Pragmatic, Randomized Optimal Platelet and Plasma Ratios
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 680
- 试验地点
- 24
- 主要终点
- 24-hour Mortality
研究概览
简要总结
Pragmatic, Randomized, Optimal Platelet and Plasma Ratios (PROPPR)is a Phase III trial designed to evaluate the difference in 24-hour and 30-day mortality among subjects predicted to receive massive transfusion ([MT] (defined as receiving 10 units or more red blood cells (RBCs) within the first 24 hours). The goal of PROPPR is to improve the basis on which clinicians make decisions about transfusion protocols for massively bleeding patients.
PROPPR is a Resuscitation Outcomes Consortium (ROC) Protocol. ROC is funded by the National Heart, Lung, and Blood Institute (NHLBI), the United States' Department of Defense (DoD) and the Defence Research and Development Canada. PROPPR will be conducted as a Phase III trial at Level I Adult Trauma Centers in North America.
详细描述
Background: Multiple observational studies have reported that blood product component ratios (i.e., plasma:platelets:RBCs) that approach the 1:1:1 ratio, found in fresh whole blood, are associated with significant decreases in truncal hemorrhagic death and in overall 24-hour and 30-day mortality among injured patients. The rationale for the 1:1:1 ratio is that the closer a transfusion regimen approximates whole blood, the faster hemostasis will be achieved with minimum risk of coagulopathy. The current DoD guideline specifies the use of 1:1:1, and this practice is followed on almost all combat casualties. In other observational studies, leading centers have reported good outcomes across a range of different blood product ratios. For example, a 1:2 plasma:RBC ratio is used with little guidance regarding platelets. The proposed randomized trial is intended to resolve debate and uncertainty regarding optimum blood product ratios.
Study Design: Randomized, two-group, controlled Phase III trial with a Vanguard stage. Equal random allocation to treatment using stratified, permuted blocks with randomly chosen block sizes and stratification by site.
Objective
To conduct a Phase III multi-site, randomized trial in subjects predicted to have a massive transfusion, comparing the efficacy and safety of 1:1:1 transfusion ratios of plasma and platelets to red blood cells (the closest approximation to reconstituted whole blood) with the 1:1:2 ratio. The co-primary outcomes will be 24-hour and 30-day mortality. The PROPPR Trial will be conducted with exception from informed consent (EFIC). Additionally, laboratory data from the trial will add to the understanding of trauma induced coagulopathy (TIC) and inflammation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 15 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subjects who require the highest trauma team activation at each participating center,
- •Estimated age of 15 years or older or greater than/equal to weight of 50 kg if age unknown,
- •Received directly from the injury scene,
- •Initiated transfusion of at least one unit of blood component within the first hour of arrival or during prehospital transport, and
- •Predicted to receive a MT by exceeding the threshold score of either the Assessment of Blood Consumption (ABC) score or the attending trauma physician's judgment criteria
排除标准
- •Received care (as defined as receiving a life saving intervention) from an outside hospital or healthcare facility (Procedures and care given at an outside health facility cannot be documented or controlled resulting in a high variability of standards of care and clinical outcomes.)
- •Moribund patient with devastating injuries and expected to die within one hour of Emergency Department (ED) admission
- •Prisoners, defined as those who have been directly admitted from a correctional facility
- •Patients requiring an emergency thoracotomy
- •Children under the age of 15 years or under 50 kg body weight if age unknown
- •Known pregnancy in the ED
- •Greater than 20% total body surface area (TBSA) burns
- •Suspected inhalation injury
- •Received greater than five consecutive minutes of cardiopulmonary resuscitation (CPR with chest compressions) in the pre-arrival or ED setting
- •Known Do Not Resuscitate (DNR) prior to randomization
- •Enrolled in a concurrent, ongoing interventional, randomized clinical trial
- •Patients who have activated the "opt-out" process or patients/legally authorized representatives that refuse blood products on arrival to ED.
研究组 & 干预措施
1:1:1 Blood Transfusion Ratio
干预措施: 1:1:1 Blood Transfusion Ratio (Biological)
1:1:2 Blood Transfusion Ratio
干预措施: 1:1:2 Blood Transfusion Ratio (Biological)
结局指标
主要结局
24-hour Mortality
时间窗: First 24 hours after ED admission
30-day Mortality
时间窗: First 30 days after ED admission
Coagulation as Indicated by Number of Participants With Reported Venous Thrombolic Events (VTE)
时间窗: From time of ED admission, for up to 72 hours
Blood samples were collected at time of ED admission and over time to determine the incidence of reported venous thrombolic events (VTE).
次要结局
- Incidence of Primary Surgical Procedure(ED admission to hospital discharge or 30 days, whichever comes first)
- Incidence of Transfusion Related Serious Adverse Events(ED admission to hospital discharge or 30 days, whichever comes first)
- ICU Free Days(first 30 days after ED admission)
- Amount of Randomized Blood Products Given to Hemostasis(24 hours from randomization)
- Hospital Free Days(first 30 days after ED admission)
- Time to Hemostasis(ED admission to hospital discharge or 30 days, whichever comes first)
- Initial Hospital Discharge Status(Hospital discharge or 30 days, whichever comes first)
- Ventilator Free Days(first 30 days after ED admission)
- Functional Status at Time of Hospital Discharge(Hospital discharge or 30 days, whichever comes first)
- Amount of Blood Products Given From Hemostasis to 24 Hours After ED Admission(24 hours after ED admission)
研究者
John Holcomb
Study Director
The University of Texas Health Science Center, Houston