|
No Adverse Event |
Major Adverse Event |
p value |
Age, mean (SD) |
31.3 (7.1) |
27.3 (5.7) |
0.050 |
Black race, n (%) |
5 (15.2) |
8 (50.0) |
0.01 |
Hypertension, n (%) |
12 (35.3) |
6 (35.3) |
1.000 |
Preeclampsia, n (%) |
8 (23.5) |
3 (17.6) |
0.630 |
Diabetes mellitus, n (%) |
6 (17.6) |
4 (23.5) |
0.618 |
Autoimmune disorder, n (%) |
0 (0.0) |
1 (5.9) |
0.153 |
Thyroid disease, n (%) |
3 (8.8) |
2 (11.8) |
0.739 |
|
EF at Diagnosis, mean (SD) |
21.0 (12.2) |
14.4 (12.0) |
0.073 |
EF at 6 months, mean (SD) |
44.8 (17.6) |
17.7 (13.0) |
<.0001 |
EF at 12 months, mean (SD) |
45.0 (21.0) |
16.1 (9.5) |
<.0001 |
Peak EF, mean (SD) |
55.3 (14.6) |
25.9 (17.7) |
<.0001 |
Final EF, mean (SD) |
49.6 (18.1) |
16.4 (12.7) |
<.0001 |
|
Beta-blocker, n (%) |
31 (91.2) |
15 (88.2) |
0.739 |
ACE-I/ARB, n (%) |
37 (93.0) |
16 (84.0) |
0.325 |
Aldosterone Antagonist, n (%) |
22 (64.7) |
13 (76.5) |
0.393 |
Diuretic, n (%) |
30 (88.2) |
16 (94.1) |
0.505 |
Digoxin, n (%) |
14 (41.2) |
14 (82.4) |
0.005 |
Bromocriptine, n (%) |
0 (0.0) |
2 (11.8) |
0.041 |
|
Months of Follow up, mean (SD) |
89.4 (56.1) |
77.6 (59.6) |
0.494 |