Literature DB >> 7432728

Phenytoin metabolism in pregnancy.

N K Kochenour, M G Emery, R J Sawchuk.   

Abstract

Approximately 45% of patients with epilepsy experience an increase in seizure frequency during pregnancy. Despite the availability of effective anticonvulsant medications, there has been no decrease in reported seizure frequency accompanying pregnancy in the past 35 years. The authors prospectively studied concentrations of phenytoin (DPH) and its metabolites in 5 patients throughout pregnancy and during the postpartum period. The concentrations of phenytoin, as well as both unconjugated and conjugated forms of its principal metabolite, 5-(4-hydroxyphenyl)-5-phenylhydantoin (4-OH-DPH), were measured in plasma and urine by a precise high-pressure liquid chromatography method. Four patients experienced a decrease in plasma DPH during gestation, 3 of whom developed seizures at a time of low plasma DPH concentration. Within the therapeutic range, small increments in dosage resulted in large increments in plasma DPH levels, and in the postpartum period high levels of DPH were encountered if the dosage was not reduced. As pregnancy progressed, there was a decrease in the percentage of the daily dosage of DPH excreted as 4-OH-DPH. Based on these observations, the authors conclude that 1) pregnancy is associated with altered DPH absorption or metabolism or both, and 2) periodic measurement of plasma DPH concentration is valuable when managing a pregnant epileptic patient.

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Year:  1980        PMID: 7432728

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  9 in total

1.  Applying organ clearance concepts in a clinical setting.

Authors:  Jorge Duconge
Journal:  Am J Pharm Educ       Date:  2008-10-15       Impact factor: 2.047

Review 2.  The significance of plasma protein binding on the fetal/maternal distribution of drugs at steady-state.

Authors:  M D Hill; F P Abramson
Journal:  Clin Pharmacokinet       Date:  1988-03       Impact factor: 6.447

Review 3.  Anticonvulsants during pregnancy and lactation. Transplacental, maternal and neonatal pharmacokinetics.

Authors:  H Nau; W Kuhnz; H J Egger; D Rating; H Helge
Journal:  Clin Pharmacokinet       Date:  1982 Nov-Dec       Impact factor: 6.447

4.  Bioavailability and pharmacokinetics of phenytoin during pregnancy.

Authors:  C M Lander; M T Smith; J B Chalk; C de Wytt; P Symoniw; I Livingstone; M J Eadie
Journal:  Eur J Clin Pharmacol       Date:  1984       Impact factor: 2.953

5.  Changes in primidone/phenobarbitone ratio during pregnancy and the puerperium.

Authors:  D Battino; S Binelli; L Bossi; M L Como; D Croci; C Cusi; G Avanzini
Journal:  Clin Pharmacokinet       Date:  1984 May-Jun       Impact factor: 6.447

6.  Phenytoin metabolism during pregnancy.

Authors:  M J Eadie; G E McKinnon; R G Dickinson; W D Hooper; C M Lander
Journal:  Eur J Clin Pharmacol       Date:  1992       Impact factor: 2.953

7.  Labetalol disposition and concentration-effect relationships during pregnancy.

Authors:  P C Rubin; L Butters; A W Kelman; C Fitzsimons; J L Reid
Journal:  Br J Clin Pharmacol       Date:  1983-04       Impact factor: 4.335

8.  The effect of pregnancy in humans on the pharmacokinetics of stable isotope labelled phenytoin.

Authors:  R G Dickinson; W D Hooper; B Wood; C M Lander; M J Eadie
Journal:  Br J Clin Pharmacol       Date:  1989-07       Impact factor: 4.335

Review 9.  Epilepsy during pregnancy: focus on management strategies.

Authors:  Laura M Borgelt; Felecia M Hart; Jacquelyn L Bainbridge
Journal:  Int J Womens Health       Date:  2016-09-19
  9 in total

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