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Case study patient consent

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BMC Palliative Care will not consider case reports describing preventive or therapeutic interventions, as these generally require stronger evidence. Case report submissions will be assessed by the Editors and will be sent for peer review if considered appropriate for the journal. Case reports should include relevant positive and negative findings from history, examination and investigation, and can include clinical photographs, provided these are accompanied by a statement that written consent to publish was obtained from the patient s. Case reports should include an up-to-date review of all previous cases in the field.
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Patient consent and confidentiality

Case study patient consent
Case study patient consent
Case study patient consent
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The 10 Questions You Should Know | Agency for Healthcare Research and Quality

In these decades, informed consent has been a significant medical issue. For example, should doctors respect the patients or the patients autonomy? Also how much information should the doctors provide their patients? In the following example, it shows a recent article that deals with informed consent.
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About CICP

Importance: Predictive factors associated with increased risk of medical malpractice litigation have been identified, including severity of injury, physician sex, and error in diagnosis. However, there is a paucity of literature investigating informed consent in spinal surgery malpractice. Objective: To investigate the failure to obtain informed consent as an allegation in medical malpractice claims for patients undergoing a spinal procedure. Design, setting, and participants: In this retrospective cohort study, a national medicolegal database was searched for malpractice claim cases related to spinal surgery for all years available ie, January 1, , through December 31, Main outcomes and measures: Failure to obtain informed consent and associated medical malpractice case verdict.
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If you would like to be involved in its development let us know. This study sought to understand how adult life was experienced by the first, pioneering, cohort of childhood liver transplant recipients in the UK. We conducted in-depth interviews with adults who had their first liver-only transplant between aged 13 or younger at the time and also with retired or practising clinicians. This project raised many ethical issues requiring us to formulate plans in advance of data collection. We had a flexible research design that allowed us to respond to unanticipated ethical issues, for example identifying and approaching participants; interviewing relevant clinicians; ensuring confidentiality; and communicating our findings to a broad audience.
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