US20140323825A1 - Systems and methods for acquiring calibration data usable in a pulse oximeter - Google Patents

Abstract

The present disclosure includes a pulse oximeter attachment having an accessible memory. In one embodiment, the pulse oximeter attachment stores calibration data, such as, for example, calibration data associated with a type of a sensor, a calibration curve, or the like. The calibration data is used to calculate physiological parameters of pulsing blood.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS
• This application is a continuation of U.S. patent application Ser. No. 13/196,732 filed Aug. 2, 2011, entitled “Systems And Methods For Acquiring Calibration Data Usable In A Pulse Oximeter,” which is a continuation of U.S. patent application Ser. No. 11/431,151, filed May 8, 2006, entitled “Systems and Methods for Acquiring Calibration Data Usable In A Pulse Oximeter,” now U.S. Pat. No. 7,991,446, which is a continuation of U.S. patent application Ser. No. 10/420,994 filed Apr. 22, 2003, entitled “Systems and Methods for Acquiring Calibration Data Usable In A Pulse Oximeter,” now U.S. Pat. No. 7,428,432, which is a continuation of U.S. patent application Ser. No. 10/153,263, filed May 21, 2002, entitled “System And Method For Altering A Display Mode Based On A Gravity-Responsive Sensor,” which is a continuation of U.S. patent application Ser. No. 09/516,110, filed Mar. 1, 2000, entitled “Universal/Upgrading Pulse Oximeter,” now U.S. Pat. No. 6,584,336, which is a continuation of U.S. patent application Ser. No. 09/491,175, filed Jan. 25, 2000, entitled “Universal/Upgrading Pulse Oximeter,” now abandoned, which claims the benefit of U.S. Provisional Application No. 60/161,565, filed Oct. 26, 1999, entitled “Improved Universal/Upgrading Pulse Oximeter, and Application No. 60/117,097, filed Jan. 25, 1999, entitled “Universal/Upgrading Pulse Oximeter.” Each of the foregoing applications is incorporated by reference herein.
BACKGROUND OF THE DISCLOSURE
• Oximetry is the measurement of the oxygen level status of blood. Early detection of low blood oxygen level is critical in the medical field, for example in critical care and surgical applications, because an insufficient supply of oxygen can result in brain damage and death in a matter of minutes. Pulse oximetry is a widely accepted noninvasive procedure for measuring the oxygen saturation level of arterial blood, an indicator of oxygen supply. A pulse oximetry system consists of a sensor applied to a patient, a pulse oximeter, and a patient cable connecting the sensor and the pulse oximeter.
• The pulse oximeter may be a standalone device or may be incorporated as a module or built-in portion of a multiparameter patient monitoring system, which also provides measurements such as blood pressure, respiratory rate and EKG. A pulse oximeter typically provides a numerical readout of the patient's oxygen saturation, a numerical readout of pulse rate, and an audible indicator or “beep” that occurs in response to each pulse. In addition, the pulse oximeter may display the patient's plethysmograph, which provides a visual display of the patient's pulse contour and pulse rate.
SUMMARY
• FIG. 1 illustrates a priorart pulse oximeter100 and associatedsensor110. Conventionally, apulse oximetry sensor110 hasLED emitters112, typically one at a red wavelength and one at an infrared wavelength, and aphotodiode detector114. Thesensor110 is typically attached to an adult patient's finger or an infant patient's foot. For a finger, thesensor110 is configured so that theemitters112 project light through the fingernail and through the blood vessels and capillaries underneath. TheLED emitters112 are activated bydrive signals122 from thepulse oximeter100. Thedetector114 is positioned at the fingertip opposite the fingernail so as to detect the LED emitted light as it emerges from the finger tissues. The photodiode generatedsignal124 is relayed by a cable to thepulse oximeter100.
• Thepulse oximeter100 determines oxygen saturation (SpO₂) by computing the differential absorption by arterial blood of the two wavelengths emitted by thesensor110. Thepulse oximeter100 contains asensor interface120, an SpO₂processor130, aninstrument manager140, adisplay150, an audible indicator (tone generator)160 and akeypad170. Thesensor interface120 providesLED drive current122 that alternately activates the sensor red andIR LED emitters112. Thesensor interface120 also has input circuitry for amplification and filtering of thesignal124 generated by thephotodiode detector114, which corresponds to the red and infrared light energy attenuated from transmission through the patient tissue site. The SpO₂processor130 calculates a ratio of detected red and infrared intensities, and an arterial oxygen saturation value is empirically determined based on that ratio. Theinstrument manager140 provides hardware and software interfaces for managing thedisplay150,audible indicator160 andkeypad170. Thedisplay150 shows the computed oxygen status, as described above. Theaudible indicator160 provides the pulse beep as well as alarms indicating desaturation events. Thekeypad170 provides a user interface for such things as alarm thresholds, alarm enablement, and display options.
• Computation of SpO₂relies on the differential light absorption of oxygenated hemoglobin, HbO₂, and deoxygenated hemoglobin, Hb, to determine their respective concentrations in the arterial blood. Specifically, pulse oximetry measurements are made at red and IR wavelengths chosen such that deoxygenated hemoglobin absorbs more red light than oxygenated hemoglobin, and, conversely, oxygenated hemoglobin absorbs more infrared light than deoxygenated hemoglobin, for example 660 nm (red) and 905 nm (IR).
• To distinguish between tissue absorption at the two wavelengths, the red andIR emitters112 are provideddrive current122 so that only one is emitting light at a given time. For example, theemitters112 may be cycled on and off alternately, in sequence, with each only active for a quarter cycle and with a quarter cycle separating the active times. This allows for separation of red and infrared signals and removal of ambient light levels by downstream signal processing. Because only asingle detector114 is used, it responds to both the red and infrared emitted light and generates a time-division-multiplexed (“modulated”)output signal124. This modulatedsignal124 is coupled to the input of thesensor interface120.
• In addition to the differential absorption of hemoglobin derivatives, pulse oximetry relies on the pulsatile nature of arterial blood to differentiate hemoglobin absorption from absorption of other constituents in the surrounding tissues. Light absorption between systole and diastole varies due to the blood volume change from the inflow and outflow of arterial blood at a peripheral tissue site. This tissue site might also comprise skin, muscle, bone, venous blood, fat, pigment, etc., each of which absorbs light. It is assumed that the background absorption due to these surrounding tissues is invariant and can be ignored. Thus, blood oxygen saturation measurements are based upon a ratio of the time-varying or AC portion of the detected red and infrared signals with respect to the time-invariant or DC portion:
• 
  RD/IR=(Red_AC/Red_DC)/(IR_AC/IR_DC).
• The desired SpO₂measurement is then computed from this ratio. The relationship between RD/IR and SpO₂is most accurately determined by statistical regression of experimental measurements obtained from human volunteers and calibrated measurements of oxygen saturation. In a pulse oximeter device, this empirical relationship can be stored as a “calibration curve” in a read-only memory (ROM) look-up table so that SpO₂can be directly read-out of the memory in response to input RD/IR measurements.
• Pulse oximetry is the standard-of-care in various hospital and emergency treatment environments. Demand has lead to pulse oximeters and sensors produced by a variety of manufacturers. Unfortunately, there is no standard for either performance by, or compatibility between, pulse oximeters or sensors. As a result, sensors made by one manufacturer are unlikely to work with pulse oximeters made by another manufacturer. Further, while conventional pulse oximeters and sensors are incapable of taking measurements on patients with poor peripheral circulation and are partially or fully disabled by motion artifact, advanced pulse oximeters and sensors manufactured by the assignee of the present disclosure are functional under these conditions. This presents a dilemma to hospitals and other caregivers wishing to upgrade their patient oxygenation monitoring capabilities. They are faced with either replacing all of their conventional pulse oximeters, including multiparameter patient monitoring systems, or working with potentially incompatible sensors and inferior pulse oximeters manufactured by various vendors for the pulse oximetry equipment in use oat the installation.
