OVARIAN CANCER and US: cancer registry

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Showing posts with label cancer registry. Show all posts
Showing posts with label cancer registry. Show all posts

Saturday, March 10, 2012

open access: Adequacy of family history taking in ovarian cancer patients: a population-based study.



Blogger's Note: repost/open access

Adequacy of family history taking in ovarian cancer patients: a population-based study

Abstract:
The aim of this study was to evaluate the adequacy of family history taking in epithelial ovarian cancer (EOC) patients and to identify factors that determine adequacy. Furthermore, the validity of family history taking was assessed by comparison with self-administered questionnaires. Medical records of all 1,112 EOC patients registered by the nation-wide cancer registry and diagnosed in eleven Dutch hospitals between 1996 and 2006 were reviewed. Adequate family history taking was defined as a written notification of the presence or absence of relatives with breast or ovarian cancer. Factors that were correlated with family history taking were identified using univariable and multivariable logistic regression. 147 patients filled in a postal questionnaire. An adequate family history was taken in 41% of all cases. Younger age, an academic hospital and having undergone surgery and/or chemotherapy were associated with adequate family history taking. The comparison with self-administered questionnaires showed a disagreement in 64% mainly due to missing data in medical records. Documentation on family history is either absent or inadequate in the medical records in the majority of EOC patients. These data urge for better uptake of hereditary cancer risk assessment. Different strategies for this assessment like improved family history taking and genetic testing in EOC patients should be explored.

Sunday, February 05, 2012

abstract: Comparability of cancer identification among death registry, cancer registry and hospital discharge registry - International Journal of Cancer



Abstract

Registry based cancer incidence and mortality data are widely used for etiologic research, cancer control and health care monitoring and planning. The complete coverage of all cases is the key criteria of data quality but it is difficult to assess because the alternative sources of data may be flawed. ..........

..........In conclusion, some 10% of cancer deaths had no cancer records in CR (cancer registry) or in HDR (hospital discharge registry), and 3.4% were missing in both sources. The identification rate depended on tumor site, age at death, and, to some extent, death outside hospital.