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March 14, 2011Clinical and Applied Thrombosis/Hemostasis103 citations

The Influence of Low Platelet Count on Whole Blood Aggregometry Assessed by Multiplate

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TSTrine StissingNDNadia DridiSOSisse Rye Ostrowski

Structured PICO

Does low platelet count influence whole blood aggregometry assessed by Multiplate?

P
Population
Heparinized and citrated whole blood samples (n=10) and platelet-rich plasma samples (n=7)
I
Intervention
Dilution with autologous plasma to lower platelet concentrations (200 to 25 × 10(9)/L in whole blood and 200 to 100 × 10(9)/L in platelet-rich plasma)
C
Comparator
Platelet-rich plasma (PRP) samples and higher platelet concentrations
O
Outcome
Platelet aggregation investigated by ADP-, ASPI-, COL-, and TRAP-testsurrogate

Platelet concentrations <150 × 10(9)/L may influence Multiplate whole blood aggregometry results, which should be considered when evaluating patients on antiplatelet therapy.

Abstract

The Multiplate, a whole blood (WB) platelet function test, has shown promising results identifying patients on antiplatelet therapy at increased risk of rethrombosis. In the present study, the influence of low platelet count on platelet aggregation was analyzed and compared with aggregation results in an artificial matrix, platelet-rich plasma (PRP). Heparinized and citrated blood was diluted with autologous plasma to platelet concentrations 200 to 25 × 10(9)/L in WB samples (n = 10) and 200 to 100 × 10(9)/L in PRP samples (n = 7). The platelet aggregation was investigated by the ADP-, ASPI-, COL-, and TRAP-test. The WB responses decreased at platelet concentration of ≤100 × 10(9)/L (all P < .03), except for heparin-TRAP (50 × 10(9)/L, P = .008) and citrate-ASPI (150 × 10(9)/L, P = .03). In general, WB samples demonstrated higher aggregation than PRP samples at platelet concentrations 200 to 100 × 10(9)/L (P < .05). In conclusion, platelet concentration of <150 × 10(9)/L may influence Multiplate which should be considered in clinical settings. Furthermore, the findings emphasize the importance of evaluating haemostasis in its natural matrix, WB.

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Cite This Study

Stissing et al. (2011) studied this question.

synapsesocial.com/papers/6a83fac5d65172829ee670c6https://doi.org/10.1177/1076029610397183
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