Literature DB >> 21427148

Register-based research: some methodological considerations.

Jørn Olsen1.   

Abstract

AIMS: Collecting new research data is often time consuming and expensive and it may be difficult to recruit volunteers to provide data for research. We should therefore make sure that we do not collect data that already are available and in the Nordic countries we have an opportunity to use national registers for certain types of research. In some situations using these population-based registers is preferable to collecting primary data since selection bias due to nonresponders is not a problem in these registers.
METHODS: Register-based data can be used in most designs available in observational studies and even add important data to randomised trials. Getting access to using the valuable data sources stored in national registers is much easier now that it was in the past. However, we still need better documentation and we should to a much larger extent be able to use research files that combine data from two or more of the Nordic countries. Linking primary research data to public registers will also provide new research opportunities.
RESULTS: Nordic registers have been used in several landmark papers over the years.
CONCLUSIONS: Register-based research can be done without risk of unwanted disclosure of personal data and it involves no invasive procedures. It is a valuable gift given by the people to be used for the people.

Entities:  

Mesh:

Year:  2011        PMID: 21427148     DOI: 10.1177/1403494811402719

Source DB:  PubMed          Journal:  Scand J Public Health        ISSN: 1403-4948            Impact factor:   3.021


  11 in total

1.  When the entire population is the sample: strengths and limitations in register-based epidemiology.

Authors:  Lau Caspar Thygesen; Annette Kjær Ersbøll
Journal:  Eur J Epidemiol       Date:  2014-01-10       Impact factor: 8.082

2.  No consensus on gestational diabetes mellitus screening regimes in Sweden: pregnancy outcomes in relation to different screening regimes 2011 to 2012, a cross-sectional study.

Authors:  Maria Lindqvist; Margareta Persson; Marie Lindkvist; Ingrid Mogren
Journal:  BMC Pregnancy Childbirth       Date:  2014-05-31       Impact factor: 3.007

3.  Population attitudes towards research use of health care registries: a population-based survey in Finland.

Authors:  Katariina Eloranta; Anssi Auvinen
Journal:  BMC Med Ethics       Date:  2015-07-17       Impact factor: 2.652

4.  Cohort profile: the Swedish Prescribed Drugs and Health Cohort (SPREDH).

Authors:  Shao-Hua Xie; Giola Santoni; Fredrik Mattsson; Eivind Ness-Jensen; Jesper Lagergren
Journal:  BMJ Open       Date:  2019-01-28       Impact factor: 2.692

5.  Return to work and sick leave patterns following a work injury among young adults: a study protocol of a Swedish multimodal study.

Authors:  Malin K Johansson; Marie Hasselberg; Ritva Rissanen
Journal:  BMJ Open       Date:  2021-06-01       Impact factor: 2.692

6.  Confounding with familial determinants affects the association between mode of delivery and childhood asthma medication - a national cohort study.

Authors:  Lennart Bråbäck; Cecilia Ekéus; Adrian J Lowe; Anders Hjern
Journal:  Allergy Asthma Clin Immunol       Date:  2013-04-16       Impact factor: 3.406

7.  Register-based data of psychosocial working conditions and occupational groups as predictors of disability pension due to musculoskeletal diagnoses: a prospective cohort study of 24,543 Swedish twins.

Authors:  Annina Ropponen; Åsa Samuelsson; Kristina Alexanderson; Pia Svedberg
Journal:  BMC Musculoskelet Disord       Date:  2013-09-16       Impact factor: 2.362

8.  Mental health and school dropout across educational levels and genders: a 4.8-year follow-up study.

Authors:  Cathrine F Hjorth; Line Bilgrav; Louise Sjørslev Frandsen; Charlotte Overgaard; Christian Torp-Pedersen; Berit Nielsen; Henrik Bøggild
Journal:  BMC Public Health       Date:  2016-09-15       Impact factor: 3.295

9.  Participating in an International Stereotactic Radiotherapy Patient Registry: The Establishment of Data Collection Pathways.

Authors:  Aylin Yahya; Eva Arneric; Elizabeth Kernutt; Fiona Baldacchino; Claire Haworth; Mary-Anne Kedda; Colin Tang; Sean Bydder; Tammy Corica
Journal:  Cureus       Date:  2017-06-29

10.  Validation of multiple sclerosis diagnoses in the Swedish National Patient Register.

Authors:  Chantelle Murley; Emilie Friberg; Jan Hillert; Kristina Alexanderson; Fei Yang
Journal:  Eur J Epidemiol       Date:  2019-09-06       Impact factor: 8.082

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