OBJECTIVE: This study tested the effects of low perfusion caused by emerging sepsis on the reliability of a new pulse oximetry technology (Masimo SET; IVY 405T) compared with a standard pulse oximeter (Nellcor N-200). DESIGN: Randomized trial. SETTING: University animal research facility. SUBJECTS: Twenty-six anesthetized, ventilated (Fio, 1.0), adult rabbits. INTERVENTIONS: Pneumonia/sepsis was induced by tracheal instillation of Escherichia coli. Oxygen saturation was measured by pulse oximetry (Spo ) and recorded continuously until death. Arterial oxygen saturation (Sao2) was measured hourly by oximetry and whenever Spo dropped to </=95%, or whenever a difference of >/=5% between devices occurred. Spo2 sensors were positioned at both forelegs and switched hourly. MEASUREMENTS AND MAIN RESULTS: The total time of signal loss was longer with the N-200 vs. the IVY: 65 (4-299) mins vs. 7 (0-97) mins [median (range)], p < 0.001. Signal loss was more prevalent during the first 80% of the experimental time with the N-200 compared with the IVY. Nineteen of 26 animals had a total of 62 episodes of a falsely low Spo2 value with either one of the two devices associated with hemodynamic deterioration. Median bias (Spo2 - Sao2) was small, but variability of bias values increased toward the end of the experimental time with both devices. CONCLUSIONS: The pulse oximeter equipped with Masimo SET was less prone to signal loss than the standard pulse oximeter in this sepsis model. Episodes of falsely low Spo2 readings may occur, and deviation of Spo2 from Sao2 may be increased with deteriorating hemodynamics with both devices.
OBJECTIVE: This study tested the effects of low perfusion caused by emerging sepsis on the reliability of a new pulse oximetry technology (Masimo SET; IVY 405T) compared with a standard pulse oximeter (Nellcor N-200). DESIGN: Randomized trial. SETTING: University animal research facility. SUBJECTS: Twenty-six anesthetized, ventilated (Fio, 1.0), adult rabbits. INTERVENTIONS:Pneumonia/sepsis was induced by tracheal instillation of Escherichia coli. Oxygen saturation was measured by pulse oximetry (Spo ) and recorded continuously until death. Arterial oxygen saturation (Sao2) was measured hourly by oximetry and whenever Spo dropped to </=95%, or whenever a difference of >/=5% between devices occurred. Spo2 sensors were positioned at both forelegs and switched hourly. MEASUREMENTS AND MAIN RESULTS: The total time of signal loss was longer with the N-200 vs. the IVY: 65 (4-299) mins vs. 7 (0-97) mins [median (range)], p < 0.001. Signal loss was more prevalent during the first 80% of the experimental time with the N-200 compared with the IVY. Nineteen of 26 animals had a total of 62 episodes of a falsely low Spo2 value with either one of the two devices associated with hemodynamic deterioration. Median bias (Spo2 - Sao2) was small, but variability of bias values increased toward the end of the experimental time with both devices. CONCLUSIONS: The pulse oximeter equipped with Masimo SET was less prone to signal loss than the standard pulse oximeter in this sepsis model. Episodes of falsely low Spo2 readings may occur, and deviation of Spo2 from Sao2 may be increased with deteriorating hemodynamics with both devices.
Authors: Helmut D Hummler; Anja Engelmann; Frank Pohlandt; Josef Högel; Axel R Franz Journal: Intensive Care Med Date: 2006-06-30 Impact factor: 17.440
Authors: Helmut D Hummler; Anja Engelmann; Frank Pohlandt; Josef Högel; Axel R Franz Journal: Intensive Care Med Date: 2004-01-13 Impact factor: 17.440