Document 2725 DOCN M94A2725 TI Performance of the Red-Dot HIV 1 & 2 assay. DT 9412 AU Abdel-Hamid M; Constantine NT; Dept. Pathology, University of Maryland School of Medicine,; Baltimore. SO Int Conf AIDS. 1994 Aug 7-12;10(1):239 (abstract no. PB0387). Unique Identifier : AIDSLINE ICA10/94369850 AB OBJECTIVES: To determine the suitability and performance of a new rapid assay to detect antibodies to HIV 1 & 2 in a hospital setting in Baltimore, MD. METHODS: A total of 91 sera (50 EIA negative, 39 EIA repeatedly reactive/Western blot (WB) confirmed, and 2 WB indeterminate) were tested by the Red-Dot HIV 1 & 2 rapid assay (CDI, CA, USA). In addition, 9 samples were included that were EIA false positive (WB negative). The Red-Dot test is a rapid membrane based assay which incorporates a synthetic peptide antigen and a protein A colloidal gold conjugate. Samples which exhibited discrepant results between the two screening tests were retested by all assays to ensure that technical error had not occurred. RESULTS: 39 sera produced reactive results by both tests and were confirmed by Western blot (WB). The Red-Dot test produced 3 false positive results (detected 56 of 59 true negatives), and no false negative results (0/39), thus yielding a specificity of 95% and a sensitivity of 100%. Both of the WB indeterminate samples produced reactive results by EIA, while only one produced a reactive result by the Red-Dot. DISCUSSION AND CONCLUSIONS: The Red-Dot HIV 1 & 2 rapid assay was easy to perform, required just minutes to complete, exhibited an excellent sensitivity and an acceptable specificity. This study should be expanded to include a larger sample size in order to verify the assay's performance. DE *AIDS Serodiagnosis *Blotting, Western Human HIV Seropositivity/*DIAGNOSIS/IMMUNOLOGY HIV-1/*IMMUNOLOGY HIV-2/*IMMUNOLOGY *Immunoenzyme Techniques Predictive Value of Tests MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).