• Hospitals and other caregivers are also plagued by the difficulty of monitoring patients as they are transported from one setting to another. For example, a patient transported by ambulance to a hospital emergency room will likely be unmonitored during the transition from ambulance to the ER and require the removal and replacement of incompatible sensors in the ER. A similar problem is faced within a hospital as a patient is moved between surgery, ICU and recovery settings. Incompatibility and transport problems are exacerbated by the prevalence of expensive and non-portable multi-parameter patient monitoring systems having pulse oximetry modules as one measurement parameter.
• The Universal/Upgrading Pulse Oximeter (UPO) according to the present disclosure is focused on solving these performance, incompatibility and transport problems. The UPO provides a transportable pulse oximeter that can stay with and continuously monitor the patient as they are transported from setting to setting. Further, the UPO provides a synthesized output that drives the sensor input of other pulse oximeters. This allows the UPO to function as a universal interface that matches incompatible sensors with other pulse oximeter instruments. Further, the UPO acts as an upgrade to existing pulse oximeters that are adversely affected by low tissue perfusion and motion artifact Likewise, the UPO can drive a SpO₂sensor input of multiparameter patient monitoring systems, allowing the UPO to integrate into the associated multiparameter displays, patient record keeping systems and alarm management functions.
• One aspect of the present disclosure is a measurement apparatus comprising a sensor, a first pulse oximeter and a waveform generator. The sensor has at least one emitter and an associated detector configured to attach to a tissue site. The detector provides an intensity signal responsive to the oxygen content of arterial blood at the tissue site. The first pulse oximeter is in communication with the detector and computes an oxygen saturation measurement based on the intensity signal. The waveform generator is in communication with the first pulse oximeter and provides a waveform based on the oxygen saturation measurement. A second pulse oximeter is in communication with the waveform generator and displays an oxygen saturation value based on the waveform. The waveform is synthesized so that the oxygen saturation value is generally equivalent to the oxygen saturation measurement.
• In another aspect of the present disclosure, a measurement apparatus comprises a first sensor port connectable to a sensor, an upgrade port, a signal processor and a waveform generator. The upgrade port is connectable to a second sensor port of a physiological monitoring apparatus. The signal processor is configured to compute a physiological measurement based on a signal input to the first sensor port. The waveform generator produces a waveform based on the physiological measurement, and the waveform is available at the upgrade port. The waveform is adjustable so that the physiological monitoring apparatus displays a value generally equivalent to the physiological measurement when the upgrade port is attached to the second sensor port.
• Yet another aspect of the present disclosure is a measurement method comprising the steps of sensing an intensity signal responsive to the oxygen content of arterial blood at a tissue site and computing an oxygen saturation measurement based on the intensity signal. Other steps are generating a waveform based on the oxygen saturation measurement and providing the waveform to the sensor inputs of a pulse oximeter so that the pulse oximeter displays an oxygen saturation value generally equivalent to the oxygen saturation measurement.
• An additional aspect of the present disclosure is a measurement method comprising the steps of sensing a physiological signal, computing a physiological measurement based upon the signal, and synthesizing a waveform as a function of the physiological measurement. A further step is outputting the waveform to a sensor input of a physiological monitoring apparatus. The synthesizing step is performed so that the measurement apparatus displays a value corresponding to the physiological measurement.
• A further aspect of the present disclosure is a measurement apparatus comprising a first pulse oximeter for making an oxygen saturation measurement and a pulse rate measurement based upon an intensity signal derived from a tissue site. Also included is a waveform generation means for creating a signal based upon the oxygen saturation measurement and the pulse rate measurement. In addition, there is a communication means for transmitting the signal to a second pulse oximeter.
• Another aspect of the present disclosure is a measurement apparatus comprising a portable portion having a sensor port, a processor, a display, and a docking connector. The sensor port is configured to receive an intensity signal responsive to the oxygen content of arterial blood at a tissue site. The processor is programmed to compute an oxygen saturation value based upon the intensity signal and to output the value to the display. A docking station has a portable connector and is configured to accommodate the portable so that the docking connector mates with the portable connector. This provides electrical connectivity between the docking station and the portable. The portable has an undocked position separate from the docking station in which the portable functions as a handheld pulse oximeter. The portable also has a docked position at least partially retained within the docking station in which the combination of the portable and the docking station has at least one additional function compared with the portable in the undocked position.
• A further aspect of the present disclosure is a measurement apparatus configured to function in both a first spatial orientation and a second spatial orientation. The apparatus comprises a sensor port configured to receive a signal responsive to a physiological state. The apparatus also has a tilt sensor providing an output responsive to gravity. In addition, there is a processor in communication with the sensor port and the tilt sensor output. The processor is programmed to compute a physiological measurement value based upon the signal and to determine whether the measurement apparatus is in the first orientation or the second orientation based upon the tilt sensor output. A display has a first mode and a second mode and is driven by the processor. The display shows the measurement value in the first mode when the apparatus is in the first orientation and shows the measurement value in the second mode when the apparatus is in the second orientation.
• Another aspect of the present disclosure is a measurement method comprising the steps of sensing a signal responsive to a physiological state and computing physiological measurement based on the signal. Additional steps are determining the spatial orientation of a tilt sensor and displaying the physiological measurement in a mode that is based upon the determining step.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a block diagram of a prior art pulse oximeter;
• FIG. 2 is a diagram illustrating a patient monitoring system incorporating a universal/upgrading pulse oximeter (UPO) according to the present disclosure;
• FIG. 3 is top level block diagram of a UPO embodiment;
• FIG. 4 is a detailed block diagram of the waveform generator portion of the UPO embodiment shown inFIG. 3;
• FIG. 5 is an illustration of a handheld embodiment of the UPO;
• FIG. 6 is a top level block diagram of another UPO embodiment incorporating a portable pulse oximeter and a docking station;
• FIG. 7 is a detailed block diagram of the portable pulse oximeter portion ofFIG. 6;
• FIG. 8A is an illustration of the portable pulse oximeter user interface, including a keyboard and display;
• FIGS. 8B-C are illustrations of the portable pulse oximeter display showing portrait and landscape modes, respectively;
• FIG. 9 is a detailed block diagram of the docking station portion ofFIG. 6;
• FIG. 10 is a schematic of the interface cable portion ofFIG. 6;
• FIG. 11A is a front view of an embodiment of a portable pulse oximeter;
• FIG. 11B is a back view of a portable pulse oximeter;
• FIG. 12A is a front view of an embodiment of a docking station;
• FIG. 12B is a back view of a docking station;
• FIG. 13 is a front view of a portable docked to a docking station; and
• FIG. 14 is a block diagram of one embodiment of a local area network interface for a docking station.
DETAILED DESCRIPTION
• FIG. 2 depicts the use of a Universal/Upgrading Pulse Oximeter (“UPO”)210 to perform patient monitoring. Apulse oximetry sensor110 is attached to a patient (not illustrated) and provides theUPO210 with a modulated red and IR photo-plethysmograph signal through apatient cable220. TheUPO210 computes the patient's oxygen saturation and pulse rate from the sensor signal and, optionally, displays the patient's oxygen status. TheUPO210 may incorporate aninternal power source212, such as common alkaline batteries or a rechargeable power source. TheUPO210 may also utilize anexternal power source214, such as standard 110V AC coupled with an external step-down transformer and an internal or external AC-to-DC converter.
