Critical Care Nurse. 2002;22: 69-74
Copyright © 2002 by the American Association of Critical-Care Nurses.
Protocols for Practice
Applying Research at the Bedside
Pulse Oximetry*
Mary Jo Grap, PhD, RN, CCRN
Mary Jo Grap is currently an associate professor in the School of Nursing, Virginia Commonwealth University, Richmond, Va.
* This article was first published in CRITICAL CARE NURSE February 1998. An update follows.
This column is designed to provide the latest research findings in patient care in a format that is easy to understand and integrate into clinical practice. The information is drawn from individual protocols in the various Protocols for Practice series available from AACN, which cover research-based practice protocols in detail.
Pulse oximetry is a noninvasive technology used to estimate oxyhemoglobin saturation. As many as 87% of nurses report that they regularly use this technology to assess the status of patients; however, a recent report of hospital staffs knowledge of pulse oximetry showed that only 36% of the nursing staff felt they had adequate training in the use of pulse oximetry. In addition, only 68.5% of all hospital staff tested (nursing and medical staff) correctly stated what pulse oximeters measure. Answers to questions regarding the principles of pulse oximetry, potential errors, normal ranges, or the physiology of oxygen hemoglobin dissociation varied but generally reflected limited understanding.1 The questions and answers presented here may enhance your understanding of this commonly used technology.
Q: What does pulse oximetry measure?
Pulse oximetry is used for continuous noninvasive measurement of arterial oxygen saturation. Most of the oxygen transported by the blood is bound to hemoglobin, and the degree of bindingthe saturationis determined by the percentage of hemoglobin that is loaded with oxygen.2 The pulse oximeter detects and calculates the absorption of light by functional hemoglobins to produce a measurement, SpO2, that is an estimate of arterial oxygen saturation (SaO2). Functional hemoglobins are those active in the transport of oxygen: oxygenated and deoxygenated (reduced) hemoglobin. Absorption of light by oxygenated hemoglobin differs from the absorption by deoxygenated hemoglobin. The pulse oximeter probe contains two light-emitting diodes on one side, which emit two wavelengths of monochromatic lightred and infraredand a photo detector on the other side (Figure 1
). The two diodes are cycling on and off 400 or 480 times per second, with only one on at a time.3 This enables a single detector to be used to sample first one wavelength and then the other.
Both wavelengths of light are also absorbed by venous blood and tissues. The hemoglobin absorption of light is analyzed over a full pulse beat to make the saturation measurement independent of these factors. The total absorption of light has a constant component from the tissue and from steadily flowing venous blood, and a changing component as a result of arterial pulsation. The constant component is subtracted from the total, so that the net absorption of each wavelength can be attributed to arterial blood only.3 A calculation based on previously determined calibration curves is used to relate this transcutaneous light absorption to directly measured SaO2. Pulse oximeters are calibrated empirically by using observations taken from healthy volunteers.4 To estimate SpO2 with a wide range of pulse amplitudes, the pulse oximeter automatically increases its amplifications as the pulse signal decreases. The saturation values that are displayed are not instantaneous but are averages taken over 3 to 10 seconds to help reduce the effect of pressure wave variations due to motion of the subject.5
Therefore, pulse oximetry measures only the percentage of hemoglobin that is carrying oxygen. It provides no specific information about the patients overall level of hemoglobin, adequacy of ventilation, or how well the oxygenated hemoglobin is being delivered to the tissues.
Q: How accurate is pulse oximetry?
Numerous studies have addressed the accuracy of pulse oximeters, primarily over the range of 70% to 100% saturation. Excellent correlation has been found between pulse oximetry and the "goldstandard" in vitro CO-oximetry measurements.68 These have been found to be accurate for SpO2 from 70% to 100% and within ± 2%. For SpO2 above 70%, approximately 68% of the data will fall within ±2% of the actual saturation, and 95% of the data will fall within ±4% of the actual saturation. For example, in a patient with a pulse oximeter reading of 92%, 95% of the time the true SaO2 value, as measured by arterial blood gases, would be between 88% and 96%. For saturations below 70%, manufacturers generally state that accuracy is "unspecified." Pulse - rate monitoring with pulse oximetry ranges from 20 to 30, to 250 beats per minute, with manufacturers accuracy statements indicating a range from ±1 to 2 beats per minute for the scale stated.9,10
Q: When should pulse oximetry be used?
