Equal Access to Healthcare in Socially Diverse Societies

Prof. Dr. Florian Steger; Prof. Mojca Ramšak; Prof. Dr. Pawel Łuków; Prof. Dr. Amir Muzur

doi:10.5771/9783495997895

Zusammenfassung

Mit der sich verändernden Zusammensetzung der Gesellschaften kommen Fragen der sozialen Vielfalt und des gleichberechtigten Zugangs von Minderheitengruppen zur Gesundheitsversorgung zunehmend ins Blickfeld. Gleichwohl gibt es weiterhin Debatten über die praktische Umsetzung der Gleichstellung im Gesundheitswesen. Ziel der Beiträge in diesem Band ist daher ein besseres Verständnis des Phänomens der Ungleichheit und Diskriminierung von Minderheitengruppen beim Zugang zur Gesundheitsversorgung aus interdisziplinären Perspektiven der Medizinethik, der öffentlichen Gesundheit und des Rechts. Ein solches Verständnis kann dazu führen, dass die besonderen Bedürfnisse von Minderheiten in Bezug auf die Gesundheitsversorgung ermittelt werden.

Schlagworte

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Bibliographische Angaben

Copyrightjahr: 2023
ISBN-Print: 978-3-495-99788-8
ISBN-Online: 978-3-495-99789-5
Verlag: Karl Alber, Baden-Baden
Reihe: Angewandte Ethik
Band: 8
Sprache: Englisch
Seiten: 290
Produkttyp: Sammelband

