Table 4.
TXA (n = 52) versus placebo (n = 56) | P | |
---|---|---|
Primary outcome | ||
Drain production in first 24 h*, † | −39 (−69, −14) | 0·001 |
Secondary outcomes ‡ | ||
Early haematoma | TXA 0 versus placebo 3# | 0·244 |
Total drain production*, † | −46 (−81, −18) | 0·001 |
Days with drain* | −23 (−83, −10) | 0·001 |
Drain removed at 24 h§ | 6·60 (2·07, 21·22) | 0·001 |
Drain volume in 24 h before removal* | −9 (−30, 9) | 0·309 |
Late haematoma, postoperative infection or wound rupture | TXA 5 versus placebo 6# | 1·000 |
Seroma ¶ | ||
Aspiration required§ | 1·11 (0·44, 2·79) | 0·821 |
≥ 5 aspirations§ | 0·47 (0·15, 1·50) | 0·203 |
Cumulative seroma ≥ 500 ml§ | 1·05 (0·38, 2·90) | 0·930 |
Chronic seroma§ | 0·18 (0·04, 0·89) | 0·035 |
Values in parentheses are 95 per cent confidence intervals.
Ratio between logarithmic mean as percentage difference; univariable general linear model adjusted for drug and wound surface area;
additionally adjusted for surgeon seniority.
Number of patients with early haematoma calculated from all patients; patients with early haematoma excluded from other secondary postoperative outcome registrations.
Odds ratio: logistic regression model adjusted for wound surface area.
Patients with early or late haematoma, infection or wound rupture excluded from seroma registrations. TXA, tranexamic acid.
Fisher's exact test owing to number of patients being too low for logistic regression analysis.