Because desaturation is detected earlier by pulse oximetry than by clinical observation,7,11,12 the use of pulse oximetry is recommended for any patient at risk for hypoxemia (Table 1
753).
Because the algorithms used for deriving SpO2 from light absorption are based on healthy volunteers, single pulse oximetry measurements for patients with low arterial saturation (less than 70%) may result in inaccuracies; however, even in these patients it is a valuable tool for showing trends.19,5456 In addition, pulse oximetry may be less useful in the presence of dyshemoglobins2,5761 such as carboxyhemoglobin, which is seen in smokers, patients suffering from carbon monoxide inhalation, and patients undergoing dapsone therapy; and methemaglobin, seen in patients undergoing nitrate, nitroprusside, or lidocaine therapy. It may also be less useful in patients with severe anemia, because the hemoglobin level may be too low to ensure proper functioning of the oximeter.6264
Q: What is the best location for the pulse oximeter probe?
Choose a site with the best pulsatile vascular bed: the finger (Figure 2
), toe, ear lobe, and bridge of the nose have been used. In infants, flexible probes work through the palm, foot, penis, or arm. The cheek or wing of the nostril have also been used. However, overall performance of finger probes is generally found to be better than performance of probes at other sites.8 However, because the ear-lobe is the least vasoactive site and is least susceptible to signal loss, it may show faster response and greater accuracy during periods of vasoconstriction and hypotension. Nose and forehead probes perform poorly when SpO2 is low. Manufacturers generally recommend use of the foot for infants56,6570 (Figure 3
).
When placing probes on fingers or toes, remove nail polish, especially blue, black, green, brown/ red, or synthetic nails; or place the probe sideways on the finger. Synthetic nails and some colors of nail polish may result in errors of 3% to 6%. In addition, SpO2 values may be lower in dependent extremities than in nondependent sites. Blood flow to the extremity where the sensor is placed should not be impeded in any way. The sensor should be placed on the extremity opposite arterial lines and noninvasive blood pressure monitoring devices so that pulsatile flow is not interrupted.2,22,7173
Q: What are normal parameters and what should also be assessed with pulse oximetry?
Optimal SpO2 is greater than 95%; SpO2 less than 90% reflects desaturation. However, SpO2 is not an adequate monitor of ventilation. In situations of ventilation or acid-base abnormalities (resulting in shifts of the oxyhemoglobin dissociation curve), arterial blood gases must also be monitored. Remember that measurements during hypoperfusion and vasoconstriction may not be accurate. Nursing care decisions should be based on SpO2 trends rather than on isolated values. If SpO2 measurements and other oxygenation assessment data conflict, obtain arterial blood gases to verify oxygenation status. Include pulse oximetry measurement as only one part of a total oxygenation and ventilation assessment. Also remember that SpO2 indicates the amount of hemoglobin that is saturated with oxygen. It does not provide any information about the amount of hemoglobin present, the adequacy of ventilation, or cardiac output. These must also be assessed on a regular basis.
In summary, pulse oximetry is an extremely valuable, noninvasive technology and with a complete understanding of its uses and limitations, this technology can assist nurses in providing comprehensive care to their patients.
This article is based on the protocol "Pulse Oximetry" by Mary Jo Grap, from the Noninvasive Monitoring series of AACNs Protocols for Practice. It can be obtained from AACN, 101 Columbia, Aliso Viejo, CA 926561491, (800) 899-AACN.
Acknowledgments
"Pulse Oximetry" by Mary Jo Grap, one of AACNs Protocols for Practice, was sponsored by Nellcor Puritan Bennett.
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