TY - JOUR
T1 - Effects of Hextend Hemodilution on Plasma Coagulation Kinetics in the Rabbit
T2 - Role of Factor XIII-Mediated Fibrin Polymer Crosslinking
AU - Nielsen, Vance G.
N1 - Funding Information:
This investigation was supported by a grant from BioTime, Inc., Berkeley, CA.
PY - 2006/5
Y1 - 2006/5
N2 - Background: Hydroxyethyl starch administration has been associated with decreases in hemostasis and has recently been demonstrated to decrease fibrinogen (FI)-thrombin-(FIIa)-Factor XIII (FXIII) interactions in vitro in human plasma. Thus, the purpose of the present study was to determine the effect of in vivo hemodilution with Hextend (6% hydroxyethyl starch, mean molecular weight 450 kDa) on plasma coagulation kinetics. Materials and methods: Eight male, New Zealand White rabbits were intravenously administered with 20 ml/kg of Hextend. Citrated plasma was obtained before, 1 min after, and 1 h after hemodilution. Thrombelastographic analyses were performed, with clot initiation (R, sec), clot propagation (α, degrees), and clot strength (shear elastic modulus, G, dynes/cm2) determined over 20 min. Samples were celite-activated and had either with addition or without additions of FI, FIIa or activated FXIII (FXIIIa) to restore protein content to prediluted values. Results: There was no significant difference in R values observed before (229 ± 30), 1 min after (241 ± 54), and 1 h after (214 ± 42) hemodilution. Prediluted α values (75.2 ± 1.9) were significantly decreased 1 min (53.3 ± 5.9) and 1 h after hemodilution (56.1 ± 10.2). Prediluted G values (1992 ± 434) were significantly reduced 1 min (532 ± 195) and 1 h after (630 ± 297) hemodilution. FI, FIIa, and FXIIIa addition significantly decreased R values after hemodilution. α and G values were significantly improved by FI and FXIIIa after hemodilution. FIIa addition did not significantly affect α or G. Conclusions: Hextend hemodilution in rabbits maintains clot initiation by diminishing both FIIa-FI and FXIIIa-fibrin interactions, whereas clot propagation and strength were reduced by diminished FXIIIa-fibrin interactions.
AB - Background: Hydroxyethyl starch administration has been associated with decreases in hemostasis and has recently been demonstrated to decrease fibrinogen (FI)-thrombin-(FIIa)-Factor XIII (FXIII) interactions in vitro in human plasma. Thus, the purpose of the present study was to determine the effect of in vivo hemodilution with Hextend (6% hydroxyethyl starch, mean molecular weight 450 kDa) on plasma coagulation kinetics. Materials and methods: Eight male, New Zealand White rabbits were intravenously administered with 20 ml/kg of Hextend. Citrated plasma was obtained before, 1 min after, and 1 h after hemodilution. Thrombelastographic analyses were performed, with clot initiation (R, sec), clot propagation (α, degrees), and clot strength (shear elastic modulus, G, dynes/cm2) determined over 20 min. Samples were celite-activated and had either with addition or without additions of FI, FIIa or activated FXIII (FXIIIa) to restore protein content to prediluted values. Results: There was no significant difference in R values observed before (229 ± 30), 1 min after (241 ± 54), and 1 h after (214 ± 42) hemodilution. Prediluted α values (75.2 ± 1.9) were significantly decreased 1 min (53.3 ± 5.9) and 1 h after hemodilution (56.1 ± 10.2). Prediluted G values (1992 ± 434) were significantly reduced 1 min (532 ± 195) and 1 h after (630 ± 297) hemodilution. FI, FIIa, and FXIIIa addition significantly decreased R values after hemodilution. α and G values were significantly improved by FI and FXIIIa after hemodilution. FIIa addition did not significantly affect α or G. Conclusions: Hextend hemodilution in rabbits maintains clot initiation by diminishing both FIIa-FI and FXIIIa-fibrin interactions, whereas clot propagation and strength were reduced by diminished FXIIIa-fibrin interactions.
KW - coagulation
KW - factor XIII
KW - fibrinogen
KW - hemodilution
KW - hydroxyethyl starch
KW - monitoring
KW - thrombelastography
KW - thrombin
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U2 - 10.1016/j.jss.2005.07.025
DO - 10.1016/j.jss.2005.07.025
M3 - Article
C2 - 16154147
AN - SCOPUS:33646007652
SN - 0022-4804
VL - 132
SP - 17
EP - 22
JO - Journal of Surgical Research
JF - Journal of Surgical Research
IS - 1
ER -