Pretrauma center red blood cell transfusion is associated with reduced mortality and coagulopathy in severely injured patients with blunt trauma

Ann Surg. 2015 May;261(5):997-1005. doi: 10.1097/SLA.0000000000000674.

Abstract

Objective: To evaluate the association of pretrauma center (PTC) red blood cell (RBC) transfusion with outcomes in severely injured patients.

Background: Hemorrhage remains a major driver of mortality. Little evidence exists supporting PTC interventions to mitigate this.

Methods: Blunt injured patients in shock arriving at a trauma center within 2 hours of injury were included from the Glue Grant database. Subjects were dichotomized by PTC RBC transfusion. Outcomes included 24-hour mortality, 30-day mortality, and trauma-induced coagulopathy [(TIC), admission international normalized ratio >1.5]. Cox regression and logistic regression determined the association of PTC RBC transfusion with outcomes. To address baseline differences, propensity score matching was used.

Results: Of 1415 subjects, 50 received PTC RBC transfusion. Demographics and injury severity score were similar. The PTC RBC group received 1.3 units of RBCs (median), and 52% were scene transports. PTC RBC transfusion was associated with a 95% reduction in odds of 24-hour mortality [odds ratio (OR) = 0.05; 95% confidence interval (CI), 0.01-0.48; P < 0.01], 64% reduction in the risk of 30-day mortality [hazard ratio = 0.36; 95% CI, 0.15-0.83; P = 0.02], and 88% reduction in odds of TIC (OR = 0.12; 95% CI, 0.02-0.79; P = 0.03). The matched cohort included 113 subjects (31% PTC RBC group). Baseline characteristics were similar. PTC RBC transfusion was associated with a 98% reduction in odds of 24-hour mortality (OR = 0.02; 95% CI, 0.01-0.69; P = 0.04), 88% reduction in the risk of 30-day mortality (hazard ratio = 0.12; 95% CI, 0.03-0.61; P = 0.01), and 99% reduction in odds of TIC (OR = 0.01; 95% CI, 0.01-0.95; P = 0.05).

Conclusions: PTC RBC administration was associated with a lower risk of 24-hour mortality, 30-day mortality, and TIC in severely injured patients with blunt trauma, warranting further prospective study.

Publication types

  • Multicenter Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Blood Coagulation Disorders / etiology
  • Blood Coagulation Disorders / therapy*
  • Emergency Medical Services*
  • Endopeptidase Clp
  • Erythrocyte Transfusion*
  • Female
  • Heat-Shock Proteins
  • Humans
  • Injury Severity Score
  • Male
  • Middle Aged
  • Propensity Score
  • Prospective Studies
  • Protozoan Proteins
  • Shock, Hemorrhagic / etiology
  • Shock, Hemorrhagic / therapy*
  • Treatment Outcome
  • Wounds, Nonpenetrating / complications*
  • Wounds, Nonpenetrating / mortality*

Substances

  • Heat-Shock Proteins
  • Protozoan Proteins
  • Endopeptidase Clp
  • ClpB protein, Leishmania