Perioperative Management of Temperature in Children and Influence of Hypothermia on Blood Clotting in Children. (Peritemp)

Brno University Hospital

Status: Completed

Conditions: Perioperative Hypothermia

Treatments: Diagnostic Test: Coagulation testing

Study type: Observational

Funder types: Other

Identifiers

NCT03273894

Temperature KDAR 2017

Details and patient eligibility

About

Perioperative hypothermia carries high risk of associated complications. In the observational study, the standard perioperative temperature management will be evaluated and the influence of the hypothermia on the coagulation system according to routine coagulation testing in combination with ROTEM will be evaluated.

Full description

Perioperative hypothermia is one of the complications of surgical interventions in total or regional anaesthesia. It is defined as a drop in body core temperature under 36°C. It occurs as a result of combination of anaesthesia, effecting of central thermoregulation control, environment temperature (i.e. operating theatre) and unsufficient isolation combined with patient's unability to actively warm up. As the body temperature drop in patients under anaesthesia is very frequent, body temperature checks became part of surgical patients care optimalisation. Furthermore, it is associated with complications, such as higher incidency of surgical wound infection, elongated healing process, longer time spent in a hospital, cardiac complications, elongated effect of most of anaesthetics, immunity and blood clotting disorders. Hypothermia elongates the initial phase of coagulation and results in thrombocytes malfunction. Normothermia reduces blood loss.

This prospective observative study has two parts. In the first one, investigators will evaluate the perioperative management of temperature in paediatric patients in Department of children anaesthesia and intensive care, University hospital Brno, Czech republic, where is intended to involve 1,000 patients. In the second phase, the patients who, based on the first phase of the study, would be the most prone to perioperative hypothermia, will be examined for any change of coagulation parameters related to the hypothermia. Investigators intend to involve 100 consecutive patients of the original group. The examined parameters are standard coagulation tests, EXTEM, FIBTEM tests obtained from a rotational thromboelastometry, or other ROTEM test related to the particular pathology. Investigators will use a standardized method of fluid management to affect dilutional coagulopathy.

Standard perioperative patient's monitoring - temperature sensor monitoring of body temperature, ECG, noninvasive blood pressure, oxygen saturation, EtCO2

Temperature management:

• the anaesthetist decides if some warming tools are needed and notes the used ones, which involve: warmed infusion, heating blanked, air warming system, infusion pipe heater, increasing of temperature in the operating theatre, covering the patient or another method of temperature management

Monitored parameters in the first phase:

• body temperature before the intervention (measured in the office previously), operating theatre's temperature at the beginning of anaesthesia
• body temperature during the intervention including the way of measuring, marked each 15 minutes
• body temperature at the end of the entire intervention, including signs of the patient's heat discomfort
• body temperature during resting time in the after-surgery resting room

Monitored parameters in the second phase:

• monitored parameters in the first phase + following:
• blood sampling for standard coagulation tests (following initial of general anaesthesia) + EXTEM, FIBTEM. In case of any pathology found here, more relevant test are run. The test is analysed by anaesthetist or ICU doctor, where the ROTEM machine is.
• blood sampling for standard coagulation tests (prior to the end of the surgical intervention) + EXTEM, FIBTEM. In case of any pathology found here, more relevant test are run. The test is analysed by anaesthetist or ICU doctor, where the ROTEM machine is.
• if body temperature is below 34°C, two sets of ROTEM tests are run: one at patient's body temperature, following by another one at a standard temperature (37°C).

Statistic evaluation:

• demographic - age, sex, type of surgery, duration of surgery, type of anaesthesia
• changes of core temperature during the perioperative care and influence of used warming tools, side effects of changes of core temperature
• laboratory tests - standard coagulation tests and ROTEM - EXTEM, FIBTEM test

Enrollment: 102 patients

Sex: All

Ages: Under 19 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• paediatric patients of age 0 - 18 years (+ 364 days) indicated to a surgical intervention with expected duration longer than 30 minutes
• informed consent of the patient's legal representative to blood sampling in order to run the coagulation tests

Exclusion criteria

• surgical intervention shorter than 20 minutes for the second phase:
• disagreement of the patient and their legal representative
• preexisting blood clotting disorder
• potential damage on the patient caused by non-indicated blood sampling (newborns with low, very low or extremely low birth weight)

Trial design

102 participants in 1 patient group

Paediatric patients undergoing surgery in general anesthesia

Description:

Paediatric patients undergoing surgery in general anesthesia with the expected duration over 30 minutes

Treatment:

Diagnostic Test: Coagulation testing