OPTICAL DETERMINATION OF BLOOD PERFUSION AND SIMILAR PARAMETERS

• US 20130053654A1
• Filed: 02/26/2010
• Published: 02/28/2013
• Est. Priority Date: 02/26/2010
• Status: Active Grant

• Current Assignee: Biosigns Pte Limited
• Original Assignee: Biovotion AG (Biofourmis AG)
• Inventors: Krebs, Hans-Joachim, Talary, Mark Stuart, Caduff, Andreas, Zakharov, Pavel
• Granted Patent: US 9,549,695 B2
• Time in Patent Office: Days
• US Class Current: 600/301
• CPC Class Codes: A61B 5/01 Measuring temperature of body parts ; Diagnostic temperature sensing, e.g. for malignant or inflamed tissue clinical contact thermometers G01K13/20
• CPC Class Codes: A61B 5/1455 using optical sensors, e.g. spectral photometrical oximeters
• CPC Class Codes: A61B 5/14552 Details of sensors specially adapted therefor
• CPC Class Codes: A61B 5/1491 Heated applicators
• CPC Class Codes: A61B 5/441 Skin evaluation, e.g. for skin disorder diagnosis

Abstract

A parameter affecting the absorptivity or the concentration of blood in tissue is measured using a semiconductor light source (7) and a light detector (8). The semiconductor light source (7) is operated at several operating conditions, at which it has different temperatures and therefore different emission spectra. In particular, the operating conditions correspond to different time intervals after switching the light source (7) on, while the light source (7) has not yet reached thermal equilibrium. This allows to perform a spectroscopic measurement using one light source only, which increases accuracy and reduces device cost.

Claims

1. A method for measuring at least one physiological parameter of tissue by means of a semiconductor light source (7) and of a light detector (8), wherein said parameter affects concentration of blood constituents, in particular different forms of hemoglobin, said method comprising the steps of

a) placing said light source (7) and said light detector (8) such that said light detector (8) measures an amount of light transmitted from said light source (7) through said tissue,

b) operating said light source (7) under a first condition where it has a first temperature, and determining a first light attenuation signal by means of said light detector (8),

c) operating said light source (7) under a second condition where it has a second temperature different from the first temperature, and determining a second light attenuation signal by means of said light detector (8),

d) determining said parameter using said first light attenuation signal and said second light attenuation signal.

2. The method of claim 1 comprising the step of varying a current through said light source (7) in order to create said different operating conditions.

3. The method of claim 2 comprising the step of switching said current from a first level to a second, different level and determining at least part of said attenuation signals at different times after switching said current while said light source (7) has not yet reached thermal equilibrium, and in particular wherein at least part of said attenuation signals are determined within 1 second from switching said current, in particular within 100 milliseconds.

4. The method of claim 1 further comprising the step of determining said parameter by calculating a difference between the first and the second light attenuation signals and/or the step of deriving said parameter from said attenuation signals using calibration data.

5. The method of claim 1 wherein said parameter is blood perfusion or any parameter depending on blood perfusion.

6. The method of claim 1 wherein said steps b) and c) are repeated for recording a time series of data, wherein a heart beat rate is derived from said time series of data.

7. The method of claim 1 comprising the step of operating said light source (7) under N conditions where it has N different temperatures and measuring an attenuation signal at each condition, wherein N>

2.

8. The method of claim 1 wherein for each operating condition said attenuation signal is determined by measuring an intensity signal by means of said light detector (8) and dividing said intensity signal by a reference signal (P_r), wherein the reference signal (P_r) corresponds to an intensity signal measured by said light detector (8) if the light from said light source (7) operating under said operating condition is reflected into said light detector (8) by means of a body whose reflectivity does not depend on the wavelength of said light source (7).

9. The method of claim 1 wherein said parameter is determined using said attenuation signals and calibration data, wherein said calibration data was obtained in a calibration procedure, which calibration procedure comprises the steps of

performing a series of calibration measurements for different states of said tissue and, for each calibration measurement, recording said attenuation signals by means of said light detector (8) and recording a value of said parameter by means of a reference method,

using multiple regression for determining said calibration data with the recorded attenuation signals being independent variables and the recorded values of said parameter being a dependent variable.

10. The method of claim 1 further comprising the step of measuring a skin temperature (T_S) of said tissue and using said skin temperature (T_S) for determining said parameter.

11. The method of claim 9 further comprising the step of using said skin temperature (T_S) as an independent variable during said multiple regression.

12. The method of claim 1 further comprising the step of monitoring light intensity signal emitted by the light source (2), in particular by means of a temperature sensor or light sensor (19), and scaling a signal from said light sensor (8) by means of said monitored light intensity signal (α

).

14. The method of claim 1 wherein said parameter is indicative of a ratio between oxygenated and non-oxygenated hemoglobin in said tissue.

15. The method of claim 1 wherein said light source (7) has a mean wavelength between 530 and 550 nm or between 560 and 580 nm, and/or wherein said light source (7) emits

between 530 and 550 nm and has a spectral half-width not larger than 20 nm, in particular not larger than 10 nm, or

between 560 and 580 nm and has a spectral half-width not larger than 20 nm, in particular not larger than 10 nm.

16. The method of claim 1, wherein said light source (7) has a mean wavelength between 520 and 540 nm or between 580 and 600 nm.

17. The method of claim 1 wherein said light source (7) is a LED or a laser diode.

19. The device of claim 18 wherein said device is adapted to carry out the method of claim 1.

13. The method of claim and 12 further comprising the step of using said monitoring signal as an independent variable during said multiple regression

18. A device for measuring in-vivo at lest one physiological parameter of tissue comprising

a housing (1) to be placed against said tissue,

a semiconductor light source (7) arranged in said housing,

a light detector (8) positioned to measure light transmitted from said light source transmitted through said tissue,

a control unit (14) for

operating said light source (7) under a first condition where it has a first temperature, and determining a first attenuation signal by means of said light detector (8),

operating said light source (7) under a second condition where it has a second temperature different from the first temperature, and determining a second attenuation signal by means of said light detector (8),

determining said parameter using said first signal and said second attenuation signal.