Clean line in the Detailed Medical Consent

Aug 6th, 2022
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How to clean line in the Detailed Medical Consent

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[Music] welcome to this lecture on medical law today we will review the case of Montgomery versus Lana Keisha Health Board we will look into how this case caused the seismic shift in informed consent again here is our legal disclaimer the information I am providing here is intended for education purposes only and with all the information being provided being well documented in the public domain under no circumstances shall we accept any liability for any loss or damage incurred as a result of improper use of this lecture if you require independent legal advice please seek professional legal opinion I am a medical doctor not your lawyer first lets review the legal position of consent as directed by the Bolam case a doctor cannot be found negligent where they have upheld a reasonable standard of care this is determined by whether a doctors actions can be supported by a body of medical experts ie held in Bolam in the case of consent where a patient claims negligence on behalf of the doc

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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.
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.
A process in which patients are given important information, including possible risks and benefits, about a medical procedure or treatment, genetic testing, or a clinical trial. This is to help them decide if they want to be treated, tested, or take part in the trial.
There are various types of consent, including explicit consent, implied consent, opt-in consent, and opt-out consent.
There are three types of patient consent you should know about for legal purposes: oral, written and implied consent. Oral consent: This type of consent comprises any verbal permission a patient gives you to conduct treatment.
A truly informed consent requires full disclosure of all relevant information by the doctor, competence of the patient to appreciate what the information signifies, understanding of the facts and issues by the patient and a voluntary non‐coerced choice by the patient leading to an autonomous authorisation for treatment
Informed consent is the process in which a health care provider educates a patient about the risks, benefits, and alternatives of a given procedure or intervention. The patient must be competent to make a voluntary decision about whether to undergo the procedure or intervention.

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