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Blunt Trauma Massive Transfusion (B-MaT) Score: A Novel Scoring Tool
Eric O Yeates1, Areg Grigorian2, Kenji Inaba3
1Department of Surgery, University of California Irvine (UCI), Orange, California.
The Journal of Surgical Research
|November 3, 2021
Summary
A new Blunt trauma Massive Transfusion (B-MaT) score predicts the need for massive transfusion in blunt trauma patients before hospital arrival. This tool identifies high-risk blunt mechanisms and vital sign abnormalities to guide early treatment.
Area of Science:
- Trauma Surgery
- Emergency Medicine
- Hemorrhagic Shock Management
Background:
- Existing massive transfusion (MT) prediction tools lack immediate variables and fail to differentiate blunt trauma mechanisms by force.
- There is a need for a specific tool to predict MT in blunt trauma patients (BTPs) considering diverse blunt force mechanisms.
Purpose of the Study:
- To develop and validate a novel scoring tool, the Blunt trauma Massive Transfusion (B-MaT) score.
- To predict the requirement for MT in BTPs prior to their arrival at the hospital.
Main Methods:
- Utilized the 2017 Trauma Quality Improvement Program database for BTPs, randomly divided into derivation and validation sets.
- Developed logistic regression models to identify independent predictors of MT (≥6 units PRBCs within 4h or ≥10 units within 24h).
- Derived the B-MaT score based on weighted predictors and calculated the area under the receiver-operating curve (AROC).
Main Results:
- Identified heart rate ≥ 120 bpm, systolic blood pressure ≤ 90 mmHg, and high-risk blunt mechanisms as key predictors for MT.
- The B-MaT score (0-9) demonstrated increasing MT rates with higher scores (e.g., score 9: 32.4% MT rate).
- Achieved an AROC of 0.86 in the derivation set and 0.85 in the validation set, indicating good predictive accuracy.
Conclusions:
- The B-MaT score is a novel, pre-arrival tool for predicting MT needs in blunt trauma patients.
- Further prospective validation is recommended to confirm accuracy and evaluate its impact on patient outcomes and blood product allocation.
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