DISPOSITION OF DIGOXIN IMMUNE FAB IN PATIENTS WITH KIDNEY FAILURE

被引:18
作者
UJHELYI, MR
ROBERT, S
CUMMINGS, DM
COLUCCI, RD
SAILSTAD, JM
VLASSES, PH
FINDLAY, JWA
ZAROWITZ, BJ
机构
[1] HARTFORD HOSP,DEPT PHARM SERV,HARTFORD,CT 06115
[2] UNIV HOSP CONSORTIUM,OAK BROOK,IL
[3] WELLCOME RES LABS,DIV PHARMACOKINET & DRUG METAB,RES TRIANGLE PK,NC 27709
[4] HENRY FORD HOSP,COLL PHARM,DETROIT,MI 48202
[5] HENRY FORD HOSP,DEPT PHARM SERV,DETROIT,MI 48202
[6] E CAROLINA UNIV,SCH MED,DEPT FAMILY MED,GREENVILLE,NC 27834
[7] HARTFORD HOSP,COLL PHARM,HARTFORD,CT 06115
[8] WAYNE STATE UNIV,DETROIT,MI 48202
[9] UNIV CONNECTICUT,STORRS,CT 06268
关键词
D O I
10.1038/clpt.1993.165
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Digoxin and digoxin immune Fab, its antidote, are eliminated renally. However, the disposition of Fab in severe kidney disease is poorly described. Therefore, the disposition of Fab and its relationship to total and free digoxin were studied in five digoxin-toxic patients with end-stage renal disease (n = 4) or severe renal dysfunction (n = 1) with a mean (+/- SD) serum creatinine of 5.9 +/- 1.2 mg/dl (four patients were receiving long-term hemodialysis). Serum was drawn after a clinically neutralizing Fab dose (80 to 160 mg) every 12 to 24 hours for 204 to 327 hours. Fab concentrations were assessed by radioimmunoassay, whereas total digoxin concentrations were assessed with a modified radioimmunoassay or fluorescence polarization immunoassay. The concentration-time profile of Fab appeared to be similar to the concentration-time profile of total digoxin. The mean (+/- SD) half-lives of the alpha and beta disposition phases of Fab were 13 +/- 5 hours and 96 +/- 31 hours, respectively, which were similar to the alpha and beta parameter estimates of total digoxin (14 +/- 4 and 123 +/- 16 hours, respectively). Steady-state volume of distribution and systemic clearance of Fab were 0.29 +/- 0.11 L/kg and 0.057 +/- 0.022 ml/min/kg, respectively. Thus, in comparison to values reported in patients with normal renal function, the elimination of Fab and total digoxin are markedly delayed in patients with end-stage renal disease, which may necessitate prolonged clinical monitoring.
引用
收藏
页码:388 / 394
页数:7
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