Pulse oximetry Flashcards
Pulse oximeter vs co-oximeter
in-vivo vs in-vitro, mechanism
Pulse oximeter is an in-vivo monitor
Co-oximeter is an in-vitro monitor which measures the concentration of different forms of haemoglobin (oxyHb, DeoxyHb, MetHb, COHb) in a haemolysed blood sample - can therefore derive oxygen saturation.
Both function by the absorption of light
* Pulse oximeter: light absorbed by whole human tissue – see diagram
* Co-oximeter: light absorbed by blood alone. Relies on the fact that there is a linear relationship between light absorbance and hte concentration of an absorbing substance, and that different haemoglobins absorb light at different frequencies.
Beer-Lambert law
There is a linear relationship between light absorbance and the concentration of an absorbing substance
Pulse oximeter probe
Structure, mechanism. At which frequencies do the LEDs emit light?
- Probe contains 2 light-emitting diodes (LED), emitting light at red (660nm) and infrared (940nm) frequencies
- There is a photodetector either on opposite side to LEDs (transmission) or same side as LEDs (reflectance) to measure the transmitted or reflected light
Measures how the two frequencies (red and infrared) of light are absorbed across a pulsatile tissue bed therefore inferring saturation
* Photodectector produces current linearly proportional to the intensity of the light striking it
* Photodetector cannot distinguish between red and infrared light, so to accomodate this, micoprocessor turns each LED on and off in sequence
* When both LEDs are off, ambient light is measured so it can be extracted from the signal
Pulse oximeter computerised unit
Basic components (5)
- Switching circuit: controls sequencing of LEDs
- Automatic gain controllers: control intensity of emitted light to compensate for thickness of finger, skin colour
- Bypass filters: extract the AC (pulsatile, due to arterial pulsation) component from the DC (constant) component -> can be displayed as pulse waveform -> pulse rate calculated from waveform
- Analogue to digital signal converters (microprocessor requires digital signal)
- Microprocessor and monitor: processes filtered data, allows setting of alarms, display shows pulse rate, saturation, plethysmograph
How is pulse rate calculated from pulse oximeter
- Photodetector generates a current proportional to the transmitted light
- Using bypass filters, computerised unit can extract pulsatile (AC) component due to arterial pulsation from the constant component (DC)
- –> plethysmograph (pulse waveform)
- Pulse rate is calculated from this waveform
Absorption spectrogram
Points of similar absorption for different forms
Absorption spectrogram shows how light at different frequencies is absorbed by haemoglobins. Note y axis is logarithmic
- Oxyhaemoglobin has much greater absorption at 940nm (infrared) than 660nm (red)
- Deoxyhaemoglobin has much greater absorption at 660nm than 940nm
- Isobestic point = 810nm, both oxyhaemoglobin and deoxyhaemoglobin have same absorption
- At 660nm carboxyhaemoglobin has similar absorption to oxyhaemoglobin, and methaemoglobin has similar absorption to deoxyhaemoglobin - therefore methaemoglobin mimics deoxyhaemoglobin and carboxyhaemoglobin mimics oxyhaemoglobin
How does the pulse oximeter calculate saturation
Formula, averaging
Processor calculates ratio of absorption at 660nm to 940nm (R/IR ratio):
R/IR = (ac660 / dc660) / (ac940/dc940)
This is compared to a ‘look up’ table pre-programmed into the machines memory. See graph of saturation vs R/IR ratio. Note curve is extrapolated below SpO2 70%
Most oximeters average out saturation readings over 5 to 20 seconds.
Accuracy of pulse oximeter
Range, acute changes, effect of poor perfusion/ venous pulsation
Accuracy of +/-2% between 100-70% SpO2. Below 70% calibration curve of R/IR vs SpO2 is extrapolated, and calibration between pulse oximeter and in-vivo oximeter is less accurate
Most oximeters average out saturation readings over 5-20 seconds - if sampling rate up to 20s, limited ability to detect acute changes
Accuracy/ measurement may be limited by conditions that affect the pulsatile (AC) component
* Poor perfusion and low BP -> pulsatile (AC) component is harder to extract - see picture
* Venous pulsation e.g. tricuspid regurgitation and impaired venous return may be misinterpreted as part of the pulsatile (AC) component
Effect of carboxyhaemoglobin and methaemoglobin on pulse oximeter readings
Carboxyhaemoglobin
* e.g. carbon monoxide poisoning and heavy smokers
* causes falsely high SpO2, as it resembles oxyhaemoglobin at 660 nm.
Methaemoglobin
* caused by drugs, such as nitrates and local anaesthetics e.g. prilocaine
* can lead to misreading as it resembles deoxyhaemoglobin at 660 nm
External causes of error in pulse oximeter readings (4)
- Excessive movement
- Poor positioning of probe
- External fluorescent lighting
- Nail polish - can cause under-reading of pulse oximeter. Especially blue and black polish. Degree of artificial desaturation correlates with the difference in the polish’s absorbance at 660nm and absorbance at 940nm. Turning oximeter through 90 degrees can eliminate problem
Complications of pulse oximeter use (2)
- Pressure sores may be caused by long term use due to local decreased perfusion from pressure on the tissues.
- Burns from the LEDs may occur
Poor perfusion is a risk factor for both
Identify the different absorption frequencies shown on the absorption spectogram.