BLOOD ANALYSIS DEVICES, SYSTEMS AND METHODS

Abstract

Methods and apparatus are provided for non-invasive blood analysis. A blood analysis device (10, 30) comprises a housing (24) for receiving a human or animal body part or a container of blood. The housing (24, 32) comprises at least one wave emitter (18) for emitting an emitted wave to target blood, and at least one wave sensor (26) for sensing a response wave after the emitted wave has interacted with the target blood. The at least one wave sensor is configured to output at least one sense signal allowing a frequency spectrum of the emitted wave to be constructed.

Claims

1. A blood analysis device, comprising: at least one wave emitter for emitting an emitted wave to target blood, and at least one wave sensor for sensing a response wave after the emitted wave has interacted with the target blood, the at least one wave sensor configured to output at least one sense signal allowing a frequency spectrum of the emitted wave to be constructed.

2. The blood analysis device of claim 1, comprising a housing operatively associated with the at least one wave emitter and adapted to receive (i) a human or animal body part, or (ii) a container of blood.

3. The blood analysis device of claim 2, wherein the housing comprises a cuff for receiving a limb of a human or animal user.

4. The blood analysis of claim 2, wherein the housing comprises a receptacle for receiving and holding the container.

5. The blood analysis device of claim 1, wherein the emitted wave is an ultrasound wave.

6. The blood analysis device of claim 5, wherein the ultrasound wave is a broadband or multispectral wave.

7. The blood analysis device of claim 1, wherein the emitted wave is an electromagnetic wave.

8. The blood analysis device of claim 7, wherein the electromagnetic wave is a broadband or multispectral electromagnetic wave.

9. The blood analysis device of claim 1, wherein the at least one wave sensor comprises a hyperspectral image sensor.

10. The blood analysis device of claim 1, wherein the at least one wave emitter comprises a plurality of wave emitters and the at least one wave sensor comprises a plurality of wave sensors so that at least two pairs of wave emitters and wave sensors are oppositely arranged about the housing.

11. The blood analysis device of claim 1, wherein the at least one wave emitter comprises at least one ultrasound wave emitter and at least one electromagnetic wave emitter and the at least one wave sensor comprises at least one ultrasound sensor and at least one hyperspectral image sensor.

12. The blood analysis device of claim 1, wherein the at least one waver sensor is configured to output a spectral image of the target blood.

13. A blood analysis system comprising: a blood analysis device according to any preceding claim; at least one blood analyzer configured to receive the at least one sense signal and to perform a frequency spectrum analysis thereon and to determine at least one blood characteristic based on the frequency spectrum analysis.

14. The blood analysis system of claim 13, wherein the at least one blood characteristic comprises at least one of: HDL—High Density Lipoprotein Level; LDL—Low Density Lipoprotein Level; Ratio of HDL and LDL; CRP—C-Reactive Protein Level of inflammation with the body; CBC—Complete Blood Count; TSH—Thyroid-stimulating hormone level; INR—International Normalized Ratio; LFT—Liver Function Test; U+E—Urea and Electrolytes; CMP—Comprehensive Metabolic Panel; WBC—White Blood Cell Count; RBC—Red Blood Cell Count; HBC—Hemoglobin Level of hemoglobin molecules; HCT—Hematocrit Level; PLT—Platelets level; sodium, potassium, chloride, bicarbonate, blood urea nitrogen (BUN), magnesium, creatinine, glucose, and/calcium; Blood Cell characteristics; Blood Cell Wall Thickness; Blood Cell Quality; Blood Cell Quantity; Blood Cell Age; Blood Cell Damage; Blood Minerals; Immune Cells; Cancer Cells; Viruses; Bacteria; Blood Pressure; triglyceride levels; carbon dioxide and/or oxygen levels; and Blood Velocity.

15. The blood analysis system of claim 13, wherein the at least one blood analyzer comprises at least one computer processor and computer processor instructions for performing the frequency spectrum analysis.

16. The blood analysis system of claim 13, wherein the at least one blood analyzer is included in the housing, remotely or a combination thereof.

17. The blood analysis system of claim 13, wherein the at least one blood analyzer is configured to compare spectral readings of the at least one sense signal with at least one reference frequency spectrum signature corresponding to the at least one least one blood characteristic.

18. A blood analysis method, comprising: providing a blood analysis device, the blood analysis device comprising at least one wave emitter, and at least one wave sensor; emitting, with the at least one emitter, an emitted wave to target blood; sensing, with the at least one waver sensor, a response wave after the emitted wave has interacted with the target blood, wherein the at least one wave sensor outputs at least one spectral sense signal; and receiving, with at least one blood analyzer, the at least one spectral sense signal, performing a frequency spectrum analysis thereon and determining at least one blood characteristic based on the frequency spectrum analysis.

