Literature DB >> 33717322

The Rhetoric of the 'Passive Patient' in Indian Medical Negligence Cases.

Supriya Subramani1.   

Abstract

In this paper, I examine the rhetoric employed by court judgements, with a particular emphasis on the narrative construct of the 'passive patient'. This construction advances and reinforces paternalistic values, which have scant regard for the patients' preferences, values, or choices within the legal context. Further, I critique the rhetoric employed and argue that the use of this rhetoric is the basis for a precedent that limits the understanding and respect of patients. Through this paper, I present the contemporary use of the 'passive patient' construct in the context of the Indian legal system and describe how such constructions have become a source of normative justification for legal reasoning that jeopardizes the patient's agency. I argue for the primacy of 'respect for persons' within Indian law and the need to treat each patient as a person who has agency, preferences, and values during clinical interactions. I conclude by suggesting that laws that adopt narratives that acknowledging the significance of patient engagement and the relevance of effective communication during clinical encounters would help cultivate a culture of patient-centred care, by moving beyond the rhetoric of 'passive patient' and the 'health/choice' dichotomy. © National University of Singapore and Springer Nature Singapore Pte Ltd. 2019.

Entities:  

Keywords:  Agency; Consent; India; Law; Patient-centred care; Respect

Year:  2019        PMID: 33717322      PMCID: PMC7747317          DOI: 10.1007/s41649-019-00106-1

Source DB:  PubMed          Journal:  Asian Bioeth Rev        ISSN: 1793-9453


  52 in total

1.  Labeling patient (in)competence: a feminist analysis of medico-legal discourse.

Authors:  B Secker
Journal:  J Soc Philos       Date:  1999

2.  The sick role and the role of the physician reconsidered.

Authors:  T Parsons
Journal:  Milbank Mem Fund Q Health Soc       Date:  1975

3.  Not so new directions in the law of consent? Examining Montgomery v Lanarkshire Health Board.

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4.  Three approaches to qualitative content analysis.

Authors:  Hsiu-Fang Hsieh; Sarah E Shannon
Journal:  Qual Health Res       Date:  2005-11

Review 5.  Socio-economic status of the patient and doctor-patient communication: does it make a difference?

Authors:  S Willems; S De Maesschalck; M Deveugele; A Derese; J De Maeseneer
Journal:  Patient Educ Couns       Date:  2005-02

6.  Capacity for Preferences: Respecting Patients with Compromised Decision-Making.

Authors:  Jason Adam Wasserman; Mark Christopher Navin
Journal:  Hastings Cent Rep       Date:  2018-05       Impact factor: 2.683

7.  Re-examining respect for human research participants.

Authors:  Neal W Dickert
Journal:  Kennedy Inst Ethics J       Date:  2009-12

Review 8.  Communicating the uncertainty of harms and benefits of medical interventions.

Authors:  Mary C Politi; Paul K J Han; Nananda F Col
Journal:  Med Decis Making       Date:  2007-09-14       Impact factor: 2.583

9.  Disclosure of information to patients in medical care.

Authors:  R R Faden; C Becker; C Lewis; J Freeman; A I Faden
Journal:  Med Care       Date:  1981-07       Impact factor: 2.983

10.  Collaborative deliberation: a model for patient care.

Authors:  Glyn Elwyn; Amy Lloyd; Carl May; Trudy van der Weijden; Anne Stiggelbout; Adrian Edwards; Dominick L Frosch; Tim Rapley; Paul Barr; Thom Walsh; Stuart W Grande; Victor Montori; Ronald Epstein
Journal:  Patient Educ Couns       Date:  2014-08-13
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