FAIR plus R: Making Clinical Data Reliable Through Qualitative Metadata

被引:0
|
作者
Boenisch, Caroline [1 ]
Kesztyues, Dorothea [1 ]
Kesztyues, Tibor [1 ]
机构
[1] Univ Med Ctr Gottingen, Dept Med Informat, Med Data Integrat Ctr, Robert Koch Str 40, D-37075 Gottingen, Germany
来源
MEDINFO 2023 - THE FUTURE IS ACCESSIBLE | 2024年 / 310卷
关键词
FAIR; metadata; data quality; reliable data;
D O I
10.3233/SHTI230935
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Metadata are often the first access to data repositories for researchers within secondary use. Through automatic metadata generation and metadata harvesting the amount of data about data has been growing ever since. In order to make data not only FAIR but also reliable, the aspect of metadata quality has to be considered. But as earlier assessments of metadata of different repositories showed, metadata quality still lacks behind its capability. Providing an extensive literature review the authors conclude nine measures to assess metadata in relation to clinical care repositories, such as Medical Data Integration Centers (MeDICs). Proceeding from these measures the authors propose an addition of the FAIR Guiding Principles by adding a fifth block for Reliability including three principles, that resulted from the measures presented. The results form the basis for the future work of an assessment of metadata, that is stored in a MeDIC.
引用
收藏
页码:99 / 103
页数:5
相关论文
共 26 条
  • [21] Understanding Mental Health Clinicians' Perceptions and Concerns Regarding Using Passive Patient-Generated Health Data for Clinical Decision-Making: Qualitative Semistructured Interview Study
    Nghiem, Jodie
    Adler, Daniel A.
    Estrin, Deborah
    Livesey, Cecilia
    Choudhury, Tanzeem
    JMIR FORMATIVE RESEARCH, 2023, 7
  • [22] Alerts and Collections for Automating Patients' Sensemaking and Organizing of Their Electronic Health Record Data for Reflection, Planning, and Clinical Visits: Qualitative Research-Through-Design Study
    Nakikj, Drashko
    Kreda, David
    Gehlenborg, Nils
    JMIR HUMAN FACTORS, 2023, 10
  • [23] Mapping the information pathways of adverse reactions through clinical event sequences, patient interactions with the healthcare system and generation of different data streams-A qualitative pilot study
    Andersen, Morten
    Hallgreen, Christine E.
    Bate, Andrew
    PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2023, 32 : 469 - 469
  • [25] Time for standardization of SBRT planning through large scale clinical data and guideline-based approachesZeit für eine Standardisierung der SBRT-Planung mithilfe großer klinischer Datenmengen und leitlinienbasierter Ansätze
    Christos Moustakis
    Oliver Blanck
    Fatemeh Ebrahimi
    Mark ka heng Chan
    Iris Ernst
    Thomas Krieger
    Marciana-Nona Duma
    Markus Oechsner
    Ute Ganswindt
    Christian Heinz
    Horst Alheit
    Hilbert Blank
    Ursula Nestle
    Rolf Wiehle
    Christine Kornhuber
    Christian Ostheimer
    Cordula Petersen
    Gerhard Pollul
    Wolfgang Baus
    Georg Altenstein
    Eric Beckers
    Katrin Jurianz
    Florian Sterzing
    Matthias Kretschmer
    Heinrich Seegenschmiedt
    Torsten Maass
    Stefan Droege
    Ulrich Wolf
    Juergen Schoeffler
    Uwe Haverkamp
    Hans Eich
    Matthias Guckenberger
    Strahlentherapie und Onkologie, 2017, 193 : 1068 - 1069
  • [26] Pediatric Dose Determinations for the Phase I Study of the DOT1L Inhibitor, EPZ-5676, in MLL-r Acute Leukemia: Leveraging Early Clinical Data in Adults through Physiologically-Based Pharmacokinetic Modeling
    Waters, Nigel J.
    Thomson, Blythe
    Gardner, Iain
    Johnson, Trevor N.
    Olhava, Edward J.
    Pollock, Roy M.
    Legler, Michelle
    Copeland, Robert A.
    Hedrick, Eric E.
    BLOOD, 2014, 124 (21)