Literature DB >> 26785952

How can the research potential of the clinical quality databases be maximized? The Danish experience.

M Nørgaard1, S P Johnsen1.   

Abstract

In Denmark, the need for monitoring of clinical quality and patient safety with feedback to the clinical, administrative and political systems has resulted in the establishment of a network of more than 60 publicly financed nationwide clinical quality databases. Although primarily devoted to monitoring and improving quality of care, the potential of these databases as data sources in clinical research is increasingly being recognized. In this review, we describe these databases focusing on their use as data sources for clinical research, including their strengths and weaknesses as well as future concerns and opportunities. The research potential of the clinical quality databases is substantial but has so far only been explored to a limited extent. Efforts related to technical, legal and financial challenges are needed in order to take full advantage of this potential.
© 2016 The Association for the Publication of the Journal of Internal Medicine.

Entities:  

Keywords:  Clinical quality; databases; registry-based; research

Mesh:

Year:  2016        PMID: 26785952     DOI: 10.1111/joim.12437

Source DB:  PubMed          Journal:  J Intern Med        ISSN: 0954-6820            Impact factor:   8.989


  8 in total

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Journal:  Clin Epidemiol       Date:  2020-07-27       Impact factor: 4.790

3. 

Authors:  Sinéad M Langan; Sigrún A J Schmidt; Kevin Wing; Vera Ehrenstein; Stuart G Nicholls; Kristian B Filion; Olaf Klungel; Irene Petersen; Henrik T Sørensen; William G Dixon; Astrid Guttmann; Katie Harron; Lars G Hemkens; David Moher; Sebastian Schneeweiss; Liam Smeeth; Miriam Sturkenboom; Erik von Elm; Shirley V Wang; Eric I Benchimol
Journal:  CMAJ       Date:  2019-06-24       Impact factor: 8.262

4.  Danish clinical quality databases - an important and untapped resource for clinical research.

Authors:  Henrik Toft Sørensen; Lars Pedersen; Jørgen Jørgensen; Vera Ehrenstein
Journal:  Clin Epidemiol       Date:  2016-10-25       Impact factor: 4.790

5.  The reporting of studies conducted using observational routinely collected health data statement for pharmacoepidemiology (RECORD-PE).

Authors:  Sinéad M Langan; Sigrún Aj Schmidt; Kevin Wing; Vera Ehrenstein; Stuart G Nicholls; Kristian B Filion; Olaf Klungel; Irene Petersen; Henrik T Sorensen; William G Dixon; Astrid Guttmann; Katie Harron; Lars G Hemkens; David Moher; Sebastian Schneeweiss; Liam Smeeth; Miriam Sturkenboom; Erik von Elm; Shirley V Wang; Eric I Benchimol
Journal:  BMJ       Date:  2018-11-14

6.  Classifying outcomes in secondary and tertiary care clinical quality registries-an organizational case study with the COMET taxonomy.

Authors:  Antero Vanhala; Anna-Rosa Lehto; Anu Maksimow; Paulus Torkki; Sanna-Maria Kivivuori
Journal:  BMC Health Serv Res       Date:  2022-06-21       Impact factor: 2.908

7.  The Danish Neuro-Oncology Registry: establishment, completeness and validity.

Authors:  Steinbjørn Hansen; Jan Nielsen; René J Laursen; Birthe Krogh Rasmussen; Bente Mertz Nørgård; Kim Oren Gradel; Rikke Guldberg
Journal:  BMC Res Notes       Date:  2016-08-30

8.  The Danish Myelodysplastic Syndromes Database: Patient Characteristics and Validity of Data Records.

Authors:  Tine Bichel Lauritsen; Jan Maxwell Nørgaard; Kirsten Grønbæk; Anders Pommer Vallentin; Syed Azhar Ahmad; Louise Hur Hannig; Marianne Tang Severinsen; Kasper Adelborg; Lene Sofie Granfeldt Østgård
Journal:  Clin Epidemiol       Date:  2021-06-14       Impact factor: 4.790

  8 in total

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