CareLit Fachartikel

Data from Population-based Cancer Registration for Secondary Data Analysis: Methodological Challenges and Perspectives

Volker Arndt,Bernd Holleczek,Hiltraud Kajüter,Sabine Luttmann,Alice Nennecke,Sylke Ruth Zeissig,Klaus Kraywinkel,Alexander Katalinic · Das Gesundheitswesen · 2020 · Heft S 1 · S. S62 bis S71

Dokument
313170
CareLit-ID
Jahr
2020
Publikation
PDF
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Metadaten
DOI
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Bibliografische Angaben

Zeitschrift
Das Gesundheitswesen
Autor:innen
Volker Arndt,Bernd Holleczek,Hiltraud Kajüter,Sabine Luttmann,Alice Nennecke,Sylke Ruth Zeissig,Klaus Kraywinkel,Alexander Katalinic
Ausgabe
Heft S 1 / 2020
Jahrgang 82
Seiten
S62 bis S71
Erschienen: 2024-03-02 07:41:14
ISSN
1439-4421

Zusammenfassung

Abstract Population-based cancer registries have a long-standing role in cancer monitoring. Scientific use of cancer registry data is one important purpose of cancer registration, but use of cancer registry data is not restricted to cancer registries. Cancer registration in Germany is currently heading towards population-based collection of detailed clinical data. This development together with additional options for record linkage and long-term follow-up will offer new opportunities for health services and outcome research. Both regional population-based registries and the German Centre for Cancer Registry Data…

Schlagworte

EVALUATION GESUNDHEITSWESEN BERLIN ENTWICKLUNG EPIDEMIOLOGIE INTERNATIONAL KARZINOM KREBS MAMMAKARZINOM ROLLE DEUTSCHLAND PUBMED PATIENTEN GLAS Das Gesundheitswesen