Methods to measure blood flow velocity of red blood cells in vivo at the microscopic level.

Several methods to measure red blood cell velocity in microvessels by electronic means are discussed. Signals are generated by the red blood cells present in the microscopic image of the microvessels. These signals can be converted to obtain an output signal proportional to the actual red blood cell velocity. The method of spatial filtering by interlacing gratings is discussed in terms of a filter with an input signal. Adaptation of optical factors that might improve the velocity measurement is obtained by a mathematical analysis. Different methods of correlation are presented. The temporal correlation (dual slit and video window) and spatial correlation methods are discussed in relation to factors influencing the quality of the correlogram, the peak of which is proportional to red blood cell velocity. The conversion of red blood cell velocity to volume flow is put in perspective.