Literature DB >> 12136066

Lamotrigine clearance during pregnancy.

T A Tran1, I E Leppik, K Blesi, S T Sathanandan, R Remmel.   

Abstract

OBJECTIVE: To evaluate changes in lamotrigine (LTG) clearance before, during, and after pregnancy.
METHODS: Twelve pregnancies that had complete steady-state data before, during, and after pregnancy were evaluated. Data included weight, LTG dose, and LTG blood levels at preconception, during pregnancy, and postpartum, and concomitant use of other antiepileptic drugs and their dosages. Apparent clearance (L/[kg.day]) of LTG was calculated by dose/level/weight for time points at preconception; during the first trimester, second trimester, and third trimester; and postpartum. Apparent clearance was compared between preconception and each of the three trimesters. Statistical analysis was performed using one-way analysis of variance, the Student-Newman-Keuls test, and the paired Student's t-test.
RESULTS: An increase in apparent clearance (>65%) was observed between preconception and the second and third trimesters (p < 0.05). Eleven pregnancies required higher doses of LTG to maintain therapeutic levels during pregnancy. There was no significant change in apparent clearance between each trimester. A decrease in apparent clearance was observed between the last two trimesters and postpartum (p < 0.05). In the postpartum period, apparent clearances returned to the preconception baseline, and LTG doses needed to be reduced.
CONCLUSION: Pregnancy increases LTG clearance by >50%. This effect occurs early in pregnancy and reverts quickly after delivery. LTG levels should be monitored before, during, and after pregnancy.

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Year:  2002        PMID: 12136066     DOI: 10.1212/wnl.59.2.251

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  46 in total

Review 1.  [Lamotrigine in women with epilepsy. Review of present data].

Authors:  B Schmitz
Journal:  Nervenarzt       Date:  2003-10       Impact factor: 1.214

2.  Anatomical, physiological and metabolic changes with gestational age during normal pregnancy: a database for parameters required in physiologically based pharmacokinetic modelling.

Authors:  Khaled Abduljalil; Penny Furness; Trevor N Johnson; Amin Rostami-Hodjegan; Hora Soltani
Journal:  Clin Pharmacokinet       Date:  2012-06-01       Impact factor: 6.447

3.  The importance of increased clearance of lamotrigine during pregnancy.

Authors:  Elinor Ben-Menachem
Journal:  Epilepsy Curr       Date:  2005 Mar-Apr       Impact factor: 7.500

4.  Do the results of pregnancy registries contradict one another?

Authors:  Cynthia L Harden
Journal:  Epilepsy Curr       Date:  2006 May-Jun       Impact factor: 7.500

Review 5.  Epilepsy in pregnancy.

Authors:  Torbjörn Tomson; Vilho Hiilesmaa
Journal:  BMJ       Date:  2007-10-13

6.  Hormones, seizures, and lamotrigine: Oh, my!

Authors:  Page B Pennell
Journal:  Epilepsy Curr       Date:  2008 Jan-Feb       Impact factor: 7.500

Review 7.  Pharmacogenetics and individualizing drug treatment during pregnancy.

Authors:  David M Haas
Journal:  Pharmacogenomics       Date:  2014-01       Impact factor: 2.533

Review 8.  Pharmacotherapy for mood disorders in pregnancy: a review of pharmacokinetic changes and clinical recommendations for therapeutic drug monitoring.

Authors:  Kristina M Deligiannidis; Nancy Byatt; Marlene P Freeman
Journal:  J Clin Psychopharmacol       Date:  2014-04       Impact factor: 3.153

9.  The management of epilepsy in pregnancy at the Whittington Hospital: a retrospective audit 2004-2006 and 2007-2010.

Authors:  Rebecca Allen; Liliana Grosu; Ishita Das; Amma Kyei-Mensah
Journal:  Obstet Med       Date:  2013-05-03

Review 10.  Do lamotrigine and levetiracetam solve the problem of using sodium valproate in women with epilepsy?

Authors:  John J Craig
Journal:  Obstet Med       Date:  2012-02-20
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