19. The blood analysis method of claim 18, wherein the blood analysis device comprises a housing operatively associated with the at least one wave emitter and adapted to receive (i) a human or animal body part, or (ii) a container of blood.

20. The blood analysis method of claim 19, wherein the housing comprises a cuff for receiving a limb of a human or animal user or wherein the housing comprises a receptacle for receiving and holding the container.

21-23. (canceled)

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0043] The present invention will hereinafter be described in conjunction with the following drawing figures, wherein like numerals denote like elements, and

[0044] FIGS. 1(a) to 1(g) are various views of a first blood analysis device, in accordance with various embodiments;

[0045] FIGS. 2(a) to 2(d) are various views of a second blood analysis device, in accordance with various embodiment;

[0046] FIG. 3(a) is a flow chart of a method of blood analysis, in accordance with various embodiments; and

[0047] FIG. 3(b) is a flow chart of another method of blood analysis, in accordance with various embodiments.

DETAILED DESCRIPTION

[0048] The following detailed description is merely exemplary in nature and is not intended to limit the invention or the application and uses of the invention. Furthermore, there is no intention to be bound by any theory presented in the preceding background or the following detailed description.

[0049] With reference to FIGS. 1 and 2, the present disclosure provides a blood analysis device 10, 30 that includes one or more imaging/sensing devices 18, 26 for imaging blood contained in a vial 28 or other container or in-vivo blood. In an embodiment according to FIG. 1, the blood analysis device 10 is operable to stand on a table or other surface and receive a vial 28 of blood for imaging. In another embodiment according to FIG. 2, the blood analysis device 30 forms a cuff and is operable to be wrapped around a limb, e.g. an arm, of a patient to image blood in-vivo. In these embodiments, blood is imaged, and the images are analyzed by an internal and/or external processing unit 22 including an image analyzer to determine blood characteristics. In embodiments, ultrasound, MRI and/or hyperspectral imaging is utilized. Imaging herein is used in a broad sense to refer to one or more sensing elements (e.g. a grid of pixels) for detecting ultrasound, electromagnetic or other waves and determining an intensity or other measurement thereof. Sensed measurements can be collected and compared with reference values forming a signature representing blood characteristics. Thus, the imaging can provide one or more measurement signatures for comparison with reference signatures.

[0050] Turning to FIGS. 1(a) to 1(g), an embodiment of a first blood analysis device 10 is shown. The blood analysis device 10 includes a housing 24, which is in a bucket shape in the exemplary embodiment. The housing 24 has a bottom configured for standing on a horizontal surface such as a table or a desk. The housing 24 includes a plurality of imaging/sensing devices 18. In particular, the imaging/sensing devices 18 include ultrasound transducers/emitters and ultrasound sensors. In the exemplary embodiment, three pairs of oppositely disposed imaging/sensing devices 18 are included. However, less or more imaging/sensing devices 18 could be included. The imaging/sensing devices 18 are circumferentially distributed about, and fixed to, the housing 24. The housing 24 further includes a different type of imaging/sensing device 26, which is a hyperspectral imaging device in the exemplary embodiment. By providing a combination of different types of imaging/sensing devices 18, 26, greater information on the target blood is available for subsequent analysis and blood characterization. Although a combination of ultrasound and hyperspectral imaging/sensing devices 18, 26 are disclosed in the present embodiment, other imaging/sensing medians are envisaged that allow blood properties to be determined such as miniature MRI devices and the like. In one embodiment, an inner space defined by the housing 24 is filled with solid silicone gel to reduce ultrasonic pressure wave impedance.

[0051] In embodiments, the hyperspectral imaging/sensing device 26 includes multiple led lights to assist hyperspectral imaging. The hyperspectral electromagnetic waves are captured by a hyperspectral camera for subsequent analysis. In embodiments, the processing unit 22 is configured to activate one ultrasound imaging/sensing device (transducer/emitter 18) to emit an ultrasound pressure wave and to sense the emitted wave using a plurality of the other ultrasound imaging/sensing devices (sensors 18) after the emitted wave has interacted with target blood in the vial 28. In this way, loss of ultrasound imaging information is minimized.

[0052] In the embodiment of FIGS. 1(a) to 1(g), the imaging/sensing devices 18, 26 are arranged on a frame 20 that supports the imaging devices and also allows imaging/sense data to be communicated there within to the processing unit 22. In some embodiments, the processing unit 22 is configured to receive and externally transmit captured imaging/sense data for external analysis. In other embodiments, the processing unit 22 is configured to analyze the captured imaging/sense data to determine blood characteristics. In embodiments, the processing unit 22 includes a microprocessor or other computer processor device and memory storing instructions thereon for controlling operation of the imaging/sensing devices 18, 26. In particular, the processing unit 22 is configured to activate the imaging/sensing devices 18, 26, to capture imaging/sense data and either to transmit the captured (and optionally pre-processed) imaging/sense data for blood analysis processing at an external blood analyzer or to analyze the imaging/sense data onboard to determine blood characteristics. In embodiments, blood analysis of the imaging/sense data includes comparing the images/sense data with a database of blood image/sense signatures to determining blood characteristics. In embodiments where ultrasound and/hyperspectral imaging/sensing is utilized, spectral components of the imaging/sense data are compared with spectral imaging/sense data stored in a reference database to characterize the blood.

