In 2004, the government amended the HIPAA privacy rule that makes it easier for relevant institutions to obtain medical information without the consent of those concerned. In their article, Herman and Peel examine the effect this rule has on the citizens and doctors who care for them, stating that the elimination of the right of consent will make it hard for patients to be truthful about their conditions, leading to unwittingly falsified data.
This article is important as it shows us clearly how HIPAA is infringing on citizens rights while claiming to be protecting them. The problem with the article is that it was written in 2004, and there may be changes in legislation six years down the line.
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