Sociološki i etički aspekti informisanog pristanka onkološkog pacijenta u pravu Republike Srbije
Sažetak
Informisani pristanak predstavlja odraz lične autonomije i samoodređenja pacijenta u odnosu na predloženu medicinsku meru, gde poseban izazov u kontekstu informisanog pristanka predstavlja oblast onkologije. Cilj rada je interdisciplinarna pravna, sociološka i etička analiza informisanog pristanka onkološkog pacijenta. U radu se analiziraju uslovi punovažnosti informisanog pristanka sa pravnog aspekta, veština komunikacija između lekara i pacijenta, kao i etičke dileme koje se odnose na autonomiju pacijenta u okviru sistema beneficijencije. Zaključeno je da informisani pristanak onkološkog pacijenta može biti smatran suštinski valjanim samo ukoliko su, pored pravnih, ispunjeni i etički i komunikacioni standardi, pri čemu je neophodno prilagoditi informacije individualnim potrebama pacijenta.
Reference
Act on the Protection of Patient Rights of the Republic of Croatia, Narodne novine, No. 169/04, 37/08. [In Croatian]
Adamson, M., Choi, K., Notaro, S., Cotoc, C. (2018). The doctor-patient relationship and information-seeking behavior: four orientations to cancer communication. J Palliat Care, 33 (2), 79–87. https://doi.org/10.1177/0825859718759881
Andersen-Watts, R. (2008). The Failure of Breast Cancer Informed Consent Statutes. Michigan Journal of Gender & Law, 14 (2), 201–222. https://repository.law.umich.edu/mjgl/vol14/iss2/2
Bury, M. (1997). Health and Illness in a Changing Society. London: Sage.
Charmaz, K. (1983). Loss of self: a fundamental form of suffering in the chronically ill. Sociology of Health & Illness, 5 (2), 168–195. doi:10.1111/1467-9566.ep10491512
Charmaz, K. (2000). Grounded theory: Objectivist and constructivist methods. In: N. K. Denzin and Y. Lincoln (eds.). The Handbook of Qualitative Research, 509–535. Thousand Oaks, CA: Sage Publications, Inc. https://qualquant.org/wp-content/uploads/text/Charmaz%202000.pdf.
Čizmić, J. (2023). The Effects of the Patient’s Information on his Health (the Patient’s Right to Information). Zbornik radova Pravnog fakulteta u Splitu, 60 (4)/2023, 669–689. https://doi.org/10.31141/zrpfs.2023.60.150.669 [In Croatian]
Čović, A. (2023a). Euthanasia: The right to die between God’s will and the will of a man. Strani pravni život, 67 (2), 229–250. https://doi.org/10.56461/SPZ_23204KJ [In Serbian]
Čović, A. (2023b). The Role of the Church in Light of Contemporary Bioethical Issues. In: Džomić, Z. Vuković (eds.). State-ecclesiastical law, 127–149. Kragujevac: Pravni fakultet Univerziteta u Kragujevcu. [In Serbian]
Daruši, D. (2014). Informed Consent or Patient Autonomy – Truths or Misconceptions. The term paper presented at the Faculty of Law, “Union” University. Beograd. [In Serbian]
Dedić, G. (2015). Medical Ethics. Beograd: Medija centar Odbrana. [In Serbian]
Dedić, G. (2019). Communication skills in medicine. Beograd: Medija centar Odbrana. [In Serbian]
Đurđević, N. (1997). Patient’s Consent to Treatment. Kragujevac: Pravni fakultet u Kragujevcu. [In Serbian]
Emanuel, E. J., Emanuel, L. L. (1992). Four models of the physician-patient relationship, JAMA, 267 (16), 2221–2226. https://doi.org/10.1001/jama.1992.03480160079038
Entwistle, V. A., Carter, S. M., Cribb, A., McCaffery, K. (2010). Supporting Patient Autonomy: The Importance of Clinician-patient Relationships, J Gen Intern Med, 25 (7), 741–745. https://pmc.ncbi.nlm.nih.gov/articles/PMC2881979/
Family Law, Narodne novine, No. 103/15, 98/19, 47/20, 49/23 and 156/23. [In Croatian]
Frank, A. W. (1995). The Wounded Storyteller: Body, Illness, and Ethics. Chicago: University of Chicago Press. https://doi.org/10.7208/chicago/9780226260037.001.0001
Goodyear-Smith, F., Buetow, S. (2001). Power Issues in the Doctor-Patient Relationship, Health Care Analysis, 9 (4), 449–462. https://doi.org/10.1023/A:1013812802937
Katz, S. J., Belkora, J., Elwyn, G. (2014). Shared Decision Making for Treatment of Cancer: Challenges and Opportunities, J Oncol Pract, 10 (3), 206–208. https://doi.org/10.1200/JOP.2014.001434
Klarić, P., Baretić, M., Nikšić, S. (2022). Compensatory Medical Law. Zagreb: Sveučilište u Zagrebu, Pravni fakultet. [In Croatian]
Lanceley, A. (2022) . Toward Personalized Informed Consent in Cancer Care. Medical Anthropology, 41, 210–214. https://doi.org/10.1080/01459740.2021.2021903
Law on Patients’ Rights, “Službeni glasnik Republike Srbije”, 45/2013 and 25/2019 – other law. [In Serbian]
Mišić Radanović, N. (2018). The Patient’s Consent to a Medical Procedure as a Reason for Excluding Illegality. Zbornik radova Pravnog fakulteta u Splitu, 130 (4), 865–892. https://doi.org/10.31141/zrpfs.2018.55.130.865 [In Croatian]
Mišić Radanović, N. (2021). Legal Aspects of Refusing a Medical Procedure. Godišnjak Akademije pravnih znanosti Hrvatske (Yearbook of the Croatian Academy of Legal Sciences), 12 (1), 263–287. https://doi.org/10.32984/gapzh.12.1.13 [In Croatian]
Mujović Zornić, H. (2005) . Patient Rights – Universality and the European Concept. Aktualnosti građanskog i trgovačkog zakonodavstva i pravne prakse, 253–273. [In Serbian]
Mujović Zornić, H. (2015). Autonomy of Will. Pravni život, 9, 303–322. [In Serbian]
Mustać, K. (2020). Parson’s concept of the sick role, Kolegij: Sociologija i zdravstvo. https://www.scribd.com/document/636766749/Parsonsov-koncept-socijalne-uloge-bolesnika. [In Croatian]
Otani, K., Buchanan, P., Desai, S., Herrmann, P. (2016). Different combining process be-tween male and female patients to reach their overall satisfaction. J Patient Exp, 3(4), 145–150. https://doi.org/10.1177/2374373516685953
Parsons, T. (1951). The Social System. London: Routledge.
