Microcor, Inc.

Allan L Kaminsky

Justin S Clark

Robert Gail Billings

Jon Neese

Paul Ruben

Ke-shieng Yang

The hematocrit of blood (i.e., the percentage of whole blood volume occupied by red blood cells) perfusing a finger is determined by stimulating the finger with two current frequencies, one relatively high (e.g., 10 MHZ) and the other relatively low (e.g., 100 KHz). Voltages induced in the finger in response to the two current frequencies are then captured and separated into baseline and pulsatile components. The hematocrit is determined as a function of the ratio of the high frequency pulsatile component to the low frequency pulsatile component, multiplied by the ratio of the square of the low frequency baseline component to the square of the high frequency baseline component. The signal-to-noise ratio of the captured voltages can be enhanced by the application of external pressure to the finger, such as by applying a pressure cuff to the finger.

System and method for in-vivo hematocrit measurement using impedance and

A method and apparatus for noninvasively determining hematocrit utilizing the frequency-dependent electrical impedance characteristics of whole blood by electrically stimulating a patient body portion containing a vascular compartment with a current source over a range of frequencies. A hematocrit measurement system includes a signal generator and demodulator (SGD) that sends an applied signal to an electrode pod that applies a current to a limb of a patient. The electrode pod receives resulting measured voltage signals and provides them to the SGD. The SGD provides to a personal computer (PC) signals indicative of the current passing through the limb of a patient and the resulting voltage. The voltage and current may be measured for various frequencies over, for example, a range from about 10 kHz to about 10 MHz. The electrical impedance from the blood alone is isolated from the total limb impedance from the blood, tissue, bone, etc. by determining the difference between measurements at different blood volumes. The hematocrit is determined by the PC based on inphase and quadrature data provided by the SGD. A neural network may be useful in determining the hematocrit from the blood impedance patterns.

Method and apparatus for noninvasively determining hematocrit

A method and apparatus for noninvasively determining hematocrit utilizing the frequency dependent electrical impedance characteristics of whole blood by electrically stimulating a patient body portion containing a pulsatile vascular compartment with a constant current source at two selected frequencies, one of which is high enough that the capacitive nature of erythrocytes will significantly affect the magnitude of the impedance of the blood. Sensed voltage across the stimulated body portion at the two frequencies is representative of the corresponding magnitudes, and the method further includes detecting the signal envelopes of the sensed voltages, isolating and converting the pulsatile components of the signal envelopes to the digital domain, normalizing each isolated converted pulsatile component against the voltage baseline of its carrier waveform and creating a ratio of the normalized isolated pulsatile components representative of the patient's hematocrit. The ratio is indexed to a look-up table constructed from clinical studies correlating such ratios at the two selected frequencies to hematocrit, and the hematocrit corresponding to the created ratio is displayed. A plurality of ratios of sets of time-matched pulsatile component segments are created and averaged using a weighted averaging technique which more heavily weights ratios created from more significant segment sets, the weighted ratio average being correlated to hematocrit via the look-up table.

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Holladay, UT, United States of America

Allan L Kaminsky