|
Group I (AmB+
|
Group II (AmB+
|
P-value
|
---|
Fluconazole + 5-FC)
|
Fluconazole + 5-FC + VPS)
|
---|
Adverse events (n, %)
|
(n = 27)
|
(n = 39)
| |
Hypokalemia
|
13 (48.1%)
|
20 (51.3%)
|
0.804
|
Transaminase elevation
|
14 (51.9%)
|
15 (38.5%)
|
0.285
|
Renal impairment
|
5 (18.5%)
|
12 (30.8%)
|
0.267
|
Hematological impairment
|
5 (18.5%)
|
14 (35.9%)
|
0.128
|
Sequelae
|
(n = 27)
|
(na = 36)
| |
Headache
|
9 (33.3%)
|
9 (25.0%)
|
0.395
|
Dizziness/vertigo
|
2 (7.4%)
|
5 (13.9%)
|
0.465
|
Hemiparesis
|
4 (14.8%)
|
5 (13.9%)
|
0.850
|
Visual
|
8 (29.6%)
|
6 (16.7%)
|
0.184
|
Auditory
|
1 (3.7%)
|
7 (19.4%)
|
0.077
|
Seizure
|
3 (11.1%)
|
2 (5.6%)
|
0.387
|
- a One patient was lost to -follow-up and two patients were death at the 10th week in Group II