Perović, S. (2012). Natural Law and Morality – speech from 2012. Besede sa Kopaonika, 900–902. [In Serbian]
Radenović, S. (2012). Bioethics and Medicine. Novi Sad: Akademska knjiga. [In Serbian]
Radišić, J. (2004). Medical Law. Beograd: Nomos. [In Serbian]
Radišić, J. (2012). Patient Consent to Treatment and Liability for Treatment Without Valid Consent. Evropska revija za pravo osiguranja, 39–48.
Regulation on the National Program “Serbia Against Cancer”. “Službeni glasnik Republike Srbije”, No. 20 of 19th March 2009. [In Serbian]
Schneider, N., Bäcker, A., Brenk-Franz, K., Keinki, C., Hübner, J., Brandt, F., Von der Winkel, G., Hager, L., Strauss, B., Altmann, U. (2020). Patient information, communication and competence empowerment in oncology (PIKKO) – evaluation of a supportive care intervention for overall oncological patients. Study protocol of a nonrandomized controlled trial. BMC Med Res Methodol, 20 (1), 1. https://pubmed.ncbi.nlm.nih.gov/32414331/ https://doi.org/10.1186/s12874-020-01002-1
Schwaegermann, M. K., Schranz, M., Moehler, M., Labenz, C., Moringlane, A., Schmidt, M., Theobald, M., Hess, G. (2021). Any progress in informed consenting for cancer treatment? Results from a cross-sectional analysis at a comprehensive cancer center. J Cancer Res Clin Oncol, 147 (7), 2117–2126. doi: 10.1007/s00432-020-03495-1. Epub 2021 Jan 9. PMID: 33420813; PMCID: PMC8164598.
Segall, A. (1976). The Sick Role Concept, Journal of Health & Social Behavior, 17 (2), 162–169. https://doi.org/10.2307/2136342
Sherlock, A., Brownie, S. Patients’ recollection and understanding of informed consent: a literature review. ANZ J Surg. 2014 Apr; 84 (4), 207–10. doi: 10.1111/ans.12555. PMID: 24812707.
Sherlock, A., Brownie, S. (2014). Patients’ recollection and understanding of informed consent: a literature review. ANZ Journal of Surgery, 84 (4), 207–210. doi: 10.1111/ans.12555.
Shrivastava, S., Shrivastava, P. B., Ramasamy, J. (2014). Exploring the dimensions of doc-tor-patient relationship in clinical practice in hospital settings, Int J Health Policy Manag, 2 (4), 159–160. https://pmc.ncbi.nlm.nih.gov/articles/PMC4025091/
Sim, D., Yuan, S. E., Yun, J. H. (2016). Health literacy and physician-patient communication: a review of the literature. The International Journal of Communication and Health, 10, 104– 106.
Stjepanović, B. (2024) . The principle of autonomy of the will and the marriage contract, Pravne praznine i punoća prava, Pravni fakultet, Istočno Sarajevo, 251–270.
Strauss, A. L., Glaser, B. G. (1975). Chronic Illness and the Quality of Life. Saint Louis: Mosby.
Turabian, J. (2019). Sociology of the Medical-Patient Relationship: Putting Flesh on the Bones of a Stick Figure, General medicine and Clinical Practice, 2 (2), https://www.researchgate.net/publication/335883386_Sociology_of_the_Medical-Patient_Relationship_Putting_Flesh_on_the_Bones_of_a_Stick_Figure
Van Roij, J., Brom, L., Youssef-El Soud M., Van de Poll- Franse, L., Raijmakers, N. J. H. (2019). Social consequences of advanced cancer in patients and their informal car-egivers: a qualitative study. Support Care Cancer, 27 (4), 1187–1195. doi: 10.1007/s00520-018-4437-1.
Vukadinović Marković, J. (2024). European Health Union. In: J. Perović Vujačić (ed.). The Right to Justice – Challenges of the Moder Age. Proceedings of the 37th Meeting of Kopaonik Natural Law School “Slobodan Perović”, 479–492. Beograd: Kopaonička škola prirodnog prava – Slobodan Perović. [In Serbian]
Wise T., Biondi M., Constantini A. (2013). Psycho-oncology, 2013, Arlington: American Psychiatric Publishing.
Young, J. T. (2004). Illness Behaviour: A Selective Review and Synthesis. Sociology of Health Illness, 26 (1), 1–31. https://doi.org/10.1111/j.1467-9566.2004.00376.x
Zick Varul, M. (2010). Talkott Parsons the Sick Role and Chronic Illness, Body and Society, 16 (2), 72–94. https://doi.org/10.1177/1357034X10364766
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