• In addition to providing pulse oximetry measurements, theUPO210 also separately generates a signal, which is received by apulse oximeter268 external to theUPO210. This signal is synthesized from the saturation calculated by theUPO210 such that theexternal pulse oximeter268 calculates the equivalent saturation and pulse rate as computed by theUPO210. Theexternal pulse oximeter268 receiving the UPO signal may be a multiparameter patient monitoring system (MPMS)260 incorporating apulse oximeter module268, a standalone pulse oximeter instrument, or any other host instrument capable of measuring SpO₂. TheMPMS260 depicted inFIG. 2 has arack262 containing a number of modules for monitoring such patient parameters as blood pressure, EKG, respiratory gas, and SpO₂. The measurements made by these various modules are shown on amultiparameter display264, which is typically a video (CRT) device. TheUPO210 is connected to an existingMPMS260 with acable230, advantageously integrating the UPO oxygen status measurements with other MPMS measurements. This allows the UPO calculations to be shown on a unified display of important patient parameters, networked with other patient data, archived within electronic patient records and incorporated into alarm management, which are all MPMS functions convenient to the caregiver.
• FIG. 3 depicts the major functions of theUPO210, including aninternal pulse oximeter310, awaveform generator320, apower supply330 and anoptional display340. Attached to theUPO210 are asensor110 and anexternal pulse oximeter260. Theinternal pulse oximeter310 provides thesensor110 with adrive signal312 that alternately activates the sensor's red and IR LEDs, as is well-known in the art. A correspondingdetector signal314 is received by theinternal pulse oximeter310. Theinternal pulse oximeter310 computes oxygen saturation, pulse rate, and, in some embodiments, other physiological parameters such as pulse occurrence, plethysmograph features and measurement confidence. Theseparameters318 are output to thewaveform generator320. A portion of these parameters may also be used to generate display drive signals316 so that patient status may be read from, for example, an LED orLCD display module340 on the UPO.
• Theinternal pulse oximeter310 may be a conventional pulse oximeter or, for upgrading anexternal pulse oximeter260, it may be an advanced pulse oximeter capable of low perfusion and motion artifact performance not found in conventional pulse oximeters. An advanced pulse oximeter for use as aninternal pulse oximeter310 is described in U.S. Pat. No. 5,632,272 assigned to the assignee of the present disclosure and incorporated herein by reference. An advanced pulse oximetry sensor for use as thesensor110 attached to theinternal pulse oximeter310 is described in U.S. Pat. No. 5,638,818 assigned to the assignee of the present disclosure and incorporated herein by reference. Further, a line of advanced Masimo SET® pulse oximeter OEM boards and sensors are available from the assignee of the present disclosure.
• Thewaveform generator320 synthesizes a waveform, such as a triangular waveform having a sawtooth or symmetric triangle shape, that is output as amodulated signal324 in response to aninput drive signal322. Thedrive input322 andmodulation output324 of thewaveform generator320 are connected to thesensor port262 of theexternal pulse oximeter260. The synthesized waveform is generated in a manner such that theexternal pulse oximeter260 computes and displays a saturation and a pulse rate value that is equivalent to that measured by theinternal pulse oximeter310 andsensor110. In the present embodiment, the waveforms for pulse oximetry are chosen to indicate to the external pulse oximeter260 a perfusion level of 5%. Theexternal pulse oximeter260, therefore, always receives a strong signal. In an alternative embodiment, the perfusion level of the waveforms synthesized for the external pulse oximeter can be set to indicate a perfusion level at or close to the perfusion level of the patient being monitored by theinternal pulse oximeter310. As an alternative to the generated waveform, adigital data output326, is connected to thedata port264 of theexternal pulse oximeter260. In this manner, saturation and pulse rate measurements and also samples of the unmodulated, synthesized waveform can be communicated directly to theexternal pulse oximeter260 for display, bypassing the external pulse oximeter's signal processing functions. The measured plethysmograph waveform samples output from theinternal pulse oximeter310 also may be communicated through thedigital data output326 to theexternal pulse oximeter260.
• It will be understood from the above discussion that the synthesized waveform is not physiological data from the patient being monitored by theinternal pulse oximeter310, but is a waveform synthesized from predetermined stored waveform data to cause theexternal pulse oximeter260 to calculate oxygen saturation and pulse rate equivalent to or generally equivalent (within clinical significance) to that calculated by theinternal pulse oximeter310. The actual physiological waveform from the patient received by the detector is not provided to theexternal pulse oximeter260 in the present embodiment. Indeed, the waveform provided to the external pulse oximeter will usually not resemble the plethysmographic waveform of physiological data from the patient being monitored by theinternal pulse oximeter260.
• The cable230 (FIG. 2) attached between thewaveform generator320 andexternal pulse oximeter260 provides amonitor ID328 to the UPO, allowing identification of predetermined external pulse oximeter calibration curves. For example, this cable may incorporate an encoding device, such as a resistor, or a memory device, such as a PROM1010 (FIG. 10) that is read by thewaveform generator320. The encoding device provides a value that uniquely identifies a particular type ofexternal pulse oximeter260 having known calibration curve, LED drive and modulation signal characteristics. Although the calibration curves of theexternal pulse oximeter260 are taken into account, the wavelengths of theactual sensor110, advantageously, are not required to correspond to the particular calibration curve indicated by themonitor ID328 or otherwise assumed for theexternal pulse oximeter260. That is, the wavelength of thesensor110 attached to theinternal pulse oximeter310 is not relevant or known to theexternal pulse oximeter260.
• FIG. 4 illustrates one embodiment of thewaveform generator portion320 of the UPO210 (FIG. 3). Although this embodiment is illustrated and described as hardware, one of ordinary skill will recognize that the functions of the waveform generator may be implemented in software or firmware or a combination of hardware, software and firmware. Thewaveform generator320 performs waveform synthesis with a waveform look-up table (“LUT”)410, awaveform shaper420 and awaveform splitter430. Thewaveform LUT410 is advantageously a memory device, such as a ROM (read only memory) that contains samples of one or more waveform portions or segments containing a single waveform. These stored waveform segments may be as simple as a single period of a triangular waveform, having a sawtooth or symmetric triangle shape, or more complicated, such as a simulated plethysmographic pulse having various physiological features, for example rise time, fall time and dicrotic notch.
• Thewaveform shaper420 creates a continuous pulsed waveform from the waveform segments provided by thewaveform LUT410. Thewaveform shaper420 has ashape parameter input422 and anevent indicator input424 that are buffered470 from theparameters318 output from the internal pulse oximeter310 (FIG. 3). Theshape parameter input422 determines a particular waveform segment in thewaveform LUT410. The chosen waveform segment is specified by the first address transmitted to thewaveform LUT410 on the address lines426. The selected waveform segment is sent to thewaveform shaper420 as a series of samples on the waveform data lines412.
• Theevent indicator input424 specifies the occurrence of pulses in the plethysmograph waveform processed by the internal pulse oximeter310 (FIG. 3). For example, the event indicator may be a delta time from the occurrence of a previously detected falling pulse edge or this indicator could be a real time or near real time indicator of the pulse occurrence. Thewaveform shaper420 accesses thewaveform LUT410 in a manner to create a corresponding delta time between pulses in the synthesizedwaveform output428. In one embodiment, the waveform shaper is clocked at a predetermined sample rate. From a known number of samples per stored waveform segment and the input delta time from the event indicator, thewaveform shaper420 determines the number of sequential addresses to skip between samples and accesses thewaveform LUT410 accordingly. This effectively “stretches” or “shrinks” the retrieved waveform segment so as to fit in the time between two consecutive pulses detected by the UPO.
