期刊论文详细信息
BMC Medical Ethics
Pharmaceutical information systems and possible implementations of informed consent - developing an heuristic
Søren Holm1  Thomas Ploug2 
[1] Center for Medical Ethics, Faculty of Medicine, University of Oslo, Oslo, Norway;Centre for Applied Ethics and Philosophy of Science, Department of Communication, Aalborg University Copenhagen, A. C. Meyers Vænge, 2450, København SV, Denmark
关键词: Routinisation;    Informed consent;    Health information systems;    Health information;    Control;    Autonomy;   
Others  :  800012
DOI  :  10.1186/1472-6939-13-30
 received in 2012-04-26, accepted in 2012-10-17,  发布年份 2012
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【 摘 要 】

Background

Denmark has implemented a comprehensive, nationwide pharmaceutical information system, and this system has been evaluated by the Danish Council of Ethics. The system can be seen as an exemplar of a comprehensive health information system for clinical use.

Analysis

The paper analyses 1) how informed consent can be implemented in the system and how different implementations create different impacts on autonomy and control of information, and 2) arguments directed towards justifying not seeking informed consent in this context.

Results and Conclusion

Based on the analysis a heuristic is provided which enables a ranking and estimation of the impact on autonomy and control of information of different options for consent to entry of data into the system and use of data from the system.

The danger of routinisation of consent is identified.

The Danish pharmaceutical information system raises issues in relation to autonomy and control of information, issues that will also occur in relation to other similar comprehensive health information systems. Some of these issues are well understood and their impact can be judged using the heuristic which is provided. More research is, however needed in relation to routinisation of consent.

【 授权许可】

   
2012 Ploug and Holm; licensee BioMed Central Ltd.

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