Join cross in the Professional Medical Consent effortlessly

Aug 6th, 2022
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How to Join cross in the Professional Medical Consent

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hi I'm dr. ha Pinto and we're going to talk today about consent and this is in continuation of our medical ethics lecture series okay so what is consent consent it defined as a permission for something to happen or an agreement to do something in the context of medicine this involves a patient providing permission or in other words consent for a treatment or an investigation gaining consent is the ethical and legal duty of that doctor okay so when a doctor requests consent from a patient this can be provided either as one written consent for example in the case of a consent form for an operation oral consent for example when we're asking if we can examine a patient it's imperative though that we ensure that this is documented clearly in the notes and three implied consent for example if we're taking our phlebotomy equipment to the patient and they lean out their arm for us to take their blood ideally this should be avoided where possible as it may be misinterpreted by the doctor we sh...

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Informed Consent Checklist (1998) A statement that the study involves research. An explanation of the purposes of the research. The expected duration of the subjects participation. A description of the procedures to be followed. Identification of any procedures which are experimental.
Consent Forms Consent Form 1 Patient agreement to investigation, treatment or procedure. Consent Form 2 Parental agreement to investigation, treatment or procedure for a child or young person. Consent Form 3 Patient Parental agreement to investigation, treatment or procedure where consciousness not impaired.
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.
Exceptions: (1) emergencies, (2) emancipated minors, (3) mature minors, (4) statutory exceptions, such as HIV testing, drug abuse testing, STD testing etc.
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
Cues for consent might look/feel like: Looking at you, smiling and nodding. Being relaxed and happy. Being enthusiastic and responsive. Kissing you back and touching you. Responding to you with their body.
Consent can also be non-verbal. There are ways to express a clear willingness to engage in sexual contact without using words.Examples of giving nonverbal consent may include: Head nod. Thumbs up. Pulling someone closer. Nodding yes. Making direct eye contact. Actively touching someone. Initiating sexual activity.
Defining consent informed the person must be given all of the information about what the treatment involves, including the benefits and risks, whether there are reasonable alternative treatments, and what will happen if treatment does not go ahead.
For consent to be considered valid: it must be voluntary. the patient must have the mental capacity to consent. the patient must be properly informed.
There are two well-recognized exceptions to the need for informed consent to medical treatment. The more common is a medical emergency, in which an unconscious or delirious patient cannot consent. The second is rare and involves certain court-ordered treatments or treatments and tests mandated by law.

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