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

Authors :
Altahan RM
Mathews N
Bourguignon A
Tasneem S
Arnold DM
Lim W
Hayward CPM
Source :
International journal of laboratory hematology [Int J Lab Hematol] 2024 Apr; Vol. 46 (2), pp. 362-374. Date of Electronic Publication: 2023 Dec 26.
Publication Year :
2024

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).<br />Methods: To further evaluate the L-PRP LTA strategy, we evaluated findings for a subsequent patient cohort.<br />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] × 10 <superscript>9</superscript> /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 × 10 <superscript>9</superscript>  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.<br />Conclusion: Diagnostic LTA with L-PRP, using a strategy that considers thrombocytopenia severity, is feasible and informative.<br /> (© 2023 The Authors. International Journal of Laboratory Hematology published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1751-553X
Volume :
46
Issue :
2
Database :
MEDLINE
Journal :
International journal of laboratory hematology
Publication Type :
Academic Journal
Accession number :
38148642
Full Text :
https://doi.org/10.1111/ijlh.14216