Low Titer Group O Whole Blood In Injured Children Requiring Massive Transfusion

Barbara A Gaines1, Mark H Yazer2, Darrell J Triulzi2

  • 1University of Pittsburgh School of Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA.

Annals of Surgery
|February 7, 2022
PubMed

Insights

Low-titer group O whole blood (LTOWB) administration in pediatric trauma patients requiring massive transfusion was linked to better survival outcomes. This approach improved 72-hour and 28-day survival rates in critically injured children.

Area of Science:

  • Emergency Medicine
  • Pediatric Critical Care
  • Trauma Surgery

Background:

  • Limited data exist on the efficacy of low-titer group O whole blood (LTOWB) in pediatric trauma resuscitation.
  • Massive transfusion protocols are critical for managing life-threatening hemorrhage in injured children.

Purpose of the Study:

  • To evaluate the survival impact of using LTOWB in pediatric patients undergoing massive transfusion after injury.
  • To compare outcomes between LTOWB and conventional component therapy in this population.

Main Methods:

  • A prospective observational study was conducted at a pediatric Level 1 trauma center.
  • Included were injured children (1-17 years) requiring >40 mL/kg of LTOWB or conventional components within 24 hours.
  • Survival analysis used Kaplan-Meier curves, log-rank tests, and Cox regression, with 28-day survival as the primary outcome.

Main Results:

  • 33% of patients (27/80) received LTOWB as part of resuscitation.
  • After adjusting for confounders, LTOWB use was associated with significantly improved 72-hour and 28-day survival (AOR 0.23, P=0.009 and AOR 0.41, P=0.02).
  • LTOWB survivors experienced reduced hospital length of stay, ICU length of stay, and ventilator days.

Conclusions:

  • LTOWB administration during hemostatic resuscitation is independently associated with improved survival in massively transfused pediatric trauma patients.
  • This finding supports the consideration of LTOWB in pediatric massive transfusion protocols.
Abstract

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