The purpose of this study is to determine whether externally warming critically ill afebrile adult septic patients will improve indices of immune function and/or clinical outcomes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
60
External warming via forced air warming to a goal body temperature 1.5°C greater than the baseline minimum temperature (within previous 24 hours) for 48 hours
Washington University School of Medicine
St Louis, Missouri, United States
Monocyte human leukocyte antigen (mHLA-DR) expression
Time frame: 48 hours hours following the start of the intervention period
Interferon (IFN)-gamma production
Time frame: 48 hours following the start of the intervention period
Number of patients who acquire nosocomial infections
Number of patients who develop a nosocomial infection (defined as a new infection diagnosed greater than 48 hours after the original sepsis diagnosis) within 30 days of the sepsis diagnosis
Time frame: 30 days after diagnosis of sepsis
Mortality
Time frame: 28 days
Number of patients in whom the intervention is stopped early secondary to hemodynamic changes related to the intervention
Time frame: Through study completion, 2 years
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