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Table 3 Clinical characteristics upon hospital admission of matched trauma patients with and without tranexamic acid administered during the prehospital phase

From: The impact of prehospital tranexamic acid on mortality and transfusion requirements: match-pair analysis from the nationwide German TraumaRegister DGU®

 

Tranexamic acid group

n = 2275

Control group

n = 2275

p value

Shock (BP ≤ 90 mmHg) (n, %)

539 (24.6%)

571 (26.4)

.185

BP on admission (mmHg), mean, SD

113 (34)

111 (35)

.108

Hemoglobin (g/dl), mean, SD

11.6 (2.7)

11.7 (2.7)

.305

Base excess (mmol/l) mean, SD

− 4.5 (6.1)

− 4.3 (6.3)

.155

INR mean, SD

1.32 (0.67)

1.32 (0.75)

.094

Fluids (ml) median, IQR

1500 (500–3000)

1000 (500–2150)

< .001

Blood transfusion until ICU (n, %)b

765 (33.9%)

694 (30.7%)

.022

FFP transfusion until ICU (n, %)

462 (20.5%)

435 (19.3%)

.307

Units of pRBCa, median, IQR

4 (2–7)

4 (2–9)

< .001

Units of FFPa, median, IQR

2 (0–6)

3 (0–7)

.023

Units of pRBCb, median, IQR

0 (0–2)

0 (0–2)

.235

Units of FFPb, median, IQR

0 (0–0)

0 (0–0)

.501

Hemostatic drugsc (n, %)

1034 (47.8%)

939 (44.2%)

.018

TXA in the ER (n, %)

749 (32.9)

798 (35.1)

.014

  1. ER, emergency room; pRBC, packed red blood cells; FFP, fresh frozen plasma
  2. aOnly cases with blood transfusion
  3. bData of all patients
  4. ci.e., fibrinogen, prothrombin concentrates (PPSB), calcium, factor VII or factor XIII