The Danish National Patient Registry: a review of content, data quality, and research potential

Национальный реестр пациентов Дании: обзор содержания, качества данных и исследовательского потенциала
Henrik Toft Sørensen, Lars Pedersen, Véra Ehrenstein, Morten Schmidt, Sigrún Alba Jóhannesdóttir Schmidt, Jakob Lynge Sandegaard
2015-11-01

Danish National Patient RegistryInternational Classification of Diseasesnationwide longitudinal registrypositive predictive valuevalidation studies
BACKGROUND: The Danish National Patient Registry (DNPR) is one of the world's oldest nationwide hospital registries and is used extensively for research. Many studies have validated algorithms for identifying health events in the DNPR, but the reports are fragmented and no overview exists. OBJECTIVES: To review the content, data quality, and research potential of the DNPR. METHODS: We examined the setting, history, aims, content, and classification systems of the DNPR. We searched PubMed and the Danish Medical Journal to create a bibliography of validation studies. We included also studies that were referenced in retrieved papers or known to us beforehand. Methodological considerations related to DNPR data were reviewed. RESULTS: During 1977-2012, the DNPR registered 8,085,603 persons, accounting for 7,268,857 inpatient, 5,953,405 outpatient, and 5,097,300 emergency department contacts. The DNPR provides nationwide longitudinal registration of detailed administrative and clinical data. It has recorded information on all patients discharged from Danish nonpsychiatric hospitals since 1977 and on psychiatric inpatients and emergency department and outpatient specialty clinic contacts since 1995. For each patient contact, one primary and optional secondary diagnoses are recorded according to the International Classification of Diseases. The DNPR provides a data source to identify diseases, examinations, certain in-hospital medical treatments, and surgical procedures. Long-term temporal trends in hospitalization and treatment rates can be studied. The positive predictive values of diseases and treatments vary widely (<15%-100%). The DNPR data are linkable at the patient level with data from other Danish administrative registries, clinical registries, randomized controlled trials, population surveys, and epidemiologic field studies - enabling researchers to reconstruct individual life and health trajectories for an entire population. CONCLUSION: The DNPR is a valuable tool for epidemiological research. However, both its strengths and limitations must be considered when interpreting research results, and continuous validation of its clinical data is essential.
1
DNPR data can identify diseases, examinations, selected in-hospital treatments, and surgical procedures, enabling analyses of long-term hospitalization and treatment trends.
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Disease and treatment coding validity varies substantially, with positive predictive values ranging from below 15% to 100%.
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Patient-level linkage with multiple Danish registries and studies enables reconstruction of population-wide individual life and health trajectories, but continuous clinical-data validation remains essential.
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The Danish National Patient Registry recorded 8,085,603 persons and millions of inpatient, outpatient, and emergency contacts during 1977–2012.
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The registry provides nationwide longitudinal administrative and clinical data, covering nonpsychiatric hospital discharges since 1977 and additional psychiatric, emergency, and specialty outpatient contacts since 1995.

The Danish National Patient Registry (DNPR) and its nationwide longitudinal patient-contact data

The DNPR's content, data quality, validation of recorded diseases and treatments, and potential for epidemiological research through linkage with other population-level data sources

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2015-11-01
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Henrik Toft Sørensen
Lars Pedersen
Véra Ehrenstein
Morten Schmidt
Sigrún Alba Jóhannesdóttir Schmidt
Jakob Lynge Sandegaard
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