TY - JOUR
T1 - What happens after an elevated PSA test
T2 - The experience of 13,591 veterans
AU - Zeliadt, Steven B.
AU - Hoffman, Richard M.
AU - Etzioni, Ruth
AU - Ginger, Van Anh T.
AU - Lin, Daniel W.
N1 - Funding Information:
This work was supported by the VA. The VA Office of Research and Development Health Services RD, Department of Veterans Affairs, Short-term Health Services Project, SHP-08-165, funded this study. Portions of the data presented here were presented at the VA Health Services RD National Meeting in February 2009 and at the Annual Meeting of the American Urological Association in April 2009.
Funding Information:
Acknowledgements: This work was supported by the VA. The VA Office of Research and Development Health Services R&D, Department of Veterans Affairs, funded this study through a Short-term Health Services Project grant: SHP-08-165. The authors are grateful to Adam Batten for data processing, and to Bruce Wynar and Carol Simons for chart review and data abstraction. The views expressed in this article are those of the authors and do not necessarily reflect the position or policy of the Department of Veterans Affairs.
PY - 2010/11
Y1 - 2010/11
N2 - BACKGROUND: The occurrence and timing of prostate biopsy following an elevated prostate-specific antigen (PSA) test varied considerably in randomized screening trials. OBJECTIVE: Examine practice patterns in routine clinical care in response to an elevated PSA test (=4 ng/μl) and determine whether time to biopsy was associated with cancer stage at diagnosis. DESIGN: Retrospective cohort study. PARTICIPANTS: All veterans (n=13,591) in the Pacific Northwest VA Network with a PSA=4 ng/μl between 1998 and 2006 and no previous elevated PSA tests or prostate biopsy. MAIN MEASURES: We assessed follow-up care including additional PSA testing, urology consults, and biopsies. We compared stage at diagnosis for men who were biopsied within 24 months vs. those men biopsied and diagnosed >24 months after the elevated PSA test. KEY RESULTS: Two-thirds of patients received follow- up evaluation within 24 months of the elevated PSA test: 32.8% of men underwent a biopsy, 15.5% attended a urology visit but were not biopsied, and 18.8% had a subsequent normal PSA test. Younger age, higher PSA levels, more prior PSA tests, no copayment requirements, existing urologic conditions, low body mass index, and low comorbidity scores were associated with more complete follow-up. Among men who underwent radical prostatectomy, a delayed diagnosis was not significantly associated with having a pathologically advanced-stage cancer (T3/T4), although we found an increased likelihood of presenting with stage T2C relative to stage T2A or T2B cancer. CONCLUSIONS: Follow-up after an elevated PSA test is highly variable with more than a third of men receiving care that could be considered incomplete. A delayed diagnosis was not associated with poorer prognosis.
AB - BACKGROUND: The occurrence and timing of prostate biopsy following an elevated prostate-specific antigen (PSA) test varied considerably in randomized screening trials. OBJECTIVE: Examine practice patterns in routine clinical care in response to an elevated PSA test (=4 ng/μl) and determine whether time to biopsy was associated with cancer stage at diagnosis. DESIGN: Retrospective cohort study. PARTICIPANTS: All veterans (n=13,591) in the Pacific Northwest VA Network with a PSA=4 ng/μl between 1998 and 2006 and no previous elevated PSA tests or prostate biopsy. MAIN MEASURES: We assessed follow-up care including additional PSA testing, urology consults, and biopsies. We compared stage at diagnosis for men who were biopsied within 24 months vs. those men biopsied and diagnosed >24 months after the elevated PSA test. KEY RESULTS: Two-thirds of patients received follow- up evaluation within 24 months of the elevated PSA test: 32.8% of men underwent a biopsy, 15.5% attended a urology visit but were not biopsied, and 18.8% had a subsequent normal PSA test. Younger age, higher PSA levels, more prior PSA tests, no copayment requirements, existing urologic conditions, low body mass index, and low comorbidity scores were associated with more complete follow-up. Among men who underwent radical prostatectomy, a delayed diagnosis was not significantly associated with having a pathologically advanced-stage cancer (T3/T4), although we found an increased likelihood of presenting with stage T2C relative to stage T2A or T2B cancer. CONCLUSIONS: Follow-up after an elevated PSA test is highly variable with more than a third of men receiving care that could be considered incomplete. A delayed diagnosis was not associated with poorer prognosis.
KW - Prostate biopsy
KW - Prostate-specific antigen (PSA)
KW - Rostate cancer
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U2 - 10.1007/s11606-010-1468-9
DO - 10.1007/s11606-010-1468-9
M3 - Article
C2 - 20697965
AN - SCOPUS:78650173035
SN - 0884-8734
VL - 25
SP - 1205
EP - 1210
JO - Journal of General Internal Medicine
JF - Journal of General Internal Medicine
IS - 11
ER -