Claims
- 1. In combination, an instrument for determining a coagulation characteristic of blood, a blood fraction or a control comprising a radiation-reflective surface, a first source for irradiating the surface, and a first detector for detecting radiation reflected from the surface, and a cuvette for holding a sample of the blood, blood fraction or control the coagulation characteristic of which is to be determined, the cuvette having two opposed walls substantially transparent to the source radiation and reflected radiation, the first source and first detector being disposed adjacent a first one of said two opposed walls and the radiation reflective surface being disposed adjacent a second of said two opposed walls.
- 2. The combination of claim 1 wherein the instrument further comprises a second source for irradiating the cuvette and a second detector for detecting when a sample has been applied to a sample application point in the cuvette, the second detector detecting radiation from the second radiation source transmitted through one of said two opposed walls of the cuvette, reflected and transmitted back through said one wall to the second detector.
- 3. The combination of claim 1 or 2 and further comprising a third source for irradiating the surface, the first detector detecting radiation from the third source reflected from the surface, the third source positioned to transmit radiation through said two opposed walls for reflection by the surface and transmission back through said two opposed walls to the first detector to indicate whether a sample has reached a first point in the cuvette.
- 4. The combination of claim 3 and further comprising a fourth source for irradiating the surface, the first detector detecting radiation from the fourth source reflected from the surface, the fourth source positioned to transmit radiation through said two opposed walls for reflection by the surface and transmission back through said two opposed walls to the first detector to indicate whether a sample has reached a second point in the cuvette.
- 5. The combination of claim 4 wherein the second point is downstream in the spread of the sample from the first point and the first point is downstream in the spread of the sample from the sample application point.
- 6. The combination of claim 1 or 2 and further comprising a heater for maintaining the blood, blood fraction or control at a desired temperature, means for mounting the heater adjacent the surface, means for providing power to the heater and means for monitoring the surface temperature and for feeding the monitored temperature back to the means for providing power to the heater.
- 7. The combination of claim 6 wherein the heater comprises an electrically resistive foil, the surface comprises a first radiation reflective surface of a tile, the tile further comprising a second surface opposite the first surface thereof, and means for mounting the electrically resistive foil to the second surface of the tile.
- 8. The combination of claim 1 or 2 wherein the instrument determines the coagulation characteristic by combining fluid blood, blood fraction or control with particles which are affected by a magnetic field so that the particles become suspended relatively freely in the fluid, the instrument further comprising means for generating a time-varying magnetic field for causing the particles to be reoriented as the magnetic field varies, with the reorientation changing as the fluid coagulates owing to the fluid's changing viscosity, and means for mounting the means for generating the time-varying magnetic field adjacent the surface.
- 9. The combination of claim 1 or 2 wherein the cuvette comprises a region for bearing a code, the instrument further comprising one or more fifth radiation sources for irradiating the code bearing region, one or more third detectors for detecting the transmission of radiation through the code bearing region, the fifth radiation source or sources and third detector or detectors mounted adjacent the code bearing region to detect the code.
- 10. The combination of claim 9 wherein there are multiple fifth radiation sources and a single third detector, the third detector having an active region which extends adjacent the code bearing region to detect the transmission of radiation from all of said fifth radiation sources, and means for activating the fifth radiation sources in a predetermined sequence to permit the detection and determination of the code borne by the code bearing region.
- 11. The combination of claim 3 wherein the cuvette comprises a region for bearing a code, the instrument further comprising one or more fifth radiation sources for irradiating the code bearing region, one or more third detectors for detecting the transmission of radiation through the code bearing region, the fifth radiation source or sources and third detector or detectors mounted adjacent the code bearing region to detect the code.
- 12. The combination of claim 11 wherein there are multiple fifth radiation sources and a single third detector, the third detector having an active region which extends adjacent the code bearing region to detect the transmission of radiation from all of said fifth radiation sources, and means for activating the fifth radiation sources in a predetermined sequence to permit the detection and determination of the code borne by the code bearing region.
- 13. The combination of claim 4 wherein the cuvette comprises a region for bearing a code, the instrument further comprising one or more fifth radiation sources for irradiating the code bearing region, one or more third detectors for detecting the transmission of radiation through the code bearing region, the fifth radiation source or sources and third detector or detectors mounted adjacent the code bearing region to detect the code.
- 14. The combination of claim 13 wherein there are multiple fifth radiation sources and a single third detector, the third detector having an active region which extends adjacent the code bearing region to detect the transmission of radiation from all of said fifth radiation sources, and means for activating the fifth radiation sources in a predetermined sequence to permit the detection and determination of the code borne by the code bearing region.
