Confusing “Consent” Terminology Emerges

In its August 19th letter to the Office of the National Coordinator, the HIT Policy Committee creates the term “meaningful consent” related to the coming choices patients will be asked to make about the sharing and use of their clinical data. In the recommendations, the committee clearly states that the recommendations apply to exchange of identifiable health information in order to meet Stage 1 meaningful use requirements. So now is the perfect time to ensure that the difference between the two types of consent remain distinct in the mind of the patient population. » Continue reading “Confusing “Consent” Terminology Emerges”

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