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In recent years concerns over the use of results of scientific
advances, expectations about how medical decisions are made, and
demographic changes have raised ethical questions about how
resources are allocated, and how the principles of beneficence, and
respect for patient autonomy are applied. The effect that bioethics
can have on policy decisions and health care delivery demand an
enhanced approach to our understanding of such complex issues. This
volume opens a window to how empirical social research can be used
to illuminate and answer such quandaries and offers a practical
resource for those wishing to engage in this type of research.
Through a thorough look at both quantitative and qualitative
methods utilized in key research investigations in bioethics, the
book examines the impact of such investigations on clinical and
policy decision-making, scholarship and on the advancement of
theory. The varied sociological and anthropological research
examples that are presented allow readers to better understand the
richness and breadth of such work as well as relevant practical and
theoretical approaches.
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