Table 2

Unadjusted outcomes during 180-day follow-up period

CharacteristicStable group, n = 2504Comparator group, n = 3569P
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 
CharacteristicStable group, n = 2504Comparator group, n = 3569P
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 

AC indicates anticoagulation.

*

Heparin or low-molecular-weight heparin.

Fisher exact test.

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