The 2023 ACR/EULAR APS classification criteria exhibit consistently excellent specificity but reduced and phenotype-dependent sensitivity, which reinforces the intended role of the criteria for classification rather than clinical diagnosis and highlight important limitations in specific APS subgroups.
Abstract
Objectives
To systematically evaluate the classification performance of the 2023 American College of Rheumatology/European Alliance of Associations for Rheumatology (ACR/EULAR) classification criteria for antiphospholipid syndrome (APS).
Methods
We conducted a systematic review of literature from August 2023 through May 2026, including studies that evaluated the ability of the 2023 ACR/EULAR APS criteria to classify patients previously classified according to expert clinical diagnosis and/or the 2006 revised Sapporo (Sydney) criteria. Data on true and false positives and negatives were extracted. Sensitivity and specificity were pooled using a bivariate random-effects model when both parameters were available; sensitivity was additionally pooled using a univariate random-effects model.
Results
Twenty four studies comprising 25 data sets were included, of which 13 incorporated non-APS control groups. In the bivariate meta-analysis, pooled sensitivity was 0.74 (95%CI 0.67-0.81) and pooled specificity was 0.99 (95% CI 0.98-1.00). Sensitivity demonstrated substantial heterogeneity across studies and varied markedly by APS phenotype. Sensitivity was low in obstetric APS (pooled sensitivity 0.20 in studies restricted to obstetric APS and 0.31 when obstetric subgroup data from additional studies were included), whereas it was higher among cases of thrombotic APS (0.82). Across cohorts, non-classification was mainly driven by isolated IgM antiphospholipid antibody positivity and obstetric APS phenotypes.
Conclusion
The 2023 ACR/EULAR APS classification criteria exhibit consistently excellent specificity but reduced and phenotype-dependent sensitivity. These findings reinforce the intended role of the criteria for classification rather than clinical diagnosis and highlight important limitations in specific APS subgroups.
Findings support using the 2023 criteria primarily to define homogeneous research cohorts rather than as a stand-alone basis for diagnosis or treatment decisions, and support using the 2023 criteria primarily to define homogeneous research cohorts.
Ting-Wei Sheng, Yu-Qi Tang, Zheng-Wei Tan et al.· Frontiers in Medicine· 0 citations
Background Antiphospholipid syndrome is an autoimmune disorder characterized by recurrent thrombotic events and/or adverse pregnancy outcomes. Although three classification criteria—the 1999 Sapporo criteria, the Revised Sapporo criteria, and the 2023 ACR/EULAR antiphospholipid syndrome classification—have been develop...
Jie Wang, Yang-Qi Yin, Jia-Qi Qu et al.· PLoS ONE· 0 citations
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Nergis Akay, S. Şahin, S. A. Uçar et al.· Rheumatology· 0 citations
BACKGROUND
Pediatric immune thrombocytopenia (ITP) usually has a favorable prognosis, although some children progress to chronic disease (>12 mo). A 2014 meta-analysis by Heitink-Pollé and colleagues identified important prognostic markers that informed tools such as the Nordic prediction score. Given advances in diagn...
Ahmad S. Ashi, O. Alshaikhi, E. Alnasser· Journal of pediatric hematol...· 0 citations
INTRODUCTION
To synthesize contemporary evidence on epidemiology, triggers and risk factors, pathophysiology, clinical presentation, diagnosis, management patterns, and outcomes in Takotsubo Syndrome (TTS) restricted to studies using the International Takotsubo (InterTAK) Diagnostic Criteria.
METHODS
A PRISMA‑guided...
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