• Thewaveform splitter430 creates afirst waveform432 corresponding to a first waveform (such a red wavelength) expected by the external pulse oximeter260 (FIG. 3) and a second waveform (such as infrared)434 expected by theexternal pulse oximeter260. The relative amplitudes of thefirst waveform432 andsecond waveform434 are adjusted to correspond to theratio output444 from acalibration curve LUT440. Thus, for every value of measured oxygen saturation at thesat input442, thecalibration curve LUT440 provides acorresponding ratio output444 that results in thefirst waveform432 and thesecond waveform434 having an amplitude ratio that will be computed by the external pulse oximeter260 (FIG. 3) as equivalent to the oxygen saturation measured by the internal pulse oximeter310 (FIG. 3).
• As described above, one particularly advantageous aspect of the UPO is that the operating wavelengths of the sensor110 (FIG. 3) are not relevant to the operating wavelengths required by the external pulse oximeter260 (FIG. 3), i.e. the operating wavelengths that correspond to the calibration curve or curves utilized by the external pulse oximeter. Thecalibration curve LUT440 simply permits generation of a synthesized waveform as expected by the external oximeter260 (FIG. 3) based on the calibration curve used by the external pulse oximeter260 (FIG. 3). Thecalibration curve LUT440 contains data about the known calibration curve of the external pulse oximeter260 (FIG. 3), as specified by themonitor ID input328. In other words, the waveform actually synthesized is not a patient plethysmographic waveform. It is merely a stored waveform that will cause the external pulse oximeter to calculate the proper oxygen saturation valve and pulse rate values. Although this does not provide a patient plethysmograph on the external pulse oximeter for the clinician, the calculated values, which is what is actually sought, will be accurate.
• Amodulator450 responds to anLED drive input322 to generate a modulatedwaveform output324 derived from thefirst waveform432 andsecond waveform434. Also, adata communication interface460 transmits as adigital data output326 the data obtained from thesat442,pulse rate462 andsynthesized waveform428 inputs.
• FIG. 5 depicts ahandheld UPO500 embodiment. Thehandheld UPO500 haskeypad inputs510, anLCD display520, an externalpower supply input530, anoutput port540 for connection to an external pulse oximeter and asensor input550 at the top edge (not visible). Thedisplay520 shows the measuredoxygen saturation522, the measuredpulse rate524, a pulsatingbar526 synchronized with pulse rate or pulse events, and aconfidence bar528 indicating confidence in the measured values of saturation and pulse rate. Also shown arelow battery572 and alarm enabled574 status indicators.
• The handheld embodiment described in connection withFIG. 5 may also advantageously function in conjunction with a docking station that mechanically accepts, and electrically connects to, the handheld unit. The docking station may be co-located with a patient monitoring system and connected to a corresponding SpO₂module sensor port, external power supply, printer and telemetry device, to name a few options. In this configuration, the handheld UPO may be removed from a first docking station at one location to accompany and continuously monitor a patient during transport to a second location. The handheld UPO can then be conveniently placed into a second docking station upon arrival at the second location, where the UPO measurements are displayed on the patient monitoring system at that location.
• FIG. 6 shows a block diagram of a UPO embodiment, where the functions of theUPO210 are split between aportable pulse oximeter610 and adocking station660. The portable pulse oximeter610 (“portable”) is a battery operated, fully functional, stand-alone pulse oximeter instrument. The portable610 connects to a sensor110 (FIG. 2) through a UPO patient cable220 (FIG. 2) attached to apatient cable connector618. The portable610 provides thesensor110 with adrive signal612 that alternately activates the sensor's red and IR LEDs, as is well-known in the art. The portable also receives acorresponding detector signal614 from the sensor. The portable can also input a sensor ID on thedrive signal line612, as described in U.S. Pat. No. 5,758,644 entitled Manual and Automatic Probe Calibration, assigned to the assignee of the present disclosure and incorporated herein by reference.
• The portable610 can be installed into thedocking station660 to expand its functionality. When installed, the portable610 can receivepower662 from thedocking station660 if thedocking station660 is connected toexternal power668. Alternately, with noexternal power668 to thedocking station660, the portable610 can supplypower662 to thedocking station660. The portable610 communicates to the docking station with a bi-directionalserial data line664. In particular, the portable610 provides the docking station with SpO₂, pulse rate and related parameters computed from thesensor detector signal614. When the portable610 is installed, thedocking station660 may drive a host instrument260 (FIG. 2) external to the portable610. Alternatively, the portable610 anddocking station660 combination may function as a standalone pulse oximeter instrument, as described below with respect toFIG. 13.
• In one embodiment, thedocking station660 does not perform any action when the portable610 is not docked. The user interface for thedocking station660, i.e. keypad and display, is on the portable610. An indicator LED on thedocking station660 is lit when the portable is docked. Thedocking station660 generates adetector signal output674 to the host instrument260 (FIG. 2) in response to LED drive signals672 from the host instrument and SpO₂values and related parameters received from the portable610. Thedocking station660 also provides aserial data output682, anurse call684 and ananalog output688.
• Aninterface cable690 connects thedocking station660 to the host instrument patient cable230 (FIG. 2). The LED drive signals672 anddetector signal output674 are communicated between thedocking station660 and the host instrument260 (FIG. 2) via theinterface cable690. Theinterface cable690 provides async data output692 to thedocking station660, communicating sensor, host instrument (e.g. monitor ID328,FIG. 3) and calibration curve data. Advantageously, this data allows thedocking station660 to appear to a particular host instrument as a particular sensor providing patient measurements.
• FIG. 7 provides further detail of the portable610. The portable components include apulse oximeter processor710, amanagement processor720, apower supply730, adisplay740 and akeypad750. Thepulse oximeter processor710 functions as an internal pulse oximeter, interfacing the portable to a sensor110 (FIG. 2) and deriving SpO₂, pulse rate, a plethysmograph and a pulse indicator. An advanced pulse oximeter for use as thepulse oximeter processor710 is described in U.S. Pat. No. 5,632,272, referenced above. An advanced pulse oximetry sensor for use as the sensor110 (FIG. 2) attached to thepulse oximeter processor710 is described in U.S. Pat. No. 5,638,818, also referenced above. Further, a line of advanced Masimo SET® pulse oximeter OEM boards and sensors are available from the assignee of the present disclosure. In one embodiment, thepulse oximeter processor710 is the Masimo SET® MS-3L board or a low power MS-5 board.
• Themanagement processor720 controls the various functions of the portable610, including asynchronousserial data communications724 with thepulse oximeter processor710 and synchronousserial communications762 with the docking station660 (FIG. 6). The physical and electrical connection to the docking station660 (FIG. 6) is via adocking station connector763 and thedocking station interface760, respectively. Theprocessor720 utilizes a real-time clock702 to keep the current date and time, which includes time and date information that is stored along with SpO₂parameters to create trend data. The processor of the portable610 and the docking station660 (FIG. 6) can be from the same family to share common routines and minimize code development time.
• Theprocessor720 also controls the user interface800 (FIG. 8A) by transferringdata742 to thedisplay740, including display updates and visual alarms, and by interpretingkeystroke data752 from thekeypad750. Theprocessor720 generates various alarm signals, when required, via an enablesignal728, which controls aspeaker driver770. Thespeaker driver770 actuates aspeaker772, which provides audible indications such as, for example, alarms and pulse beeps. Theprocessor720 also monitors system status, which includesbattery status736, indicating battery levels, and docked status764, indicating whether the portable610 is connected to the docking station660 (FIG. 6). When the portable610 is docked and is on, theprocessor720 also decides when to turn on or off docking station power732.
