantable medical devices: learning the lessons from the vaginal mesh scandal 247
Jean V. McHale
14 Consent for data and tissue research 266
Angela Ballantyne
PART IV CONSENT AT THE MARGINS
15 British abortion law and the challenges of consent 290
Rachel Arkell and Clare Murphy
16 Adolescent consent to treatment for gender dysphoria in England and Wales 310
Emma Cave
17 Consent in emergency medicine 328
Rebecca Whiticar
18 Informed consent at the end of life 346
Rob Heywood
PART V PROXY CONSENT
19 What's the harm? An analysis of best interests through the lens of harm reduction and relative harm in the context of disagreement in the care of critically ill children 368
Peta Coulson-Smith and Emma Nottingham
20 The role and influence of social media on medical treatment decisions for critically ill children 394
Neera Bhatia
21 Consent and mental capacity law: a story of (dis)empowerment and medical dominance 412
Beverley Clough and Ruby Reed-Berendt
22 Proxy consent for the elderly: a relational autonomy perspective 442
Roy Gilbar
23 Conclusion: (re)considering consent in medicine - the role of the law, patient autonomy, and consent 459
Sara Fovargue
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Informed Consent; Proxy Consent; Consent to Innovative Treatments; Guidelines and Consent; Montgomery v Lanarkshire; Autonomy and Consent