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. 2020 Jul 21;6:104. doi: 10.1186/s40814-020-00643-9

Table 4.

Clinical outcomes in TXA trial

Outcomes TXA (N = 49) Placebo (N = 51) HR (95% CI)
Composite outcome within 30 days after surgerya, n (%) 1 (2.0%) 6 (11.8%) 0.16 (0.02–1.34)
 Vascular mortality, n (%) 0 (0.0) 1 (2.0)b
 Non-fatal myocardial infarction, n (%) 1 (2.0%) 3 (5.9%)
 Stroke, n (%) 0 (0.0) 0 (0.0)
 Pulmonary embolism, n (%) 0 (0.0) 0 (0.0)
 Deep vein thrombosis, n (%) 0 (0.0) 1 (2.0)
 Life-threatening bleeding, n (%) 0 (0.0) 2 (3.9)
 Non-fatal major bleeding, n (%) 0 (0.0) 1 (2.0)
All-cause mortality, n (%) 0 (0.0) 1 (2.0) c
Myocardial infarction, n (%) 1 (2.0%) 4 (7.8%) 0.23 (0.03–2.07)
MINS, n (%) 0 (0.0%) 6 (11.8%) c
Cardiac revascularization, n (%) 0 (0.0) 1 (2.0) c
Postoperative infection, n (%) 6 (12.2) 7 (13.7) 0.77 (0.26–2.30)
Postoperative sepsis, n (%) 1 (2.0) 4 (7.8) 0.23 (0.03–2.04)
Congestive heart failure, n (%) 1 (2.0) 0 (0.0) c
Re-hospitalization for vascular reason, n (%) 0 (0.0) 1 (2.0) c
Seizure, n (%) 0 (0.0) 0 (0.0) c

TXA tranexamic acid, HR hazard ratio, CI confidence interval, MINS myocardial injury after noncardiac surgery

aComposite outcome of vascular mortality, non-fatal myocardial infarction, non-fatal stroke, non-fatal cardiac arrest, non-fatal pulmonary embolism, non-fatal deep vein thrombosis, non-fatal life-threatening bleeding, and non-fatal major bleeding

bDue to myocardial infarction

cNot determinable