Prevalence Survey in France of Unintentional Perioperative Hypothermia and Its Impact on Two Outcomes
- Conditions
- Hypothermia, Perioperative
- Registration Number
- NCT02790086
- Lead Sponsor
- Société Française d'Anesthésie et de Réanimation
- Brief Summary
The primary objectives of the study are
* to perform a survey on the clinical management of unintentional hypothermia during surgery in France.
* to assess the impact of perioperative hypothermia on anemia and myocardial injury.
- Detailed Description
100 investigation centers in metropolitan France will participate in the study, targeting 2000 included patients (20 surgical interventions in each center). The duration of inclusion in each center should last at most 2 weeks.
The selected surgical interventions will be those performed with a high frequency, practiced in all types of hospitals (public, private, university hospital or not), and requiring anesthesia of at leat 30 minutes (general, epidural or intrathecal anesthesia).
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 2000
Not provided
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Core temperature up to 24 hours The temperature will be measured with the same type of thermometer in all investigator sites: SpotOn™ (3M France).
blood loss up to 24 hours Blood loss will be assessed by haemoglobin variation between preoperative and the first post-operative day.
myocardial injury up to 48 hours Troponin T will be measured after the surgical intervention (at least 6 hours after the end of the surgery) and on the second postoperative day (when the patient remains hospitalized).
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Service d'Anesthésie-Réanimation Chirurgicale, Hôpital Cochin
🇫🇷Paris, Ile de France, France