Literature DB >> 2370566

Monitoring of phenytoin in epileptic children: value of the single morning sample.

A S Naglo1, A Nergårdh, L O Boréus.   

Abstract

The intra-individual variation in plasma concentration of phenytoin was studied in ten clinically well controlled children on monotherapy. The drug concentration was determined in routine pre-dose samples taken on three to five different mornings. On two of these occasions, plasma phenytoin was also determined at 0.5, 1, 2, 3, 5 and 7 h after the dose. The difference between the highest and lowest morning concentrations in a patient varied between 7.5 and 40 mumol/l (mean 20.1 mumol/l). Half of all morning concentration values were lower than 40 mumol/l. This often-recommended lower limit for good seizure control should therefore be reconsidered. The two concentration versus time curves in each patient during 7 h after administration differed considerably in shape, and the first curve could not be used for prediction of the second curve. The ratio between unbound and total drug was very stable and amounted to 9.4, SD 0.94% (n = 168). It is concluded that the conventional single morning sample is satisfactory for routine monitoring in well-controlled children on monotherapy with phenytoin. In problem patients, and during combination therapy, however, more extensive investigation will be necessary, including repeated morning samples as well as determination of dose-interval curves and protein binding.

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Year:  1990        PMID: 2370566     DOI: 10.1007/bf00314592

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  17 in total

1.  A study of the pharmacokinetics of phenytoin (diphenylhydantoin) in epileptic patients, and the development of a nomogram for making dose increments.

Authors:  A Richens
Journal:  Epilepsia       Date:  1975-11       Impact factor: 5.864

2.  Phenytoin kinetics in children.

Authors:  R G Curless; P D Walson; D E Carter
Journal:  Neurology       Date:  1976-08       Impact factor: 9.910

Review 3.  Should we measure free antiepileptic drug levels?

Authors:  W H Theodore
Journal:  Clin Neuropharmacol       Date:  1987       Impact factor: 1.592

4.  A comparison between microcrystalline and conventional phenytoin preparations: relative bioavailability and steady-state plasma concentrations.

Authors:  L O Boréus; A Nergårdh; M Ehrnebo; K Theorell
Journal:  J Neurol       Date:  1980       Impact factor: 4.849

5.  Identifying patients who might benefit from free phenytoin monitoring.

Authors:  J Baird-Lambert; M P Manglick; M Wall; N Buchanan
Journal:  Ther Drug Monit       Date:  1987-06       Impact factor: 3.681

Review 6.  Circadian changes of drug disposition in man.

Authors:  A Reinberg; M H Smolensky
Journal:  Clin Pharmacokinet       Date:  1982 Sep-Oct       Impact factor: 6.447

7.  Diphenylhydantoin elimination kinetics in overdosed children.

Authors:  L K Garrettson; W J Jusko
Journal:  Clin Pharmacol Ther       Date:  1975-04       Impact factor: 6.875

8.  Is free fraction measurement of phenytoin always necessary in pediatric epileptic patients?

Authors:  I Johno; T Kuzuya; K Suzuki; M Hasegawa; T Nakamura; S Kitazawa; K Aso; K Watanabe
Journal:  Ther Drug Monit       Date:  1988       Impact factor: 3.681

9.  Absorption and metabolism of phenytoin from tablets and capsules.

Authors:  T C Smith; A Kinkel
Journal:  Clin Pharmacol Ther       Date:  1976-12       Impact factor: 6.875

10.  The rate of decline of diphenylhydantoin in human plasma.

Authors:  K Arnold; N Gerber
Journal:  Clin Pharmacol Ther       Date:  1970 Jan-Feb       Impact factor: 6.903

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  1 in total

Review 1.  Clinical pharmacokinetics of antiepileptic drugs in paediatric patients. Part II. Phenytoin, carbamazepine, sulthiame, lamotrigine, vigabatrin, oxcarbazepine and felbamate.

Authors:  D Battino; M Estienne; G Avanzini
Journal:  Clin Pharmacokinet       Date:  1995-11       Impact factor: 6.447

  1 in total

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