Assessment of attitudes toward patient rights of people live from a Turkey town and migrating to Belgium

IF 1.2 Q4 HEALTH POLICY & SERVICES International Journal of Human Rights in Healthcare Pub Date : 2022-10-14 DOI:10.1108/ijhrh-12-2021-0204
Vahide Korkmaz, Nilufer Demirsoy
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Abstract

Purpose The purpose of this study is to assess the attitudes of individuals living in Belgium and in Emirdag in regard to patient rights and the effect of cultural differences in developing the attitude. This study measures the attitudes of two groups of people living in different geographies, “individuals living in Emirdag and Individuals emigrated from Emirdag to Belgium,” and yet having the same ethnic origin, common social and cultural capital. Design methodology/approach Implementing quantitative research, the data for the current study was obtained from a total of 1,043 participants, who were administered the Likert type “Patient Rights Attitude Scale” along with demographic questionnaire. Findings The total score mean of the scale is 126.09 ± 15.21 in the Emirdag group, whereas in the Belgian group, it is 129.78 ± 13.356. While the attitude with the highest mean score about patient rights in both groups observed under “the right to seek medical attention” and “the right to consent in medical and drug researches” items and thusthese items are considered as a common denominator, the two groups differed in the scale items that received the lowest average. Social implications It is important to determine the effects of attitudes toward patient rights and cultural differences on the development of attitudes, to determine the problems in the delivery of health services and health service procurement. Originality/value The structures that direct the choices and decisions of individuals in critical subjects such as organ transplantation and euthanasia, and thus having different practices in the doctrine, can be affected by individuals and even society’s rules, beliefs and values. It was concluded that immigrant participants’ dominating culture and related beliefs, rules and values play a role in the making of decision and choice.
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对土耳其城镇移民到比利时的患者权利态度的评估
目的本研究的目的是评估生活在比利时和埃米尔当的个人对患者权利的态度,以及文化差异对培养这种态度的影响。这项研究测量了生活在不同地理位置的两组人的态度,“生活在埃米尔当的个人和从埃米尔当移民到比利时的个人”,但具有相同的种族血统、共同的社会和文化资本。设计方法/方法实施定量研究,本研究的数据来自1043名参与者,他们接受了Likert型“患者权利态度量表”和人口统计问卷。结果:阿联酋组的总分平均值为126.09±15.21,而比利时组为129.78±13.356。虽然在“寻求医疗护理的权利”和“医学和药物研究中的同意权”项目下观察到的两组患者对患者权利的态度平均得分最高,因此这些项目被视为一个共同点,但两组在平均得分最低的量表项目上存在差异。社会含义重要的是确定对患者权利的态度和文化差异对态度发展的影响,确定提供医疗服务和医疗服务采购中的问题。独创性/价值观在器官移植和安乐死等关键学科中指导个人选择和决策的结构,因此在学说中有不同的实践,可能会受到个人甚至社会规则、信仰和价值观的影响。研究表明,移民参与者的主导文化以及相关的信仰、规则和价值观在决策和选择中发挥着作用。
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来源期刊
CiteScore
2.90
自引率
7.10%
发文量
48
期刊介绍: nternational Journal of Human Rights in Healthcare (IJHRH) is an international, peer reviewed journal with a unique practical approach to promoting race equality, inclusion and human rights in health and social care. The journal publishes scholarly and double blind peer-reviewed papers of the highest standard, including case studies and book reviews. IJHRH aims include: -To explore what is currently known about discrimination and disadvantage with a particular focus on health and social care -Push the barriers of the human rights discourse by identifying new avenues for healthcare practice and policy internationally -Create bridges between policymakers, practitioners and researchers -Identify and understand the social determinants of health equity and practical interventions to overcome barriers at national and international levels. The journal welcomes papers which use varied approaches, including discussion of theory, comparative studies, systematic evaluation of interventions, analysis of qualitative data and study of health and social care institutions and the political process. Papers published in IJHRH: -Clearly demonstrate the implications of the research -Provide evidence-rich information -Provoke reflection and support critical analysis of both challenges and strengths -Share examples of best practice and ‘what works’, including user perspectives IJHRH is a hugely valuable source of information for researchers, academics, students, practitioners, managers, policy-makers, commissioning bodies, social workers, psychologists, nurses, voluntary sector workers, service users and carers internationally.
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