Transform your daily workflows and Modify Physical Exam Consent

Aug 6th, 2022
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Simple guide on how to Modify Physical Exam Consent

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How to Modify Physical Exam Consent

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hey guys welcome back to the channel and today ill be going through what you need to know when it comes to consenting your patients and ill also be covering some of the trickiest situations like gillick competence and the mental capacity act for vulnerable adults so my name is ali and im a final year dental student studying at newcastle and todays video as ive already mentioned well be covering obtaining valid consent which is the third gdc principle well be covering a quick history on english taught law cases to do with negligence and then well talk a bit about what valid consent actually is followed by consenting children under 16 and then well finish off by talking about consenting vulnerable adults who dont have the capacity to consent for themselves there are timestamps on the screen now and in the description so if you have anything that youre specifically after feel free to skip around lets get started so im not gonna bore you guys for t

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To the general rule that consent must always be obtained before any treatment is administered, there is an important exception. In cases of medical emergency when the patient (or substitute decision maker) is unable to consent, a physician has the duty to do what is immediately necessary without consent.
Implied Consent. Participation in a certain situation is sometimes considered proof of consent. Explicit Consent. Active Consent. Passive Consent. Opt-Out Consent.
Holding out an arm to have a blood pressure taken is implicit consent, whereas an ECG or blood gases may require explicit consent.
Good practice in consent It is a general legal and ethical principle that valid consent must be obtained before commencing an examination, starting treatment or physical investigation, or providing personal care.
Obtaining informed consent in medicine is process that should include: (1) describing the proposed intervention, (2) emphasizing the patients role in decision-making, (3) discussing alternatives to the proposed intervention, (4) discussing the risks of the proposed intervention and (5) eliciting the patients
Consent information must include the: ∎ nature of the treatment or care; ∎ expected benefits; ∎ the material risks and side effects; ∎ alternative courses of action; and ∎ likely consequences of not receiving the treatment.
3 key elements: it must be voluntary. the patient must have the capacity to consent. the patient must be properly informed.
In an emergency, if a person is unconscious and in danger of death or other serious outcomes if medical care is not given right away, informed consent may not be required before treatment.

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