Serologic test for syphilis as a surrogate marker for human immunodeficiency virus infection among United States blood donors

G. A. Herrera, E. M. Lackritz, R. S. Janssen, V. P. Raimondi, R. Y. Dodd, J. Aberle-Grasse, L. R. Petersen

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

BACKGROUND: This study evaluated the usefulness of the serologic test for syphilis (STS) in preventing the transmission of human immunodeficiency virus (HIV), hepatitis B and C viruses, and human T-lymphotropic virus via the transfusion of seronegative, infectious window-period blood. STUDY DESIGN AND METHODS: Demographic and laboratory information on blood donations made between January 1992 and June 1994 in 18 American Red Cross regions was analyzed. It was assumed that the same proportion of HIV-positive and HIV- infectious window-period donations reacted on STS and were negative on ether screening tests (hepatitis B and C viruses and human T-lymphotropic virus). This proportion multiplied by the estimated number of HIV-infectious window- period donations is the number of post-screening HIV-infectious donations removed by STS. RESULTS: Of 4,468,570 donations, 12,145 (0.27%) were STS positive and 377 (0.008%) were HIV positive. Among donations that were negative on other screening tests, STS-reactive donations were 12 times more likely to be HIV positive (odds ratio = 11.9; 95% CI = 5,26). However, of an estimated 13 infectious window-period donations, 0.2 would have been removed because of a reactive STS, at a cost of over $16 million. CONCLUSION: STS is a poor marker and a costly strategy for preventing post-screening HIV infections and other blood-borne diseases.

Original languageEnglish (US)
Pages (from-to)836-840
Number of pages5
JournalTransfusion
Volume37
Issue number8
DOIs
StatePublished - Aug 1997
Externally publishedYes

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