“A key component of informed consent to participate in medical research is the understanding that research is not the same as treatment.” – J Jaxen
A monumental ethical issue is hovering over the entire medical establishment in the United States that threatens its integrity and trust. The human element is being removed from the equation, replaced by computers to give us our options, and legislation to remove our choice. Somewhere in the shuffle, the individual’s informed consent was broken down, lost in the paperwork, and made irrelevant.
Informed consent is the process by which the treating health care provider discloses appropriate information to their patient so that the patient may make a voluntary choice to accept or refuse treatment. It originates from the legal and ethical right that the patient has to direct what happens to their body, and from the ethical duty of the physician to involve the patient in their health care. Concerning the current hot button area of vaccination in the United States, the patient is not given proper informed consent of side effects or the actual vaccine inserts to look at prior to injection. If they did receive the insert, they would quickly see the repeated words “there have been no controlled trials” and “safety and effectiveness have not been established.” Continue reading