Literature DB >> 35190833

Development of a framework to assess the quality of data sources in healthcare settings.

Sepideh Hooshafza1,2, Louise Mc Quaid1, Gaye Stephens2, Rachel Flynn1, Laura O'Connor1.   

Abstract

OBJECTIVE: The purpose of this study was to develop a framework to assess the quality of healthcare data sources.
MATERIALS AND METHODS: First, a systematic review was performed and a thematic analysis of included literature conducted to identify items relating to the quality of healthcare data sources. Second, expert advisory group meetings were held to explore experts' perception of the results of the review and identify gaps in the findings. Third, a framework was developed based on the findings.
RESULTS: Synthesis of the review results and expert advisory group meetings resulted in 8 parent themes and 22 subthemes. The parent themes were: Governance, leadership, and management; Data; Trust; Context; Monitoring; Use of information; Standardization; Learning and training. The 22 subthemes were: governance, finance, organization, characteristics, time, data management, data quality, ethics, access, security, quality improvement, monitoring and feedback, dissemination, analysis, research, standards, linkage, infrastructure, documentation, definitions and classification, learning, and training. DISCUSSION: The herein presented framework was developed using a robust methodology which included reviewing literature and extracting data source quality items, filtering, and matching items, developing a list of themes, and revising them based on expert opinion. To the best of our knowledge, this study is the first to apply a systematic approach to identify aspects related to the quality of healthcare data sources.
CONCLUSIONS: The framework, can assist those using healthcare data sources to identify and assess the quality of a data source and inform whether the data sources used are fit for their intended use.
© The Author(s) 2022. Published by Oxford University Press on behalf of the American Medical Informatics Association. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  data source; healthcare; quality assessment

Mesh:

Year:  2022        PMID: 35190833      PMCID: PMC9006677          DOI: 10.1093/jamia/ocac017

Source DB:  PubMed          Journal:  J Am Med Inform Assoc        ISSN: 1067-5027            Impact factor:   4.497


  13 in total

1.  Analyzing data and data sources towards a unified approach for ensuring end-to-end data and data sources quality in healthcare 4.0.

Authors:  Argyro Mavrogiorgou; Athanasios Kiourtis; Konstantinos Perakis; Dimitrios Miltiadou; Stamatios Pitsios; Dimosthenis Kyriazis
Journal:  Comput Methods Programs Biomed       Date:  2019-06-29       Impact factor: 5.428

Review 2.  Secondary data sources for health services research in urologic oncology.

Authors:  Alexander P Cole; David F Friedlander; Quoc-Dien Trinh
Journal:  Urol Oncol       Date:  2017-09-12       Impact factor: 3.498

3.  Moving Towards an EHR Data Quality Framework: The MIRACUM Approach.

Authors:  Lorenz A Kapsner; Marvin O Kampf; Susanne A Seuchter; Gaetan Kamdje-Wabo; Tobias Gradinger; Thomas Ganslandt; Sebastian Mate; Julian Gruendner; Detlef Kraska; Hans-Ulrich Prokosch
Journal:  Stud Health Technol Inform       Date:  2019-09-03

4.  Patient registries in primary care: essential element for quality improvement.

Authors:  Elizabeth I Molina-Ortiz; Aida C Vega; Neil S Calman
Journal:  Mt Sinai J Med       Date:  2012 Jul-Aug

5.  Operating principles for running a clinical quality registry: are they feasible?

Authors:  Michelle Ogilvy; James Kollias
Journal:  ANZ J Surg       Date:  2012-09-03       Impact factor: 1.872

6.  Clinical data integration of distributed data sources using Health Level Seven (HL7) v3-RIM mapping.

Authors:  Teeradache Viangteeravat; Matthew N Anyanwu; Venkateswara Ra Nagisetty; Emin Kuscu; Mark Eijiro Sakauye; Duojiao Wu
Journal:  J Clin Bioinforma       Date:  2011-11-21

7.  Utility of registries for post-marketing evaluation of medicines. A survey of Swedish health care quality registries from a regulatory perspective.

Authors:  Nils Feltelius; Rolf Gedeborg; Lennart Holm; Björn Zethelius
Journal:  Ups J Med Sci       Date:  2017-03-03       Impact factor: 2.384

Review 8.  The importance of effective registries in pulmonary diseases and how to optimize their output.

Authors:  Joanna Chorostowska-Wynimko; Marion Wencker; Ildikó Horváth
Journal:  Chron Respir Dis       Date:  2019 Jan-Dec       Impact factor: 2.444

9.  Developing a Preliminary Conceptual Framework for Guidelines on Inclusion of Patient Reported-Outcome Measures (PROMs) in Clinical Quality Registries.

Authors:  Rasa Ruseckaite; Ashika D Maharaj; Karolina Krysinska; Joanne Dean; Susannah Ahern
Journal:  Patient Relat Outcome Meas       Date:  2019-12-10

10.  The REporting of studies Conducted using Observational Routinely-collected health Data (RECORD) statement.

Authors:  Eric I Benchimol; Liam Smeeth; Astrid Guttmann; Katie Harron; David Moher; Irene Petersen; Henrik T Sørensen; Erik von Elm; Sinéad M Langan
Journal:  PLoS Med       Date:  2015-10-06       Impact factor: 11.069

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.