Abstract

Patients should not always receive hard data about the risks and benefits of a medical intervention. That information should always be available to patients who expressly ask for it, but it should be part of standard disclosure only sometimes, and only for some patients. And even then, we need to think about how to offer it.

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Additional Information

ISSN
1552-146X
Print ISSN
0093-0334
Pages
pp. 30-39
Launched on MUSE
2011-03-20
Open Access
No
Archive Status
Archived 2012
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