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Protamine reversal of heparin affects platelet aggregation and activated clotting time after cardiopulmonary bypass.

Publication ,  Journal Article
Mochizuki, T; Olson, PJ; Szlam, F; Ramsay, JG; Levy, JH
Published in: Anesth Analg
October 1998

UNLABELLED: Bleeding after cardiopulmonary bypass (CPB) is related to multiple factors. Excess protamine weakens clot structure and decreases platelet function; therefore, an increased activated clotting time (ACT) after protamine reversal of heparin may be misinterpreted as residual heparin anticoagulation. We evaluated the effects of protamine, recombinant platelet factor 4 (rPF4), and hexadimethrine on ACT in blood obtained after CPB. In addition, we examined the effect of protamine on in vitro platelet aggregation. Incremental doses of protamine, rPF4, and hexadimethrine were added to heparinized blood from CPB, and ACTs were performed. Incremental concentrations of protamine were added to heparinized platelet-rich plasma, and aggregometry was induced by adenosine diphosphate (ADP) and collagen. The mean heparin concentration at the end of CPB was 3.3 U/mL. Protamine to heparin ratios >1.3:1 produced a significant prolongation of the ACT that was not seen with rPF4 and was observed only with 5:1 hexadimethrine to heparin ratios. ADP-induced platelet aggregation was reduced with protamine administration > or =1.3:1. Excessive protamine reversal of heparin prolongs ACT and alters ADP-induced platelet aggregation in a dose-dependent manner in vitro. Additional protamine administered to treat a prolonged ACT may further increase clotting time, reduce platelet aggregation, and potentially contribute to excess bleeding after CPB. IMPLICATIONS: We found that excess protamine prolonged the activated clotting time and altered platelet function after cardiopulmonary bypass, whereas heparin antagonists, such as recombinant platelet factor 4 and hexadimethrine, exhibited a wider therapeutic range without adversely affecting the activated clotting time. Approaches to avoid excess protamine or use of alternative heparin antagonists after cardiopulmonary bypass may be beneficial.

Duke Scholars

Published In

Anesth Analg

DOI

ISSN

0003-2999

Publication Date

October 1998

Volume

87

Issue

4

Start / End Page

781 / 785

Location

United States

Related Subject Headings

  • Whole Blood Coagulation Time
  • Recombinant Proteins
  • Protamines
  • Platelet Factor 4
  • Platelet Aggregation Inhibitors
  • Platelet Aggregation
  • In Vitro Techniques
  • Humans
  • Hexadimethrine Bromide
  • Heparin Antagonists
 

Citation

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Mochizuki, T., Olson, P. J., Szlam, F., Ramsay, J. G., & Levy, J. H. (1998). Protamine reversal of heparin affects platelet aggregation and activated clotting time after cardiopulmonary bypass. Anesth Analg, 87(4), 781–785. https://doi.org/10.1097/00000539-199810000-00008
Mochizuki, T., P. J. Olson, F. Szlam, J. G. Ramsay, and J. H. Levy. “Protamine reversal of heparin affects platelet aggregation and activated clotting time after cardiopulmonary bypass.Anesth Analg 87, no. 4 (October 1998): 781–85. https://doi.org/10.1097/00000539-199810000-00008.
Mochizuki T, Olson PJ, Szlam F, Ramsay JG, Levy JH. Protamine reversal of heparin affects platelet aggregation and activated clotting time after cardiopulmonary bypass. Anesth Analg. 1998 Oct;87(4):781–5.
Mochizuki, T., et al. “Protamine reversal of heparin affects platelet aggregation and activated clotting time after cardiopulmonary bypass.Anesth Analg, vol. 87, no. 4, Oct. 1998, pp. 781–85. Pubmed, doi:10.1097/00000539-199810000-00008.
Mochizuki T, Olson PJ, Szlam F, Ramsay JG, Levy JH. Protamine reversal of heparin affects platelet aggregation and activated clotting time after cardiopulmonary bypass. Anesth Analg. 1998 Oct;87(4):781–785.

Published In

Anesth Analg

DOI

ISSN

0003-2999

Publication Date

October 1998

Volume

87

Issue

4

Start / End Page

781 / 785

Location

United States

Related Subject Headings

  • Whole Blood Coagulation Time
  • Recombinant Proteins
  • Protamines
  • Platelet Factor 4
  • Platelet Aggregation Inhibitors
  • Platelet Aggregation
  • In Vitro Techniques
  • Humans
  • Hexadimethrine Bromide
  • Heparin Antagonists