Save time with DocHub and Save Detailed Medical Consent in DOC

Aug 6th, 2022
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How to Save Detailed Medical Consent in DOC

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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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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.
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.
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.
Informed consent is documented by the use of a written consent form approved by the IRB and signed and dated by the subject or the subjects legally authorized representative at the time of consent. A copy of the signed and dated consent form must be given to the person signing the form.
In general, informed consent of the subjects, or parental permission for children involved in research, must be sought and documented in ance with, and to the extent required by, HHS regulations at 45 CFR 46.116 and 45 CFR 46.117 respectively.
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.
In general, informed consent of the subjects, or parental permission for children involved in research, must be sought and documented in ance with, and to the extent required by, HHS regulations at 45 CFR 46.116 and 45 CFR 46.117 respectively.
Informed Consent Basics Outline the risks, benefits, alternative treatment available. Involve the patient in decision making. Communicate at a level the patient can understand. Contain enough information for the patient to make an informed decision. Explain refusal of care and the risks associated.

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