• Advantageously, the caregiver can set (i.e. configure or program) the behavior of theportable display740 and alarms when the docked portable610 senses that aninterface cable690 has connected thedocking station660 to an external pulse oximeter, such as a multiparameter patient monitoring system. In one user setting, for example, theportable display740 stops showing the SpO₂811 (FIG. 8) and pulse rate813 (FIG. 8) values when connected to an external pulse oximeter to avoid confusing the caregiver, who can read equivalent values on the patient monitoring system. Thedisplay740, however, continues to show the plethysmograph815 (FIG. 8) and visual pulse indicator817 (FIG. 8) waveforms. For one such user setting, the portable alarms remain active.
• Another task of theprocessor720 includes maintenance of a watchdog function. Thewatchdog780 monitors processor status on thewatchdog data input782 and asserts the :Preset output784 if a fault is detected. This resets themanagement processor720, and the fault is indicated with audible and visual alarms.
• The portable610 gets its power from batteries in thepower supply730 or frompower766 supplied from the docking station660 (FIG. 6) via thedocking station interface760. Apower manager790 monitors the on/off switch on thekeypad750 and turns-on the portable power accordingly. Thepower manager790 turns off the portable on command by theprocessor720. DC/DC converters within thepower supply730 generate the requiredvoltages738 for operation of the portable610 and docking station power732. The portable batteries can be either alkaline rechargeable batteries or another renewable power source. The batteries of thepower supply730 supply docking station power732 when the docking station660 (FIG. 6) is without external power. A battery charger within the docking station power supply provides charging current768 to rechargeable batteries within thepower supply730. The docking station power supply990 (FIG. 9) monitorstemperature734 from a thermistor in the rechargeable battery pack, providing an indication of battery charge status.
• Anon-volatile memory706 is connected to themanagement processor720 via a high-speed bus722. In the present embodiment, thememory706 is an erasable and field re-programmable device used to store boot data, manufacturing serial numbers, diagnostic failure history, adult SpO₂and pulse rate alarm limits, neonate SpO₂and pulse rate alarm limits, SpO₂and pulse rate trend data, and program data. Other types of non-volatile memory are well known. The SpO₂and pulse rate alarm limits, as well as SpO₂related algorithm parameters, may be automatically selected based on the type of sensor110 (FIG. 2), adult or neonate, connected to the portable610.
• TheLCD display740 employs LEDs for a backlight to increase its contrast ratio and viewing distance when in a dark environment. The intensity of the backlight is determined by the power source for the portable610. When the portable610 is powered by either a battery pack within itspower supply730 or a battery pack in the docking station power supply990 (FIG. 9), the backlight intensity is at a minimum level. When the portable610 is powered by external power668 (FIG. 6), the backlight is at a higher intensity to increase viewing distance and angle. In one embodiment, button on the portable permits overriding these intensity settings, and provides adjustment of the intensity. The backlight is controlled in two ways. Whenever any key is pressed, the backlight is illuminated for a fixed number of seconds and then turns off, except when the portable is docked and derives power from an external source. In that case, the backlight is normally on unless deactivated with a key on the portable610.
• FIG. 8A illustrates theportable user interface800, which includes adisplay740 and akeypad750. In one embodiment, thedisplay740 is a dot matrix LCD device having160 pixels by480 pixels. Thedisplay740 can be shown in portrait mode, illustrated inFIG. 8B, or in landscape mode, illustrated inFIG. 8C. A tilt sensor950 (FIG. 9) in the docking station660 (FIG. 6) or a display mode key on the portable610 (FIG. 6) determines portrait or landscape mode. The tilt sensor950 (FIG. 9) can be a gravity-activated switch or other device responsive to orientation and can be alternatively located in the portable610 (FIG. 6). In a particular embodiment, the tilt sensor950 (FIG. 9) is a non-mercury tilt switch, part number CW 1300-1, available from Comus International, Nutley, N.J. (www.comus-intl.com). The tilt sensor950 (FIG. 9) could also be a mercury tilt switch.
• Examples of how the display area can be used to displaySpO₂811,pulse rate813, aplethysmographic waveform815, avisual pulse indicator817 and softkey icons820 in portrait and landscape mode are shown inFIGS. 8B and 8C, respectively. The software program of the management processor720 (FIG. 7) can be easily changed to modify the category, layout and size of the display information shown inFIGS. 8B-C. Other advantageous information for display is SpO₂limits, alarm, alarm disabled, exception messages and battery status.
• Thekeypad750 includessoft keys870 and fixedkeys880. The fixedkeys880 each have a fixed function. Thesoft keys870 each have a function that is programmable and indicated by one of the softkey icons820 located next to thesoft keys870. That is, a particular one of the softkey icons820 is in proximity to a particular one of thesoft keys870 and has a text or a shape that suggests the function of that particular one of thesoft keys870. In one embodiment, the button portion of each key of thekeypad750 is constructed of florescent material so that thekeys870,880 are readily visible in the dark.
• In one embodiment, thekeypad750 has one row of foursoft keys870 and one row of three fixedkeys880. Other configurations are, of course, available, and specific arrangement is not significant. The functions of the three fixedkeys880 are power, alarm silence and light/contrast. The power function is an on/off toggle button. The alarm silence function and the light/contrast function have dual purposes depending on the duration of the key press. A momentary press of the key corresponding to the alarm silence function will disable the audible alarm for a fixed period of time. To disable the audible alarm indefinitely, the key corresponding to the alarm silence function is held down for a specified length of time. If the key corresponding to the alarm silence function is pressed while the audible alarm has been silenced, the audible alarm is reactivated. If the key corresponding to the light/contrast function is pressed momentarily, it is an on/off toggle button for the backlight. If the key corresponding to the light/contrast function is held down, the display contrast cycles through its possible values.
• In this embodiment, the default functions of the foursoft keys870 are pulse beep up volume, pulse beep down volume, menu select, and display mode. These functions are indicated on the display by the up arrow, down arrow, “menu” and curved arrow softkey icons820, respectively. The up volume and down volume functions increase or decrease the audible sound or “beep” associated with each detected pulse. The display mode function rotates thedisplay740 through all four orthogonal orientations, including portrait mode (FIG. 8B) and landscape mode (FIG. 8C), with each press of the corresponding key. The menu select function allows the functionality of thesoft keys870 to change from the default functions described above. Examples of additional soft key functions that can be selected using this menu feature are set SpO₂high/low limit, set pulse rate high/low limit, set alarm volume levels, set display to show trend data, print trend data, erase trend data, set averaging time, set sensitivity mode, perform synchronization, perform rechargeable battery maintenance (deep discharge/recharge to remove battery memory), and display product version number.
• FIG. 9 provides further details of thedocking station660, which includes adocking station processor910, anon-volatile memory920, awaveform generator930, aPROM interface940, atilt sensor950, aportable interface970 and associatedconnector972,status indicators982, aserial data port682, anurse call output684, ananalog output688 and apower supply990. In one embodiment, thedocking station660 is intended to be associated with a fixed (non-transportable) host instrument, such as a multiparameter patient monitoring instrument in a hospital emergency room. In a transportable embodiment, thedocking station660 is movable, and includes a battery pack within thepower supply990.
• Thedocking station processor910 orchestrates the activity on thedocking station660. Theprocessor910 provides thewaveform generator930 withparameters932 as discussed above forFIGS. 3 and 4. Theprocessor910 also provides asynchronousserial data912 for communications with external devices and synchronousserial data971 for communications with the portable610 (FIG. 6). In addition, theprocessor910 determines system status includingsync status942,tilt status952 andpower status992. The portable management processor720 (FIG. 7) performs the watchdog function for thedocking station processor910. Thedocking station processor910 sends watchdog messages to the portable processor720 (FIG. 7) as part of the synchronousserial data972 to ensure the correct operation of thedocking station processor910.
