PF4-dependent P-selectin expression assay in comparison to the heparin-induced platelet activation assay for the diagnosis of heparin-induced thrombocytopenia
Research article published in Transfusion (2025)
Abstract
BACKGROUND: Heparin-induced thrombocytopenia (HIT) is a severe complication characterized by thrombocytopenia and thrombosis. The presence of antibodies against heparin/platelet factor 4 (PF4) complexes is a key indicator for HIT. Diagnostic laboratory testing generally includes detection of anti-heparin/PF4 and/or functional testing such as the heparin-induced platelet activation assay (HIPAA). However, current functional tests are time-consuming and require specific technical skills. The PF4-dependent P-selectin expression assay (PEA) is a flow cytometry-based test that evaluates activation of donor platelets in the presence of HIT patient serum. METHODS: We conducted the PEA with 23 patient sera that were positive in both the anti-PF4/heparin enzyme-linked immunosorbent assay (ELISA) and HIPAA and 26 sera that tested negative in the anti-PF4/heparin ELISA. We next compared the PEA to the HIPAA using a retrospective clinical cohort of 195 sera of suspected HIT patients and tested the reproducibility of the PEA. RESULTS: The PEA was found to have a sensitivity of 73.9% and a specificity of 73.1% compared to the HIPAA. In our retrospective clinical cohort, we found that 74.4% (145 out of 195 samples) had identical results in both the HIPAA and PEA, with a specificity of 64.94% and sensitivity of 80.51% for the PEA compared to the HIPAA. Reproducibility testing of the PEA across three independent runs demonstrated consistent results in 83.3% (30 out of 36 samples). DISCUSSION: These findings suggest that the PEA is a promising functional test for HIT laboratory diagnostics based on the relatively high sensitivity; however, further studies are needed to validate its clinical applicability.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Summary
Peer-reviewed clinical and outcomes research relevant to anticoagulation, leech therapy, and microsurgical flap management. Indexed in PubMed and verified against the NCBI record.
Why This Matters for Hirudotherapy
This diagnostic-accuracy study compared a flow-cytometry PF4-dependent P-selectin expression assay (PEA) against the established heparin-induced platelet activation assay (HIPAA) for diagnosing heparin-induced thrombocytopenia, reporting in a retrospective cohort of 195 suspected-HIT sera that the two tests agreed in 74.4% of samples, with the PEA showing 80.51% sensitivity and 64.94% specificity versus HIPAA, and the authors concluding it is a promising but not-yet-validated functional test. For hirudotherapy this is background to the HIT field: better, faster HIT diagnosis matters precisely because confirmed HIT mandates non-heparin anticoagulation, the clinical niche that direct thrombin inhibitors such as the leech-derived hirudin were developed to fill. Caveat: this is a laboratory method-comparison study against an imperfect reference standard, the authors flag the need for further validation, and it does not study leech therapy.
Citation
PF4-dependent P-selectin expression assay in comparison to the heparin-induced platelet activation assay for the diagnosis of heparin-induced thrombocytopenia.
Meier et al. · Transfusion, 2025
Added to ASH library: May 28, 2026 · Site last updated: June 18, 2026