TY - JOUR
T1 - Continuous Arteriovenous Hemofiltration of Aminoglycoside Antibiotics in Critically Ill Patients
AU - Zarowitz, Barbara J.
AU - Anandan, J. V.
AU - Dumler, Francis
AU - Jayashankar, J.
AU - Levin, Nathan
PY - 1986
Y1 - 1986
N2 - The effect of continuous arteriovenous hemofiltration on the clearance of either tobramycin or gentamicin (mean dose, 1.65 ± 0.36 mg/kg) was studied in eight critically ill patients. Mean aminoglycoside clearance by hemofiltration was 3.47 ± 1.93 mL/min and total body clearance was 11.92 ± 3.51 mL/min. Hemofiltration clearance (HFCL) was directly correlated with hemofiltration flow rate (HFQR): HFCL (mL/min) = 1.03 HFQR (mL/min) − 0.88 (R = .89). Mean volume of distribution was 0.31 ± 0.08 L/kg, and the elimination rate constant was 0.020 ± 0.01 hr−1. Continuous arteriovenous hemofiltration was responsible for the removal of between 3% and 36% of each aminoglycoside dose in 24 hours. In critically ill patients with changing hemofiltration flow rates, measurement of multiple serum aminoglycoside concentrations is necessary to accurately assess dosing requirements and avoid ototoxicity and nephrotoxicity. 1986 American College of Clinical Pharmacology
AB - The effect of continuous arteriovenous hemofiltration on the clearance of either tobramycin or gentamicin (mean dose, 1.65 ± 0.36 mg/kg) was studied in eight critically ill patients. Mean aminoglycoside clearance by hemofiltration was 3.47 ± 1.93 mL/min and total body clearance was 11.92 ± 3.51 mL/min. Hemofiltration clearance (HFCL) was directly correlated with hemofiltration flow rate (HFQR): HFCL (mL/min) = 1.03 HFQR (mL/min) − 0.88 (R = .89). Mean volume of distribution was 0.31 ± 0.08 L/kg, and the elimination rate constant was 0.020 ± 0.01 hr−1. Continuous arteriovenous hemofiltration was responsible for the removal of between 3% and 36% of each aminoglycoside dose in 24 hours. In critically ill patients with changing hemofiltration flow rates, measurement of multiple serum aminoglycoside concentrations is necessary to accurately assess dosing requirements and avoid ototoxicity and nephrotoxicity. 1986 American College of Clinical Pharmacology
UR - http://www.scopus.com/inward/record.url?scp=0023025765&partnerID=8YFLogxK
U2 - 10.1002/j.1552-4604.1986.tb02973.x
DO - 10.1002/j.1552-4604.1986.tb02973.x
M3 - Article
C2 - 3793961
AN - SCOPUS:0023025765
SN - 0091-2700
VL - 26
SP - 686
EP - 689
JO - Journal of Clinical Pharmacology
JF - Journal of Clinical Pharmacology
IS - 8
ER -