• Thedocking station processor910 accessesnon-volatile memory920 over a high-speed bus922. Thenon-volatile memory920 is re-programmable and contains program data for theprocessor910 including instrument communication protocols, synchronization information, a boot image, manufacturing history and diagnostic failure history.
• Thewaveform generator930 generates a synthesized waveform that a conventional pulse oximeter can process to calculate SpO₂and pulse rate values or exception messages, as described above with respect toFIG. 4. However, in the present embodiment, as explained above, the waveform generator output does not reflect a physiological waveform. It is merely a waveform constructed to cause the external pulse oximeter to calculate the correct saturation and pulse rate. In an alternative embodiment, physiological data could be provided to the external pulse oximeter, but the external pulse oximeter would generally not be able to calculate the proper saturation values, and the upgrading feature would be lost. Thewaveform generator930 is enabled if an interface cable690 (FIG. 6), described below with respect toFIG. 10, with valid synchronization information is connected. Otherwise, the power to thewaveform generator930 is disabled.
• Thestatus indicators982 are a set of LEDs on the front of thedocking station660 used to indicate various conditions including external power (AC), portable docked, portable battery charging, docking station battery charging and alarm. Theserial data port682 is used to interface with either a computer, a serial port of conventional pulse oximeters or serial printers via a standard RS-232 DB-9connector962. Thisport682 can output trend memory, SpO₂and pulse rate and support the system protocols of various manufacturers. Theanalog output688 is used to interface with analog input chart recorders via aconnector964 and can output “real-time” or trend SpO₂and pulse rate data. Thenurse call output684 from aconnector964 is activated when alarm limits are exceeded for a predetermined number of consecutive seconds. In another embodiment, data, including alarms, could be routed to any number of communications ports, and even over the Internet, to permit remote use of the upgrading pulse oximeter.
• ThePROM interface940 accessessynchronization data692 from the PROM1010 (FIG. 10) in the interface cable690 (FIGS. 6,10) and providessynchronization status942 to thedocking station processor910. Theportable interface970 provides the interconnection to the portable610 (FIG. 6) through the docking station interface760 (FIG.
• 7).
• As shown inFIG. 9,external power668 is provided to thedocking station660 through astandard AC connector968 and on/offswitch969. When thedocking station660 hasexternal power668, thepower supply990 charges the battery in the portable power supply730 (FIG. 7) and the battery, if any, in the dockingstation power supply990. When the portable610 (FIG. 6) is either removed or turned off, thedocking station power973 is removed and thedocking station660 is turned off, except for the battery charger portion of thepower supply990. Thedocking station power973 and, hence, thedocking station660 turn on whenever a docked portable610 (FIG. 6) is turned on. The portable610 (FIG. 6) supplies power for an embodiment of thedocking station660 without a battery whenexternal power668 is removed or fails.
• FIG. 10 provides further detail regarding theinterface cable690 used to connect between the docking station660 (FIG. 6) and the patient cable230 (FIG. 2) of a host instrument260 (FIG. 2). Theinterface cable690 is configured to interface to a specific host instrument and to appear to the host instrument as a specific sensor. APROM1010 built into theinterface cable690 contains information identifying a sensor type, a specific host instrument, and the calibration curve of the specific host instrument. The PROM information can be read by the docking station660 (FIG. 6) assynchronization data692. Advantageously, thesynchronization data692 allows the docking station660 (FIG. 6) to generate a waveform to the host instrument that causes the host instrument to display SpO₂values equivalent to those calculated by the portable610 (FIG. 6). Theinterface cable690 includes anLED drive path672. In the embodiment shown inFIG. 10, theLED drive path672 is configured for common anode LEDs and includes IR cathode, red cathode and common anode signals. Theinterface cable690 also includes adetector drive path674, including detector anode and detector cathode signals.
• A menu option on the portable610 (FIG. 6) also allows synchronization information to be calculated in the field. With manual synchronization, the docking station660 (FIG. 6) generates a waveform to the host instrument260 (FIG. 2) and displays an expected SpO₂value. The user enters the SpO₂value displayed on the host instrument using the portable keypad750 (FIG. 7). These steps are repeated until a predetermined number of data points are entered and the SpO₂values displayed by the portable and the host instrument are consistent.
• FIGS. 11A-B depict an embodiment of the portable610, as described above with respect toFIG. 6.FIGS. 12A-B depict an embodiment of thedocking station660, as described above with respect toFIG. 6.FIG. 13 depicts an embodiment of theUPO210 where the portable610 is docked with thedocking station660, also as described above with respect toFIG. 6.
• FIG. 11A depicts theportable front panel1110. The portable610 has apatient cable connector618, as described above with respect toFIG. 6. Advantageously, theconnector618 is rotatably mounted so as to minimize stress on an attached patient cable (not shown). In one embodiment, theconnector618 can freely swivel between a plane parallel to thefront panel1110 and a plane parallel to theside panel1130. In another embodiment, theconnector618 can swivel between, and be releasably retained in, three locked positions. A first locked position is as shown, where the connector is in a plane parallel to thefront panel1110. A second locked position is where theconnector618 is in a plane parallel to theside panel1130. Theconnector618 also has an intermediate locked position 45° between the first and the second locked positions. Theconnector618 is placed in the first locked position for attachment to thedocking station660.
• Shown inFIG. 11A, theportable front panel1110 also has aspeaker772, as described with respect toFIG. 7. Further, thefront panel1110 has a row ofsoft keys870 and fixedkeys880, as described above with respect toFIG. 8. In addition, thefront panel1110 has a finger actuatedlatch1120 that locks onto a corresponding catch1244 (FIG. 12A) in thedocking station660, allowing the portable610 to be releasably retained by thedocking station660. An OEM label can be affixed to a recessedarea1112 on thefront panel1110.
• FIG. 11B depicts theportable back panel1140. Theback panel1140 has asocket763, a poleclamp mating surface1160, and abattery pack compartment1170. Thesocket763 is configured to mate with a corresponding docking station plug972 (FIG. 12A). Thesocket763 and plug972 (FIG. 12A) provide the electrical connection interface between the portable610 and the docking station660 (FIG. 12A). Thesocket763 houses multiple spring contacts that compress against plated edge-connector portions of the docking station plug972 (FIG. 12A). A conventional pole clamp (not shown) may be removably attached to themating surface1160. This conveniently allows the portable610 to be held to various patient-side or bedside mounts for hands-free pulse oximetry monitoring. The portable power supply730 (FIG. 7) is contained within thebattery pack compartment1170. Thecompartment1170 has aremovable cover1172 for protection, insertion and removal of the portable battery pack. Product labels, such as a serial number identifying a particular portable, can be affixed with theback panel indent1142.
• FIG. 12A depicts thefront side1210 of thedocking station660. Thefront side1210 has adocking compartment1220, apole clamp recess1230, pivots1242, acatch1244, aplug connector972 andLED status indicators982. Thedocking compartment1220 accepts and retains the portable610 (FIGS. 11A-B), as shown inFIG. 13. When the portable610 (FIGS. 11A-B) is docked in thecompartment1220, thepole clamp recess1230 accommodates a pole clamp (not shown) attached to the portable's pole clamp mating surface1160 (FIG. 11B), assuming the pole clamp is in its closed position. The portable610 (FIGS. 11A-B) is retained in thecompartment1220 bypivots1242 that fit into corresponding holes in the portable'sside face1130 and acatch1244 that engages the portable's latch1120 (FIG. 11A). Thus, the portable610 (FIGS. 11A-B) is docked by first attaching it at one end to thepivots1242, then rotating it about thepivots1242 into thecompartment1220, where it is latched in place on thecatch1244. The portable610 (FIGS. 11A-B) is undocked in reverse order, by first pressing the latch1120 (FIG. 11A), which releases the portable from thecatch1244, rotating the portable610 (FIGS. 11A-B) about thepivots1242 out of thecompartment1220 and then removing it from thepivots1242. As the portable is rotated into the compartment, thedocking station plug972 inserts into the portable socket763 (FIG. 11B), providing the electrical interface between the portable610 and thedocking station660. Thestatus indicators982 are as described above with respect toFIG. 9.
