Introduction

Pulse oximetry is sometimes referred to as the fifth vital sign; it is a quick and non-invasive monitoring technique that measures the oxygen saturation in the blood by shining light at specific wavelengths through tissue, most commonly the fingernail bed. Deoxygenated and oxygenated hemoglobin absorb light at different wavelengths, 660 nm, and 940 nm, respectively. The absorbed light is processed by a proprietary algorithm in the pulse oximeter to display a saturation value. In most developed countries, pulse oximetry is the standard of care to use pulse oximetry to monitor oxygen saturation for patients receiving anesthesia.[1][2] 

Pulse oximetry is also used in emergency departments, hospital wards, and ambulances to assess blood oxygenation in patients with respiratory difficulties or to monitor the potential respiratory depressant effects of pain medications. Since the widespread use of pulse oximetry in hospitals was instituted, the incidence of unrecognized oxygen desaturation has decreased significantly.[3] 

In addition to hospital-grade pulse oximeters, newer and much smaller consumer-grade models are rapidly gaining popularity in sports, private aviation, mountain climbing, and other recreational activity communities. Because of the size and cost of consumer-grade models, many patients with chronic respiratory illnesses purchase these devices to monitor their oxygen saturation or to titrate their medications or oxygen flow at home. Of note, the Food and Drug Administration has not evaluated most consumer-grade devices regarding their reliability to diagnose or treat diseases. 

Specimen Collection

Pulse oximeters are well-tolerated medical devices that provide rapid data using noninvasive technology. The most commonly used sites for application are the fingernail and toenail beds. The machine algorithm detects arterial pulsations of very small caliber in arteriolar and capillary tissue beds. Consequently, a reliable signal may not easily be obtained in patients with low tissue perfusion or excessive movement of the extremities. Other sites, including the earlobe, forehead, nasal alar, and lips, have been utilized with success.[4]

In infants, the palm, foot, arm, cheek, tongue, penis, or nasal septum also may be used for probe placement. Site-specific sensors have been developed and calibrated and should be used for those applications whenever available. In addition to collecting light absorption spectra, most pulse oximeters also capture pulse wave activity and display the plethysmographic waves from which the clinician can gain additional valuable information. 

Procedures

The spectrophotometry technique is used to determine the peripheral arterial blood oxygen saturation (SpO2) as a marker for the oxygenation of tissues using the Beer-Lambert Law. Pulse oximeter probes have two light emitters and one light detector or sensor aligned to capture the light on the other side of the tissue bed or the reflection of light from a site such as the forehead. Pulse oximeter probes come in single-use adhesive probes or multi-use clips.[5] 

However, due to infection control concerns, single-use patient clips have been introduced to the market for specific anatomical sites. Different application sites have specific probes optimized for that site and should be used when available. 

Indications

Pulse oximetry is a noninvasive means to rapidly and accurately determine oxygen saturation. This modality is one of the standard monitor parameters used in the critical care setting and during anesthesia cases and is recommended by the American Society of Anesthesiologists.[6]

In addition, pulse oximetry should be used for hospitalized patients receiving medications that may impair their respiration, such as opioids. All patients with acute respiratory disease should be monitored with pulse oximetry, regardless of the setting. Pulse oximetry is used to diagnose hypoxia rapidly and to titrate oxygen supplementation when used with ventilator support and in various disease states.[7] 

Avoiding hyperoxia is essential as it may lead to increased morbidity and mortality.[8] Prior to the institution of pulse oximeters, arterial blood gas analysis was used to detect hypoxemia. This technique is painful, and complications may occur, including hematoma, vasospasm, occlusion, thrombus or air embolism, infection, needle-stick injury to the healthcare provider, vessel laceration, hemorrhage, pain, or vasovagal response. 

Potential Diagnosis

Conventional pulse oximeters are used to diagnose hypoxia. Recent technological developments in certain pulse oximeters have allowed the assessment of other parameters such as methemoglobin and carboxyhemoglobin levels, total hemoglobin, and oxygen levels above 100% saturation. Pulse wave activity parameters can display volume status in intubated patients, and specific devices display respiratory rate by detecting pulse pressure variation within the respiratory cycle.[9]

The perfusion index (PI), which measures peripheral perfusion, has been used to diagnose the success of increased blood flow after a sympathectomy.[10] The PI can also be used as an indicator of pain in critically ill patients, and there is an apparent inverse relationship between painful stimuli and decreased PI.[11]

Normal and Critical Findings

Oxygen saturation levels between 96% and 100% are considered normal at sea level. Healthy individuals living at higher elevations may have lower oxygen saturation levels. Pulse oximeters are usually calibrated to a range of saturation from 70% to 100% with an accuracy of between 2% and 4%, indicating a pulse oximeter reading lower than 70% may not be accurately compared to the gold standard invasive blood gas measurement.[8]

While a pulse oximeter may not demonstrate absolute accuracy, it usually still tracks oxygen saturation and will display lower numbers. Technical reasons exist for the 70% calibration; however, at that low number, patients usually will have clinical signs of hypoxemia that would not necessitate invasive clinical confirmation.

Treatment for that degree of hypoxia would not differ from that for a patient with a saturation of 70%. Critical findings prompting intervention for most patients likely would be in the mid to high 80% range at sea level as the partial pressure of oxygen would be in the 60 mmHg range. However, critical numbers requiring treatment for patients with hypoxic heart defects may be lower at higher altitudes where venous and arterial blood are mixed when entering the systemic circulation. 

