© 2004 American Public Health Association
Evelyn C. Y. Chan and Chul Ahn are with the Division of General Internal Medicine, University of TexasHouston Medical School. Sally W. Vernon is with the Center for Health Promotion and Prevention Research, University of TexasHouston School of Public Health. Anthony Greisinger is with Kelsey Research Foundation and Kelsey-Seybold Clinic, Houston, Tex. Correspondence: Requests for reprints should be sent to Evelyn C. Y. Chan, MD, Biomedical Ethics, Division of General Internal Medicine, University of TexasHouston Medical School, 6431 Fannin, 1.122 MSB, Houston, TX 77030 (e-mail: evelyn.c.chan{at}uth.tmc.edu).
This study determined the accuracy of self-reports of prostatespecific antigen (PSA) testing. Men (N = 402) attending 2 outpatient clinics were asked: "Did you have a PSA test today?" and their medical records were checked. Concordance, sensitivity, and false-negative values were 65%, 67%, and 33%, respectively, at 1 clinic site and 88%, 64%, and 36% at the other. The accuracy of self-reports of PSA testing should be interpreted with caution.
Screening for prostate cancer with prostate-specific antigen (PSA) is controversial because it is not clear whether regular testing reduces mortality.15 Therefore, professional organizations recommend informed decisionmaking for PSA testing.610 To promote educational efforts for informed decisionmaking and to determine screening prevalence, which often relies on selfreported data, investigators need data on the accuracy of self-reports of PSA testing. We hypothesized that the accuracy of self-reports of PSA testing would be high if patients were asked about testing on the same day as their clinic visit. We determined whether any demographic, knowledge, or experience variables predicted accurate self-reports.
Study participants were enrolled in another study11 and attended the general internal medicine outpatient clinics at Kelsey-Seybold Clinic in Houston, Tex, and the University of TexasHouston. Men attending KelseySeybold Clinic were scheduled for an annual health maintenance examination. Men attending the University of TexasHouston were scheduled for nonurgent care visits. From April to July 2001, we approached 677 men aged 50 years or older on-site after they had visited with their physician. To be eligible, men had to have no history of prostate cancer and at least a sixth-grade education. Ninety men were ineligible, and 157 refused to participate, resulting in a sample of 430 men. Each participant was paid $10 to complete a self-administered survey. A medical record review between January and March 2002 by an internal medicine physician was used as the gold standard to determine whether men had received a PSA test with their visit. After participants with unavailable records were excluded, 265 men from Kelsey-Seybold Clinic and 137 men from the University of TexasHouston remained. We used sections of a survey from another study.11 The main dependent variable was concordance12 of patient self-reports of PSA testing to the following question: "Did you have a PSA test today?" Independent variables were demographic, knowledge, and experience variables. We excluded from our analysis 46 men at Kelsey-Seybold Clinic (17%) and 7 men from the University of TexasHouston (5%) who responded "dont know" to "Did you have a PSA test today?"
We conducted
Respondents at the Kelsey-Seybold Clinic had a higher annual household income than did respondents at the University of TexasHouston but otherwise had similar demographic characteristics (Table 1
In response to the question "Did you have a PSA test today?" at Kelsey-Seybold Clinic, 145 men responded "yes" and 74 men responded "no." At the University of TexasHouston, 25 men responded "yes" and 105 men responded "no." The concordance was 65% at Kelsey-Seybold Clinic and 88% at the University of TexasHouston. The sensitivity and false-negative values were 67% and 33%, respectively, at Kelsey-Seybold Clinic and 64% and 36%, respectively, at the University of TexasHouston. The specificity and false-positive values were 43% and 57%, respectively, at KelseySeybold Clinic and 98% and 2%, respectively, at the University of TexasHouston.
At Kelsey-Seybold Clinic, 5 variables were significantly associated with accurate self-reports of PSA testing: (1) more education, (2) "ever heard of a PSA," (3) "ever been told to have a PSA," (4) "ever had a PSA," and (5) "doctor recommended a PSA today" (Table 2
The prevalence of PSA testing was 90% at Kelsey-Seybold Clinic and 28% at the University of TexasHouston by medical record review. Among the 53 men who responded "dont know" to the question "Did you have a PSA test today?", the prevalence of PSA testing was 91% at Kelsey-Seybold Clinic and 28% at the University of TexasHouston. Among the 220 men who responded "yes" to the question "Did your doctor recommend a PSA test today?", the prevalence of PSA testing was 93% at Kelsey-Seybold Clinic and 64% at the University of TexasHouston. Among the 146 men who responded "yes" to the question "Did your doctor discuss the advantages and disadvantages of the PSA test with you?", the prevalence of PSA testing was 88% at Kelsey-Seybold Clinic and 38% at the University of TexasHouston.
Our findings and those of others13,14 suggest that the sensitivity of asking a man whether he had completed a PSA test is relatively low, regardless of the time frame for self-reporting a test. We found a false-negative response rate of one third, which is of concern because of the potential harm that may arise when men must cope with the consequences of a test that they did not even realize they had taken. Because professional organizations recommend informed decisionmaking before PSA testing, future studies should focus on improving physicianpatient communication. We recommend caution when interpreting the accuracy of self-reports of PSA testing.
This study was funded by National Cancer Institute grant K08-CA78615, awarded to Dr Chan as a clinical scientist award, and by Centers for Disease Control and Prevention/Association of Schools of Public Health grant S1171-19/20. Additional technical support was provided by National Institutes of Health grant M01-RR02558 to the Clinical Research Center at The University of TexasHouston. This brief was presented at the annual meeting of the American Public Health Association, San Francisco, Calif, November 17, 2003. We appreciate the assistance of Dr Donnie Aga of Kelsey-Seybold Clinic, Houston, Tex.
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Contributors E. C. Y. Chan supervised the study and with S. W. Vernon conceived the study design and collected and analyzed the data. C. Ahn analyzed the data. A. Greisinger assisted with data collection. All authors contributed to revisions of the brief and approved the final version. Accepted for publication November 6, 2003.
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