Section Translational Medical Ethics – Focus: Ethics and Patient oriented Care in Oncology (EPOC)
Section Leader: Prof. Dr. med. Dr. phil. Eva Winkler
- Media and News
Due to the impressing medical & technological progress fostered by structural and systemic changes in health care, ethical issues in oncology and research constantly gain importance. Such issues include, for instance, the informed consent process in research, patient’s rights and the right to self-determination or the ethical justification of expensive treatments facing limited resources in health care.
The concept of Empirical Ethics combines empirical studies in patient care and research with ethical analysis (cf. figure 1).
- The concept of empirical ethics starts with a clinical or research question that causes moral distress.
- In a first step, the empirical research allows for a detailed account of the ethical questions at stake.
- The ethical analysis weighs the values and ethical principles affected in order to develop an ethically sound recommendation.
- To close the concept, this recommendation aims at informing our decisions in the clinical or research context - be it as an aid in decision-making, as an advice or a counselling service.
NCT-EPOC research, teaching and clinical activities focus on:
- End-of-Life Decision Making (EPAL)
- Ethical issues of the use of electronic health records (INFOPAT)
- Ethical issues in the care for elderly (PAC-E)
- Ethical guideline for advanced care planning in Oncology – adaptation and implementation (ELBA)
- HiGHmed – WP 7: Ethics and Stakeholders
- Preference-based decision aid to support participatory decisions about tumor-specific and palliative therapy in the last months of life (PETUPAL)
- Economic factors influencing doctors’ medical decisions-making: Ethical responsibility in modern cancer medicine (ELABORATE)
- Genomic NEWborn screening programs – Legal Implications, Value, Ethics and Society (NEW_LIVES)
- Research Ethics and ethical requirements for the informed consent process in Next Generation Sequencing (EURAT)
- Big Data in Systems Medicine. Normative and Social Aspects for Physicians, Scientists, Patients and Society (DASYMED)
- CoNfirm – Subproject 3: Data Sharing and Data Protection
- Learning from Clinical Data. Ethical, Social and Legal Aspects (LinCDat)
- Comparative Assessment of Genome and Epigenome Editing in Medicine: Ethical, Legal and Social Implications (COMPASS-ELSI)
- FAIR-Data Spaces (FAIR-DS)
- German Human Genome-Phenome Archive (GHGA)
- Marsilius-Project: "Treuhand" (Fiduciary relationships in medical ethics)