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The new subjective medicine: taking the patient's point of view on health care and health

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  • Sullivan, Mark

Abstract

Calls to respect patient autonomy and produce patient-centered outcomes have recently brought the patient's point of view back into the center of clinical medicine. Bioethics has argued that patient values must be respected in health care decisions. But it has generally not questioned medicine's goals, including its definition of health. For bioethics, health has remained an objective biological fact. However, pressures to improve the cost-effectiveness of medical care have increased interest in the subjective health and quality of life of patients. Perceived health, health-related quality of life, and health-state utilities bring health assessment progressively closer to the patient's perspective. Now even death's harm to patients is qualified by the value patients place on their health state. Medicine's epidemiological transition from acute to chronic disease is thus prompting an epistemological transition from primarily objective to primarily subjective evidence of health and health care effectiveness. Now some of the most important patient outcomes, like patient choices before them, are valid because they are subjective. Pathophysiology is appropriately becoming a means to produce health as it is defined from the patient's point of view. The physicians' job description will be changed to focus on patients' lives rather than patients' bodies. Definitive evaluations of medical effectiveness will occur within patients' lives rather than within doctors' hospitals. This further incorporation of patient subjectivity should carry us well beyond informed consent and the other protections for patient autonomy bequeathed to us by bioethics.

Suggested Citation

  • Sullivan, Mark, 2003. "The new subjective medicine: taking the patient's point of view on health care and health," Social Science & Medicine, Elsevier, vol. 56(7), pages 1595-1604, April.
  • Handle: RePEc:eee:socmed:v:56:y:2003:i:7:p:1595-1604
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    2. Juan Oliva-Moreno & Julio López-Bastida & Pedro Serrano-Aguilar & Lilisbeth Perestelo-Pérez, 2010. "Determinants of health care costs of HIV-positive patients in the Canary Islands, Spain," The European Journal of Health Economics, Springer;Deutsche Gesellschaft für Gesundheitsökonomie (DGGÖ), vol. 11(4), pages 405-412, August.
    3. Lehoux, Pascale & Poland, Blake & Daudelin, Genevieve, 2006. "Focus group research and "the patient's view"," Social Science & Medicine, Elsevier, vol. 63(8), pages 2091-2104, October.
    4. Henry S. Perkins, 2014. "The Varied Understandings of “Terminal Cancer†and Their Implications for Clinical Research and Patient Care," Medical Decision Making, , vol. 34(6), pages 696-698, August.
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    6. Finn, Mark & Sarangi, Srikant, 2008. "Quality of life as a mode of governance: NGO talk of HIV 'positive' health in India," Social Science & Medicine, Elsevier, vol. 66(7), pages 1568-1578, April.
    7. Erik Berglund & Emilie Friberg & Monika Engblom & Åsa Andersén & Veronica Svärd, 2022. "Coordination and Perceived Support for Return to Work: A Cross-Sectional Study among Patients in Swedish Healthcare," IJERPH, MDPI, vol. 19(7), pages 1-11, March.
    8. Gisquet, Elsa, 2008. "Cerebral implants and Parkinson's disease: A unique form of biographical disruption?," Social Science & Medicine, Elsevier, vol. 67(11), pages 1847-1851, December.
    9. Ahmad Shahabeddin Parizi & Paul F. M. Krabbe & Erik Buskens & Stephan J. L. Bakker & Karin M. Vermeulen, 2019. "A Scoping Review of Key Health Items in Self-Report Instruments Used Among Solid Organ Transplant Recipients," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 12(2), pages 171-181, April.
