Blot dot in the Professional Medical Consent in a few clicks

Aug 6th, 2022
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How to blot dot in the Professional Medical Consent

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[Music] welcome to this lecture on medical law today we will review the case of Montgomery versus Lana Keisha Health Board we will look into how this case caused the seismic shift in informed consent again here is our legal disclaimer the information I am providing here is intended for education purposes only and with all the information being provided being well documented in the public domain under no circumstances shall we accept any liability for any loss or damage incurred as a result of improper use of this lecture if you require independent legal advice please seek professional legal opinion I am a medical doctor not your lawyer first lets review the legal position of consent as directed by the Bolam case a doctor cannot be found negligent where they have upheld a reasonable standard of care this is determined by whether a doctors actions can be supported by a body of medical experts ie held in Bolam in the case of consent where a patient claims negligence on behalf of the doc

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There are 4 components of informed consent including decision capacity, documentation of consent, disclosure, and competency. Doctors will give you information about a particular treatment or test in order for you to decide whether or not you wish to undergo a treatment or test.
In 1980, the Supreme Court of Canada rendered two landmark decisions pertaining to the related matters of the duty of a physician to make disclosure to the patient and the requirement of informed consent of the patient to a surgical procedure.
Implied consent is consent that is not given explicitly, but which can be inferred based on the individuals actions and the facts of a particular situation. You may imply consent for the use of personal information if you collected it directly and to provide a service.
In ordinary medical practice the consent given by a patient to a physician or surgeon, to be effective, must be an informed consent freely given. It is the duty of the physician to give a fair and reasonable explanation of the proposed treatment including the probable effect and any special or unusual risks.
The 4 types of consent are: express consent, implied consent, opt in consent and opt out consent.
There is no stipulated age of consent for treatment. The Medical Consent of Minors Act provides that minors who are 16 years old may consent to medical treatment in the same manner as they would having attained the age of majority.
Valid informed consent for research must include three major elements: (1) disclosure of information, (2) competency of the patient (or surrogate) to make a decision, and (3) voluntary nature of the decision. US federal regulations require a full, detailed explanation of the study and its potential risks.
A physician must answer any specific questions posed by the patient as to the risks involved in the proposed treatment. Always the patient must be given the opportunity to ask questions. The patient should be told about the consequences of leaving the ailment untreated.

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