Figure 7.
Correction of ATC-associated changes in coagulation parameters by superFVa treatment. Severe bleeding was induced by a midline laparotomy followed by liver laceration (LL) involving the removal of 75% of the left lobe of the liver (supplemental Figure 6). Control mice (No LL) underwent the same procedures except liver laceration. superFVa (SFVa) therapy (0.8 mg/kg) or saline control (0 mg/kg SFVa) was initiated 30 minutes after the induction of liver laceration and administered as a continuous infusion at a rate of 5 µL/min for 20 minutes. Plasma samples were collected 30 and 60 minutes after liver laceration (representing the before and after superFVa therapy time points). Shown are the plasma activity levels of (A) FV (n = 4-7), (B) FVIII (n = 4-5), and (C) plasma TAT levels (n = 3-5). Results are shown as mean ± SD. Statistical significance was determined by 1-way ANOVA with Dunnett’s multiple comparisons test. ****P < .0001.

Correction of ATC-associated changes in coagulation parameters by superFVa treatment. Severe bleeding was induced by a midline laparotomy followed by liver laceration (LL) involving the removal of 75% of the left lobe of the liver (supplemental Figure 6). Control mice (No LL) underwent the same procedures except liver laceration. superFVa (SFVa) therapy (0.8 mg/kg) or saline control (0 mg/kg SFVa) was initiated 30 minutes after the induction of liver laceration and administered as a continuous infusion at a rate of 5 µL/min for 20 minutes. Plasma samples were collected 30 and 60 minutes after liver laceration (representing the before and after superFVa therapy time points). Shown are the plasma activity levels of (A) FV (n = 4-7), (B) FVIII (n = 4-5), and (C) plasma TAT levels (n = 3-5). Results are shown as mean ± SD. Statistical significance was determined by 1-way ANOVA with Dunnett’s multiple comparisons test. ****P < .0001.

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