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. 2013 Nov 22;13:20. doi: 10.1186/1471-227X-13-20

Table 2.

Study outcomes

Outcomes TXA
Placebo
RD
RR
(n = 120) (n = 118) [95% CI] [95% CI]
Progressive intracranial haemorrhage (PIH)
21 (18%)
32 (27%)
−0.10
0.65
moderate TBI (n = 24)
7 (6%)
17 (14%)
[(−0.20)-
[0.40-1.05]
severe TBI (n = 20)
9 (8%)
11 (9%)
(−0.01)]
 
indicated neurosurgery
6 (5%)
6 (5%)
 
 
Increase in pressure effect*
*11 (10%)
12 (11%)
−0.01
0.91
[(−0.09) – 0.07]
[0.42-1.97]
Improved GCS motor score at 24 hours
37 (31%)
37 (31%)
−0.01
0.98
[(−0.12) – 0.11]
[0.67-1.44]
Neurosurgical intervention
3 (3%)
0
0.03
---
[(−0.00) – 0.05]
---
Blood products transfusion
31 (26%)
33 (28%)
−0.02
0.92
[(−0.13) – 0.09]
[0.61-1.40]
Death
12 (10%)
17 (14%)
−0.04
0.69
[(−0.13) – 0.04]
[0.35-1.39]
Unfavorable (GOS) outcome
21 (18%)
27 (23%)
−0.05
0.76
[(−0.16) – 0.05]
[0.46-1.27]
Adverse events
 
 
Stroke
0
3
---
---
Pulmonary embolus
0
0
---
---
Deep vein thrombosis
0
0
---
---
Gastrointestinal bleeding 0 1 --- ---

*Denominator for outcomes is 114 for TXA group and 115 for placebo group. This is an analysis based on complete case analysis that is not assumed the missing outcome.