The normal oxygen levels displayed on a pulse oximeter commonly range from 95% to 100%. Hypoxemia is an oxygen saturation of less than 90%. Healthcare providers must pay attention to oxygenation trends and respond if readings are inconsistent with clinical findings. Because there are several contributing factors, there is no definitive oxygen saturation value below which hypoxia of tissues occurs, nor is there a standard value above which hyperoxia of tissues occurs. 

Interfering Factors

Pulse oximetry relies on light absorption through a tissue bed with pulsating blood. Therefore factors that interfere with those parameters can interfere with the readings of pulse oximeters. Pulse oximeter readings may be less accurate at colder temperatures. A temperature of approximately 33 degrees Celsius (91.4 degrees Fahrenheit) should be maintained for reliable readings.

One commonly implicated interfering factor is black or blue nail polish or artificial fingernails, although some studies investigating this topic have been inconclusive.[12][13] If the sensor is placed on a finger with black or blue nail polish or an artificial nail and does not give a reading, placing the sensor sideways on the finger bed has been associated with some success. However, this will be outside that sensor's calibration.

The oxygen saturation of patients with dark skin tones may be overestimated by approximately 2% and varies depending on the device used. This may lead to increased rates of unrecognized hypoxemia.[14]

Intravenous dyes such as methylene blue or indocyanine green, sometimes used for surgical or diagnostic procedures, will color the serum in the blood and may interfere with the light absorption spectrum, resulting in falsely low readings.[15][16]

Dyshemoglobinemias, such as carboxyhemoglobinemia, methemoglobinemia, and others, will change blood color and absorption spectrum and lead to false readings. In these cases, confirmation with a co-oximeter should be obtained. In addition, some of the newer pulse oximeters that utilize multiple wavelengths may display methemoglobinemia.

Light pollution into the sensor of the probe due to ambient light or light from another probe may produce an inaccurate reading. This should be avoided by covering the site or the probe itself.

As stated, pulsating blood is necessary for an accurate pulse oximeter reading. The pulse amplitude in a tissue bed accounts only for 5% of available pulse oximeter signals for analysis. Decreased pulse wave amplitude due to severe hypotension, cold extremities, Raynaud disease, or excessive motion may interfere with an accurate reading.[17]

Hospital-grade pulse oximeters can read through perfusing cardiac arrhythmias such as atrial fibrillation and premature atrial or ventricular contractions. In addition to the oxygen saturation value, most pulse oximeters display the plethysmographic waveform, an additional parameter ensuring accuracy. 

Pulse oximeter manufacturers are working to mitigate these factors using different strategies with hardware sensors and software algorithm improvements. Therefore, publications reporting limitations of certain pulse oximeters may be specific to that manufacturer or model. 

If a healthcare provider believes the pulse oximeter reading is inaccurate or inconsistent with other clinical findings, the pulse oximeter probe can be placed on the provider's finder to ensure functioning equipment.

Complications

Pulse oximeters are a noninvasive device and are very well tolerated. They are used in all age groups ranging from neonates to geriatric populations. Energy transfer to patients is low. While heat blisters with prolonged use of specific sensors are possible, most complaints come from allergic reactions to the adhesives or the mechanical adhesive properties of the single-use sensors. Pressure injury from clip sensors is possible but rare and can be minimized using adhesive probes. Generally, pulse oximeters are very well tolerated and have a very low risk of complication compared with arterial blood gas measurements.

Patient Safety and Education

No specific patient education is needed beyond explaining the sensor measures the oxygen level in the patient’s blood. The risk with these devices is minimal, as mentioned above. However, the care provider should instruct patients to report any discomfort experienced. 

Clinical Significance

Pulse oximetry is part of standard intra-operative monitoring and is recommended by the ASA, the World Federation of Societies of Anesthesiologists, and the World Health Organization.[18] With the use of pulse oximeters as a standard of care for all patients receiving anesthesia, for several categories of patients in emergency and urgent care settings, and to monitor a significant percentage of hospitalized patients, the rate of undiagnosed hypoxic events leading to adverse outcomes has decreased significantly as we can monitor oxygen saturation continuously.[19] Evidence suggests using pulse oximetry in children reduces mortality rates when used in conjunction with oxygen administration.[20]

Spot checks in hospitalized patients are less optimal, as breathing and oxygenation are dynamic processes and can change rapidly. One challenge with employing devices that continuously monitor parameters is that healthcare professionals must monitor the device. Fortunately, sophisticated monitoring stations are available that alarm when a critical value is reached and can notify the patient care provider by phone or pager. Individualized alarm settings should be used for pulse oximeter alarm parameters to minimize false alarms and associated alarm fatigue. 

Limitations of pulse oximetry include the inability to detect hyperoxemia and the inability to measure ventilation or arterial oxygen tension. 

Interestingly, no clinical trials show a definitive benefit on mortality or resource allotment when pulse oximetry is utilized. 

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Disclosure: Klaus Torp declares no relevant financial relationships with ineligible companies.

Disclosure: Pranav Modi declares no relevant financial relationships with ineligible companies.

Disclosure: Elizabeth Pollard declares no relevant financial relationships with ineligible companies.

Disclosure: Leslie Simon declares no relevant financial relationships with ineligible companies.