Cited by 11Systemic Lupus Erythematosus ResearchClinical Laboratory Practices and Quality ControlBlood Coagulation and Thrombosis Mechanisms

Variable Performance of Lupus Anticoagulant Testing: The Australasian/Asia-Pacific Experience

Favaloro, Emmanuel J., Dean, Elysse, Arunachalam, Sandya·2024·Seminars in Thrombosis and Hemostasis

Abstract

Lupus anticoagulant (LA) is one of three tests identified as laboratory criteria for definite antiphospholipid syndrome (APS). The other two tests are anticardiolipin antibody (aCL) and anti-β2-glycoprotein I (aβ2GPI) antibody. The presence of LA is assessed using clot-based tests, while the presence of aCL and aβ2GPI is assessed by immunological assays. Since no test can be considered 100% sensitive or specific for LA, current guidelines recommend using two different clot-based assays reflecting different principles, with the dilute Russell viper venom time (dRVVT) and activated partial thromboplastin time (aPTT) recommended. Initially, LA-sensitive reagents are used to screen for LA, and then, in "screen-positive" samples, LA-"insensitive" reagents are used to confirm LA. Because LA assays are based on clot detection, anything that can interfere with fibrin clot development may affect test results. In particular, in addition to LA, the tests are also sensitive to the presence of a wide range of clinical anticoagulants, reflecting preanalytical issues for testing. We provide updated findings for LA testing in our geographic region, using recent data from the Royal College of Pathologists of Australasia Quality Assurance Programs, an international external quality assessment program with approximately 120 participants. Data show a wide variety of assays in use, especially for aPTT testing, and variable outcomes in reported numerical values with these assays when assessing pro…

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Crossref · 10.1055/s-0043-1776406

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  • The aPTT reagent pair used in this study (Actin FSL for screening and Actin FS for confirmation) is one of only a few paired aPTT reagents offered by commercial manufacturers, with most manufacturers of silica-based aPTT assays offering an LA-sensitive reagent, but not providing an LA insensitive silica-based paired reagent.

    “On the other hand, the aPTT reagent pair used in this study (Actin FSL for screening and Actin FS for confirmation) is one of only a few paired aPTT reagents offered by commercial manufacturers, with most manufacturers of silica-based aPTT assays offering an LA-sensitive reagent, but not providing an LA insensitive silica-based paired reagent [32].”

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Authors
Favaloro, E. J., Dean, E., & Arunachalam, S.
Affiliations
  • The University of Sydney (AU)
  • Royal College of Pathologists of Australasia (AU)
Corresponding author
Favaloro, Emmanuel J.
Venue
Seminars in Thrombosis and Hemostasis
Published
2023-11-15
Volume
50
Issue
08
Pages
1103-1113
ISSN
  • 0094-6176 (ISSN-L)
  • 1098-9064
OpenAlex
W4388714363
Cited by
11
References
4
Citations by year
2026: 1 · 2025: 3 · 2024: 7
FWCI
0.48
Type
journal article
Language
en
Open access
closed
Locations
  • Seminars in Thrombosis and Hemostasis (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Rheumatology › Systemic Lupus Erythematosus Research
  • Health Sciences › Medicine › Physiology › Clinical Laboratory Practices and Quality Control
  • Health Sciences › Medicine › Hematology › Blood Coagulation and Thrombosis Mechanisms
Keywords
lupus anticoagulant, antiphospholipid syndrome, dilute Russell viper venom time, activated partial thromboplastin time, assay variability, external quality assessment, anticoagulants
MeSH terms
Blood Coagulation Tests, Female, Humans, Partial Thromboplastin Time, Lupus Coagulation Inhibitor, Antiphospholipid Syndrome, Australasia

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