- 15. The combination of claim 5 wherein the cuvette comprises a region for bearing a code, the instrument further comprising one or more fifth radiation sources for irradiating the code bearing region, one or more third detectors for detecting the transmission of radiation through the code bearing region, the fifth radiation source or sources and third detector or detectors mounted adjacent the code bearing region to detect the code.
- 16. The combination of claim 15 wherein there are multiple fifth radiation sources and a single third detector, the third detector having an active region which extends adjacent the code bearing region to detect the transmission of radiation from all of said fifth radiation sources, and means for activating the fifth radiation sources in a predetermined sequence to permit the detection and determination of the code borne by the code bearing region.
- 17. The combination of claim 11 and further comprising a heater for maintaining the blood, blood fraction or control at a desired temperature, means for mounting the heater adjacent the surface, means for providing power to the heater and means for monitoring the surface temperature and for feeding the monitored temperature back to the means for providing power to the heater.
- 18. The combination of claim 17 wherein the heater comprises an electrically resistive foil, the surface comprises a first radiation reflective surface of a tile, the tile further comprising a second surface opposite the first surface thereof, and means for mounting the electrically resistive foil to the second surface of the tile.
- 19. The combination of claim 11 wherein the instrument determines the coagulation characteristic by combining fluid blood, blood fraction or control with particles which are affected by a magnetic field so that the particles become suspended relatively freely in the fluid, the instrument further comprising means for generating a time-varying magnetic field for causing the particles to be reoriented as the magnetic field varies, with the reorientation changing as the fluid coagulates owing to the fluid's changing viscosity, and means for mounting the means for generating the time-varying magnetic field adjacent the surface.
- 20. The combination of claim 13 and further comprising a heater for maintaining the blood, blood fraction or control at a desired temperature, means for mounting the heater adjacent the surface, means for providing power to the heater and means for monitoring the surface temperature and for feeding the monitored temperature back to the means for providing power to the heater.
- 21. The combination of claim 20 wherein the heater comprises an electrically resistive foil, the surface comprises a first radiation reflective surface of a tile, the tile further comprising a second surface opposite the first surface thereof, and means for mounting the electrically resistive foil to the second surface of the tile.
- 22. The combination of claim 13 wherein the instrument determines the coagulation characteristic by combining fluid blood, blood fraction or control with particles which are affected by a magnetic field so that the particles become suspended relatively freely in the fluid, the instrument further comprising means for generating a time-varying magnetic field for causing the particles to be reoriented as the magnetic field varies, with the reorientation changing as the fluid coagulates owing to the fluid's changing viscosity, and means for mounting the means for generating the time-varying magnetic field adjacent the surface.
- 23. The combination of claim 15 and further comprising a heater for maintaining the blood, blood fraction or control at a desired temperature, means for mounting the heater adjacent the surface, means for providing power to the heater and means for monitoring the surface temperature and for feeding the monitored temperature back to the means for providing power to the heater.
- 24. The combination of claim 23 wherein the heater comprises an electrically resistive foil, the surface comprises a first radiation reflective surface of a tile, the tile further comprising a second surface opposite the first surface thereof, and means for mounting the electrically resistive foil to the second surface of the tile.
- 25. The combination of claim 15 wherein the instrument determines the coagulation characteristic by combining fluid blood, blood fraction or control with particles which are affected by a magnetic field so that the particles become suspended relatively freely in the fluid, the instrument further comprising means for generating a time-varying magnetic field for causing the particles to be reoriented as the magnetic field varies, with the reorientation changing as the fluid coagulates owing to the fluid's changing viscosity, and means for mounting the means for generating the time-varying magnetic field adjacent the surface.
- 26. The combination of claim 9 and further comprising a user-insertable key having non-volatile memory containing data representative of instrument operating parameters, a port for receiving the key, means for comparing the code to the data representative of instrument operating parameters contained on the user-insertable key, and means for disabling the instrument if the comparison of the code and the data representative of instrument operating parameters contained on the user-insertable key is unfavorable.
- 27. The combination of claim 10 and further comprising a user-insertable key having non-volatile memory containing data representative of instrument operating parameters, a port for receiving the key, means for comparing the code to the data representative of instrument operating parameters contained on the user-insertable key, and means for disabling the instrument if the comparison of the code and the data representative of instrument operating parameters contained on the user-insertable key is unfavorable.
- 28. The combination of claim 11 and further comprising a user-insertable key having nonvolatile memory containing data representative of instrument operating parameters, a port for receiving the key, means for comparing the code to the data representative of instrument operating parameters contained on the user-insertable key, and means for disabling the instrument if the comparison of the code and the data representative of instrument operating parameters contained on the user-insertable key is unfavorable.
