Introduction: Transcatheter Aortic Valve Replacement (TAVR) procedures at our institution were complicated by perioperative hypothermia despite use of the standard of care forced-air convective warming device (the BairHugger, Augustine Medical Inc, Eden Prairie, MN, USA). To remedy this problem, we initiated a quality improvement process that investigated the use of a conductive warm water-circulating device (the Allon ThermoWrap, Menen Medical Corporation, Trevose, PA, USA), and hypothesized that it would decrease the incidence of perioperative hypothermia.
Methods: We compared two different intraoperative warming devices using a historic control. We retrospectively reviewed intraoperative records of 80 TAVRs between 6/2013 and 6/2015, 46 and 34 of which were done with the forced-air and water-circulating devices, respectively. Continuous temperature data obtained from pulmonary artery catheter, temperature upon arrival to cardiothoracic ICU (CTU), age, BSA, height, and BMI were compared.
Results: Patients warmed with both devices were similar in terms of demographic characteristics. First recorded intraoperative temperature (mean 36.26 ± SD 0.61 vs. 35.95 ± 0.46°C, p = 0.02), lowest intraoperative temperature (36.01 ± 0.58 vs. 34.89 ± 0.76°C, p<0.001), temperature at the end of the procedure (36.47 ± 0.51 vs. 35.17 ± 0.75°C, p<0.001), and temperature upon arrival to the CTU (36.35 ± 0.44 vs. 35.07 ± 0.78°C, p<0.001) were significantly higher in the water-circulating group as compared to the forced-air group.
Conclusion: A quality improvement process led to selection of a new warming device that virtually eliminated perioperative hypothermia at our institution. Patients warmed with the new device were significantly less likely to experience intraoperative hypothermia and were significantly more likely to be normothermic upon arrival to the CTU.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5456084 | PMC |
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0178600 | PLOS |
PLoS One
September 2017
Department of Anesthesiology and Perioperative Medicine, Tufts Medical Center, Boston, MA, United States of America.
Introduction: Transcatheter Aortic Valve Replacement (TAVR) procedures at our institution were complicated by perioperative hypothermia despite use of the standard of care forced-air convective warming device (the BairHugger, Augustine Medical Inc, Eden Prairie, MN, USA). To remedy this problem, we initiated a quality improvement process that investigated the use of a conductive warm water-circulating device (the Allon ThermoWrap, Menen Medical Corporation, Trevose, PA, USA), and hypothesized that it would decrease the incidence of perioperative hypothermia.
Methods: We compared two different intraoperative warming devices using a historic control.
Crit Care Med
August 2015
1Department of Neurology, Weill Cornell Medical College of Weill Cornell University, New York Presbyterian Hospital, New York, NY. 2Department of Neurosciences, Weill Cornell Medical College of Weill Cornell University, New York Presbyterian Hospital, New York, NY. 3Department of Pharmacy, Weill Cornell Medical Center, New York Presbyterian Hospital, New York, NY. 4Department of Nursing, Weill Cornell Medical College of Weill Cornell University, New York Presbyterian Hospital, New York, NY. 5Department of Neurology, Neurosurgery and Biomedical Sciences, Cedars Sinai Medical Center, Los Angeles, CA.
Objective: We performed a systematic review of the published evidence regarding nonpharmacologic antishivering interventions in various clinical settings.
Data Sources: Studies through November 2014 were identified using predefined search terms in electronic databases, including PubMed, the Cochrane Library, EMBASE: Excerpta Medica (Ovid), and Web of Science.
Study Selection: All identified articles were critically analyzed by applying prespecified criteria.
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