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. 2020 Jul 27;9(8):451. doi: 10.3390/antibiotics9080451

Table 3.

Factors potentially associated with acute kidney injury in patients with high-dose polymyxin B therapy.

Variable
Median (IQR) or No. (%)
Univariate Analysis Multivariable Analysis
No AKI
(n = 18)
AKI
(n = 25)
p Value Adjusted OR (95% CI) p Value
Demographics and Infection Characteristics
Age (years) 55 (27–66) 54 (36–66) 0.89
Male gender 12 (66.7) 18 (72.0) 0.71
Age-adjusted Charlson comorbidity index 3 (1–6) 3 (0–4) 0.21
APACHE II at infection onset 16 (12–22) 19 (11–21) 0.74
APACHE II at high-dose PMB initiation 17 (12–22) 22 (15–24) 0.22
Renal insufficiency at high-dose PMB initiation 5 (27.8) 3 (12.0) 0.20
In-hospital 30-day all-cause mortality 3 (16.7) 5 (20.0) 0.78
Details of PMB dosing prior to time at risk a
Duration of PMB (days) 12 (7–20) 12 (8–14) 0.68
Overall average daily PMB dose (IU/kg) 30 273 (29 126–33 333) 33 708 (30 000–37 037) 0.04 1.01 (1.00–1.02) 0.04
Overall cumulative PMB (MIU) 20 (12–30) 23 (16–27) 0.95
Use of combination therapy 17 (94.4) 23 (92.0) 0.76
Use of concomitant nephrotoxins
Diuretics 5 (27.8) 12 (48.0) 0.19
Vancomycin 16 (88.9) 24 (96.0) 0.39
Aminoglycosides 7 (38.9) 14 (56.0) 0.27
Intravenous contrast 4 (22.2) 11 (44.0) 0.15
Total number of nephrotoxins 2 (1–2) 3 (2–3) 0.04 2.14 (1.03–4.45) 0.04

a Time at risk was defined as the time from admission to development of AKI for patients who developed AKI due to high-dose PMB, and the time from admission to death or discharge for those who did not develop AKI due to high-dose PMB; NOTE: IU, international units; MIU, million international units; PMB, polymyxin B.