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Equal Access to Healthcare in Socially Diverse Societies / Addresses for correspondence
Equal Access to Healthcare in Socially Diverse Societies / Addresses for correspondence
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1–10
Titelei/Inhaltsverzeichnis
1–10
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11–24
Introduction
Florian Steger, Mojca Ramšak, Paweł Łuków, Amir Muzur
Florian Steger, Mojca Ramšak, Paweł Łuków, Amir Muzur
11–24
Details
27–152
I. Vulnerable groups
27–152
27–58
The role of Patient Autonomy and Informed Consent for equal access to healthcare: A conceptual inquiry of contemporary bioethical debate
Julia Alessandra Harzheim
Julia Alessandra Harzheim
27–58
Details
1. Introduction
2. Methods and Materials
2.1. Systematic literature review
2.2. Non-systematic documentary evaluation
3. Results
3.1. Overview of research literature and categorical evaluation
3.1.1. Level one: implementation, concrete observation, evaluation
3.1.2. Level two: meta level – underlying mechanisms, dynamics, interactions
3.1.3. Level three: conceptual level – re-assessing concepts, terms and definitions
3.2. Research on Social Diversity and Minority Health: The relevance of Patient Autonomy and Informed Consent
3.3. The concept of Patient Autonomy: Terms, definitions and normative claims
3.3.1. Autonomy as individual right to rational decision making: defying paternalism
3.3.2. Kantian autonomy as an inherent status sui generis
4. Discussion
4.1. Patient Autonomy and Informed Consent in individual medical encounters
4.2. Re-definition of Minority Groups in the light of the findings
4.3. Expanding the results to systematic problems of access to public healthcare
4.4. The significance of Informed Consent for justice in public healthcare: a critical revision
5. Limitations
6. Conclusion
59–82
Disparities in women’s access to reproductive healthcare
Nika Pavlović
Nika Pavlović
59–82
Details
1. Introduction
2. Method
3. Differences in health systems
4. Overcoming disparities in women access to reproductive healthcare
4.1. Croatia
4.2. Germany
4.3. Poland
4.4. Slovenia
5. Access to reproductive healthcare during COVID-19 pandemic
6. Conclusion
83–110
Exercise of children’s participatory rights in the healthcare system of the Republic of Croatia
Gordana Šimunković, Ivana Borić
Gordana Šimunković, Ivana Borić
83–110
Details
1. Introduction – Vulnerability of children
2. Method and materials
3. Participation of children
4. Participation of children in healthcare
5. Relationship between protection and participation of children
6. International researches in participation of children in healthcare
7. Participation of children in healthcare in Croatia
8. Conclusion and recommendations
111–134
»Doctors don’t listen to us or the things we need.« Experiences of heteronormative healthcare and its aftermath for LGBATIQ patients in Germany
Ann Kristin Augst, Annika Spahn
Ann Kristin Augst, Annika Spahn
111–134
Details
1. Introduction
1.1. Heteronormativity as a theoretical framework
1.2. Heteronormativity in the German healthcare system
2. Methods and Materials
2.1 Types of interviews and their analysis
2.2. Sample
3. Preliminary Results and Findings
3.1. Asexual people’s experiences in healthcare
3.2. Trans people’s experiences in healthcare
4. Discussion
5. Conclusion
135–152
Becoming a parent as a lesbian in Poland: an autoethnographic narrative
Marta Lewandowska
Marta Lewandowska
135–152
Details
1. Background
2. Autoethnographic narrative as a method
3. Our story
3.1. Doubts and fears related to reproduction decisions – before it all began
3.2. Getting knowledge – stepping into the underworld
3.3. Clinical support in Poland – being a stranger
3.4. The Danish experience – a breath of fresh air
3.5. Labor and birth – the bitter-sweet taste of privilege
4. The privileged
5. The lesson
155–212
II. Minorities
155–212
155–178
Provision of healthcare for culturally diverse populations: Insights from a qualitative study on dementia care with the members of the Turkish immigrant community in Germany
