Publication of medical case reports and consent

The Committee on Publication Ethics (COPE) published guidance on consent for publishing medical case reports in 2016 [1]. Paragraph 26 of the Declaration of Helsinki version 7 2013 states the following [2]: ‘In medical research involving human subjects capable of giving informed consent, each potential subject must be adequately informed of the aims, methods, sources of funding, any possible conflicts of interest, institutional affiliations of the researcher, the anticipated benefits and potential risks of the study and the discomfort it may entail, post-study provisions and any other relevant aspects of the study. The potential subject must be informed of the right to refuse to participate in the study or to withdraw consent to participate at any time without reprisal. Special attention should be given to the specific information needs of individual potential subjects as well as to the methods used to deliver the information. After ensuring that the potential subject has understood the information, the physician or another appropriately qualified individual must then seek the potential subject's freely-given informed consent, preferably in writing. If the consent cannot be expressed in writing, the non-written consent must be formally documented and witnessed. All medical research subjects should be given the option of being informed about the general outcome and results of the study.’ Being assured that consent has been obtained is important as journals need to know that the individuals or their legal representatives who give consent to publication have been: