From: Vancomycin dosing design method considering risk factors for nephrotoxicity
Low Risk groups | High Risk groups | p-value | |||||
---|---|---|---|---|---|---|---|
(n = 108) | (n = 104) | ||||||
Renal impairment | 14 | (13.5%) | 33 | (31.7%) | 0.001‡) | ||
Age (years) | 76 | [33–95] | 83 | [19–98] | 0.004†) | ||
Sex (M/F) | 54/54 | 63/41 | - | ||||
Height (cm) | 160 | [138–180] | 160 | [137–175] | 0.988†) | ||
Weight (kg) | 51.7 | [29.2-124.6] | 48.9 | [27.0-135.7] | 0.451†) | ||
Ccr (mL/min) | 55.3 | [14.0-120] | 46.9 | [4.9–120] | 0.045†) | ||
BMI | 20.2 | [12.5–47.5] | 20.0 | [11.7–49.8] | 0.478†) | ||
Dehydration‖) | 70 | (64.8%) | 81 | (77.9%) | 0.036‡) | ||
BUN (mg/dL) | 18.7 | [4.3–81.5] | 22.3 | [6.5–145.0] | 0.004†) | ||
Cr (mg/dL) | 0.72 | [0.26–6.7] | 0.74 | [0.25–5.04] | 0.505†) | ||
Initial Dose (mg/kg) | 24.9 | [9.0-46.7] | 26.3 | [7.5–55.6] | 0.181†) | ||
Maintenance Dose (mg/kg/day) | 28.8 | [7.4–63.9] | 23.7 | [3.5–62.3] | 0.004†) | ||
Peak blood concentration (µg/mL) | 25.5 | [12.1–56.8] | 26.5 | [8.5-120.4] | 0.162†) | ||
Trough blood concentration (µg/mL) | 15.6 | [3.0-42.1] | 16.4 | [4.8–49.8] | 0.060†) | ||
Initial Blood Sampling Measured AUC (mg·h/L) | 492 | [259–1291] | 552 | [237–1975] | 0.095†) | ||
AUCss (mg·h/L) | 572 | [306–1217] | 573 | [230–1984] | 0.500†) | ||
Cumulative AUC(mg·h/L) ¶) | 5754 | [1117–26181] | 6402 | [1011–37078] | 0.349†) | ||
Days of administration (days) | 11.5 | [3–47] | 13.0 | [3–47] | 0.196†) | ||
Periods before the onset of nephrotoxicity (days) | 11 | [3–41] | 11.5 | [3–47] | 0.689†) | ||
Dosing for more than 14 days | 36 | (33.3%) | 47 | (45.2%) | 0.077‡) |