    10. Cho, Sun Mi & Park, Chan-ung & Song, Min, 2020. "The evolution of social health research topics: A data-driven analysis," Social Science & Medicine, Elsevier, vol. 265(C).
    11. Ulrike Ravens-Sieberer & Michael Erhart & Nora Wille & Ralf Wetzel & Jennifer Nickel & Monika Bullinger, 2006. "Generic Health-Related Quality-of-Life Assessment in Children and Adolescents," PharmacoEconomics, Springer, vol. 24(12), pages 1199-1220, December.
    12. Martina F. Baumann & Daniel Frank & Lena-Charlotte Kulla & Thomas Stieglitz, 2020. "Obstacles to Prosthetic Care—Legal and Ethical Aspects of Access to Upper and Lower Limb Prosthetics in Germany and the Improvement of Prosthetic Care from a Social Perspective," Societies, MDPI, vol. 10(1), pages 1-20, January.
    13. Daniela R. Bien & Marion Danner & Vera Vennedey & Daniele Civello & Silvia M. Evers & Mickaël Hiligsmann, 2017. "Patients’ Preferences for Outcome, Process and Cost Attributes in Cancer Treatment: A Systematic Review of Discrete Choice Experiments," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 10(5), pages 553-565, October.
    14. Christen, Regula Nelly & Alder, Judith & Bitzer, Johannes, 2008. "Gender differences in physicians' communicative skills and their influence on patient satisfaction in gynaecological outpatient consultations," Social Science & Medicine, Elsevier, vol. 66(7), pages 1474-1483, April.
    15. Natasa Sedlar & Mitja Lainscak & Jerneja Farkas, 2020. "Living with Chronic Heart Failure: Exploring Patient, Informal Caregiver, and Healthcare Professional Perceptions," IJERPH, MDPI, vol. 17(8), pages 1-16, April.
    16. Paul F M Krabbe & Ruslan Jabrayilov & Patrick Detzel & Livia Dainelli & Karin M Vermeulen & Antoinette D I van Asselt, 2020. "A two-step procedure to generate utilities for the Infant health-related Quality of life Instrument (IQI)," PLOS ONE, Public Library of Science, vol. 15(4), pages 1-14, April.
    17. Fernández, Andrés & Oviedo, Enrique, 2010. "Information and communication technologies in the health sector: opportunities and challenges for the reduction of inequalities in Latin America and the Caribbean," Políticas Sociales 6178, Naciones Unidas Comisión Económica para América Latina y el Caribe (CEPAL).
    18. Peña-Longobardo, L.M. & Rodríguez-Sánchez, B. & Oliva-Moreno, J., 2021. "The impact of widowhood on wellbeing, health, and care use: A longitudinal analysis across Europe," Economics & Human Biology, Elsevier, vol. 43(C).
    19. Thompson, Andrew G.H., 2007. "The meaning of patient involvement and participation in health care consultations: A taxonomy," Social Science & Medicine, Elsevier, vol. 64(6), pages 1297-1310, March.
    20. Eissens van der Laan, M.R. & van Offenbeek, M.A.G. & Broekhuis, H. & Slaets, J.P.J., 2014. "A person-centred segmentation study in elderly care: Towards efficient demand-driven care," Social Science & Medicine, Elsevier, vol. 113(C), pages 68-76.
    21. Gill Hubbard & Nicola Illingworth & Neneh Rowa‐Dewar & Liz Forbat & Nora Kearney, 2010. "Treatment decision‐making in cancer care: the role of the carer," Journal of Clinical Nursing, John Wiley & Sons, vol. 19(13‐14), pages 2023-2031, July.
    22. Murali Sundaram & Jan Kavookjian & Julie Patrick, 2009. "Health-Related Quality of Life and Quality of Life in Type 2 Diabetes," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 2(2), pages 121-133, June.
    23. Adilson Marques & Yolanda Demetriou & Riki Tesler & Élvio R. Gouveia & Miguel Peralta & Margarida Gaspar de Matos, 2019. "Healthy Lifestyle in Children and Adolescents and Its Association with Subjective Health Complaints: Findings from 37 Countries and Regions from the HBSC Study," IJERPH, MDPI, vol. 16(18), pages 1-14, September.

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