The Effects of Ambient Temperature and Forced-air Warming on Intraoperative Core Temperature

Overview

The purpose of this study is to determine: 1. the effect of ambient temperature on the rate of core temperature change from 1 to 3 hours after induction of anesthesia (linear phase of the hypothermia curve) in major operations lasting at least a couple of hours and 2. whether the relationship between ambient temperature and rate of core temperature change is different for patients who are or are not warmed with forced-air.

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Factorial Assignment
    • Primary Purpose: Supportive Care
    • Masking: None (Open Label)
  • Study Primary Completion Date: December 2016

Detailed Description

Each patient will be randomly assigned to ambient temperature of 19°C, 21°C, or 23°C. Using a factorial approach, patients will also be randomly assigned to passive insulation or forced-air warming, stratified by the three types of surgery listed below. Group allocation will be based on computer generated codes (randomly permuted block sizes) prepared by Department of OUTCOMES RESEARCH statisticians using SAS statistical software. Allocation of consented patients to designated ambient temperature and forced-air vs. passive insulation will be via a web site that will be accessed by investigators in Bejing about 90 minutes before surgery. Patients assigned to passive insulation will be covered as usual with a cotton gown and single layer of cloth surgical draping. Patients assigned to forced-air warming will also be covered with a gown and surgical drapes, but a forced-air cover (Bair hugger 63500, 3M) will be inserted between the gown and the skin surface. A lower-body cover (about 91 by 221 cm) will be positioned so the lower end of the forced-air segments extend from the ankles upward for the entire length of the cover in thoracic and abdominal cases. The cover's foot drape will extend over the feet, and in turn be covered by the surgical drape. An upper-body forced-air cover will similarly be applied for patients having hip arthroplasties. The forced-air cover will be connected to a Bair Hugger blower and #635 covers set to "high" (≈43°C). Ambient temperature will be adjusted to the designated temperature about an hour before a patient enters the operating room and adjusted as necessary to maintain the designated temperature throughout surgery. General anesthesia will be induced as per usual clinical routine. Neuraxial (epidural or spinal) and other regional blocks are permitted. Any patients whose core temperature decreases to less than 34.5°C will be actively warmed with forced air and the ambient temperature increases to the extent practical.

Interventions

  • Other: Ambient Temperature 19°C
    • Ambient Temperature 19°C
  • Other: Ambient Temperature 21°C
    • Ambient Temperature 21°C
  • Other: Ambient Temperature 23°C
    • Ambient Temperature 23°C
  • Device: Forced-air cover (Bair hugger 63500, 3M)
    • Patients assigned to forced-air warming will also be covered with a gown and surgical drapes, but a forced-air cover (Bair hugger 63500, 3M) will be inserted between the gown and the skin surface.
  • Other: Passive insulation
    • Patients assigned to passive insulation will be covered as usual with a cotton gown and single layer of cloth surgical draping.

Arms, Groups and Cohorts

  • Experimental: Ambient Temp 19°C & Passive Insulation
    • Ambient Temperature 19°C and Passive Insulation: patients assigned to passive insulation will be covered as usual with a cotton gown and single layer of cloth surgical draping.
  • Experimental: Ambient Temp 19°C & Forced-air Warming
    • Ambient Temperature 19°C and Forced-air Warming: patients assigned to forced-air warming will also be covered with a gown and surgical drapes, but a forced-air cover (Bair hugger 63500, 3M) will be inserted between the gown and the skin surface.
  • Experimental: Ambient Temp 21°C & Passive Insulation
    • Ambient Temperature 21°C and Passive Insulation: patients assigned to passive insulation will be covered as usual with a cotton gown and single layer of cloth surgical draping.
  • Experimental: Ambient Temp 21°C & Forced-air Warming
    • Ambient Temperature 21°C and Forced-air Warming: patients assigned to forced-air warming will also be covered with a gown and surgical drapes, but a forced-air cover (Bair hugger 63500, 3M) will be inserted between the gown and the skin surface.
  • Experimental: Ambient Temp 23°C & Passive Insulation
    • Ambient Temperature 23°C and Passive Insulation: patients assigned to passive insulation will be covered as usual with a cotton gown and single layer of cloth surgical draping.
  • Experimental: Ambient Temp 23°C & Forced-air Warming
    • Ambient Temperature 23°C and Forced-air Warming: patients assigned to forced-air warming will also be covered with a gown and surgical drapes, but a forced-air cover (Bair hugger 63500, 3M) will be inserted between the gown and the skin surface.

Clinical Trial Outcome Measures

Primary Measures

  • Rate of Core Temperature Change
    • Time Frame: from 1 to 3 hours after induction of anesthesia
    • Rate of core temperature change from 1 to 3 hours after induction of anesthesia (°C/hour ) linear mixed-effects model to assess the effects of ambient temperature, forced-air warming and their interaction on the rate of core temperature change during 1 to 3h after induction

Participating in This Clinical Trial

Inclusion Criteria

  • Adults scheduled for major open thoracic surgery or video assist thoracic surgery or major abdominal surgery under general anesthesia expected to last at least two hours Exclusion Criteria:

  • Special risk for bleeding or myocardial infarction (as determined by the attending anesthesiologist) – Patients who would otherwise have been actively warmed

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 80 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Peking Union Medical College Hospital
  • Collaborator
    • The Cleveland Clinic
  • Provider of Information About this Clinical Study
    • Principal Investigator: Lijian Pei, Associate Professor – Peking Union Medical College Hospital
  • Overall Official(s)
    • LiJian Pei, MD, Principal Investigator, Associate Prof. of Dept. of Anesthesiology, PUMCH
    • Yuguang Huang, MD, Study Chair, Chair of Dept. of Anesthesiology, PUMCH
    • Daniel I Sessler, MD, Study Director, Chair of Dept. of Outcomes Research, Anesthesiology Institute, Cleveland Clinic

References

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