- 29. The combination of claim 12 and further comprising a user-insertable key having non-volatile memory containing data representative of instrument operating parameters, a port for receiving the key, means for comparing the code to the data representative of instrument operating parameters contained on the user-insertable key, and means for disabling the instrument if the comparison of the code and the data representative of instrument operating parameters contained on the user-insertable key is unfavorable.
- 30. The combination of claim 13 and further comprising a user-insertable key having non-volatile memory containing data representative of instrument operating parameters, a port for receiving the key, means for comparing the code to the data representative of instrument operating parameters contained on the user-insertable key, and means for disabling the instrument if the comparison of the code and the data representative of instrument operating parameters contained on the user-insertable key is unfavorable.
- 31. The combination of claim 14 and further comprising a user-insertable key having non-volatile memory containing data representative of instrument operating parameters, a port for receiving the key, means for comparing the code to the data representative of instrument operating parameters contained on the user-insertable key, and means for disabling the instrument if the comparison of the code and the data representative of instrument operating parameters contained on the user-insertable key is unfavorable.
- 32. The combination of claim 15 and further comprising a user-insertable key having non-volatile memory containing data representative of instrument operating parameters, a port for receiving the key, means for comparing the code to the data representative of instrument operating parameters contained on the user-insertable key, and means for disabling the instrument if the comparison of the code and the data representative of instrument operating parameters contained on the user-insertable key is unfavorable.
- 33. The combination of claim 16 and further comprising a user-insertable key having non-volatile memory containing data representative of instrument operating parameters, a port for receiving the key, means for comparing the code to the data representative of instrument operating parameters contained on the user-insertable key, and means for disabling the instrument if the comparison of the code and the data representative of instrument operating parameters contained on the user-insertable key is unfavorable.
- 34. A method for determining a coagulation characteristic of blood, a blood fraction or a control comprising irradiating a radiation-reflective surface through a cuvette for holding a sample of the blood, blood fraction or control the coagulation characteristic of which is to be determined using a first radiation source, and detecting radiation reflected from the surface using a first radiation detector, the cuvette having two opposed walls substantially transparent to the source radiation and reflected radiation.
- 35. A method of determining whether a fluid sample applied to a surface is a sample of a more readily flowable first fluid or a sample of a less readily flowable second fluid, the method comprising the steps of irradiating the surface at a first point, detecting the radiation from the first point, determining from the detected radiation when the sample has reached the first point, irradiating the surface at a second point downstream in the flow path of the fluid sample from the first point, detecting the radiation from the second point, determining from the detected radiation when the sample has reached the second point, establishing a threshold time, and comparing the time between when the sample is determined to have reached the first point and when the sample is determined to have reached the second point to the threshold time.
- 36. The method of claim 35 wherein the first fluid comprises a control and the second fluid comprises a blood fraction.
- 37. The method of claim 36 wherein the second fluid comprises blood.
- 38. A method of immunizing an instrument which determines a coagulation characteristic of blood, a blood fraction or a control against noise, the instrument including a surface upon which a user deposits a sample of blood, a blood fraction or control the coagulation characteristic of which is to be determined, the instrument irradiating the sample and detecting radiation from the sample to determine the coagulation characteristic, the method comprising the steps of monitoring the detected radiation a first time to determine if the detected radiation is increasing or decreasing, forming a first change in detected radiation from said first monitoring, subsequently monitoring the detected radiation a second time to determine if the detected radiation is increasing or decreasing, forming a second change in detected radiation from said second monitoring, establishing a first threshold, establishing a second threshold, comparing the first change to the first threshold, comparing the second change to the first threshold, if the magnitudes of both the first and second changes are greater than the first threshold, comparing the detected change in radiation to the second threshold, and determining the coagulation characteristic if the magnitudes of the first and second changes are greater than the first threshold and the detected change is greater than the second threshold.
Parent Case Info
[0001] This is a related application to U.S. Ser. No. ______, titled ANALOG HEATER-CONTROL FOR MEDICAL INSTRUMENT, U.S. Ser. No. ______, titled POWER SUPPLY MONITOR AND CONTROL FOR MEDICAL INSTRUMENT, U.S. Ser. No. ______, titled MAGNETIC SYSTEM FOR MEDICAL INSTRUMENT, U.S. Ser. No. ______, titled REAGENT AND METHOD OF ITS USE, and U.S. Ser. No. ______, titled METHOD AND APPARATUS FOR OPERATING A MEDICAL INSTRUMENT, all filed on the same date as this application and assigned to the same assignee, the disclosure of which is incorporated herein by reference.
Continuations (1)
|
Number |
Date |
Country |
Parent |
09724133 |
Nov 2000 |
US |
Child |
10357934 |
Feb 2003 |
US |