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Aug 6th, 2022
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How to Work in formula in the Detailed Medical Consent

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hi Im dr. ha Pinto and were 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 were asking if we can examine a patient its imperative though that we ensure that this is documented clearly in the notes and three implied consent for example if were 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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Types of consent include implied consent, express consent, informed consent and unanimous consent.
Key components of consent that respect the research participants and their autonomy are disclosure, capacity and voluntariness. All relevant information required for a potential research participant to make an informed decision is necessary and should be disclosed.
What are the Different Types of Consent? Informed consent. Implied consent. Explicit consent. Active consent. Passive consent. Opt-Out consent. Key takeaway.
Types of consent include implied consent, express consent, informed consent and unanimous consent.
Among the surveyed psychotherapists, there was a high consensus on important information that should be communicated to patients in the context of informed consent. Almost all psychotherapists rated confidentiality and its exemptions (95%) and self-determined decision-making (97%) as important.
A patients informed consent can be gathered one of two ways: through implied consent or express consent.
The most important part of the consent process is informing the patient about the proposed treatment and what to expect. This includes informing the patient about: the nature of the treatment, risks and side effects of the treatment.
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.
Participants indicate their willingness to participate by agreeing to a specific statement, and then are included in the study. This is the most common, and recommended, form of consent for research.
B. Basic Elements of Informed Consent Description of Clinical Investigation. Risks and Discomforts. Benefits. Alternative Procedures or Treatments. Confidentiality. Compensation and Medical Treatment in Event of Injury. Contacts. Voluntary Participation.

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