Skip to main navigation Skip to search Skip to main content

Reference range determination for whole-blood platelet aggregation using the multiplate analyzer

  • Ellinor I. B. Peerschke*
  • , Donna D. Castellone
  • , A. K. Stroobants
  • , John Francis
  • *Corresponding author for this work
  • Memorial Sloan-Kettering Cancer Center
  • Hoffmann-La Roche Inc.
  • AdventHealth Orlando

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Objectives: To develop reference ranges for platelet aggregation using the Multiplate analyzer (Roche Diagnostics, Mannheim, Germany) in blood anticoagulated with sodium citrate (Na-citrate), lithium heparin (Li-heparin), or hirudin. Methods: The study was performed at three sites on consented, healthy adults (n = 193) not taking antiplatelet medication. Platelet aggregation was evaluated in response to adenosine-5'-diphosphate, arachidonic acid, collagen, thrombin receptor activating peptide, ristocetin, and adenosine-5'-diphosphate combined with prostaglandin E1. Precision testing was conducted using healthy donors and donors taking aspirin. Results: Whole-blood platelet aggregation showed anticoagulant-dependent differences in platelet responses to all agonists. Samples collected in Na-citrate demonstrated the lowest responses to all agonists. The highest responses were obtained using Li-heparin. Precision testing revealed high variability in platelet aggregation at lower agonist doses, regardless of anticoagulant. Highest platelet response variations occurred in response to arachidonic acid in blood anticoagulated with hirudin from participants taking aspirin. Conclusions: These data demonstrate the importance of establishing locally relevant reference ranges.
Original languageEnglish
Pages (from-to)647-656
JournalAmerican journal of clinical pathology
Volume142
Issue number5
DOIs
Publication statusPublished - 1 Nov 2014

Fingerprint

Dive into the research topics of 'Reference range determination for whole-blood platelet aggregation using the multiplate analyzer'. Together they form a unique fingerprint.

Cite this