跳至主要内容
临床试验/NCT05819788
NCT05819788招募中不适用

Outcomes of Fresh Frozen Plasma Usage During Cardiopulmonary Bypass in Congenital Cardiac Surgery.

University of Alberta1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2023年8月28日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
500
试验地点
1
主要终点
Transfusion

研究概览

简要总结

When small children undergo heart surgery with the heart-lung machine, in the past, blood products to help the blood clot such as Fresh Frozen Plasma (FFP) was routinely used in children under 10kg. With blood clot monitoring technology, we feel that it might not be necessary to expose all children to FFP. We want to determine if those children who did not receive FFP bleed more or require more blood products as compared to those who did receive FFP while on the heart lung machine.

详细描述

This will be a single center, retrospective study. Our cohort will include pediatric patients between 4 and 8 kilograms undergoing congenital cardiac surgery with cardiopulmonary bypass between January 2019 and January 2023. Patients will be divided into two groups: FFP given at onset of CPB and no FFP given intraoperatively. Patients requiring FFP for heparin resistance and anti-thrombin III deficiency will be excluded. Patient clinical, surgical, and bypass characteristics, transfusion, and bleeding outcomes will be collected using REDCAP and via chart review using Connect Care.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

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

入选标准

  • pediatric patients between 4 and 8 kilograms undergoing congenital cardiac surgery with cardiopulmonary bypass

排除标准

  • Patients requiring FFP for heparin resistance and anti-thrombin III deficiency will be excluded

结局指标

主要结局

Transfusion

时间窗: 24 hours

Units of blood products transfused

Bleeding

时间窗: 24 hours

Chest tube output

次要结局

  • Length of stay(5 days)
  • Length of ventilation(5 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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