• FIG. 12B depicts theback side1260 of thedocking station660. Theback side1260 has a serial (RS-232 or USB)connector962, an analog output andnurse call connector964, anupgrade port connector966, anAC power plug968, an on/offswitch969 and aground lug1162. Ahandle1180 is provided at one end andfan vents1170 are provided at the opposite end. A pair offeet1190 are visible near theback side1260. A corresponding pair of feet (not visible) are located near the front side1210 (FIG. 12A). The feet near thefront side1210 extend so as to tilt the front side1210 (FIG. 12A) upward, making the display740 (FIG. 13) of a docked portable610 (FIG. 13) easier to read.
• FIG. 13 illustrates both the portable610 and thedocking station660. The portable610 anddocking station660 constitute three distinct pulse oximetry instruments. First, the portable610 by itself, as depicted inFIGS. 11A-B, is a handheld pulse oximeter applicable to various patient monitoring tasks requiring battery power or significant mobility, such as ambulance and ER situations. Second, the portable610 docked in thedocking station660, as depicted inFIG. 13, is a standalone pulse oximeter applicable to a wide-range of typical patient monitoring situations from hospital room to the operating room. Third, the portable610 docked and the upgrade port966 (FIG. 12B) connected with an interface cable to the sensor port of a conventional pulse oximeter module268 (FIG. 2) within a multiparameter patient monitoring instrument260 (FIG. 2) or other conventional pulse oximeter, is a universal/upgrading pulse oximeter (UPO)instrument210, as described herein. Thus, the portable610 anddocking station660 configuration of theUPO210 advantageously provides a three-in-one pulse oximetry instrument functionality.
• Another embodiment of thedocking station660 incorporates an input port that connects to a blood pressure sensor and an output port that connects to the blood pressure sensor port of a multiparameter patient monitoring system (MPMS). Thedocking station660 incorporates a signal processor that computes a blood pressure measurement based upon an input from the blood pressure sensor. Thedocking station660 also incorporates a waveform generator connected to the output port that produces a synthesized waveform based upon the computed measurement. The waveform generator output is adjustable so that the blood pressure value displayed on the MPMS is equivalent to the computed blood pressure measurement. Further, when the portable610 is docked in thedocking station660 and the blood pressure sensor is connected to the input port, the portable displays a blood pressure value according to the computed blood pressure measurement. Thus, in this embodiment, thedocking station660 provides universal/upgrading capability for both blood pressure and SpO₂.
• Likewise, thedocking station660 can function as an universal/upgrading instrument for other vital sign measurements, such as respiratory rate, EKG or EEG. For this embodiment, thedocking station660 incorporates related sensor connectors and associated sensor signal processors and upgrade connectors to an MPMS or standalone instrument. In this manner, a variety of vital sign measurements can be incorporated into thedocking station660, either individually or in combination, with or without SpO₂as a measurement parameter, and with or without the portable610. In yet another embodiment, thedocking station660 can be configured as a simple SpO₂upgrade box, incorporating a SpO₂processor and patient cable connector for a SpO₂sensor that functions with or without the portable610.
• Unlike a conventional standalone pulse oximeter, the standalone configuration shown inFIG. 13 has arotatable display740 that allows the instrument to be operated in either a vertical or horizontal orientation. A tilt sensor950 (FIG. 9) indicates when the bottom face1310 is placed along a horizontal surface or is otherwise horizontally-oriented. In this horizontal orientation, thedisplay740 appears in landscape mode (FIG. 8C). The tilt sensor950 (FIG. 9) also indicates when the side face1320 is placed along a horizontal surface or is otherwise horizontally oriented. In this vertical orientation, thedisplay740 appears in portrait mode (FIG. 8B). Asoft key870 on the portable610 can override the tilt sensor, allowing the display to be presented at any 90° orientation, i.e. portrait, landscape, “upside-down” portrait or “upside-down” landscape orientations. The handheld configuration (FIG. 11A), can also present thedisplay740 at any 90° orientation using asoft key870. In the particular embodiment described above, however, the portable610 does not have a tilt sensor and, hence, relies on asoft key870 to change the orientation of the display when not docked.
• FIG. 14 illustrates thedocking station660 incorporated within a local area network (LAN). The LAN shown is Ethernet-based1460, using acentral LAN server1420 to interconnectvarious LAN clients1430 and other system resources such as printers and storage (not shown). AnEthernet controller module1410 is incorporated with thedocking station660. Thecontroller module1410 can be incorporated within thedocking station660 housing or constructed as an external unit. In this manner, the UPO, according to the present disclosure, can communicate with other devices on the LAN or over theInternet1490.
• TheEthernet controller module1410 can be embedded with web server firmware, such as the Hewlett-Packard (HP) BFOOT-10501. Themodule1410 has both a 10 Base-T Ethernet interface for connection to theEthernet1460 and a serial interface, such as RS-232 or USB, for connection to thedocking station660. The module firmware incorporates HTTP and TCP/IP protocols for standard communications over the World Wide Web. The firmware also incorporates a micro web server that allows custom web pages to be served to remote clients over the Internet, for example. Custom C++ programming allows expanded capabilities such as data reduction, event detection and dynamic web page configuration.
• As shown inFIG. 14, there are many applications for thedocking station660 to Ethernet interface. Multiple UPOs can be connected to a hospital's LAN, and a computer on the LAN could be utilized to upload pulse rate and saturation data from the various UPOs, displaying the results. Thus, this Ethernet interface could be used to implement a central pulse oximetry monitoring station within a hospital. Further, multiple UPOs from anywhere in the world can be monitored from a central location via the Internet. Each UPO is addressable as an individual web site and downloads web pages viewable on a standard browser, the web pages displaying oxygen saturation, pulse rate and related physiological measurements from the UPO. This feature allows a caregiver to monitor a patient regardless of where the patient or caregiver is located. For example a caregiver located at home in one city or at a particular hospital could download measurements from a patient located at home in a different city or at the same or a different hospital. Other applications include troubleshooting newly installed UPOs or uploading software patches or upgrades to UPOs via the Internet. In addition alarms could be forwarded to the URL of the clinician monitoring the patient.
• The UPO may have other configurations besides the handheld unit described in connection withFIG. 5 or the portable610 anddocking station660 combination described in connection withFIGS. 11-13. The UPO may be a module, with or without a display, that can be removably fastened to a patient via an arm strap, necklace or similar means. In a smaller embodiment, this UPO module may be integrated into a cable or connector used for attaching a sensor to a pulse oximeter. The UPO may also be a circuit card or module that can externally or internally plug into or mate with a standalone pulse oximeter or multiparameter patient monitoring system. Alternatively, the UPO may be configured as a simple standalone upgrade instrument.
• Further, although a universal/upgrading apparatus and method have been mainly described in terms of a pulse oximetry measurement embodiment, the present disclosure is equally applicable to other physiological measurement parameters such as blood pressure, respiration rate, EEG and ECG, to name a few. In addition, a universal/upgrading instrument having a single physiological measurement parameter or a multiple measurement parameter capability and configured as a handheld, standalone, portable, docking station, module, plug-in, circuit card, to name a few, is also within the scope of the present disclosure.
• The UPO has been disclosed in detail in connection with various embodiments of the present disclosure. These embodiments are disclosed by way of examples only and are not to limit the scope of the present disclosure, which is defined by the claims that follow. One of ordinary skill in the art will appreciate many variations and modifications within the scope of this disclosure.

