Unadjusted outcomes during 180-day follow-up period
Characteristic . | Stable group, n = 2504 . | Comparator group, n = 3569 . | P . |
---|---|---|---|
Received heparin,* % | 0.3 | 3.2 | < .001 |
Deceased, n, % | 10, 0.4 | 58, 1.6 | < .001 |
AC-related death, n, % | 1, 0.04 | 5, 0.1 | .411† |
AC-related thrombosis, n, % | 10, 0.4 | 26, 0.7 | .100 |
AC-related bleeding, n, % | 19, 0.8 | 101, 2.8 | < .001 |
AC-related bleeding or thrombosis, n, % | 28, 1.1 | 127, 3.6 | < .001 |
Characteristic . | Stable group, n = 2504 . | Comparator group, n = 3569 . | P . |
---|---|---|---|
Received heparin,* % | 0.3 | 3.2 | < .001 |
Deceased, n, % | 10, 0.4 | 58, 1.6 | < .001 |
AC-related death, n, % | 1, 0.04 | 5, 0.1 | .411† |
AC-related thrombosis, n, % | 10, 0.4 | 26, 0.7 | .100 |
AC-related bleeding, n, % | 19, 0.8 | 101, 2.8 | < .001 |
AC-related bleeding or thrombosis, n, % | 28, 1.1 | 127, 3.6 | < .001 |