Overview
This study aims to investigate whether intraoperative administration of tranexamic acid based on ROTEMĀ® (Rotational Thromboelastometry), in pediatric patients undergoing scoliosis surgery, results in a difference in intraoperative blood loss when compared to the prophylactic administration of tranexamic acid.
Eligibility
Inclusion Criteria:
- Children undergoing scoliosis surgery under the age of 18
Exclusion Criteria:
- Patients with coagulation disorders
- Patients at an increased risk of thrombosis
- Patients with a history of epilepsy or brain surgery
- Patients with a previous allergic reaction or anaphylaxis history to tranexamic acid
- Severe liver or kidney impairment
- Other cases deemed inappropriate by the researcher