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. 2015 Oct 13;59(11):6913–6921. doi: 10.1128/AAC.01079-15

TABLE 2.

Incidence and time to AmB-induced AKI according to different definitions, stratified by type of AmB preparationa

Patient group No. of patients with AKI/total no. tested (%) by:
Binary criteria
KDIGO stage
Time to AKI (days) by the following criterion:
NT2× NT0.5 KDIGObin Stage 1 Stage 2 Stage 3 NT2× NT0.5 KDIGObin
All (n = 24) 4/24 (16.7) 15/24 (62.5) 17/24 (70.8) 13/24 (54.2) 4/24 (16.7) 0/24 (0.0) 10.3 ± 3.4 (n = 4) 8.0 ± 3.4 (n = 15) 7.2 ± 3.1 (n = 17)
Deoxycholate AmB (n = 12) 3/12 (25.0) 9/12 (75.0) 10/12 (83.3) 7/12 (58.3) 3/12 (25.0) 0/12 (0.0) 9.3 ± 3.5 (n = 3) 7.3 ± 3.5 (n = 9) 7.1 ± 3.6 (n = 10)
Liposomal AmB (n = 12) 1/12 (8.3) 6/12 (50.0) 7/12 (58.3) 6/12 (50.0) 1/12 (8.3) 0/12 (0.0) 13.0 (n = 1) 9.0 ± 3.4 (n = 6) 7.3 ± 2.6 (n = 7)
a

Continuous data are expressed as means ± standard deviations. AmB, amphotericin B; NT2×, traditional nephrotoxicity criterion that requires at least doubling of the SCr level; NT0.5, traditional nephrotoxicity criterion that requires an absolute increase in the SCr level of at least 0.5 mg/dl; KDIGObin, Kidney Disease: Improving Global Outcomes criterion that requires an increase in the SCr level by ≥0.3 mg/dl within 48 h or an increase in the SCr level to ≥1.5 times the baseline level which is known or presumed to have occurred within the prior 7 days. KDIGO stage 1 required an increase in the SCr level by ≥0.3 mg/dl or to a level 1.5 to 1.9 times the baseline level; stage 2 required an increase in the SCr levels to 2.0 to 2.9 times the baseline level, and stage 3 required an increase in the SCr level to a level ≥3.0 times the baseline level or initiation of dialysis.