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Pharmaceutical information systems and possible implementations of informed consent -- developing an heuristic.
1Centre for Applied Ethics and Philosophy of Science, Department of Communication, Aalborg University Copenhagen, A, C, Meyers Vænge, 2450, København SV, Denmark. ploug@hum.aau.dk
BMC Medical Ethics
|November 20, 2012
Summary
Informed consent in Denmark's national pharmaceutical system impacts patient autonomy and information control. A new heuristic helps assess these impacts, highlighting the risk of routine consent processes.
Area of Science:
- Health Informatics
- Bioethics
Background:
- Denmark's comprehensive national pharmaceutical information system serves as a model for clinical health information systems.
- The system's ethical implications have been evaluated by the Danish Council of Ethics.
Purpose of the Study:
- To analyze informed consent implementation within the Danish pharmaceutical information system.
- To evaluate the effects of different consent models on patient autonomy and information control.
- To examine justifications for waiving informed consent in this context.
Main Methods:
- Analysis of informed consent implementation strategies.
- Assessment of impacts on autonomy and information control.
- Development of a heuristic for ranking consent options.
Main Results:
- Different informed consent implementations significantly affect patient autonomy and control over health information.
- A heuristic tool is provided to rank and estimate the impact of various consent options.
- The risk of 'routinisation of consent' is identified as a significant ethical concern.
Conclusions:
- The Danish pharmaceutical information system presents challenges to autonomy and information control, relevant to similar health information systems.
- The provided heuristic aids in understanding and managing these ethical issues.
- Further research is necessary to address the implications of routine consent procedures.
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