Table 2.

Time-course changes in surface coverage in perfusion of blood from type 2A and 2B VWD patients and from controls under a high shear rate (1500 s−1)

Patient1-minute perfusion, %7-minute perfusion, %
2A-1 0.9 ± 0.3 10.2 ± 2.4* 
 -2 0.2 ± 0.05 7.6 ± 3.0* 
 -3 0.1 ± 0.05 2.6 ± 0.3* 
2B-1 0.2 ± 0.15 8.5 ± 3.2* 
 -2 0.1 ± 0.05 12.7 ± 1.5* 
 -3 0.5 ± 0.1 38.2 ± 5.6 
 -4 0.7 ± 0.2 43.6 ± 5.5 
Control-1 0.6 ± 0.25 37.3 ± 6.6 
 -2 1.1 ± 0.3 42.4 ± 8.5 
 -3 0.8 ± 0.2 48.3 ± 8.2 
 -4 0.5 ± 0.15 40.1 ± 2.2 
 -5 1.5 ± 0.4 42.7 ± 3.4 
Patient1-minute perfusion, %7-minute perfusion, %
2A-1 0.9 ± 0.3 10.2 ± 2.4* 
 -2 0.2 ± 0.05 7.6 ± 3.0* 
 -3 0.1 ± 0.05 2.6 ± 0.3* 
2B-1 0.2 ± 0.15 8.5 ± 3.2* 
 -2 0.1 ± 0.05 12.7 ± 1.5* 
 -3 0.5 ± 0.1 38.2 ± 5.6 
 -4 0.7 ± 0.2 43.6 ± 5.5 
Control-1 0.6 ± 0.25 37.3 ± 6.6 
 -2 1.1 ± 0.3 42.4 ± 8.5 
 -3 0.8 ± 0.2 48.3 ± 8.2 
 -4 0.5 ± 0.15 40.1 ± 2.2 
 -5 1.5 ± 0.4 42.7 ± 3.4 

Whole blood containing mepacrine-labeled platelets was perfused through a collagen-coated glass surface under a shear rate of 1500 s−1. Surface coverage by thrombi within a defined area (211 × 317 μm each) was evaluated based on epifluorescence images taken at 1 and 7 minutes after the beginning of platelet-surface interaction during perfusion. Data represent the mean ± SD of 5 areas randomly selected in each single perfusion.

*

Statistically significant differences from controls (P< .01) by 1-way factorial analysis of variance (ANOVA) and the Scheffé method as described in the legend to Figure 4.

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