1993
DOI: 10.1093/ije/22.3.369
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Completeness of Cancer Registration in Limburg, the Netherlands

Abstract: The completeness of cancer registration in the IKL (Integraal Kankercentrum Limburg) cancer registry, Limburg, the Netherlands, was evaluated for the years 1988-1990 by means of the independent case ascertainment method. This study was performed in co-operation with the Registration Network of Family Practices (RNFP) of the University of Limburg. The RNFP is a centralized database used by general practitioners (GP), containing their patients' background variables and diagnoses. The contents of the two database… Show more

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Cited by 342 publications
(198 citation statements)
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“…[27] Quality of the data is high [28] and completeness is estimated to be at least 95%. [29] Patients All patients with an invasive colon carcinoma, diagnosed in the period 2001-2006 were selected from the NCR. Diagnoses without histological confirmation, diagnoses based only on autopsy findings, patients living abroad and incomplete records were excluded from analyses.…”
Section: Netherlands Cancer Registrymentioning
confidence: 99%
“…[27] Quality of the data is high [28] and completeness is estimated to be at least 95%. [29] Patients All patients with an invasive colon carcinoma, diagnosed in the period 2001-2006 were selected from the NCR. Diagnoses without histological confirmation, diagnoses based only on autopsy findings, patients living abroad and incomplete records were excluded from analyses.…”
Section: Netherlands Cancer Registrymentioning
confidence: 99%
“…Additional information could be collected from medical specialists, GPs and registration of the Comprehensive Cancer Centre North Netherlands, which records about 96% of all cancer incidences in the Netherlands [38]. Table 1 gives the premorbid characteristics of the cancer patients.…”
Section: Patientsmentioning
confidence: 99%
“…The conceptually simplest and most definitive method to check completeness of cancer registration is to identify a series of cases from an independent source, e.g. lists of probands in clinical trials or other research studies, and to assess how many have been registered (Goldberg et al, 1980;Nwene and Smith, 1982;Mattson et al, 1985;Hunt and Coleman, 1987;Villard-Mackintosh et al, 1988;Swerdlow et al, 1993;Schouten et al, 1993). Such independent lists are often unavailable, however.…”
mentioning
confidence: 99%