Evaluation of a diagnostic platelet aggregation test strategy for platelet rich plasma samples with low platelet counts

Int J Lab Hematol. 2024 Apr;46(2):362-374. doi: 10.1111/ijlh.14216. Epub 2023 Dec 26.

Abstract

Introduction: Light transmission aggregometry (LTA) is important for diagnosing platelet function disorders (PFD) and von Willebrand disease (VWD) affecting ristocetin-induced platelet aggregation (RIPA). Nonetheless, data is lacking on the utility of LTA for investigating thrombocytopenic patients and platelet rich plasma samples with low platelet counts (L-PRP). Previously, we developed a strategy for diagnostic LTA assessment of L-PRP that included: (1) acceptance of referrals/samples, regardless of thrombocytopenia severity, (2) tailored agonist selection, based on which are informative for L-PRP with mildly or severely low platelet counts, and (3) interpretation of maximal aggregation (MA) using regression-derived 95% confidence intervals, determined for diluted control L-PRP (C-L-PRP).

Methods: To further evaluate the L-PRP LTA strategy, we evaluated findings for a subsequent patient cohort.

Results: Between 2008 and 2021, the L-PRP strategy was applied to 211 samples (11.7% of all LTA samples) from 192 unique patients, whose platelet counts (median [range] × 109 /L) for blood and L-PRP were: 105 [13-282; 89% with thrombocytopenia] and 164 [17-249], respectively. Patient-L-PRP had more abnormal MA findings than simultaneously tested C-L-PRP (p-values <0.001). Among patients with accessible electronic medical records (n = 181), L-PRP LTA uncovered significant aggregation abnormalities in 45 (24.9%), including 18/30 (60%) with <80 × 109 platelets/L L-PRP, and ruled out PFD, and VWD affecting RIPA, in others. The L-PRP LTA strategy helped diagnose VWD affecting RIPA, Bernard Soulier syndrome, familial platelet disorder with myeloid malignancy, suspected ITGA2B/ITGB3-related thrombocytopenia, and acquired PFD.

Conclusion: Diagnostic LTA with L-PRP, using a strategy that considers thrombocytopenia severity, is feasible and informative.

Keywords: hemostatic disorders; platelet aggregation; platelet count; platelet function tests; thrombocytopenia.

MeSH terms

  • Blood Platelet Disorders* / diagnosis
  • Blood Platelets / pathology
  • Humans
  • Platelet Aggregation
  • Platelet Count
  • Platelet Function Tests
  • Platelet-Rich Plasma*
  • Thrombocytopenia* / diagnosis
  • Thrombocytopenia* / pathology
  • von Willebrand Diseases* / diagnosis

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