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Aug 6th, 2022
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How to Edit note 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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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.
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. US federal regulations require a full, detailed explanation of the study and its potential risks.
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.
These barriers include the fact that treatment decisions take place over a long period; there are often many decisions to be made; although patients want information about treatment, they typically believe that decision making is the physicians task; physicians do not understand the rationale for the patients role in
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.
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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