CREATININE CLEARANCE DURING CIMETIDINE ADMINISTRATION FOR MEASUREMENT OF GLOMERULAR-FILTRATION RATE

被引:145
作者
VANACKER, BAC [1 ]
KOOMEN, GCM [1 ]
KOOPMAN, MG [1 ]
DEWAART, DR [1 ]
ARISZ, L [1 ]
机构
[1] UNIV AMSTERDAM,ACAD MED CTR,DEPT CLIN CHEM,1105 AZ AMSTERDAM,NETHERLANDS
关键词
D O I
10.1016/0140-6736(92)92502-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Creatinine clearance inaccurately estimates true glomerular filtration rate (GFR) because of tubular secretion of creatinine. We studied the ability of oral cimetidine, a blocker of tubular creatinine secretion, to improve the accuracy of measuring creatinine clearance. Clearances of inulin and endogenous creatinine were simultaneously measured in 16 patients with renal disease before administration of cimetidine and during 8 successive 3 h clearance periods with cimetidine 400 mg as priming dose followed by 200 mg every 3 h. At baseline, creatinine relative to inulin clearance (Cl(C)/Cl(I)) ranged from 1.14 to 2.27. With cimetidine, Cl(C)/Cl(I) approached unity in 8 patients (mean 1.02 [SD 0.03]), but considerably exceeded unity in 8 others (1.33 [0.14]). Plasma cimetidine/creatinine ratio was smaller in this second group, due to significantly higher renal clearance of cimetidine (333 [136] vs 165 [89] ml/min, p=0.01). In a further study, cimetidine dose and, consequently plasma cimetidine concentration, was increased in 6 additional patients who had incomplete inhibition previously. This increased dose completely inhibited tubular creatinine secretion in the third until the sixth hour, so that creatinine clearance equalled GFR. Provided an adequate dose of cimetidine is given, 24 h creatinine clearance during administration of drug measures GFR accurately in patients with renal disease. However, because of the maximum daily dose of cimetidine that is advised, short clearance times (3 h) are recommended.
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页码:1326 / 1329
页数:4
相关论文
共 22 条
[11]   CIRCADIAN-RHYTHM OF GLOMERULAR-FILTRATION RATE IN NORMAL INDIVIDUALS [J].
KOOPMAN, MG ;
KOOMEN, GCM ;
KREDIET, RT ;
DEMOOR, EAM ;
HOEK, FJ ;
ARISZ, L .
CLINICAL SCIENCE, 1989, 77 (01) :105-111
[12]   CHANGES IN COMPOSITION OF THE URINE IN URETER AND BLADDER AT LOW URINE FLOW [J].
LEVINSKY, NG ;
BERLINER, RW .
AMERICAN JOURNAL OF PHYSIOLOGY, 1959, 196 (03) :549-553
[13]   The renal excretion of endogenous creatinine in man comparison with exogenous creatinine and inulin [J].
Miller, BF ;
Winkler, AW .
JOURNAL OF CLINICAL INVESTIGATION, 1938, 17 (01) :31-40
[14]   SERIAL ASSESSMENT OF GLOMERULAR-FILTRATION RATE IN LUPUS NEPHROPATHY [J].
PETRI, M ;
BOCKENSTEDT, L ;
COLMAN, J ;
WHITINGOKEEFE, Q ;
FITZ, G ;
SEBASTIAN, A ;
HELLMANN, D .
KIDNEY INTERNATIONAL, 1988, 34 (06) :832-839
[15]   ORAL CIMETIDINE IMPROVES THE ACCURACY AND PRECISION OF CREATININE CLEARANCE IN LUPUS NEPHRITIS [J].
ROUBENOFF, R ;
DREW, H ;
MOYER, M ;
PETRI, M ;
WHITINGOKEEFE, Q ;
HELLMANN, DB .
ANNALS OF INTERNAL MEDICINE, 1990, 113 (07) :501-506
[16]   The renal excretion of creatinine in man [J].
Shannon, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1935, 14 (04) :403-410
[17]   LIMITATIONS OF CREATININE AS A FILTRATION MARKER IN GLOMERULOPATHIC PATIENTS [J].
SHEMESH, O ;
GOLBETZ, H ;
KRISS, JP ;
MYERS, BD .
KIDNEY INTERNATIONAL, 1985, 28 (05) :830-838
[18]   CLINICAL PHARMACOKINETICS OF CIMETIDINE [J].
SOMOGYI, A ;
GUGLER, R .
CLINICAL PHARMACOKINETICS, 1983, 8 (06) :463-495
[19]  
VANACKER BAC, 1992, J LAB CLIN MED, V120, P400
[20]   SATURABLE PHARMACOKINETICS IN THE RENAL EXCRETION OF DRUGS [J].
VANGINNEKEN, CAM ;
RUSSEL, FGM .
CLINICAL PHARMACOKINETICS, 1989, 16 (01) :38-54