Predicting human immunodeficiency virus type 1-positive sera by using two enzyme immunoassay kits in a parallel testing format

J Clin Microbiol. 1991 Nov;29(11):2507-12. doi: 10.1128/jcm.29.11.2507-2512.1991.

Abstract

Two algorithms for screening sera for antibody to human immunodeficiency virus type 1 were compared for their efficiency in identifying a true-positive sample in a population with heterogeneous risk factors, using the criteria of specificity and positive predictive value (PPV). In the first algorithm, all sera were screened by using a single enzyme immunoassay (EIA) kit, and a specificity of 98.6% and a PPV of 69.3% was calculated for true-positive sera. The second algorithm employed two different EIA kits in parallel to screen each sample. In the first instance, a specificity and a PPV of 100% was calculated if a positive sample was defined as reactive by both EIA kits; in the second, a specificity of 99.97% and a PPV of 99.4% was obtained if this criterion was extended to include a combination of one reactive and one equivocal result obtained with the two EIA kits.

Publication types

  • Comparative Study

MeSH terms

  • Algorithms
  • Diagnostic Errors
  • Evaluation Studies as Topic
  • HIV Antibodies / blood*
  • HIV Seropositivity / diagnosis*
  • HIV Seropositivity / immunology
  • HIV-1 / immunology*
  • Humans
  • Immunoenzyme Techniques* / statistics & numerical data
  • Risk Factors
  • Sensitivity and Specificity

Substances

  • HIV Antibodies