Median tacrolimus trough during admission, ng/ml |
Alternative therapy during admission |
5 (13.2%) |
4 (14.8%) |
1 (9.1%) |
.77 |
1.0‐5.0 |
10 (26.3%) |
7 (25.9%) |
3 (27.3%) |
5.1‐10.0 |
19 (50.0%) |
14 (51.9%) |
5 (45.5%) |
>10.0 |
4 (10.5%) |
2 (7.4%) |
2 (18.2%) |
Percentage reduction in median tacrolimus trough |
Alternative therapy prior to admission |
6 (15.8%) |
5 (18.5%) |
1 (9.1%) |
.83 |
No reduction |
15 (39.5%) |
10 (37.0%) |
5 (45.5%) |
10%‐30% |
12 (31.6%) |
8 (29.6%) |
4 (36.4%) |
>30% |
5 (13.2%) |
4 (14.8%) |
1 (9.1%) |
Percentage change in tacrolimus trough (IQR) |
−11% (−26% to 17%) |
−11% (−28% to 11%) |
−6% (−22% to 33%) |
.32 |
Mycophenolate dose |
Off antimetabolite |
4 (10.5%) |
2 (7.4%) |
2 (18.2%) |
.68 |
Same dose |
1 (2.6%) |
1 (3.7%) |
0 (0.0%) |
50%‐75% dose reduction |
20 (52.6%) |
14 (51.9%) |
6 (54.5%) |
Hold antimetabolite |
13 (34.2%) |
10 (37.0%) |
3 (27.3%) |
Total prednisone equivalents administered during hospitalization, mg |
<500 |
25 (65.8%) |
20 (74.1%) |
5 (45.5%) |
.15 |
500‐1000 |
8 (21.1%) |
5 (18.5%) |
3 (27.3%) |
>1000 |
5 (13.2%) |
2 (7.4%) |
3 (27.3%) |
Mean prednisone equivalents per day during hospitalization, mg |
17.2 ± 18.6 |
12.9 ± 16.5 |
27.7 ± 19.2 |
.04 |
Enrolled in clinical trial |
4 (10.5%) |
4 (14.8%) |
0 (0.0%) |
.18 |
Antiviral and immunomodulatory therapies |
Hydroxychloroquine |
26 (68.4%) |
18 (66.7%) |
8 (72.7%) |
.71 |
Azithromycin |
22 (57.9%) |
14 (51.9%) |
8 (72.7%) |
.24 |
Remdesivir |
3 (7.9%) |
2 (7.4%) |
1 (9.1%) |
.86 |
IL‐6 or IL‐1 inhibitor |
3 (7.9%) |
2 (7.4%) |
1 (9.1%) |
.86 |
Convalescent plasma |
10 (26.3%) |
6 (22.2%) |
4 (36.4%) |
.37 |
Anticoagulation therapy |
None |
2 (5.3%) |
1 (3.7) |
1 (9.1%) |
.37 |
Prophylactic dose |
16 (42.1%) |
13 (48.1%) |
3 (27.3%) |
Treatment dose |
20 (52.6%) |
13 (48.1%) |
7 (63.6%) |
Prescription of anti‐Xa inhibitor |
10 (26.3%) |
8 (29.6%) |
2 (18.2%) |
.46 |