[0053] The blood analysis device 10 of the exemplary embodiment of FIGS. 1(a) to 1(g) includes a cover 12 that allows the housing 24 to be closed during activation of the imaging/sensing devices 18, 26. In the illustrated exemplary embodiment, first and second covers 12a, 12b open and close by sliding atop housing 24. The specific mechanism shown is a sliding cooperation of brackets 14, 15 of the housing 24 and the cover 12 and a sliding cooperation of projection and guide 16, 17 between the housing 24 and the cover 12. Other cooperative structures for allowing the cover first and second covers 12a, 12b to slide away and towards one another when opening and closing are envisaged. Further, alternative opening and closing structures can be provided such as hinges to allow for a vertical opening and closing. In the exemplary embodiment of FIG. 1, the cover 12 opens and closes by manual operation. However, an electrified (e.g. motor operated) cover 12 is possible.

[0054] The blood analysis device 10 could include a (rechargeable) battery for supplying the imaging/sensing devices 18, 26 with power. Alternatively, a power cord socket could be included for the supply of electrical power.

[0055] With reference to FIGS. 2(a) to 2(d), an embodiment of a second blood analysis device 30 is illustrated. The blood analysis device 30 includes a housing 32 in the shape of a cuff for wrapping around a limb of a subject, such as the upper arm. The housing 32 includes first and second housing parts 48a, 48b that are connected at a hinge 42 to allow the housing 32 to open to receive the upper arm and to close about the upper arm. The housing 32 includes a latch 34 to hold the housing 32 in the closed configuration. The latch 34 includes a first arm 36 and a second arm 44 connected at the ends of respective housing parts 48a, 48b. The second arm 44 includes a plate 39 connected thereto and the plate 39 has a plurality of ribs 40 respectively defining differing degrees of closure of the housing 32 when engaged by the first arm 36. A release tab 41 is included on an outside of the plate 39 to facilitate release of the latch 34 to open the housing 32. Thus, the latch 34 has different latch positions (provided in one embodiment by ribs 40) so that the housing 32 can accommodate different size upper arms.

[0056] In embodiments, the housing 32 holds a plurality of imaging/sense devices 38, 46. In some embodiments, different types of imaging/sense devices 38, 46 are included in housing 32. In one exemplary embodiment, one or more ultrasound devices 38 are included and one or more hyperspectral imaging/sense devices 46 are included. MRI imaging and other suitable imaging/sense medians could be used. The imaging/sense devices 38, 46 are directed toward the inside of the cuff shaped housing to image/sense blood flowing within veins of a subject.

[0057] Although not shown in FIGS. 2(a) to 2(d), a processing unit is included in the housing 32 for controlling activation of the imaging/sense devices 38, 46 and for controlling capture of imaging/sense data. The processing unit is configured to process the imaging/sense data to determine blood characteristics or to transmit the captured imaging/sense data (optionally after pre-processing) to an external processor for analysis to determine blood characteristics. Further, the blood analysis device 30 includes a battery (e.g. a rechargeable battery) for supplying power to the imaging/sense devices 38, 46 and the processing unit.

[0058] FIG. 3 is a flow chart of one exemplary operation of the blood analysis devices 10, 30 described herein.

[0059] Steps 100 and 102 are concerned with the blood analysis device 10 of FIG. 1. In step 100, a bar code on the vial or test tube 28 is scanned by a bar code scanner (not shown), which can be internal to the blood analysis device 10 or a peripheral device. Other ways of uniquely identifying vial 28 are envisaged such as QR codes, and alphanumeric serial codes. In step 102, the vial 28 containing target blood is inserted into a receptacle defined by silicone gel included within the housing 24. Thus, the cover 12 is slid horizontally open with respect to the housing 24. For the blood analysis device 30 of FIG. 2, steps 100 and 102 are replaced with placing the housing 32 about the arm or leg of a subject and engaging the latch 34 at a latch position corresponding to a snug fit of the housing 32 to the subject body part. The remaining steps of the flow chart of FIG. 3 are common to both blood analysis devices 10. 30.

