The pharmacokinetics of Cetirizine, a histamine H1-receptor antagonist, were investigated in five renal failure patients undergoing chronic haemodialysis therapy. The patients received one 10 mg cetirizine dihydrochloride capsule 3 h before haemodialysis. Concentrations of cetirizine in serum and di
Ceforanide pharmacokinetics in haemodialysis: The effect of ultrafiltration
✍ Scribed by José M. Lanao; Consuelo R. De Prada; Alfonso Dominguez-Gil; José M. Tabernero; Jesús Martín; Juan R. Gómez
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 505 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0142-2782
No coin nor oath required. For personal study only.
✦ Synopsis
The kinetics of ceforanide in plasma and dialysate was studied in 8 patients with terminal renal impairment after undergoing haemodialysis sessions lasting between 4 and 5 h. All patients received a single i.v. dose of 15mg kg-' of the drug at the start of the session. The dialysers used in this study were Spiraflow capillar 1.3m2, Travenol plates 1.4m2, and PAN plates. Blood flow ranged between 200 and 300ml min-' and dialysate flow between 500-650ml min-'. Plasma ceforanide levels were measured at the input and output of the dialyser and the antibiotic levels in dialysate were determined coinciding with the withdrawal times of the blood samples. A microbiologic plate diffusion method was used to determine the antibiotic concentrations.
The mean values of some pharmacokinetic parameters of ceforanide calculated with a non-linear regression program from the data obtained from arterial blood were the following: (Y (h-') = 4.14 k 1-32; p (h-') = 0.26 f 0.07; tlh p (h) = 2.82 f 0.82; Vd,, (I) From the relationships between the antibiotic concentrations at the input and output of the dialyser it was possible to calculate an extraction coeffficient of 0.11 f 0.06. The dialysis clearance of ceforanide was calculated from the determination of the extraction coefficient and from the measuring of antibiotic in dialysate, though different results were obtained with the two methods. Dialysis clearance calculated from the extraction coefficient showed a mean value of 18.68 k 12.161~11 min-', significantly lower (p < 0.01) than that established by analysis of the antibiotic in dialysate, which was 41-55 f 15433ml min-'. These differences may be attributed to problems related to the determination of blood flow and to the ultrafiltration capacity of the dialysis membranes. A linear relationship was established between the percentage error in the observed and predicted extraction coefficients and the ultrafiltration rate. The results obtained suggest that the simultaneous measurement of = 10-24 f 2.14.
📜 SIMILAR VOLUMES
The pharmacokinetics and pharmacodynamics of fosinoprilat, the diacid of fosinopril sodium (a new angiotensin-converting enzyme (ACE) inhibitor), were investigated in six haemodialysis patients. Intravenous 14C-fosinoprilat (7.5 mg), oral 14C-fosinopril sodium (10 mg) and oral fosinopril sodium (10
We have studied the pharmacokinetics of fluconazole in five patients on long-term haemodialysis. The single-pass extraction rate of the dialyzer was 59 (3.5)% (n = 4), and the serum concentration was reduced by haemodialysis for 3 or 4 h by 26 (3.2)% (n = 5) and 39 (2.2)% (n = 9) respectively. The e