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Tag: newborn disease screening

Ethical debate: Patient consent and medical progress

Posted on February 10, 2010April 16, 2010 By David Shiffman 60 Comments on Ethical debate: Patient consent and medical progress
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Image from Unt.edu

The interwebs are abuzz with glowing reviews for Rebecca Skloot’s new book “The Immortal Life of Henrietta Lacks”. I’m currently #37 on the library reserve list (sorry, Rebecca, but I’m a poor grad student and I can’t afford to buy it). The book tells the story of the HeLa cell line, which are cells that were taken from a patient without her consent. These cells have led to important medical breakthroughs. But how isolated of an incident is this?

Read More “Ethical debate: Patient consent and medical progress” »

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