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Canterbury v. Spence (464 F.2d. 772, 782 D.C. Cir. 1972) was a landmark federal case decided by the United States Court of Appeals for the District of Columbia Circuit that significantly reshaped malpractice law in the United States. [1] [2] It established the idea of "informed consent" to medical procedures.
The informed consent doctrine is generally implemented through good healthcare practice: pre-operation discussions with patients and the use of medical consent forms in hospitals. However, reliance on a signed form should not undermine the basis of the doctrine in giving the patient an opportunity to weigh and respond to the risk.
Informed consent to medical treatment case country location year summary Christiane Völling: Germany 2011 Informed consent and involuntary sex reassignment in the case of an adult intersex woman. Gillick competence: England 1985 The right of minors to request contraception from their doctor without parental consent.
This helped establish what was required to be disclosed before a procedure, helping to set the boundaries of informed consent. Negligence could be used in informed consent cases. Cobbs v. Grant: 1972 This case caused the courts to define consent as being patient-based: "what would a competent patient need to know to make a rational decision."
Reibl v Hughes [1980] 2 S.C.R. 880 is a leading decision of the Supreme Court of Canada on negligence, medical malpractice, informed consent, the duty to warn, and causation. The case settled the issue of when a physician may be sued for battery and when it is more appropriate to sue the doctor in negligence. The Court wrote unanimously that ...
In medicine, a case report is a detailed report of the symptoms, signs, diagnosis, treatment, and follow-up of an individual patient. Case reports may contain a demographic profile of the patient, but usually describe an unusual or novel occurrence. Some case reports also contain a literature review of other reported cases.
A case report form (or CRF) is a paper or electronic questionnaire specifically used in clinical trial research. [1] The case report form is the tool used by the sponsor of the clinical trial to collect data from each participating patient.
The Belmont Report allows for the protection of participants in clinical trials and research studies. Seven things nurses, as primary caregivers for individuals participating in a study, must do to ensure the rights of the participant are met are. [9] Ensure the study is approved by an IRB; Get informed consent from the patient