Literature DB >> 17470503

Theory and practice of informed consent in the Czech Republic.

Eva Krizova1, Jiri Simek.   

Abstract

The large-scale change of Czech society since 1989 has involved the democratic transformation of the health system. To empower the patient was one important goal of the healthcare reform launched immediately after the Velvet Revolution. The process has been enhanced by the accession of the Czech Republic to the European Union and the adoption of important European conventions regulating the area. The concept of informed consent and a culture of negotiation are being inserted into a traditionally paternalistic culture. Our article describes the current situation on the issue of the communication of information on state of health and treatment, and on the question of the participation of the patient in decisions on treatment. We present empirical results of a public opinion survey on this issue. The results show a still prevailing submissive attitude towards the physicians, despite the fact that the concept of informed consent has become more and more publicly familiar (42% of respondents gave the completely correct answer regarding informed consent). The impact of age, education and sex on answers to the questionnaire was analysed. Men, younger and more educated respondents were more likely to show the autonomous attitude, whereas women, older and less educated people tended to show the traditional submissive attitude. Further, our article raises the question of the cultural and historical background within which the current ethically and legally binding norms (products of western democracies, in fact) are interpreted. The question is how far cultural modifications are tolerable in the practical implementation of universal ethical constructs (informed consent).

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Year:  2007        PMID: 17470503      PMCID: PMC2598120          DOI: 10.1136/jme.2005.015164

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  6 in total

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Journal:  J Int Bioethique       Date:  2004 Jun-Sep

4.  Should cancer patients be informed about their diagnosis and prognosis? Future doctors and lawyers differ.

Authors:  Bernice S Elger; T W Harding
Journal:  J Med Ethics       Date:  2002-08       Impact factor: 2.903

5.  Limits of patient autonomy. Physician attitudes and practices regarding life-sustaining treatments and euthanasia.

Authors:  T R Fried; M D Stein; P S O'Sullivan; D W Brock; D H Novack
Journal:  Arch Intern Med       Date:  1993-03-22

6.  Convention for the protection of human rights and dignity of the human being with regard to the application of biology and medicine: convention on human rights and biomedicine (adopted by the Committee of Ministers on 19 November 1996). Council of Europe Convention of Biomedicine.

Authors: 
Journal:  Hum Reprod       Date:  1997-09       Impact factor: 6.918

  6 in total
  3 in total

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2.  Are physician-patient communication practices slowly changing in Croatia? -- a cross-sectional questionnaire study.

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Journal:  Croat Med J       Date:  2013-04       Impact factor: 1.351

3.  Limited family members/staff communication in intensive care units in the Czech and Slovak Republics considerably increases anxiety in patients' relatives--the DEPRESS study.

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  3 in total

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