Effect of Active Warming on Surgical Site Infections
Surgical Site Infection, Ventral Hernia
About this trial
This is an interventional prevention trial for Surgical Site Infection focused on measuring Hypothermia, Surgical Wound Infection, Herniorrhaphy, Nursing care
Eligibility Criteria
Inclusion Criteria:
- Patients with American Society of Anesthesiologists score I-II-III,
- 18-70 years old,
- Patients undergoing abdominal surgery (ventral hernia)
- Patients whose operation lasts longer than 30 minutes and less than 3 hours
Exclusion Criteria:
- Patients with American Society of Anesthesiologists score IV-V
- Patients with morbid obese (BMI> 40kg / m^2)
- Patients with neurological, psychiatric, neuromuscular disease
- Alcohol and drug addict patients
- Mental retarded patients
- Patients taking medications that affect thermoregulation, such as vasodilators
- Patients with a history of thyroid disease
- Pregnant women
- Patients undergoing pre-intra-post-blood transfusion
- Patients with blood glucose levels above 200 mg / dl
Sites / Locations
- Muğla Sıtkı Koçman University Training and Research HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
No Intervention
Experimental
Experimental
Control Group
Underbody Blanket Group
Surgical Access Blanket Group
Body temperature of the patients will be measured in the pre-operative service and in the waiting room. Sociodemographic characteristics form, preoperative, intra and postoperative evaluation forms will be completed. Body temperature, blood pressure, respiratory rate, heart rate and O2 saturation of the patients will be monitored every 15 minutes during the operation and postoperative 2 hours and data will be recorded on the data collection form.
Patients with hypothermia (<36C) will be warmed by air blown underbody blanket before the surgical procedure. Warming procedure will be continued during and postoperative 2 hours of surgery. Body temperature will be measured by tympanic temperature gauge. Intravenous fluid, antiseptic solutions and irrigation fluids will be given to the patients during surgery by heating before administering. Body temperature, blood pressure, respiratory rate, heart rate and O2 saturation of the patients will be monitored every 15 minutes during the operation and postoperative 2 hours and data will be recorded on the data collection form.
Patients with hypothermia (<36C) will be warmed by air blown surgical access blanket before the surgical procedure. Warming procedure will be continued during and postoperative 2 hours of surgery. Body temperature will be measured by tympanic temperature gauge. Intravenous fluid, antiseptic solutions and irrigation fluids will be given to the patients during surgery by heating before administering. Body temperature, blood pressure, respiratory rate, heart rate and O2 saturation of the patients will be monitored every 15 minutes during the operation and postoperative 2 hours and data will be recorded on the data collection form.