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
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
44
Experimental
Comparator
Westmead Childrens Hospital
Sydney, New South Wales, Australia
RECRUITINGRoyal Brisbane and Women's Hospital
Brisbane, Queensland, Australia
RECRUITINGLady Cilento Children's Hospital
Brisbane, Queensland, Australia
RECRUITINGPrincess Alexandra Hospital
Brisbane, Queensland, Australia
RECRUITINGCairns Hospital
Cairns, Queensland, Australia
RECRUITINGGold Coast University Hospital
Gold Coast, Queensland, Australia
RECRUITINGMackay Base Hospital
Mackay, Queensland, Australia
RECRUITINGRockhampton Hospital
Rockhampton, Queensland, Australia
RECRUITINGTownsville Hospital
Townsville, Queensland, Australia
RECRUITINGRoyal Adelaide Hospital
Adelaide, South Australia, Australia
RECRUITINGTime to administration of fibrinogen replacement from time of identification of hypofibrinogenaemia requiring fibrinogen replacement
Time to fibrinogen replacement
Time frame: 3 Hours
Transfusion Requirements
In number of units of Packed Red Blood Cells, Plasma, FC, Cryoprecipitate, Platelets, Prothrombin Complex Concentrate at 4, 6, 24, 48hrs
Time frame: Up to 48 hours after Trauma Unit presentation
Duration of bleeding episode or time until surgical control
Duration bleeding episode
Time frame: It is anticipated that haemorrhage control will be achieved within 12 hours
Intensive Care Unit LOS
ICU LOS
Time frame: 1 Year
Hospital LOS
Hospital LOS
Time frame: 1 Year
Adverse Events
Transfusion related adverse events, Sepsis, Multiple Organ Failure, Acute Renal Failure, Symptomatic Thromboembolic Complications
Time frame: 1 Year
All Cause Mortality
Mortality at 4, 6, 24 hours and up to 90 days
Time frame: Up to 90 Days
Functional Outcomes GOS-E Paediatrics
Functional Outcome Measures at 60 and 90 Days
Time frame: Up to 90 Days
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