Abstract

The protection of patient dignity and autonomy forms the cornerstone of a just healthcare system. In India, the recognition of patients’ rights has evolved from moral discourse to a constitutional and legal imperative. This paper presents a multidimensional study of patients’ rights through four core dimensions: ethical foundations, technological transformation, social equity, and legal enforcement. The first dimension traces the journey from compassion to codification, examining how moral and philosophical ideals rooted in Kantian respect for persons and bioethical principles of consent, beneficence, and non-maleficence—have shaped the jurisprudential understanding of patient dignity under Articles 14, 19, and 21 of the Indian Constitution. The second explores the emergence of the digital dignity paradigm, analysing how telemedicine, artificial intelligence, and electronic health data systems have redefined privacy, consent, and accountability. It highlights the regulatory challenges posed by digital health innovations in light of the Digital Personal Data Protection Act, 2023 and the GDPR framework. The third dimension addresses intersectional inequalities that continue to obstruct equal realization of patients’ rights among women, rural populations, Dalits, persons with disabilities, and LGBTQ+ individuals. It underscores how systemic discrimination erodes both dignity and access to care. The final dimension moves from rights to remedies, proposing enforceable models such as an independent Patient Rights Commission or Healthcare Ombudsman, drawing insights from the UK’s NHS Charter and WHO Patients’ Rights Framework. Through this integrated analysis, the paper argues that protecting patients’ rights requires an ethically grounded, technologically responsive, socially inclusive, and legally enforceable approach, where dignity is not only recognized in law but genuinely realized in practice.

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