TY - JOUR
T1 - Comparing dichotomous screening tests when individuals negative on both tests are not verified
AU - Chock, Catherine
AU - Irwig, Les
AU - Berry, Geoffrey
AU - Glasziou, Paul
N1 - Funding Information:
We wish to thank Judy Simpson, John Carlin, and Stephen Walter for their constructive comments on drafts of this paper. Catherine Chock WAS a recipient of a National Health and Medical Research Council Public Health Research and Development Committee research Scholar-
PY - 1997/11
Y1 - 1997/11
N2 - Two dichotomous screening tests are often compared by performing both tests in a sampled population, and submitting positive results on either test to verification by the reference standard. Unbiased estimates of the true positive and false positive rates of each test cannot be estimated directly. However, unbiased estimates of the relative true positive and relative false positive rates may be obtained. When one test has a higher true positive rate at the expense of a higher false positive rate, the trade off is represented by the ratio of extra false positives detected to extra true positives detected. A 95% confidence interval for this ratio is derived. This ratio is prevalence dependent and only applies to the sampled population. For target populations of different prevalence, estimates of the ratio may be obtained if one of the following applies: (i) the test characteristics of one test are known; (ii) the relative prevalence is known; and (iii) certain assumptions are made.
AB - Two dichotomous screening tests are often compared by performing both tests in a sampled population, and submitting positive results on either test to verification by the reference standard. Unbiased estimates of the true positive and false positive rates of each test cannot be estimated directly. However, unbiased estimates of the relative true positive and relative false positive rates may be obtained. When one test has a higher true positive rate at the expense of a higher false positive rate, the trade off is represented by the ratio of extra false positives detected to extra true positives detected. A 95% confidence interval for this ratio is derived. This ratio is prevalence dependent and only applies to the sampled population. For target populations of different prevalence, estimates of the ratio may be obtained if one of the following applies: (i) the test characteristics of one test are known; (ii) the relative prevalence is known; and (iii) certain assumptions are made.
UR - http://www.scopus.com/inward/record.url?scp=0030728169&partnerID=8YFLogxK
U2 - 10.1016/S0895-4356(97)00122-4
DO - 10.1016/S0895-4356(97)00122-4
M3 - Article
C2 - 9393377
AN - SCOPUS:0030728169
SN - 0895-4356
VL - 50
SP - 1211
EP - 1217
JO - Journal of Clinical Epidemiology
JF - Journal of Clinical Epidemiology
IS - 11
ER -