Zümrüt Alpinar-Sencan
Zümrüt Alpinar-Sencan
155–178
Details
1. Introduction
1.1. Migration and dementia
1.2. Provision of and access to dementia care for and by culturally diverse populations
1.3. Culture’s role in healthcare ethics
2. Methods
2.1. Recruitment process
2.2. Study design
2.3. Data collection and analysis
3. Findings
3.1. There is a need for support, guidance and information
3.2. The disease is not well-known
3.3. Being a foreigner had led to a sense of discrimination
3.4. Living and working conditions have an impact on the initiation of the disease
3.5. The care is offered by the family members
4. Discussion
4.1. Need for culturally sensitive care to promote better access and provision of healthcare
4.2. Culture’s role in shaping one’s health-related phenomena
4.3. Impact of migration experience on one’s mental health
4.4. Willingness to care for the family
5. Limitations
6. Conclusion
179–192
Kidney transplantation in Jehovah’s Witnesses – the Croatian perspective
Dean Markić, Lada Zibar
Dean Markić, Lada Zibar
179–192
Details
1. Introduction
2. Patients and Methods
3. Results
4. Discussion
5. Conclusion
193–212
Health status and access to the healthcare system of members of the Roma national minority in the Republic of Croatia
Suzana Kunac, Aleksandar Racz
Suzana Kunac, Aleksandar Racz
193–212
Details
1. Introduction
2. Materials and method
3. Roma in the healthcare system in the Republic of Croatia
3.1 Roma access to the healthcare system in the Republic of Croatia
3. Conclusion
215–284
III. Healthcare professionals
215–284
215–240
Diversity-sensitive healthcare delivery across Poland’s clinical landscapes
Ewa Nowak, Anna-Maria Barciszewska, Karolina Napiwodzka
Ewa Nowak, Anna-Maria Barciszewska, Karolina Napiwodzka
215–240
Details
1. Theoretical background
2. Objectives
3. Method and procedure
3.1. Sample
4. Results
5. Discussion
6. Conclusion
241–252
Educational needs of nurses in intensive therapy units to improve attitudes towards interculturally diverse patients in Slovenia
Bojana Filej, Mojca Poredoš, Boris Miha Kaučič
Bojana Filej, Mojca Poredoš, Boris Miha Kaučič
241–252
Details
1. Background
2. Methods and materials
3. Results
4. Discussion
5. Conclusion
253–266
The importance of improving education of healthcare professionals on communication with minorities – experience with Roma in the Croatian healthcare system
Sanja Pleština, Sandra Karabatić
Sanja Pleština, Sandra Karabatić
253–266
Details
1. Introduction
2. Methods and Materials
3. Results
4. Discussion
5. Conclusion
267–284
Improving access to healthcare for minority groups: qualitative study with social workers in Croatia
Vanja Branica, Ivana Mošić Pražetina
Vanja Branica, Ivana Mošić Pražetina
267–284
Details
1. Introduction
2. Methods and Materials
3. Results
3.1. Patients from diverse cultural background
3.1.1. Foreigners
3.1.2. Roma minority
3.2. Perception of working with patients from diverse cultural background
3.3. Access to hospital healthcare
3.3.1. Good access to healthcare
3.3.2. Social works access to patients and patients’ access to social workers
3.4. Role of social workers
3.4.1. Getting to know the patient
3.4.2. Developing the helping relationship with patient and family members
3.4.3. Administrative and formal tasks and procedures
3.4.4. Bridge between hospital, patient and professionals in other institution
3.5. Impeding factors in provision of social work services
3.5.1. Lack of procedure and protocols
3.5.2. Time
3.5.3. Language barriers
3.6. Examples of good practice
4. Discussion
5. Limitations
6. Conclusion
285–290
Addresses for correspondence
285–290
Details
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Equal Access to Healthcare in Socially Diverse Societies , page 285 - 290
Addresses for correspondence
Autoren
Florian Steger (Ed.)
Mojca Ramšak (Ed.)
Pawel Łuków (Ed.)
Amir Muzur (Ed.)
DOI
doi.org/10.5771/9783495997895-285
ISBN print: 978-3-495-99788-8
ISBN online: 978-3-495-99789-5
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doi.org/10.5771/9783495997895-285
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