Replace phone in the Detailed Medical Consent effortlessly

Aug 6th, 2022
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How to Replace phone in the Detailed Medical Consent

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my name is Veera Loza Im a gastroenterologist a physician but more importantly Im a son a brother an uncle and also like many of you a patient let me tell you two stories first is that of a young six-year-old boy who stopped his father from going to work by simply saying daddy I cant breathe his father rushed over to hit to his son noticed he was gasping for air took him to the emergency room where it followed by a nurse walked into the emergency room and listened to his chest his heart and lungs they turned to the family and said this is nothing this is only asthma we will give him some treatment and he will be fine and then they walked out of the room the second is that of a young doctor in training who walks into a patients room confidently to describe a procedure known as an endoscopic retrograde cholangiopancreatography kudos to anybody who can spell that he walks into the patients room and looks to the patient and her family and says so looks like theres a stone stuck in y

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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
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.
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.
The informed consent process may be conducted over the phone or via video conference (e.g. Zoom). The participant signs and dates a hard copy of the consent form and returns it to the study team via email, fax, mail, or at their first in-person visit.
Consent information must include the: ∎ nature of the treatment or care; ∎ expected benefits; ∎ the material risks and side effects; ∎ alternative courses of action; and ∎ likely consequences of not receiving the treatment.

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