TY - JOUR
T1 - Cimetidine Disposition in Patients Undergoing Continuous Ambulatory Peritoneal Dialysis
AU - KOGAN, FREDERICK J.
AU - SAMPLINER, RICHARD E.
AU - MAYERSOHN, MICHAEL
AU - KAZAMA, RODNEY M.
AU - PERRIER, DONALD
AU - JONES, WILLIAM
AU - MICHAEL, ULRICH F.
PY - 1983
Y1 - 1983
N2 - Abstract: Cimetidine disposition was determined in six patients undergoing continuous ambulatory peritoneal dialysis to ascertain the need for modification of conventional dosing regimens. Blood, dialysis fluid, and urine were collected for 48 hours after administration of a single intravenous dose of cimetidine. The following values were obtained: elimination half‐life, 4.3 hours; systemic or total body clearance, 191 ± 55 ml/min; and dialysis clearance, 4.2 ± 3.1 ml/min. Approximately 2% of a cimetidine dose is removed by dialysis, indicating that there is no need to adjust the conventional renal failure dosing regimen in patients undergoing continuous ambulatory peritoneal dialysis. 1983 American College of Clinical Pharmacology
AB - Abstract: Cimetidine disposition was determined in six patients undergoing continuous ambulatory peritoneal dialysis to ascertain the need for modification of conventional dosing regimens. Blood, dialysis fluid, and urine were collected for 48 hours after administration of a single intravenous dose of cimetidine. The following values were obtained: elimination half‐life, 4.3 hours; systemic or total body clearance, 191 ± 55 ml/min; and dialysis clearance, 4.2 ± 3.1 ml/min. Approximately 2% of a cimetidine dose is removed by dialysis, indicating that there is no need to adjust the conventional renal failure dosing regimen in patients undergoing continuous ambulatory peritoneal dialysis. 1983 American College of Clinical Pharmacology
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U2 - 10.1002/j.1552-4604.1983.tb02732.x
DO - 10.1002/j.1552-4604.1983.tb02732.x
M3 - Article
C2 - 6875024
AN - SCOPUS:0020639938
SN - 0091-2700
VL - 23
SP - 252
EP - 256
JO - The Journal of Clinical Pharmacology
JF - The Journal of Clinical Pharmacology
IS - 5-6
ER -