Inhaltsverzeichnis

KapitelSeiten

Titelei/InhaltsverzeichnisSeiten 1 - 10 Download Kapitel (PDF)
IntroductionSeiten 11 - 24 Florian Steger, Mojca Ramšak, Paweł Łuków, Amir Muzur Download Kapitel (PDF)
1. Julia Alessandra Harzheim Download Kapitel (PDF)
  1. 1. Introduction
  2. 1. 2.1. Systematic literature review
    2. 2.2. Non-systematic documentary evaluation
  3. 1. 1. 3.1.1. Level one: implementation, concrete observation, evaluation
      2. 3.1.2. Level two: meta level – underlying mechanisms, dynamics, interactions
      3. 3.1.3. Level three: conceptual level – re-assessing concepts, terms and definitions
    2. 3.2. Research on Social Diversity and Minority Health: The relevance of Patient Autonomy and Informed Consent
    3. 1. 3.3.1. Autonomy as individual right to rational decision making: defying paternalism
      2. 3.3.2. Kantian autonomy as an inherent status sui generis
  4. 1. 4.1. Patient Autonomy and Informed Consent in individual medical encounters
    2. 4.2. Re-definition of Minority Groups in the light of the findings
    3. 4.3. Expanding the results to systematic problems of access to public healthcare
    4. 4.4. The significance of Informed Consent for justice in public healthcare: a critical revision
  5. 5. Limitations
  6. 6. Conclusion
2. Nika Pavlović Download Kapitel (PDF)
  1. 1. Introduction
  2. 2. Method
  3. 3. Differences in health systems
  4. 1. 4.1. Croatia
    2. 4.2. Germany
    3. 4.3. Poland
    4. 4.4. Slovenia
  5. 5. Access to reproductive healthcare during COVID-19 pandemic
  6. 6. Conclusion
3. Gordana Šimunković, Ivana Borić Download Kapitel (PDF)
  1. 1. Introduction – Vulnerability of children
  2. 2. Method and materials
  3. 3. Participation of children
  4. 4. Participation of children in healthcare
  5. 5. Relationship between protection and participation of children
  6. 6. International researches in participation of children in healthcare
  7. 7. Participation of children in healthcare in Croatia
  8. 8. Conclusion and recommendations
4. Ann Kristin Augst, Annika Spahn Download Kapitel (PDF)
  1. 1. 1.1. Heteronormativity as a theoretical framework
    2. 1.2. Heteronormativity in the German healthcare system
  2. 1. 2.1 Types of interviews and their analysis
    2. 2.2. Sample
  3. 1. 3.1. Asexual people’s experiences in healthcare
    2. 3.2. Trans people’s experiences in healthcare
  4. 4. Discussion
  5. 5. Conclusion
5. Marta Lewandowska Download Kapitel (PDF)
  1. 1. Background
  2. 2. Autoethnographic narrative as a method
  3. 1. 3.1. Doubts and fears related to reproduction decisions – before it all began
    2. 3.2. Getting knowledge – stepping into the underworld
    3. 3.3. Clinical support in Poland – being a stranger
    4. 3.4. The Danish experience – a breath of fresh air
    5. 3.5. Labor and birth – the bitter-sweet taste of privilege
  4. 4. The privileged
  5. 5. The lesson
1. Zümrüt Alpinar-Sencan Download Kapitel (PDF)
  1. 1. 1.1. Migration and dementia
    2. 1.2. Provision of and access to dementia care for and by culturally diverse populations
    3. 1.3. Culture’s role in healthcare ethics
  2. 1. 2.1. Recruitment process
    2. 2.2. Study design
    3. 2.3. Data collection and analysis
  3. 1. 3.1. There is a need for support, guidance and information
    2. 3.2. The disease is not well-known
    3. 3.3. Being a foreigner had led to a sense of discrimination
    4. 3.4. Living and working conditions have an impact on the initiation of the disease
    5. 3.5. The care is offered by the family members
  4. 1. 4.1. Need for culturally sensitive care to promote better access and provision of healthcare
    2. 4.2. Culture’s role in shaping one’s health-related phenomena
    3. 4.3. Impact of migration experience on one’s mental health
    4. 4.4. Willingness to care for the family
  5. 5. Limitations
  6. 6. Conclusion
2. Dean Markić, Lada Zibar Download Kapitel (PDF)
  1. 1. Introduction
  2. 2. Patients and Methods
  3. 3. Results
  4. 4. Discussion
  5. 5. Conclusion
3. Suzana Kunac, Aleksandar Racz Download Kapitel (PDF)
  1. 1. Introduction
  2. 2. Materials and method
  3. 1. 3.1 Roma access to the healthcare system in the Republic of Croatia
  4. 3. Conclusion
1. Ewa Nowak, Anna-Maria Barciszewska, Karolina Napiwodzka Download Kapitel (PDF)
  1. 1. Theoretical background
  2. 2. Objectives
  3. 1. 3.1. Sample
  4. 4. Results
  5. 5. Discussion
  6. 6. Conclusion
2. Bojana Filej, Mojca Poredoš, Boris Miha Kaučič Download Kapitel (PDF)
  1. 1. Background
  2. 2. Methods and materials
  3. 3. Results
  4. 4. Discussion
  5. 5. Conclusion
3. Sanja Pleština, Sandra Karabatić Download Kapitel (PDF)
  1. 1. Introduction
  2. 2. Methods and Materials
  3. 3. Results
  4. 4. Discussion
  5. 5. Conclusion
4. Vanja Branica, Ivana Mošić Pražetina Download Kapitel (PDF)
  1. 1. Introduction
  2. 2. Methods and Materials
  3. 1. 1. 3.1.1. Foreigners
      2. 3.1.2. Roma minority
    2. 3.2. Perception of working with patients from diverse cultural background
    3. 1. 3.3.1. Good access to healthcare
      2. 3.3.2. Social works access to patients and patients’ access to social workers
    4. 1. 3.4.1. Getting to know the patient
      2. 3.4.2. Developing the helping relationship with patient and family members
      3. 3.4.3. Administrative and formal tasks and procedures
      4. 3.4.4. Bridge between hospital, patient and professionals in other institution
    5. 1. 3.5.1. Lack of procedure and protocols
      2. 3.5.2. Time
      3. 3.5.3. Language barriers
    6. 3.6. Examples of good practice
  4. 4. Discussion
  5. 5. Limitations
  6. 6. Conclusion
Addresses for correspondenceSeiten 285 - 290 Download Kapitel (PDF)