Volume 49, Issue 4 pp. 696-703

Thrombin generation and clot formation in methylene blue–treated plasma and cryoprecipitate

Rebecca Cardigan

Rebecca Cardigan

From NHS Blood & Transplant, Brentwood; and the Department of Haematology, Addenbrookes Hospital, Cambridge, UK.

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Katherine Philpot

Katherine Philpot

From NHS Blood & Transplant, Brentwood; and the Department of Haematology, Addenbrookes Hospital, Cambridge, UK.

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Philip Cookson

Philip Cookson

From NHS Blood & Transplant, Brentwood; and the Department of Haematology, Addenbrookes Hospital, Cambridge, UK.

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Roger Luddington

Roger Luddington

From NHS Blood & Transplant, Brentwood; and the Department of Haematology, Addenbrookes Hospital, Cambridge, UK.

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First published: 20 March 2009
Citations: 34
Dr Rebecca Cardigan, NHS Blood & Transplant, Long Road, Cambridge CB2 2PT, UK; e-mail: [email protected].

Abstract

BACKGROUND: Methylene blue (MB) treatment of plasma is known to reduce the activity of clotting factors, but its effect on thrombin generation and clot formation is not well documented.

STUDY DESIGN AND METHODS: Individual clotting factors and inhibitors and global tests of thrombin generation and clot formation using rotational thrombelastometry (ROTEM) were assessed in a paired study of standard or MB plasma and cryoprecipitate (n = 20 each).

RESULTS: MB treatment resulted in a 10 percent reduction in endogenous thrombin potential and 30 percent decrease in peak thrombin as well as the expected 20 to 35 percent loss of Factor (F)VIII, fibrinogen, and FXI activity. MB treatment had no effect on the rate of clot formation and increased the clot firmness by 20 percent as assessed by ROTEM. There were minimal further changes in either coagulation factor levels or thrombin generation when thawed plasma was stored for an additional 24 hours. FVIII and fibrinogen content of MB cryoprecipitate was reduced by 30 and 40 percent, respectively, but this was not associated with altered clot time or rate of clot formation by ROTEM and only an 8 percent decrease in clot firmness.

CONCLUSIONS: It is concluded that MB treatment is associated with a reduction in the thrombin-generating capacity of plasma, but has very little effect on the strength of clot formation as assessed by thrombelastometry. The thrombin-generating capacity of standard and MB plasma is relatively unaltered by subsequent storage of thawed plasma at 4°C for 24 hours.

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