跳至主要内容
临床试验/NCT05874843
NCT05874843招募中不适用

Validation of Point-of-care Thromboelastography (TEG 6s) in Pediatric Patients

Indiana University1 个研究点 分布在 1 个国家目标入组 125 人开始时间: 2023年9月11日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
125
试验地点
1
主要终点
TEG 6s viscoelastic measurement, angle, in pediatric surgical patients

研究概览

简要总结

The goal of this observational study is to learn about the performance of the TEG6s in normal pediatric patients. The main questions it aims to answer are: What are the normal TEG 6S lab results in normal pediatric patients and how do they compare to existing published reference ranges. Participants and their guardians will be asked to submit a small amount of blood at the beginning of an elective operation for analysis in the TEG 6s machine.

详细描述

Trauma is the leading cause of death in children. Researchers, starting with Trunkey et al., have described three general time points of mortality after trauma - in the field, early secondary to hemorrhage and late due to infectious complications. Early mortality after trauma is specifically linked to hemorrhage. Trauma-induced coagulopathy is a multifactorial phenomenon present after trauma in both children and adults that can worsen hemorrhage and ultimately lead to increased mortality. Classical laboratory measurements of the coagulation pathway (PT, PTT, INR, fibrinogen, platelet count) have shown derangement after trauma and are correlated with mortality. However, these traditional tests of coagulation function take time to run as they are drawn and sent to a laboratory for evaluation and therefore provide a delayed snapshot of a potentially evolving coagulopathy scenario. Adult trauma centers have increasingly incorporated viscoelastic measures of the coagulation cascade to evaluate for and subsequently treat trauma-induced coagulopathy. One such test is thromboelastography (TEG) which is a whole blood assay that assesses functional clot kinetics and stability. It provides information on how various hemostatic factors, including coagulation factors, platelets, and fibrinogen, contribute to the clot. A 2016 randomized-controlled trial in adult trauma patients who met criteria for the institutions massive transfusion protocol were randomized to transfusion guided by TEG or by conventional measure of coagulopathy. The authors found increased survival in the TEG group as well as less transfusion of platelets and fresh frozen plasma.

TEG assesses the clot rate, clot strength, and clot stability, which then assists the clinician in choosing appropriate blood component therapy. The American College of Surgeons Trauma Quality Improvement Program recommends the use of thromboelastography when patients are at risk for trauma-induced coagulopathy. Visicoeslastic evaluation of the coagulation pathway has become the standard of care in adult trauma patients to provide information on a patient's coagulation status, particularly when the patient is requiring multiple blood products. This allows the physician to deliver a targeted hemostatic resuscitation appropriate for the patient needs in real-time. This can result in a decrease of blood products and quicker reversal of the trauma induced coagulopathy.

Riley Hospital for Children at IU Health has a TEG 5000 machine (Haemonetics Corp.) which performs the coagulation tests needed to help guide the resuscitation of a critical trauma patient. While an improvement over previous tests (such as INR, platelet count, PTT), the TEG 5000 still takes 45-60 minutes to get the results needed to guide fluid/blood resuscitation, making the results outdated as the patient has potentially received multiple units of blood products and/or had additional bleeding during that time. The TEG 5000 machine also has very specific environmental, and preparation needs (i.e. flat surface which is not bumped; controlled pipetting (dropping) of blood products into machine as well as mixing of reagents) that is very difficult to do in a busy trauma bay/emergency department with a critical patient.

The TEG 6s assays are performed in a microfluidic cartridge which only requires a small amount of a patient's blood be transferred to the cartridge for analysis. The vibration frequency of the blood meniscus at which resonance occurs is used to create a clot dynamics tracing. The sample is drawn automatically into the testing chambers rather than requiring manual pipetting, leading to less user variability. This simpler operation provides results in 15-20 minutes, making the test more clinically useful in guiding transfusion therapy during active bleeding.

TEG 6s and TEG 5000 have been evaluated in adult patients with good agreement between the modalities. More specifically, the TEG 6s has been validated in adult trauma patients. However, few pediatric studies exist.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
3 Months 至 18 Years(Child, Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients less than 18 years of age undergoing elective pediatric surgical care in the operating room at Riley Hospital for Children

排除标准

  • •Known disorder of coagulation pathway(s)
  • •Administration of medications that may alter the coagulation cascade
  • •Patients in foster care or wards of the court

研究组 & 干预措施

Pediatric Participants

Other

Pediatric surgery patients undergoing elective pediatric surgical cases under anesthesia will be invited to participate in this prospective laboratory test validation study. The results of the interventional test will not be used in clinical decision making for the participant.

干预措施: Thromboelastography (TEG 6S) (Diagnostic Test)

结局指标

主要结局

TEG 6s viscoelastic measurement, angle, in pediatric surgical patients

时间窗: Day 1, sample drawn at the time of clinical IV placement and evaluated within 1-4 hours of collection

To validate the TEG 6S measurement values in pediatric patients by comparing its viscoelastic values with those existing published reference ranges

TEG 6s viscoelastic measurements, R time, in pediatric surgical patients

时间窗: Day 1, sample drawn at the time of clinical IV placement and evaluated within 1-4 hours of collection

To validate the TEG 6S measurement values in pediatric patients by comparing its viscoelastic values with those existing published reference ranges

TEG 6s viscoelastic measurement, maximum amplitude, in pediatric surgical patients

时间窗: Day 1, sample drawn at the time of clinical IV placement and evaluated within 1-4 hours of collection

To validate the TEG 6S measurement values in pediatric patients by comparing its viscoelastic values with those existing published reference ranges

TEG 6s viscoelastic measurement, lysis at 30 minutes, in pediatric surgical patients

时间窗: Day 1, sample drawn at the time of clinical IV placement and evaluated within 1-4 hours of collection

To validate the TEG 6S measurement values in pediatric patients by comparing its viscoelastic values with those existing published reference ranges

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Matthew Landman

Associate Professor of Surgery

Indiana University

研究点 (1)

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