Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (14)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Etzioni, R. D.
Right arrow Articles by Welss, N. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Etzioni, R. D.
Right arrow Articles by Welss, N. S.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

American Journal of Epidemiology Vol. 148, No. 3: 292-297
Copyright © 1998 by The Johns Hopkins University School of Hygiene and Public Health


other

Analysis of Case-Control Studies of Screening: Impact of Misspecifying the Duration of Detectable Preclinical Pathologic Changes

Ruth D. Etzioni1 and Noel S. Welss2

1 Program in Biostatistics, Fred Hutchinson Cancer Research Center Seattle, WA
2 Department of Epidemiology, School of Public Health and Community Medicine, University of Washington, and Program in Epidemiology, Fred Hutchinson Cancer Research Center Seattle, WA

Reprint requests to Dr. Ruth Etzioni, Program in Biostatistics, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue N, MP-665, P.O. Box 19024, Seattle, WA 98109-1024.

In case-control studies of screening to prevent cancer mortality, exposure is ideally defined as screening that takes place within that period prior to diagnosis during which the cancer is potentially detectable using the screening modality under study. This interval has been called the detectable preclinical period (DPP). Mis-specifying the duration of the DPP can bias the results of such studies. This article quantifies the impact of incorrectly estimating the duration of the DPP or using the correct average DPP but failing to consider its variability. The authors developed a computer simulation model of disease incidence and mortality with and without screening. The authors then selected cases and controls from the generated population and compared their screening histories. The results indicate that underestimation of the duration of the DPP generally leads to greater bias than does overestimation, but in both instances the extent of the bias is modified by the relative length of the DPP and the average interscreening interval. In practice, the authors recommend that to prevent a falsely low estimate of the effectiveness of a screening test in reducing mortality, a high percentile of the DPP distribution be used when analyzing the results of case-control studies of screening. Am J Epidemiol 1998;148:292–7.

case-control studies; mass screening


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Am J EpidemiolHome page
A. R. Localio, L. Zhou, and S. A. Norman
Measuring Screening Intensity in Case-Control Studies of the Efficacy of Mammography
Am. J. Epidemiol., August 1, 2006; 164(3): 272 - 281.
[Abstract] [Full Text] [PDF]


Home page
Arch Intern MedHome page
J. Concato, C. K. Wells, R. I. Horwitz, D. Penson, G. Fincke, D. R. Berlowitz, G. Froehlich, D. Blake, M. A. Vickers, G. A. Gehr, et al.
The Effectiveness of Screening for Prostate Cancer: A Nested Case-Control Study
Arch Intern Med, January 9, 2006; 166(1): 38 - 43.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.