Comparison of Nasal and Forehead Oximetry in Critically Ill Patients at Risk for Decreased Peripheral Perfusion

Last updated: May 8, 2017
Sponsor: Washington University School of Medicine
Overall Status: Completed

Phase

N/A

Condition

Circulation Disorders

Pressure Ulcer

Dizzy/fainting Spells

Treatment

N/A

Clinical Study ID

NCT02382133
201408123
  • Ages 18-90
  • All Genders

Study Summary

Continuous pulse oximetry monitoring is the standard of care in critically ill patients in emergency departments, operating rooms and intensive care units. In patients with poor peripheral perfusion (low blood flow) due to peripheral vascular disease, low body temperature, or shock and the use of medications to raise the blood pressure, clinicians have difficulty obtaining an accurate measurement. This study compares the accuracy of forehead oximetry sensors to nasal alar sensors to lab oximetry measures and on the rate of device related pressure ulcers with both.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Presence of an existing arterial catheter for blood sampling and one of the following:

  2. Difficulty obtaining a consistent signal from a digit or ear sensor or

  3. On pressors of at least 0 .10 mcg/kg/min of norepinephrine or

  4. Core temperature < or equal to 35 degrees C

Exclusion

Exclusion Criteria:

  1. Anatomic impediments (burns, wounds, dressings, etc.) to placement of the sensor onthe forehead or nasal alar

  2. History of known dyshemoglobinemias evidenced by carboxyhemoglobin levels > 10% ormethemoglobin level > 2%

  3. Severe anemia with hemoglobin < 5 g/dL

  4. Pregnant women

Study Design

Total Participants: 43
Study Start date:
October 01, 2014
Estimated Completion Date:
September 30, 2016

Study Description

Continuous pulse oximetry monitoring is the standard of care in critically ill patients in emergency departments, operating rooms and intensive care units. In patients with poor peripheral perfusion (low blood flow) due to peripheral vascular disease, low body temperature, or shock and the use of medications to raise the blood pressure, clinicians have difficulty obtaining an accurate measurement. Several studies have demonstrated the utility of forehead sensor measurements under these clinical conditions. Forehead sensor measurement is considered to be a more central measurement than with digit or ear sensors. However the sensor requires a head band for accurate measurement. On a regular basis, the forehead sensor has led to pressure ulcer development at Barnes-Jewish Hospital despite following vendor recommendations for alternating placement every 8 hours from one side of the forehead to the other. An alternate sensor placed on the nose has recently demonstrated rapid detection of induced drops in oxygen saturation. It has also demonstrated correlation with arterial oxygen saturation measured in a clinical laboratory. The oxygen saturation measurement from the nose is also considered a central measurement. However, studies of the nose sensor were conducted in healthy subjects or during anesthesia care over several hours. Therefore, research is needed to examine the accuracy of the nose sensor in the ICU patient population. In addition, due to concerns for sensor related pressure ulcers in patients with decreased perfusion, the sensor needs to be evaluated for extended periods of time.

Connect with a study center

  • Barnes-Jewish Hospital at Washington University

    Saint Louis, Missouri 63110
    United States

    Site Not Available

  • Barnes-Jewish Hospital at Washington University

    St. Louis, Missouri 63110
    United States

    Site Not Available

Map preview placeholder

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.