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Emergency Hemorrhage Control
Joe Sherrell
EMS Officer
Tulsa Fire Department
(918) 596-9808
jsherrell@cityoftulsa.org
The student shall be able to effectively
recognize uncontrolled hemorrhage and
immediately provide the indicated
treatment.
Upon completion of this course, the student will be able to:
1. Recognize uncontrolled hemorrhage
2. Identify the proper method of treatment
3. Discuss the indication for tourniquet use
4. Demonstrate the proper use of a tourniquet
Objectives
5. Discuss the indication for the use of Combat Gauze
6. Demonstrate the proper use of Combat Gauze
7. Discuss the indication for the use of Phenylephrine
8. Demonstrate the proper use of Phenylephrine
9. Discuss the indication and use of TXA
Lacerations
Penetrations
Amputations
Assessment
Scene Safety & PPE
Primary Survey
Hospital Notification
Primary Survey Care
Control Arterial Bleeding
Open and Maintain Airway
Minimize on scene time
En Route Care
Reassess
Oxygenation/Ventilation
Vascular Access
Secondary Survey
BLS Skills
Identification
Tourniquet
Hemostatic Agent
Hospital Notification
BLS Before ALS
Battlefield tested
Endorsed by PHTLS
Associated complications <1.5%
Uncontrollable Hemorrhage
How long does it take for death to occur due to
complete femoral artery and vein dissection?
As little as
3 minutes
Combat Application Tourniquet
(C-A-T)
Apply just proximal to the bleeding wound
Route the band around the extremity
Pass the band through the outside slit of buckle
The friction adaptor buckle locks the band in place
Pull the self-adhering band tight and secure
Twist the rod until the bleeding has stopped.
Lock the rod in place with the windlass clip
Secure the rod with the strap
Indicate the time of tourniquet application
Leave area uncovered
TK 0945
Video
Eliminate distal pulse
Do not loosen
Second tourniquet may be required
Conscious patients may experience pain
Utilize pain management protocol
Combat Gauze
Mechanism of Action
Impregnated with Kaolin
Promotes activation of Factor XII
Initiates the clotting cascade
Indication
Hemorrhage not controllable with tourniquet or
other means
C-A-T ineffective
Wound location does not allow use of a C-A-T
Application
Remove pooled blood
Pack gauze into wound
Hold pressure over bleeding source
3 minutes or hemostasis
Apply pressure bandage
The Newest Kid on the Block
274 Hospitals
40 Countries
20,211 adult trauma patients
With, or risk of, significant bleeding
HR > 110, SBP <90, clinical judgement
Treatment within 8 hours of injury
TXA or placebo
Death in hospital within 4 weeks
Bleeding
Vascular Occlusion (MI, Stroke, PE)
Multiorgan Failure
Head Injury
Other
Vascular Occlusive Events
Need for blood/surgery
All Cause Mortality
9.1% Increase in survival
Bleeding
8.5% Increase in survival
Did Not reduce
the need for blood
the need for surgery
Did increase survival
TXA is Safe
TXA Makes a Difference
TXA Increases Survival
TXA doesn’t create clots in bad places
Retrospective
Combat Casualties in Afghanistan
British Helo Physicians
TXA vs No TXA
1+ unit(s) PRBC
10+ units of PRBC
896 Patients
293 received TXA
Characterize TXA use in combat injury care
Effect of TXA on
Blood Product Use
Bad Clots
Mortality (24 hrs., 48hrs., 30 days)
~7 times more likely to survive with TXA
Slight increase in DVT & PE formation
Higher Injury = Increase Risk of Clots
Military Theater – penetrating/ortho
Survival allows DVT/PE to be diagnosed
Increase Survival
Massive Transfusion
TXA independent predictor of survival
Benefit shown after 48 hours
Possible anti-inflammatory component
Earlier is Better
If a casualty is anticipated to need
significant blood transfusion:
presents with hemorrhagic shock
one or more major amputations
Penetrating torso trauma
Evidence of severe bleeding
Administer 1 gram of tranexamic acid in 100 cc
Normal Saline or Lactated Ringers as soon as
possible but NOT later than 3 hours after injury.
Begin second infusion of 1 gm TXA after Hextend
or other fluidtreatment.
Formulary
 Anti-Fibrinolytic
Promotes clot formation
Hemorrhagic shock
Trauma < 3 hours old
Suspected need for massive blood transfusion
 In metropolitan Tulsa:
sustained tachycardia ≥ 110
AND
sustained hypotension systolic BP≤ 90
Non-hemorrhagic shock
Non-traumatic hemorrhagic shock
Hemorrhagic shock stabilized with other hemostatic
agents/measures
Onset of action within 4 hours after IV administration
Delayed effects up to 48 hours consistent with anti-
inflammatory actions.
While a theoretical concern, TXA has not been shown
to cause significant increase in:
deep venous thrombosis
pulmonary embolism
myocardial infarction
stroke
 1 gram IVPB over 10 minutes.
Administer in 100 mL or 250 mL NS.
 The CRASH-2 Collaborators. Effects of tranexamic acid on death,
vascular occlusive events, and blood transfusion in trauma patients
with signifcant hemorrhage (CRASH-2): a randomised, placebo-
controlled trial. Lancet 2010; 376: 23–32.
 Jonathan J. Morrison; Joseph J. Dubose; Todd E. Rasmussen; Mark J.
Midwinter. Military Application of Tranexamic Acid in Trauma
Emergency Resuscitation (MATTERs) Study. Arch Surg. 2011
 Medical Control Board. EMS Protocols for Metropolitan Oklahoma
City and Tulsa. 2013.
 Tactical Combat Casualty Care Guidelines. Prehospital Trauma Life
Support. 2012.

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