Nordic Cancer Registries – an overview of their procedures and data comparability
The Nordic Cancer Registries are among the oldest population-based registries in the world, with more than 60 years of complete coverage of what is now a combined population of 26 million. However, despite being the source of a substantial number of studies, there is no published paper comparing the...
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| Published in | Acta oncologica Vol. 57; no. 4; pp. 440 - 455 |
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| Main Authors | , , , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
England
03.04.2018
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| Subjects | |
| Online Access | Get full text |
| ISSN | 0284-186X 1651-226X 1651-226X |
| DOI | 10.1080/0284186X.2017.1407039 |
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| Abstract | The Nordic Cancer Registries are among the oldest population-based registries in the world, with more than 60 years of complete coverage of what is now a combined population of 26 million. However, despite being the source of a substantial number of studies, there is no published paper comparing the different registries. Therefore, we did a systematic review to identify similarities and dissimilarities of the Nordic Cancer Registries, which could possibly explain some of the differences in cancer incidence rates across these countries.
We describe and compare here the core characteristics of each of the Nordic Cancer Registries: (i) data sources; (ii) registered disease entities and deviations from IARC multiple cancer coding rules; (iii) variables and related coding systems. Major changes over time are described and discussed.
All Nordic Cancer Registries represent a high quality standard in terms of completeness and accuracy of the registered data.
Even though the information in the Nordic Cancer Registries in general can be considered more similar than any other collection of data from five different countries, there are numerous differences in registration routines, classification systems and inclusion of some tumors. These differences are important to be aware of when comparing time trends in the Nordic countries. |
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| AbstractList | The Nordic Cancer Registries are among the oldest population-based registries in the world, with more than 60 years of complete coverage of what is now a combined population of 26 million. However, despite being the source of a substantial number of studies, there is no published paper comparing the different registries. Therefore, we did a systematic review to identify similarities and dissimilarities of the Nordic Cancer Registries, which could possibly explain some of the differences in cancer incidence rates across these countries.
We describe and compare here the core characteristics of each of the Nordic Cancer Registries: (i) data sources; (ii) registered disease entities and deviations from IARC multiple cancer coding rules; (iii) variables and related coding systems. Major changes over time are described and discussed.
All Nordic Cancer Registries represent a high quality standard in terms of completeness and accuracy of the registered data.
Even though the information in the Nordic Cancer Registries in general can be considered more similar than any other collection of data from five different countries, there are numerous differences in registration routines, classification systems and inclusion of some tumors. These differences are important to be aware of when comparing time trends in the Nordic countries. The Nordic Cancer Registries are among the oldest population-based registries in the world, with more than 60 years of complete coverage of what is now a combined population of 26 million. However, despite being the source of a substantial number of studies, there is no published paper comparing the different registries. Therefore, we did a systematic review to identify similarities and dissimilarities of the Nordic Cancer Registries, which could possibly explain some of the differences in cancer incidence rates across these countries.BACKGROUNDThe Nordic Cancer Registries are among the oldest population-based registries in the world, with more than 60 years of complete coverage of what is now a combined population of 26 million. However, despite being the source of a substantial number of studies, there is no published paper comparing the different registries. Therefore, we did a systematic review to identify similarities and dissimilarities of the Nordic Cancer Registries, which could possibly explain some of the differences in cancer incidence rates across these countries.We describe and compare here the core characteristics of each of the Nordic Cancer Registries: (i) data sources; (ii) registered