• Nancy M Richards, Karen K Giuliano, and Philip G Jones.
• Mid America Heart Institute, Saint Luke's Hospital, 4401 Wornall Road, Kansas City, MO 64111, USA. nrichards@saint-lukes.org
• Resp Care. 2006 Jan 1; 51 (1): 29-35.

ObjectiveTo assess the clinical performance of 3 new-generation pulse-oximetry signal-processing software systems (Philips FAST, Masimo SET, and Nellcor N-3000) during ambulation after open-heart surgery.DesignProspective, convenience sample.SettingCardiac surgical progressive care unit in a 629-bed, not-for-profit, tertiary-care teaching hospital.PatientsStatus post-cardiac-surgery patients (n = 36) during their first postoperative ambulation.InterventionsNone.ProtocolRandomization was used for digit and hand selection, and all 3 devices were used continuously during ambulation. Data on dropouts, false alarms, and correlation with heart rate were recorded. We continuously measured arterial oxygen saturation via pulse oximetry during ambulation with all 3 devices.ResultsPairwise comparisons indicated significant differences among the 3 devices for data dropout and false alarm. In repeated-measures analysis, the Nellcor N-3000 had the greatest likelihood of data dropout (odds ratio of 31.9 to Masimo and 5.6 to Philips, at the 95% confidence interval). However, the converse was true for false alarms; the Masimo had the most false alarms, with an odds ratio of 17.9 to Nellcor and 2.3 to Philips, at the 95% confidence interval. There were also significantly more dropouts with all 3 devices when readings were taken on a hand on an arm from which a radial graft had been taken (p = 0.004). For heart-rate correlation, the mean absolute difference among the 3 devices was similar: Philips = 4.3 beats/min, Masimo = 5.1 beats/min, and Nellcor = 3.0 beats/min.ConclusionsThere are significant differences among the 3 devices with regard to dropout and false alarms. High numbers of dropouts are problematic because no pulse-oximetry patient information is available during dropout. However, false alarms are even more problematic, because they desensitize clinicians to alarms and call into question the accuracy of displayed data. While our data highlight the statistical differences between the studied oximeters, the clinical implications of these differences warrant further study.

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