1 US5746206A - Isolated Layer Pulse Oximetry - Google Patents
Audrea Hillen edited this page 2025-08-14 10:28:24 +08:00


Another disadvantage is that the calculated oxygen saturation worth is influenced by pulsatile sign contributions from many differing tissue layers, including the skin or floor tissue layer. U.S. Pat. No. 5,188,108 issued to Secker suggests the use of a plurality of emitters and/or receivers to supply a number of emitter/receiver combination. Specifically, BloodVitals SPO2 the current invention permits for pulsed oximetry measurement which isolates arterial saturation levels for specific ranges of tissue layers which rejects saturation ranges of the tissue above or below the tissue of interest by using a number of spaced detectors and/or emitters. FIG. 4 is an overall block diagram displaying the foremost components of an operational system using the current invention. FIG. 6 is a graph of absorptivity vs. FIG. 7 is a graph comprising calculated oxygen saturation values using the rules of the invention for deep and shallow tissue measurements, and BloodVitals tracker values obtained with out utilizing the rules of the invention. FIG. 1A is a schematic diagram exhibiting the rules of operation of the present invention.


10 at subdermal tissue level 12 having gentle absorption properties u b . 14 Interposed between the non-invasive monitoring and measurement system (not proven) and subdermal tissue level 12, is pores and skin or floor tissue degree 14 having light absorption properties u a . It's deemed desirable to measure arterial oxygen saturation in the tissue layer 12 or blood oxygen monitor the tissue layer 14 independently. 16 transmits electromagnetic radiation in the seen and close to infrared region at two predetermined wavelengths (e.g. 660 nm and 905 nm). Emitter 16 is proven as a single entity in this instance. However, totally different emitters may be used for the totally different predetermined wavelengths, if desired. If more than one emitter is used, it's most convenient that they be co-positioned to simulate a single point source. LED's are a most well-liked type of emitter. Sixteen travel usually along path 18 to a primary detector 20 and alongside path 22 to a second detector 24 as shown.


18 within layer 12 (with absorption u b ) is proven as L 1 and the size of path 22 inside layer 12 is proven as L 2 . Detector BloodVitals insights 20 is spaced a distance of r 1 from emitter sixteen and detector 24 is spaced at a distance of r 2 . 18 and path 22 traverse skin layer 14 twice. Furthermore, as a result of paths 18 and 22 traverse pores and skin layer 14 using approximately the identical angle, the first distinction between paths 22 and 18 is the difference between length L 2 and length L 1 traversing subdermal layer 12, which is the tissue layer of interest. Therefore, it can be assumed that the difference in absorption between path L 2 and path L 1 is instantly attributable to subdermal layer 12, the tissue layer of curiosity, corresponding to the different spacings r 2 and r 1 . 12 could also be represented by l and the deeper path by means of the subdermal tissue by L 1 and L 2 , depending on which detector is considered.


Equation eight is equivalent to standard pulse oximetry if the second detector is eradicated. 16,20 (i.e. r 1 ) and the second emitter/detector pair 16,24 (i.e. r 2 ) needs to be larger than a number of occasions the pores and skin thickness (i.e. r 1 ,r 2 much higher than d) in order that the 4 occurrences of are all approximately equal, or a minimum of have equivalent counterparts influencing the 2 detectors. If the detectors are too close to each other, ⁇ FIG. 1B is a schematic diagram, just like FIG. 1A, displaying the current invention employing multiple emitters 16 and 17 and a single detector 24. Those of talent in the artwork will respect that the operation is just like that described above. FIG. 2 is a perspective view of the preferred mode of patient interface machine 26 employing the current invention. Planar surface 28 is positioned into contact with the pores and skin of the patient during monitoring and measurement.


If desirable, this place could also be maintained by way of adhesive or home SPO2 device different mechanical means identified in the art. Further, if fascinating, surface 28 may have a curvature, and could also be either flexible or inflexible. 16, detector 20, and detector 24 are as previously discussed. Wiring electrically couples emitter 16, detector BloodVitals tracker 20, and detector 24 to the circuitry which performs the monitoring capabilities. FIG. Three is a partially sectioned view displaying patient interface gadget 26 in operational position. Cable 32 conducts the electrical signals to and from the monitoring circuitry as described below. All other parts are as previously described. FIG. Four is a block diagram displaying your complete monitoring and BloodVitals tracker measurement system using the present invention. 36 and two wavelength driver 34 alternately turn on the purple and infrared LED's 16 at a desired chop frequency (e.g. 1,600 hz). CPU forty eight for calculating arterial oxygen saturation. PCT/US94/03546, the disclosure of which is included herein by reference. Alternate control electronics are identified within the artwork and could be used, if desired.