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Aug 6th, 2022
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How to Clean background 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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The underlying principle of consent isnt particularly complicated: Patients have a right to make an informed, voluntary decision about their care. That means they need to know the nature, risks, and benefits of their options which includes declining treatment.
Required Components. Generally, three conditions must be met for informed consent to be considered validthe participants must understand the information presented, the consent must be given voluntary, and the participant must be competent to give consent.
Types of consent include implied consent, express consent, informed consent and unanimous consent.
ETHICAL ANGLE The concept of consent arises from the ethical principle of patient autonomy[1] and basic human rights. [2] Patients has all the freedom to decide what should or should not happen to his/her body and to gather information before undergoing a test/procedure/surgery.
The consent form should be written in the second person and include all the elements of informed consent arranged sequentially. The Purpose of the Study should be restricted to a statement of the scientific purpose. The Documentation of Informed Consent should contain the subjects concluding consent statement.
The informed consent process makes sure that your health care provider has given you information about your condition along with testing and treatment options before you decide what to do.
The underlying principle of consent isnt particularly complicated: Patients have a right to make an informed, voluntary decision about their care. That means they need to know the nature, risks, and benefits of their options which includes declining treatment.

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