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Fibrinogen Early In Severe Trauma studY Junior

只有註冊用戶可以翻譯文章
登陸註冊
鏈接已保存到剪貼板
狀態招聘中
贊助商
Gold Coast Hospital and Health Service
合作者
Emergency Medicine Foundation
National Blood Authority
Australian Red Cross

關鍵詞

抽象

1. Haemorrhage in severe trauma is a significant cause of mortality and is potentially the most preventable cause of death in paediatric trauma patients
2. Trauma Induced Coagulopathy (TIC) is a complex coagulopathy associated with severe trauma
3. Hypo/dysfibrinogenaemia plays an important role in TIC
4. Early replacement of fibrinogen may improve outcomes
5. Fibrinogen replacement is potentially inadequate in standard fixed ratio Major Haemorrhage Protocols (MHP) utilising Plasma and/or Cryoprecipitate
6. The majority of centres utilise cryoprecipitate for additional fibrinogen supplementation as part of a MHP
7. Cryoprecipitate administration is often delayed (between 60 - 120 minutes) in a fixed ratio MHP
8. It is clear early intervention in severe traumatic haemorrhage is associated with improved outcomes - CRASH 2 and PROPPR studies
9. Increasing interest in the use of Fibrinogen Concentrate (FC) in severe bleeding but not supported by high level evidence
10. Benefits of FC - viral inactivation, known dose, easily reconstituted, can be administered quickly in high dose and stored at room temperature in the trauma resuscitation bay
12. No previous studies comparing FC and Cryoprecipitate in bleeding paediatric trauma patients 13. Fibrinogen supplementation will be guided by an accepted ROTEM targeted treatment algorithm 14. Pilot, multi-centre randomised controlled trial comparing FC to Cryoprecipitate (current standard practise in fibrinogen supplementation) 15. Hypothesis: Fibrinogen replacement in severe traumatic haemorrhage can be achieved quicker with a more predictable dose response using Fibrinogen Concentrate compared to Cryoprecipitate 16. It is imperative that robust and clinically relevant trials are performed to investigate fibrinogen supplementation in paediatric trauma patients before widespread adoption makes performing such studies unfeasible

日期

最後驗證: 05/31/2020
首次提交: 03/22/2018
提交的預估入學人數: 04/15/2018
首次發布: 04/24/2018
上次提交的更新: 06/24/2020
最近更新發布: 06/28/2020
實際學習開始日期: 06/30/2018
預計主要完成日期: 06/29/2021
預計完成日期: 06/29/2021

狀況或疾病

Trauma
Hemorrhage
Coagulopathy
Pediatrics

干預/治療

Drug: Fibrinogen Concentrate

Drug: Cryoprecipitate

相 2

手臂組

干預/治療
Experimental: Fibrinogen Concentrate
Fibrinogen Replacement using Fibrinogen Concentrate as per ROTEM (FIBTEM) FIBTEM A5 0mm = 60mg/kg FC FIBTEM A5 1-4mm = 50mg/kg FC FIBTEM A5 5-6mm = 40mg/kg FC FIBTEM A5 7-8mm = 30mg/kg FC FIBTEM A5 9-10mm = 20mg/kg FC
Drug: Fibrinogen Concentrate
Experimental
Active Comparator: Cryoprecipitate
Fibrinogen Replacement using Cryoprecipitate as per ROTEM (FIBTEM) FIBTEM A5 0mm = 6ml/kg Cryoprecipitate FIBTEM A5 1-4mm = 5ml/kg Cryoprecipitate FIBTEM A5 5-6mm = 4ml/kg Cryoprecipitate FIBTEM A5 7-8mm = 3ml/kg Cryoprecipitate FIBTEM A5 9-10mm = 2ml/kg Cryoprecipitate
Drug: Cryoprecipitate
Comparator

資格標準

有資格學習的年齡 3 Months 至 3 Months
有資格學習的性別All
接受健康志願者
標準

Inclusion Criteria:

1. Child affected by trauma (3 months to 18 years)

2. Judged to have significant haemorrhage OR predicted to require significant transfusion by the treating clinician

3. Activation of Local MHP or transfusion of emergency red blood cells (Pre-hospital or at Trauma Centre)

Exclusion Criteria:

1. Injury judged incompatible with survival

2. Randomisation unable to occur within 6 hours of hospital admission

3. Pregnancy

4. Known personal or parental objection to blood products

5. Known coagulation disorder (i.e. haemophilia, von Willebrand disease)

6. Previous dedicated fibrinogen replacement this admission

7. Pre-Trauma Centre dedicated fibrinogen replacement

8. Participation in competing study

結果

主要結果指標

1. Time to administration of fibrinogen replacement from time of identification of hypofibrinogenaemia requiring fibrinogen replacement [3 Hours]

Time to fibrinogen replacement

次要成果指標

1. Transfusion Requirements [Up to 48 hours after Trauma Unit presentation]

In number of units of Packed Red Blood Cells, Plasma, FC, Cryoprecipitate, Platelets, Prothrombin Complex Concentrate at 4, 6, 24, 48hrs

2. Duration of bleeding episode or time until surgical control [It is anticipated that haemorrhage control will be achieved within 12 hours]

Duration bleeding episode

3. Intensive Care Unit LOS [1 Year]

ICU LOS

4. Hospital LOS [1 Year]

Hospital LOS

5. Adverse Events [1 Year]

Transfusion related adverse events, Sepsis, Multiple Organ Failure, Acute Renal Failure, Symptomatic Thromboembolic Complications

6. All Cause Mortality [Up to 90 Days]

Mortality at 4, 6, 24 hours and up to 90 days

7. Functional Outcomes GOS-E Paediatrics [Up to 90 Days]

Functional Outcome Measures at 60 and 90 Days

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