Pharmacokinetics of once-daily IP gentamicin in CAPD patients

被引:0
作者
Low, CL
Bailie, GR
Evans, A
Eisele, G
Venezia, RA
机构
[1] ALBANY COLL PHARM,ALBANY,NY 12208
[2] ALBANY MED COLL,ALBANY,NY
来源
PERITONEAL DIALYSIS INTERNATIONAL | 1996年 / 16卷 / 04期
关键词
pharmacokinetics; intraperitoneal; peritonitis; dosing; treatment; residual renal function; gentamicin;
D O I
暂无
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objective:This study aimed to investigate the pharmacokinetic characteristics of once-daily intraperitoneal (IF) gentamicin in continuous ambulatory peritoneal dialysis (CAPD) patients. Design: Prospective, nonrandomized, open study. Setting: CAPD outpatient clinic in a teaching hospital. Patients: Ten volunteer CAPD patients without peritonitis. Interventions: Each patient received a single IP dose of 0.6 mg/kg of gentamicin. Blood and dialysate samples were collected at 0, 0.5, 1, 2, 3, 6 (end of first dwell), and 24 hours after the administration of IP gentamicin. Any urine produced over the 24-hour study period was also collected. The dialysate concentration/time data were fitted to a monoexponential curve for all patients. Results: The bioavailability was 56+/-11% over a six-hour dwell. The mean serum elimination half-life (t(1/2)) was 35.8 hours. The volume of distribution was 0.23+/-0.08 L/kg. Equilibration of gentamicin across the peritoneal membrane was rapid, with a t(1/2) equilibration of 4.5 hours. The peritoneal clearance was 5.74+/-1.5 mL/min. Patients with residual renal function had significantly higher systemic gentamicin clearances (7.36+/-1.46 mL/min) than those of anuric patients (4.76+/-1.08 mL/min, p < 0.024). Conclusion: Currently recommended doses of once-daily IP gentamicin for the treatment of peritonitis may not produce the desired therapeutic serum and dialysate concentrations over 24 hours for effective treatment of peritonitis.
引用
收藏
页码:379 / 384
页数:6
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