2017
DOI: 10.1080/0284186x.2017.1407039
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Nordic Cancer Registries – an overview of their procedures and data comparability

Abstract: 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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Cited by 244 publications
(335 citation statements)
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“…22 The quality of data originates in part in the civil registration system, which is based on personal identity codes and multiple population-based registries, which make record linkage possible. 22 The quality of data originates in part in the civil registration system, which is based on personal identity codes and multiple population-based registries, which make record linkage possible.…”
Section: Discussionmentioning
confidence: 99%
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“…22 The quality of data originates in part in the civil registration system, which is based on personal identity codes and multiple population-based registries, which make record linkage possible. 22 The quality of data originates in part in the civil registration system, which is based on personal identity codes and multiple population-based registries, which make record linkage possible.…”
Section: Discussionmentioning
confidence: 99%
“…22 According to a recent report by the United Nations, Nordic populations have been ranked the happiest worldwide. The strengths of the current study included the 3-country population-based setting with all patients included, a cohort that therefore was free of selection or participation bias.…”
Section: Discussionmentioning
confidence: 99%
“…The Swedish Family‐Cancer Database includes data on the Swedish population collated in family and is linked to the Swedish Cancer Registry, which was founded in 1958 and covers the entire population with more than 2 million cancers . The registry is based on compulsory cancer notifications made by clinicians and pathologists/cytologists . Since the mid‐1980s, there are six regional registries associated with the oncological centers in each medical region of Sweden where the registration, coding and major check‐up and correction work is performed.…”
Section: Methodsmentioning
confidence: 99%
“…The Swedish Family‐Cancer Database includes the whole Swedish population organized in families and linked to the national Cancer Registry with more than 2 million cancers registered since 1958 . The registry is based on compulsory cancer notifications from clinicians and pathologists/cytologists . All registered NHL cases were histologically verified.…”
Section: Methodsmentioning
confidence: 99%