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    Passive Patient Culture in India

    Disrespect in Law and Medicine

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    Author(s)
    Subramani, Supriya
    Language
    English
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    Abstract
    In a society shaped by deep inequalities, where healthcare and legal systems often reinforce class, caste, religion, and gender hierarchies, this book offers a powerful examination of patienthood in India. Through its critical approach, it seeks to disrupt binaries—such as universalistic and particularistic values and data versus theory—while decentering normative discourses by foregrounding lived experiences within the context. It offers philosophical and conceptual insights that extend far beyond local variations and contexts, challenging dominant narratives in global discourses on medical decision-making and concepts such as informed consent, autonomy, and respect. This book critiques the archetype of the “passive patient” entrenched in both medicine and law in India — an image that undermines agency, diminishes self-respect, and sustains a culture of disrespect. Chapters of the book unpacks the intersections of power, social categories, and patienthood, exposing how marginalized communities face everyday indignities in healthcare and law. It explores law and medicine’s role in maintaining presumed 'passive patient' archetype, especially through legal judgements and healthcare encounters. This book advocates for reimagining patienthood as centered on self-respect, recognition, and agency, arguing that the “passive patient” is not an isolated phenomenon but an outcome of broader, oppressive structures. Contributing to robust debates in medical sociology, bioethics, and social justice, this book is essential reading for those interested in the intersections of these fields, along with applied ethics, health services research, and law. This book is freely available as downloadable Open Access PDFs at http://www.taylorfrancis.com under a Creative Commons Attribution-Non Commercial-No Derivatives (CC-BY-NC-ND) 4.0 license.
    URI
    https://library.oapen.org/handle/20.500.12657/100109
    Keywords
    Bio Ethics; Human Rights; Consent Law; Medical Ethics; patient autonomy; Patient-centred care; physician-patient encounter; patient stereotypes
    DOI
    10.4324/9781003129998
    ISBN
    9780367655365, 9781040335772, 9781003129998
    Publisher
    Taylor & Francis
    Publisher website
    https://taylorandfrancis.com/
    Publication date and place
    Oxford, 2025
    Imprint
    Routledge
    Series
    Routledge Research in Health Law,
    Classification
    Medical and healthcare law
    Medical sociology
    Sociology
    Ethics and moral philosophy
    Nursing
    International law
    Regional / International studies
    Pages
    198
    Rights
    https://creativecommons.org/licenses/by-nc-nd/4.0/
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    License

    • If not noted otherwise all contents are available under Attribution 4.0 International (CC BY 4.0)

    Credits

    • logo EU
    • This project received funding from the European Union's Horizon 2020 research and innovation programme under grant agreement No 683680, 810640, 871069 and 964352.

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