Claims (18)

What is claimed is:

1. A method for communicating a physiological waveform indicative of a physiological condition to a patient monitor, the method comprising:

obtaining a sensor signal indicative of a physiological parameter;

calculating a first physiological measurement using a first processor;

communicating the physiological measurement to a second processor;

constructing an output signal indicative of the physiological measurement; and

communicating the output signal to the sensor input of a patient monitoring device for recalculation and display of the physiological measurement.

2. The method ofclaim 1, further comprising displaying the calculated physiological measurement on a first display associated with the first processor.

3. The method ofclaim 1, wherein the physiological measurement comprises at least one of blood oxygen levels, blood pressure, ECG, and pulse rate.

4. The method ofclaim 1, wherein the output signal is configured to cause a patient monitor not associated with the first processor to calculate a second physiological measurement substantially equivalent to the first physiological measurement.

5. The method ofclaim 1, wherein the second processor comprises a waveform generator.

6. The method ofclaim 1, wherein the second processor is comprised within a docking station.

7. A system for communicating a physiological waveform indicative of a physiological condition to a patient monitor, the system comprising:

a sensor input configured to obtain a sensor signal indicative of a physiological parameter;

a first processor configured to calculate a first physiological measurement;

a second processor in communication with the first processor;

wherein the second processor is configured to construct an output signal indicative of the physiological measurement; and

an output configured to communicate the output signal to a patient monitoring device for recalculation and display of the first physiological measurement.

8. The method ofclaim 7, further comprising a first display in communication with the first processor, wherein the display is configured to display the calculated physiological measurement.

9. The method ofclaim 7, wherein the physiological measurement comprises at least one of blood oxygen levels, blood pressure, ECG, and pulse rate.

10. The method ofclaim 7, wherein the output signal is configured to cause a patient monitor not associated with the first processor to calculate a second physiological measurement substantially equivalent to the first physiological measurement.

11. A method for communicating a physiological waveform indicative of a physiological condition to a patient monitor, the method comprising:

obtaining a sensor signal indicative of a physiological parameter;

displaying information about the sensor signal on a first display;

constructing an output signal indicative of the sensor signal and

communicating the output signal to a patient monitoring device for recalculation and display of the physiological parameter, wherein the patient monitoring device communicates with a second display.

12. The method ofclaim 11, further comprising calculating a first physiological measurement using a first processor.

13. The method ofclaim 12, further communicating the first physiological measurement to a second processor.

14. The method ofclaim 12, further comprising displaying the physiological measurement on the first display.

15. The method ofclaim 11, wherein information comprises a power on indication.

16. The method ofclaim 11, wherein information comprises signal quality information.

17. The method ofclaim 11, wherein information comprises a physiological measurement.

18. A system for communicating a physiological waveform indicative of a physiological condition to a patient monitor, the system comprising:

a sensor input configured to obtain a sensor signal indicative of a physiological parameter;

a first display configured to display calculated information about the sensor signal;

a processor configured to construct an output signal indicative of the sensor signal based on the calculated information; and

an output configured to communicate the output signal to a patient monitoring device, wherein the patient monitoring device communicates with a second display.

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