Protection of Personal Information in Medical Journal Publications
10.5469/neuroint.2019.00031
- Author:
Sun HUH
1
Author Information
1. Department of Parasitology and Institute of Medical Education, Hallym University College of Medicine, Chuncheon, Korea. shuh@hallym.ac.kr
- Publication Type:Review
- Keywords:
Informed consent;
Personally identifiable information;
Privacy;
Republic of Korea;
Ethics committees, Research
- MeSH:
Bioethics;
Computer Security;
Consent Forms;
Ethics;
Ethics Committees, Research;
Humans;
Informed Consent;
Jurisprudence;
Korea;
Personally Identifiable Information;
Privacy;
Publications;
Republic of Korea;
Retrospective Studies
- From:Neurointervention
2019;14(1):1-8
- CountryRepublic of Korea
- Language:English
-
Abstract:
It aimed to present the definition of personal information based on Korean laws that protect personal information and the process of protection of personal information in journal publishing based on the guidelines of the International Committee of Medical Journal Editors and Committee of Publication Ethics. Two Korean laws relate to the protection of personal information in human subject research: the Personal Information Protection Act and the Bioethics and Safety Act. These laws were enacted to prevent the unauthorized use of Koreans’ personal information including medical information. Personal information can be divided into personally identifiable information including resident registration numbers and sensitive information including health information. To protect personal information in journal publishing, institutional review board (IRB) approval and obtaining informed consent from patients is recommended or mandatory in clinical studies. However, retrospective chart reviews may be exempted from IRB approval, while obtaining informed consent is recommended for all case reports. Journal policies may vary with regard to whether a copy of the informed consent form is collected from authors, since the Committee of Publication Ethics guideline does not specifically recommend collecting it. In discussions of adopting clinical data-sharing policies, transfer of data including nonidentifiable personal information to another country is an unresolved issue. Furthermore, a public data repository site should be established in Korea for data to be deposited. To protect subjects’ privacy and to prevent legal issues potentially arising from privacy concerns, editors and publishers should do their best to publish articles with appropriate oversight on subjects’ personal information.