disease entities and deviations from IARC multiple cancer coding rules; (iii) variables and related coding systems. Major changes over time are described and discussed.METHODSWe describe and compare here the core characteristics of each of the Nordic Cancer Registries: (i) data sources; (ii) registered disease entities and deviations from IARC multiple cancer coding rules; (iii) variables and related coding systems. Major changes over time are described and discussed.All Nordic Cancer Registries represent a high quality standard in terms of completeness and accuracy of the registered data.RESULTSAll Nordic Cancer Registries represent a high quality standard in terms of completeness and accuracy of the registered data.Even though the information in the Nordic Cancer Registries in general can be considered more similar than any other collection of data from five different countries, there are numerous differences in registration routines, classification systems and inclusion of some tumors. These differences are important to be aware of when comparing time trends in the Nordic countries.CONCLUSIONSEven though the information in the Nordic Cancer Registries in general can be considered more similar than any other collection of data from five different countries, there are numerous differences in registration routines, classification systems and inclusion of some tumors. These differences are important to be aware of when comparing time trends in the Nordic countries. |
| Author | Højsgaard Schmidt, Lise Kristine Lambe, Mats Khan, Staffan Pettersson, David Engholm, Gerda Malila, Nea Tryggvadóttir, Laufey Pukkala, Eero Johannesen, Tom Børge Virtanen, Anni Hakanen, Tiina Ursin, Giske Ólafsdóttir, Elínborg Storm, Hans Larønningen, Siri |
| Author_xml | – sequence: 1 givenname: Eero surname: Pukkala fullname: Pukkala, Eero organization: Finnish Cancer Registry, Institute for Statistical and Epidemiological Cancer Research, Helsinki, Finland;, Faculty of Social Sciences, University of Tampere, Tampere, Finland – sequence: 2 givenname: Gerda surname: Engholm fullname: Engholm, Gerda organization: Danish Cancer Society, Copenhagen, Denmark – sequence: 3 givenname: Lise Kristine surname: Højsgaard Schmidt fullname: Højsgaard Schmidt, Lise Kristine organization: Danish Cancer Registry, The Danish Health Data Authority, Copenhagen, Denmark – sequence: 4 givenname: Hans surname: Storm fullname: Storm, Hans organization: Danish Cancer Society, Copenhagen, Denmark – sequence: 5 givenname: Staffan surname: Khan fullname: Khan, Staffan organization: Swedish Cancer Registry, the Swedish National Board of Health and Welfare, Stockholm, Sweden – sequence: 6 givenname: Mats surname: Lambe fullname: Lambe, Mats organization: Regional Cancer Centre Uppsala-Örebro, Uppsala, Sweden;, Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden – sequence: 7 givenname: David surname: Pettersson fullname: Pettersson, David organization: Swedish Cancer Registry, the Swedish National Board of Health and Welfare, Stockholm, Sweden – sequence: 8 givenname: Elínborg surname: Ólafsdóttir fullname: Ólafsdóttir, Elínborg organization: Icelandic Cancer Registry, Icelandic Cancer Society, Reykjavik, Iceland – sequence: 9 givenname: Laufey surname: Tryggvadóttir fullname: Tryggvadóttir, Laufey organization: Icelandic Cancer Registry, Icelandic Cancer Society, Reykjavik, Iceland;, Faculty of Medicine, University of Iceland, Reykjavik, Iceland – sequence: 10 givenname: Tiina surname: Hakanen fullname: Hakanen, Tiina organization: Finnish Cancer Registry, Institute for Statistical and Epidemiological Cancer Research, Helsinki, Finland – sequence: 11 givenname: Nea surname: Malila fullname: Malila, Nea organization: Finnish Cancer Registry, Institute for Statistical and Epidemiological Cancer Research, Helsinki, Finland;, Faculty of Social Sciences, University of Tampere, Tampere, Finland – sequence: 12 givenname: Anni surname: Virtanen fullname: Virtanen, Anni organization: Finnish Cancer Registry, Institute for Statistical and Epidemiological Cancer Research, Helsinki, Finland;, Department of Pathology, University of Helsinki and HUSLAB, Helsinki University Hospital, Helsinki, Finland – sequence: 13 givenname: Tom Børge surname: Johannesen fullname: Johannesen, Tom Børge organization: Cancer Registry of Norway, Oslo, Norway – sequence: 14 givenname: Siri surname: Larønningen fullname: Larønningen, Siri organization: Cancer Registry of Norway, Oslo, Norway – sequence: 15 givenname: Giske surname: Ursin fullname: Ursin, Giske organization: Cancer Registry of Norway, Oslo, Norway |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29226751$$D View this record in MEDLINE/PubMed http://kipublications.ki.se/Default.aspx?queryparsed=id:137856980$$DView record from Swedish Publication Index |
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