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- C M Morrison, Q S Ringenberg, V Gerhard, S Anderson, D C Doll, and J W Yarbro.
- Department of Medicine, University of Missouri-Columbia School of Medicine 65212.
- J Cancer Educ. 1987 Jan 1; 2 (4): 233-8.
AbstractTumor registries provide a valuable source of treatment, survival, and epidemiologic data but have been faulted for incomplete and insufficient collection of data. An eight page, 38-item Cancer Patient Questionnaire (CPQ) was developed to collect more extensive information for the tumor registry. The CPQ identified significantly more patients with a family history of cancer than had previously been detected by chart review by the tumor registrar. The CPQ agreed with data collected by the tumor registry in 96% of cases for place of birth, 84% of cases for occupational history, 91% of cases for tobacco use, and 88% of cases for number of pregnancies or live births. The Cancer Patient Questionnaire is complete and easy to use and may replace the chart review in the collection of these data.
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