Case report consent form 2025

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Generally, a case report should be short and focussed, with its main components being the abstract, introduction, case description, and discussion.
Case report: Detailed report on an individual patient (e.g. presentation, diagnosis, treatment, response and follow-up). Ethics committee/IRB approval is often not required; consent should be obtained for publication of patient information.
Which medical procedures or tests require informed consent? In general, the following procedures and tests require informed consent: Anesthesia. Any transfer of your personal information to another person or place like diagnoses, medical treatments or prognoses.
To be valid, consent must be voluntary, informed, specific, current, and given by a person with capacity. Unless otherwise indicated, consent can be express or implied, written or verbal.
Historically, case reports were published without consent of the patient. However, standards have been evolving in law and ethics such that consent should now be viewed as mandatory.

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Although not technically required, especially if the case report does not include any identifying information, some journals require informed consent for all case reports before publishing. The CARE guidelines recommend obtaining informed consent AND the patients perspective on the treatment/outcome (if possible).
Informed consent in an ethical requirement for most studies involving humans, so before you start writing your case report, take a written consent from the patient as most journals require that you provide it at the time of manuscript submission. In case the patient is a minor, parental consent is required.
Follow these steps to write an effective consent form. Step 1: Title and introduction. Step 2: Description of the activity. Step 3: Risks and benefits. Step 4: Confidentiality and data handling. Step 5: Voluntary participation and withdrawal. Step 6: Consent statement. Step 7: Signature and date. Step 8: Contact information.

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