Executive Summary

The appropriateness of a pulse oximeter sensor varies significantly based on the type of patient being monitored and the intended sensor application site. The choice of an inappropriate sensor can result in erroneous oxygen saturation readings, leading to false alarms or to a failure to alarm. Likewise, putting a sensor on the wrong site will affect the amount of light that reaches the photodetector, possibly leading to erroneous readings. To avoid placement problems, check a sensor's labeling for its intended site, and follow the supplier's directions. Also, check the labeling to determine the patient weight ranges for which the sensor is approved.

When using transmittance-based sensors, aligning the LEDs and photodetectors directly across from one another enables the maximum amount of emitted light from the LED to be sensed by the detector and helps prevent false readings.

Who Should Read This

Table of Contents

It's important that the type of pulse oximetry sensor is appropriate to its intended location on the patient and to the type of patient being monitored. The choice of an inappropriate sensor can result in erroneous oxygen saturation readings, leading to false alarms or to a failure to alarm when a patient is at risk.

 

Pulse Oximeter Sensor Selection

Although all pulse oximetry sensors perform the same basic function, they vary in terms of where on a patient they are to be placed. For example, a finger sensor may be used for an adult patient, whereas a forehead sensor may be chosen for a neonatal patient. Therefore, sensor designs take into account factors such as the size of the intended site (e.g., finger, foot). For instance, with disposable sensors, the shape and length of the adhesive bandage depend on where they are designed to be applied. 

 

Sensor Application

Often, it's physically possible to put a sensor on the wrong site. For instance, a neonatal foot sensor can be placed on an infant's toe, and it might seem to fit well when used this way. But doing so may produce inaccurate readings because the distance between a sensor's LED and photodetector is based on the dimensions of the body part for which that sensor is designed. Putting a sensor on the wrong site will affect the amount of light that reaches the photodetector, possibly leading to erroneous readings.

Placement is also a concern with forehead sensors. Products designed for a patient's ear, finger, nose, or toe are transmittance sensors, which use red/infrared (R/IR) light that is transmitted through tissue and then detected. However, products designed for the forehead are reflectance sensors—the R/IR signal is emitted, passes through the tissue, and is then reflected back to the detector side of the sensor. Although it's possible to apply an opened disposable finger sensor by laying it flat across the forehead, any saturation readings obtained from doing so may be incorrect.

A similar problem can occur if the sensor is inappropriate for the patient, such as when an adult finger sensor is placed on a pediatric patient's finger. In addition, because patient weight affects the distance that light must travel between the LED and photodetector, using the right sensor for the patient's weight is important. To avoid placement problems, check a sensor's labeling for its intended site, and follow the supplier's directions. Also, check the labeling to determine the patient weight ranges for which the sensor is approved.

 

Appropriate Alignment of Disposable Transmittance-Based Sensors

Incorrect sensor alignment is a common problem with using disposable transmittance-based sensors and leads to the generation of false readings. When these sensors are applied, the LEDs and photodetectors should be aligned directly across from one another. (See the figure.)

A finger with a disposable adhesive sensor attached. Top: A properly applied sensor. The LED and photodetector are correctly aligned. Bottom: An improperly applied sensor. The LED and photodetector are misaligned, which can lead to problems such as optic bypass.

 

Applying the sensors in this way enables the maximum amount of emitted light from the LED to be sensed by the detector. If an LED and photodetector are misaligned, hospitals may encounter a problem known as optic bypass, which occurs when the light emitted from the LED doesn't properly pass through the tissue's arterial bed before reaching the photodetector. There are markers on most adhesive disposable sensors to indicate when the LED is properly aligned with the photodetector. (Clip-on, reusable finger probes are constructed with the LED and photodetector already aligned.) Note that this is not just a concern during application: Once a sensor is on a patient, clinicians should periodically check it to ensure that proper alignment is maintained.

Glossary

Bibliography

References

Resource List

Topics and Metadata

Topics

Alarm Management; Biomedical Engineering; Technology Management; Technology Selection

Caresetting

Ambulatory Care Center; Ambulatory Surgery Center; Assisted-living Facility; Behavioral Health Facility; Dialysis Facility; Emergency Department; Endoscopy Facility; Home Care; Hospice; Hospital Inpatient; Hospital Outpatient; Imaging Center; Independent Living Facility; Physician Practice; Short-stay Facility; Skilled-nursing Facility; Substance Abuse Treatment Facility; Trauma Center; Rehabilitation Facility

Clinical Specialty

Cardiothoracic Surgery; Cardiovascular Medicine; Critical Care; Nursing

Roles

Biomedical/Clinical Engineer; Materials Manager/Procurement Manager; Nurse

Information Type

Guidance

Phase of Diffusion

 

Technology Class

 

Clinical Category

 

SourceBase Supplier

Product Catalog

MeSH

ICD9/ICD10

FDA SPN

SNOMED

HCPCS

Disease/Condition

 

Publication History