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Published on: July 28, 2020
Novel concepts for damage control resuscitation in trauma
Philbert Y Van1, John B Holcomb, Martin A Schreiber
1aDivision of Trauma, Critical Care and Acute Care Surgery, Oregon Health and Science University, Portland, Oregon bDivision of Acute Care Surgery, University of Texas Health Science Center at Houston, Houston, Texas, USA.
Damage control resuscitation for trauma involves a 1:1:1 ratio of plasma, platelets, and red blood cells. Alternatives like low titer O whole blood and cold-stored platelets can be used when plasma and platelets are scarce.
Area of Science:
- Trauma resuscitation
- Hemorrhagic shock management
- Blood product transfusion
Background:
- Traumatic injuries are a leading cause of global mortality.
- Damage control resuscitation (DCR) with a 1:1:1 ratio of plasma, platelets, and red blood cells is standard for exsanguinating hemorrhage.
- Availability of plasma and platelets can be challenging in certain settings.
Purpose of the Study:
- To review literature on alternatives for achieving the 1:1:1 transfusion ratio in trauma resuscitation.
- To explore substitutes for plasma and platelets when they are not readily available.
Main Methods:
- Literature review of studies on trauma resuscitation and blood product alternatives.
- Analysis of findings regarding the efficacy and logistics of different transfusion strategies.
Main Results:
- Liquid and freeze-dried plasma (FDP) offer logistical advantages and potential superiority over fresh frozen plasma.
- Cold-stored platelets (CSPs) exhibit enhanced hemostatic properties and better resistance to bacterial contamination.
- Low titer type O whole blood is a safe option for civilian trauma patients.
Conclusions:
- Resuscitation for traumatic hemorrhagic shock should prioritize a 1:1:1 plasma, platelet, and red blood cell ratio with minimal crystalloids.
- When plasma and platelets are limited, low titer type O whole blood, liquid plasma, FDP, or CSPs are viable alternatives.
- CSPs may offer superior hemostatic function compared to room temperature platelets.
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Assessment:
1. Clinical Evaluation:
History:
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