[0060] Step 104 includes activating the imaging/sensing devices 18, 26, 38, 46. In some embodiments, activating the imaging/sensing devices 18, 26, 38, 46 includes emitting ultrasonic waves from one or more ultrasonic imaging/sensing devices 18, 38 in sub-step 104a. Additionally or alternatively, activating the imaging/sensing devices 18, 26, 38, 46 includes emitting electromagnetic radiation hyperspectral imaging devices 26, 46 in sub-step 104b. In step 106 imaging/sense data of target blood is captured with a sensor 18, 26, 38, 46. In some embodiments, capturing imaging/sense data includes step 106b capturing hyperspectral data that has interacted with blood using hyperspectral imaging camera/sensor 26, 46. Additionally or alternatively, ultrasonic pressure waves that have interacted with target blood is detected using ultrasonic sensor/camera 18, 38 in step 106b. In step 108, plural imaging/sensing devices 18, 26, 38, 46 are sequentially activated and imaging data is captured from one or more image sensing devices 18, 26, 38, 46.

[0061] In step 110, the imaging data that has been captured in foregoing steps is processed. In one embodiment, step 110 includes transmitting the captured image/sense data to an external processor or performing processing using processing unit 22. Transmission of imaging/sense data can use wifi, Bluetooth, Zigbee or any other data transmission scheme. Processing is performed on the captured image/sense data. In one example, spectrally focused (e.g. narrowband focused) imaging/sense data is identified that corresponds to known signatures for blood characteristics. One or more spectral filters may be used to spectrally focus the captured imaging data. In embodiments processing step 110 results in multiple spectrally focused imaging/sense data components corresponding to known signatures of blood characteristics. For example, step 110 includes providing normalized intensity values at different frequency points in the measured data for comparison in step 112 (described below) with reference values corresponding a signature for a particular blood characteristic.

[0062] In step 112, spectrally focused imaging data is compared to reference signature data obtained from reference database 111 (which may be updated from the cloud 113 periodically). That is, reference image/sense signatures including data points at a plurality of specific frequencies (e.g. narrowband signatures) are compared to imaging/sense data from step 110 having data points at corresponding specific frequencies to determine matching data that is indicative of blood characteristics. In this way, blood characteristics as described herein are determined in step 116.

[0063] In step 118, the blood analysis results from step 116 are stored and reported. In one example, a cloud-based results database is accessed to retrieve the blood analysis, for example using a unique code associated with the patient or the vial 28 (e.g. as obtained from the bar code). In embodiments, the blood analysis report is printed on physical medium or displayed on a screen.

[0064] FIG. 3(b) illustrates another exemplary embodiment of blood analysis using an MRI method. MRI data capture could be used additionally or alternatively to the ultrasound or hyperspectral sensing methods described above with respect to FIG. 3(a). The method is largely the same as that described with respect to FIG. 3(a). As such, the process will not be further described expect with regard to steps 104′, 106′ 110′ and 112′. In these steps, MRI data capture (step 106′) is used on target blood in a vial or in a limb of a patient. Different aspects (e.g. measurements at different frequency combinations) of the MRI data are grouped into measurement signatures for comparison with reference signatures in steps 110′ and 112′ to determine values for respective blood characteristics. Thus, blood analysis values are determined in step 116′ and reported in step 118′.

[0065] In a non-illustrated embodiment there is disclosed a blood analysis device for use in a doctor's waiting room and adapted to perform diagnostics on patients in the waiting room. The blood analysis device may for example be placed on a reception desk or mounted to a wall. The blood analysis device includes at least one wave emitter for emitting an emitted wave to a patient (target blood) and at least one wave sensor, here a hyperspectral image sensor for sensing a response wave after the emitted wave has interacted with the patient in the waiting room. The at least one wave sensor is configured to output at least one sense signal allowing a frequency spectrum of the emitted wave to be constructed. In this embodiment blood of a patient is imaged, and the images are analyzed by a processing unit including an image analyzer to determine blood characteristics. In this embodiment hyperspectral imaging is utilized to detect waves and determining an intensity or other measurement thereof. Such sensed measurements are collected and compared with reference values forming a signature representing blood characteristics. Thus, the imaging can provide one or more measurement signatures for comparison with reference signatures making it possible to detect diseases while a patient is waiting in the waiting room. It will be appreciated that use of the blood analysis device need not be limited to doctors' waiting rooms but could be employed in public spaces and be employed for detecting diseases in animals.

[0066] While at least one exemplary aspect has been presented in the foregoing detailed description of the invention, it should be appreciated that a vast number of variations exist. It should also be appreciated that the exemplary aspect or exemplary aspects are only examples, and are not intended to limit the scope, applicability, or configuration of the invention in any way. Rather, the foregoing detailed description will provide those skilled in the art with a convenient road map for implementing an exemplary aspect of the invention. It being understood that various changes may be made in the function and arrangement of elements described in an exemplary aspect without departing from the scope of the invention as set forth in the appended claims.