Literature DB >> 6510463

Pharmacokinetic study of the new sulfamethopyrazine-trimethoprim combination (kelfiprim) in renal insufficiency.

A Cantaluppi, G Graziani, C Ponticelli, S Grasso, G Meinardi, F Piaia, V Tamassia.   

Abstract

The combination of trimethoprim (TMP) and sulfamethopyrazine (SMP) has been successfully used to treat chronic urinary tract infections. Since parenchymal involvement associated with renal insufficiency of varying degree is not infrequent in these patients, it was considered important to study the pharmacokinetics of TMP and SMP in a fixed dose combination. Four groups of patients were studied: 1) 4 patients with endogenous creatinine clearance (CLcR) between 80 and 40 ml/min; 2) 3 patients with CLcR between 40 and 10 ml/min; 3) 3 patients on chronic peritoneal dialysis (CAPD); and 4) 3 patients on haemodialysis. A single oral dose of 250 mg TMP and 200 mg SMP was given to each patient. Multiple samples were collected over 9 days and the following pharmacokinetic parameters were calculated: total area under the plasma level curve, slow disposition rate constant beta and the corresponding t1/2 beta, plasma clearance and the apparent volume of distribution. The results show that the two moieties of the TMP-SMP combination behaved differently in uraemic patients as fas as elimination rate was concerned. TMP was eliminated more slowly both in patients with diminished renal function and in those subjected to haemo- or peritoneal dialysis. The reduction in the rate of elimination of TMP was significantly correlated with the degree of renal impairment. The elimination of SMP, however, was not significantly affected by the reduced renal function; indeed a tendency to increase was noted, at least in dialyzed patients.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1984        PMID: 6510463     DOI: 10.1007/bf00542173

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  9 in total

Review 1.  Synergy of trimethoprim-sulfamethoxazole.

Authors:  S R Bushby
Journal:  Can Med Assoc J       Date:  1975-06-14       Impact factor: 8.262

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Authors:  G Schioppacassi; V Mandelli; R Mazzoleni; E Morvillo
Journal:  G Ital Chemioter       Date:  1979 Jan-Dec

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Authors:  G P Wormser
Journal:  N Y State J Med       Date:  1978-10

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Authors:  S R Bushby; G H Hitchings
Journal:  Br J Pharmacol Chemother       Date:  1968-05

5.  The renal handling of trimethoprim and sulphamethoxazole in man.

Authors:  P Sharpstone
Journal:  Postgrad Med J       Date:  1969-11       Impact factor: 2.401

6.  Pharmacokinetic study of a sulfametopyrazine/trimethoprim combination (Kelfiprim) in human volunteers.

Authors:  D S Reeves; M J Bywater; D W Bullock; H A Holt
Journal:  J Antimicrob Chemother       Date:  1980-09       Impact factor: 5.790

7.  Evaluation of slow infusions of co-trimoxazole by using predictive pharmacokinetics.

Authors:  D J Morgan; K Raymond
Journal:  Antimicrob Agents Chemother       Date:  1980-02       Impact factor: 5.191

8.  Quantitative determination of the bacteriostatically active fraction of sulfonamides and the sum of their inactive metabolites in the body fluids.

Authors:  J Rieder
Journal:  Chemotherapy       Date:  1972       Impact factor: 2.544

9.  Serum and saliva levels of a trimethoprim-sulfamethopyrazine combination in man.

Authors:  A Sardi; M P Vettaro; R Alesina; S Grasso; G Meinardi; I de Carneri; V Tamassia
Journal:  Eur J Clin Pharmacol       Date:  1981       Impact factor: 2.953

  9 in total
  1 in total

Review 1.  Clinical pharmacokinetics of antibiotics in patients with impaired renal function.

Authors:  W L St Peter; K A Redic-Kill; C E Halstenson
Journal:  Clin Pharmacokinet       Date:  1992-03       Impact factor: 6.447

  1 in total

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