Do you need consent to write a case report 2025

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A case report on one or two patients is generally not considered research. However, any PHI disclosed in case reports is subject to the Privacy Rule.
Case reports typically do not need IRB approval. Only patient consent. Depending on the kind of data used (its not mandated in all cases, but even the slightest personally identifiable information as defined by COPE will mandate it), you might need written consent.
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.
The primary (first) author should be the person who made the diagnosis, had direct patient contact, and wrote the largest share of the report. If that person is not interested in publishing, the case can be deferred to a peer who was also directly involved in the care of the patient.
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.

People also ask

Good practice case studies In many cases you will see that copyright is closely associated with obtaining ethical approval for your study and consent or release from the individual or organisation involved, so they understand what you wish to do with their content.

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