Literature DB >> 73850

Salivary phenytoin concentrations in epilepsy and in chronic renal failure.

F Reynolds, P N Ziroyanis, N F Jones, S E Smith.   

Abstract

Plasma total, plasma unbound (free, therapeutically active), and salivary phenytoin concentrations have been measured in seventeen epileptics and in seven patients with chronic renal failure on long-term phenytoin therapy. Patients with chronic renal failure had low plasma total, but disproportionately high plasma free, drug concentrations indicating impaired protein binding. Even so, their plasma free drug concentrations never fell within the predicted therapeutic range on conventional phenytoin dosage. Salivary drug concentrations correlated closely with plasma free drug concentrations. These observations suggest that phenytoin therapy could be more appropriately monitored by measurement of salivary, rather than plasma, drug concentrations. Avoidance of blood-sampling would be an added advantage, particularly in children and in uraemia. The present results suggest that the optimal therapeutic range of salivary phenytoin would be 4-10 mumol/1.

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Year:  1976        PMID: 73850     DOI: 10.1016/s0140-6736(76)92404-1

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  24 in total

Review 1.  Therapeutic drug monitoring in saliva. An update.

Authors:  R K Drobitch; C K Svensson
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2.  A comparison of serum and saliva paracetamol concentrations.

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Journal:  Br J Clin Pharmacol       Date:  1991-05       Impact factor: 4.335

Review 3.  Therapeutic drug monitoring in pregnancy: rationale and current status.

Authors:  C Knott; F Reynolds
Journal:  Clin Pharmacokinet       Date:  1990-12       Impact factor: 6.447

4.  Use of saliva in monitoring carbamazepine medication in epileptic children.

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Review 5.  The use of kinetic-dynamic interactions in the evaluation of drugs.

Authors:  D B Campbell
Journal:  Psychopharmacology (Berl)       Date:  1990       Impact factor: 4.530

Review 6.  Therapeutic drug monitoring in saliva.

Authors:  M Danhof; D D Breimer
Journal:  Clin Pharmacokinet       Date:  1978 Jan-Feb       Impact factor: 6.447

7.  Overuse of monitoring of blood concentrations of antiepileptic drugs.

Authors:  D W Chadwick
Journal:  Br Med J (Clin Res Ed)       Date:  1987-03-21

8.  Unbound phenytoin plasma concentrations in patients comedicated with sodium valproate--the predictive value of plasma albumin concentration.

Authors:  G J Johnson; C J Kilpatrick; R W Bury; R O Fullinfaw; R F Moulds
Journal:  Br J Clin Pharmacol       Date:  1989-06       Impact factor: 4.335

Review 9.  Oral absorption and secretion of drugs.

Authors:  C F Speirs
Journal:  Br J Clin Pharmacol       Date:  1977-04       Impact factor: 4.335

10.  Comparison of phenytoin determinations in plasma, plasma dialysate and saliva for control of antiepileptic therapy in children.

Authors:  G Brügmann; E Kleinau; R Nolte; F Petruch
Journal:  Klin Wochenschr       Date:  1979-01-15
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