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      Seven year overview (2007-2013) of ethical transgressions by registered healthcare professionals in South Africa

      research-article
      ,
      Health SA Gesondheid (Online)
      Elsevier
      Ethical transgression, HPCSA, Complaints

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          Abstract

          A move has taken place internationally in the delivery and "consumption" of health care where if clients and patients (health care consumers) hold the opinion that the health care professionals/providers' behaviour has had a negative effect, impact or outcome on them, they may lodge a complaint with the relevant health professional regulatory body. Ethical transgressions of health care providers can generally be clustered into the following three categories: a) Competence and conduct with clients (e.g. abandonment, sexual intimacies, dishonesty, disclosure of information); b) Business practices (e.g. billing, reports, documentation); and c) Professional practice (e.g. referral upon termination, obtaining appropriate potential employment opportunities, nonprofessional relationships). The primary objective of this study was to analyse the ethical transgressions of registered members of the twelve professional boards in the Health Professions Council of South Africa (HPCSA) in the period 2007 to 2013. A mixed methods approach was followed in this study which specifically focused on a historical research approach. The results indicate that the boards with the highest number of transgressions per the registered practitioners were firstly the Medical and Dental practitioners, closely followed by the Optometry and Dispensing Opticians Board. The predominantly complaint made against members of both these boards was for fraudulent conduct (collectively totalling to 85% of all fraudulent cases during the period) and included actions such as charging for non-rendered services, issuing false statements and submitting fraudulent medical aid claims. Cognisance needs to be taken that the South African public will increasingly demand better services and that since they are being better informed via the media of their rights and have access to a broader database of knowledge (rightly or wrongly so the internet) practitioners' opinions will not necessarily be accepted outright and that they (the public) will challenge it accordingly. This raises the concern that practitioners need to take on the responsibility to communicate with their patients/clients in order to educate them and keep them informed.

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          Most cited references22

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          Social Research Methods Qualitative and Quantitative Approaches.

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            Revolution or evolution: the challenges of conceptualizing patient and public involvement in a consumerist world.

            Changing the relationship between citizens and the state is at the heart of current policy reforms. Across England and the developed world, from Oslo to Ontario, Newcastle to Newquay, giving the public a more direct say in shaping the organization and delivery of healthcare services is central to the current health reform agenda. Realigning public services around those they serve, based on evidence from service user's experiences, and designed with and by the people rather than simply on their behalf, is challenging the dominance of managerialism, marketization and bureaucratic expertise. Despite this attention there is limited conceptual and theoretical work to underpin policy and practice. This article proposes a conceptual framework for patient and public involvement (PPI) and goes on to explore the different justifications for involvement and the implications of a rights-based rather than a regulatory approach. These issues are highlighted through exploring the particular evolution of English health policy in relation to PPI on the one hand and patient choice on the other before turning to similar patterns apparent in the United States and more broadly. A framework for conceptualizing PPI is presented that differentiates between the different types and aims of involvement and their potential impact. Approaches to involvement are different in those countries that adopt a rights-based rather than a regulatory approach. I conclude with a discussion of the tension and interaction apparent in the globalization of both involvement and patient choice in both policy and practice.
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              Social Research Methods: Qualitative and Quantitative Approaches

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                Author and article information

                Contributors
                Role: ND
                Role: ND
                Journal
                hsa
                Health SA Gesondheid (Online)
                Health SA Gesondheid (Online)
                Elsevier (Cape Town, Western Cape, South Africa )
                1025-9848
                2071-9736
                2016
                : 21
                : 1
                : 46-53
                Affiliations
                [02] orgnameTshwane University of Technology South Africa
                [01] orgnameUniversity of the Western Cape South Africa
                Article
                S2071-97362016000100005
                10.1016/j.hsag.2015.11.004
                c9ba3d26-62e9-4fad-9066-045ad6553e76

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

                History
                : 16 November 2015
                : 31 March 2015
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 17, Pages: 8
                Product

                SciELO South Africa


                Ethical transgression,HPCSA,Complaints
                Ethical transgression, HPCSA, Complaints

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