To the Editor: Accurate and precise temperature measurement, which is an important part of a patient’s clinical examination, can be obtained from several locations, including the distal esophagus, rectum, bladder, and pulmonary artery. However, measuring temperature in these locations is invasive and impractical for most patients. A simple reliable accurate and non-invasive method for measuring temperature is needed in clinical practice. Finvers et al. developed a novel non-invasive continuous temperature assessment method using a wireless temporal artery bandage thermometer (WiTAT). Given the potential value of WiTAT but the absence of clinical data about its precision and accuracy, we performed a prospective evaluation of the agreement in temperature assessment between WiTAT and an established method of core temperature thermometry (bladder). After Ethics Committee approval and patients’ written informed consent, we recruited five males and nine females based on an estimate that a minimum of 14 patients with 12 temperature measurements would be needed to have 90% power to detect a 0.25 C difference in measured temperatures. The patients, ranging in age from 19 to 74 yr and with a minimum range of 1 C in their recorded temperatures in the 72 hr prior to consent, were admitted to a medical-surgical intensive care unit (ICU). Temperature measurements were performed hourly and in a rapid sequential manner from the skin overlying the temporal artery (WiTAT) and from within the bladder (Level 1 Foley Catheter temperature Sensor, Smiths Group PLC., Rockland, MA, USA) as part of routine clinical monitoring performed by bedside nurses. Wireless temporal artery bandage thermometer temperatures were recorded at foursecond intervals directly into a closed and locked bedside laptop computer (to blinded clinicians and investigators) whose clock was synchronized with that of the ICU’s electronic patient information system. Bladder temperature measurements (manufacturer documented accuracy ± 0.2 C in the range of 5-45 C) were displayed continually on the bedside monitor and were recorded hourly directly into the ICU’s electronic patient information system with a time stamp. Temperature measurement agreement between WiTAT and the bladder thermometer was analyzed using the procedures described by Bland and Altman. Limits of agreement were clinically (±0.5 C) defined. Mean differences in measured temperatures were calculated along with the standard deviations of the differences using a one-way repeated measures analysis of variance with patient as the classification variable. Statistical analysis was performed using R, version 2.9 (R Foundation for Statistical Computing, Vienna, Austria). For analysis, we used 999 WiTAT-bladder temperature observations that were recorded within one minute of each other (Figure). The mean difference between temperatures measured by WiTAT and the bladder thermometer was 0.09 C (95% confidence interval [CI], 0.02 C to 0.16 C). Agreement between the two devices was better for normothermia (36.0 C to \38.3 C) (mean 0.28 C; 95% CI, 0.21 C to 0.35 C) than for hypothermia (\36 C) (mean H. T. Stelfox, MD, PhD (&) J. Conly, MD J. Haslett, PhD S. Zwierzchowski, M Eng University of Calgary, Calgary, AB, Canada e-mail: tom.stelfox@albertahealthservices.ca