Informed Consent

Informed consent is a process for getting permission before conducting a healthcare intervention on a person, or for disclosing personal information. A health care provider may ask a patient to consent to receive therapy before providing it, or a clinical researcher may ask a research participant before enrolling that person into a clinical trial. Informed consent is collected according to guidelines from the fields of medical ethics and research ethics.

An informed consent can be said to have been given based upon a clear appreciation and understanding of the facts, implications, and consequen
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The Immortal Life of Henrietta Lacks
Uprooted by Peter J. BoniWonder Drug by Jennifer VanderbesThe Immortal Life of Henrietta Lacks by Rebecca SklootThe Good Doctor by Barron H. LernerFor the Public Good by Belle Boggs
Medical Ethics
10 books — 35 voters


Susan McCutcheon
Drugs and medical technology can be enormously beneficial when used to take care of real complications, but too often they are abused when applied to women birthing normally. These women are thus subjected to unnecessary risks. The key to this problem is informed consent, an ideal too seldom realized. Informed consent means that no woman during pregnancy or labor should ever be deceived into thinking that any drug or procedure (Demerol, Seconal, spinals, caudals, epidurals, paracervical block, e ...more
Susan McCutcheon, Natural Childbirth the Bradley Way

Stephen Fry
The uncomfortable, as well as the miraculous, fact about the human mind is how it varies from individual to individual. The process of treatment can therefore be long and complicated. Finding the right balance of drugs, whether lithium salts, anti-psychotics, SSRIs or other kinds of treatment can be a very hit or miss heuristic process requiring great patience and classy, caring doctoring. Some patients would rather reject the chemical path and look for ways of using diet, exercise and talk-ther ...more
Stephen Fry

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