Remove Line in the Physical Exam Consent

Aug 6th, 2022
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How to Remove Line in the Physical Exam Consent

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[Music] Im mark Pepin Im an MD PhD student here at UAB School of Medicine this is Aaron Dorman PA student here and today well be teaching you through the heent exam before you enter the rooms is important to know you have the proper equipment to perform this exam so what I have with me is a tuning fork specifically the 512 Hertz secondly I have a pen light here also a tongue depressor and I also have an HR 2 types of ID charts notice the different sizes in the lowest font here maybe you cant see that from there but its important to read the small font basically at the very bottom of each of these charts one of them so this one requires you to hold the chart at 16 inches 16 to 18 inches so at basically at arms length have the patient hold it the second one here is actually at the foot of the bed or about six feet from the patient so you yourself would hold this and ask the patient to read it so just kind of a thing to note on what you actually have with you the last thing here sho

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What does consent to treatment mean? Giving consent to treatment for mental health means both that: You agree with a health professional about a treatment theyve suggested for you. You have given your consent verbally or in writing to receiving that treatment.
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.
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.
To be valid, consent must be given voluntarily and freely, without pressure or undue influence being exerted on the person either to accept or refuse treatment. Such pressure can come from partners or family members, as well as health or care practitioners.
The informed consent process involves three key features: (1) disclosing to potential research subjects information needed to make an informed decision; (2) facilitating the understanding of what has been disclosed; and (3) promoting the voluntariness of the decision about whether or not to participate in the research.
Consent to treatment means a person must give permission before they receive any type of medical treatment, test or examination. This must be done on the basis of an explanation by a clinician. Consent from a patient is needed regardless of the procedure, whether its a physical examination or something else.
A person may indicate consent non-verbally (for example by presenting their arm for their pulse to be taken), verbally, or in writing. For the consent to be valid, the person must have capacity to make the particular decision with sufficient and appropriate information and not be acting under duress.
It is the patients right to refuse consent. When that happens, carefully document the refusal and inform the patient of the potential health issues involved because treatment was refused.
However, there are a number of circumstances where the practitioner can reasonably override such a decision, including: the person lacks the mental capacity to make that decision this must be properly explored and recorded in line with the Mental Capacity Act. other people are, or may be, at risk, including children.

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