Literature DB >> 34100760

Secondary Use of Clinical Data in Data-Gathering, Non-Interventional Research or Learning Activities: Definition, Types, and a Framework for Risk Assessment.

Martin Jungkunz1, Anja Köngeter1, Katja Mehlis1, Eva C Winkler1, Christoph Schickhardt2.   

Abstract

BACKGROUND: The secondary use of clinical data in data-gathering, non-interventional research or learning activities (SeConts) has great potential for scientific progress and health care improvement. At the same time, it poses relevant risks for the privacy and informational self-determination of patients whose data are used.
OBJECTIVE: Since the current literature lacks a tailored framework for risk assessment in SeConts as well as a clarification of the concept and practical scope of SeConts, we aim to fill this gap.
METHODS: In this study, we analyze each element of the concept of SeConts to provide a synthetic definition, investigate the practical relevance and scope of SeConts through a literature review, and operationalize the widespread definition of risk (as a harmful event of a certain magnitude that occurs with a certain probability) to conduct a tailored analysis of privacy risk factors typically implied in SeConts.
RESULTS: We offer a conceptual clarification and definition of SeConts and provide a list of types of research and learning activities that can be subsumed under the definition of SeConts. We also offer a proposal for the classification of SeConts types into the categories non-interventional (observational) clinical research, quality control and improvement, or public health research. In addition, we provide a list of risk factors that determine the probability or magnitude of harm implied in SeConts. The risk factors provide a framework for assessing the privacy-related risks for patients implied in SeConts. We illustrate the use of risk assessment by applying it to a concrete example.
CONCLUSIONS: In the future, research ethics committees and data use and access committees will be able to rely on and apply the framework offered here when reviewing projects of secondary use of clinical data for learning and research purposes. ©Martin Jungkunz, Anja Köngeter, Katja Mehlis, Eva C Winkler, Christoph Schickhardt. Originally published in the Journal of Medical Internet Research (https://www.jmir.org), 08.06.2021.

Entities:  

Keywords:  clinical data; electronic health records; ethics; patient data; privacy; research; risk assessment; risk factors; risks; secondary use

Year:  2021        PMID: 34100760     DOI: 10.2196/26631

Source DB:  PubMed          Journal:  J Med Internet Res        ISSN: 1438-8871            Impact factor:   5.428


  1 in total

1.  Patients' Willingness to Provide Their Clinical Data for Research Purposes and Acceptance of Different Consent Models: Findings From a Representative Survey of Patients With Cancer.

Authors:  Katja Mehlis; Eva C Winkler; Anja Köngeter; Christoph Schickhardt; Martin Jungkunz; Susanne Bergbold
Journal:  J Med Internet Res       Date:  2022-08-25       Impact factor: 7.076

  1 in total

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