Ethics and Informed Consent for Comparative Effectiveness Research With Prospective Electronic Clinical Data

Medical Care ◽  
2013 ◽  
Vol 51 ◽  
pp. S53-S57 ◽  
Author(s):  
Ruth Faden ◽  
Nancy Kass ◽  
Danielle Whicher ◽  
Walter Stewart ◽  
Sean Tunis
2017 ◽  
Vol 45 (3) ◽  
pp. 352-364 ◽  
Author(s):  
Lois Shepherd

This paper explains why informed consent for randomized comparative effectiveness research (CER) must include risks of standard care. Disclosures of such risks are both legally and ethically required and, for reasons discussed in the paper, should remain so.


Medical Care ◽  
2012 ◽  
Vol 50 ◽  
pp. S49-S59 ◽  
Author(s):  
Dean F. Sittig ◽  
Brian L. Hazlehurst ◽  
Jeffrey Brown ◽  
Shawn Murphy ◽  
Marc Rosenman ◽  
...  

2017 ◽  
Vol 2 (2) ◽  
pp. e10047 ◽  
Author(s):  
Stephanie R. Morain ◽  
Ellen Tambor ◽  
Rachael Moloney ◽  
Nancy E. Kass ◽  
Sean Tunis ◽  
...  

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