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Should the Use of Patient Medical Information in Research Require the Approval of Attending Physicians?

研究成果: Article査読

抄録

Retrospective observational studies using medical records require researchers to guarantee the right to opt out of the study. However, is it also necessary to confirm whether the medical professionals who created those medical records permit their use as well? In this article, we consider possible options based on a fictitious scenario. Based on our deliberations, we recommend that the information be disclosed on the hospital’s homepage or in leaflets (principal investigator: hospital director), and, similar to patients, attending physicians should be given the opportunity to opt out. We also recommend that an application be submitted to the hospital’s research ethics committee. In this paper, we address the public interest aspect of the use of patient information as a primary item for ethical scrutiny. In addition to research ethics, this particular point underscores the importance of public health ethics, particularly as they pertain to the conflict between individual freedom and public interest.

本文言語English
論文番号27
ジャーナルPublications
10
3
DOI
出版ステータスPublished - 2022 9月

UN SDG

この成果は、次の持続可能な開発目標に貢献しています

  1. SDG 3 - すべての人に健康と福祉を
    SDG 3 すべての人に健康と福祉を

ASJC Scopus subject areas

  • ビジネスおよび国際経営
  • 通信
  • メディア記述
  • コンピュータ サイエンスの応用
  • 図書館情報学

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