Skip to main content
. 2021 Nov 2;12:761167. doi: 10.3389/fphar.2021.761167

TABLE 1.

Characteristics and outcomes of DILI caused by tigecycline.

Variables Pattern of liver injury
Hep (n = 10) Mix (n = 4) Chol (n = 41)
Causality assessment
 Highly probable, n (%) 3 (30.0%) 0 (0.0%) 6 (14.6%)
 Probable, n (%) 7 (70.0%) 4 (100.0%) 35 (85.4%)
Liver injury during tigecycline treatment, n (%) 7 (70.0%) 3 (75.0%) 32 (78.0%)
 Withdrawal tigecycline after liver injury, n (%) 3 (30.0%) 2 (50.0%) 20 (48.8%)
 Reduction tigecycline dosage after liver injury, n (%) 0 (0.0%) 0 (0.0%) 3 (7.3%)
 Continuous treatment without adjustment, n (%) 4 (40.0%) 1 (25.0%) 9 (22.0%)
Liver injury within 3 days of discontinuation of tigecycline, n (%) 3 (30.0%) 1 (25.0%) 9 (22.0%)
Latency time of liver injury, median (IQR), days 4.5 (2.0–7.4) 6.5 (1.8–12.0) 12.0 (9.0–16.0)
Re-exposure to tigecycline and recurrent ALT or ALP increase, n (%) 0 (0.0%) 0 (0.0%) 2 (4.9%)
Drugs for treatment
 Anti-inflammation, n (%) 5 (50.0%) 2 (50.0%) 16 (39.0%)
 Antioxidants, n (%) 8 (80.0%) 3 (75.0%) 31 (75.6%)
 Phospholipids, n (%) 3 (30.0%) 2 (50.0%) 4 (9.8%)
 Cholagogue, n (%) 3 (30.0%) 2 (50.0%) 19 (46.3%)
Outcome of liver injury*
 Recovery, n (%) 7 (70.0%) 2 (50.0%) 17 (41.5%)
 Improvement, n (%) 1 (10.0%) 1 (25.0%) 5 (12.2%)
 No improvement, n (%) 1 (10.0%) 0 (0.0%) 15 (36.6%)
 Aggravation, n (%) 0 (0.0%) 1 (25.0%) 0 (0.0%)
Time to recovery, median (range, min-max), days 11.0 (4.0–37.0) 13.5 (2.0–25.0) 24.0 (8.0–66.0)
30-day all-cause mortality, n (%) 2 (20.0%) 1 (25.0%) 3 (7.3%)
Length of stay in hospital, median (IQR), days 42.0 (20.3–59.3) 33.5 (24.0–62.5) 46.0 (38.0–63.5)

* One of patients with hepatocellular injury pattern lack of outcome data, while eight of patients with cholestatic injury pattern. DILI, drug-induced liver injury; Hep, hepatocellular injury pattern; Mix, mixed injury pattern; Chol, cholestatic injury pattern; IQR, interquartile ranges; ALT, alanin aminotransferase; ALP, alkalinephosphatase; min, minimal; max, maximal.