Coherent light scattered from an ensemble of moving scatterers produces a time-varying speckle pattern. The intensity fluctuations observed in a single speckle can be regarded either as a time-varying interference effect or as a Doppler beating effect. Techniques based on each of these approaches have been developed to analyze the fluctuations in an attempt to measure the velocities of the scatterers. Most of these methods measure the temporal statistics of the intensity fluctuations in a single speckle, i.e., at a single point. If a map of the velocity distribution is required, some form of scanning must be introduced. One way of avoiding the need to scan is to make use of the spatial statistics of time-integrated speckle. This is the basis of a technique, already described in the literature, called laser speckle contrast analysis (LASCA). In this article, we present a brief review of the theory linking the intensity fluctuations to the velocity and of the various techniques that have been proposed to measure them. We then describe the present configuration of our LASCA technique and describe some recent developments in our search for a real-time, noninvasive, full-field technique for visualizing capillary blood flow. © 1999 Society of Photo-Optical Instrumentation Engineers.

We have developed a technique, called Laser Speckle Contrast Analysis (LASCA), to monitor capillary blood flow. Like the earlier method 'single-exposure speckle photography' it uses the phenomenon of time-varying speckle, drawing on models that relate the statistics ofthe speckle pattern, especially the contrast, to the velocity ofthe scatterers. Temporal variations in the pattern blur the captured image, whether photographic or digital, reducing the contrast. LASCA is a fully-digitized, fullfield, non-invasive technique and operates in quasi-real-time: it grabs an image and then produces a 2-dimensional map of contrast variations representing differing velocities. Previously the data had been stretched, as a full range of contrasts could not be achieved. This problem has been addressed and we believe solved, thus giving us a full range of contrasts. In this paper we look at the effects ofchanging the exposure time. If it is varied it should be possible, according to the models used, to look at different ranges of velocity. Also we hope to show that by using different wavelengths together it is possible to distinguish between flow at different depths in the skin. We illustrate the validity of our technique with some of our results and then compare these to other methods ofmeasuring capillary blood flow.

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