Abstract

BackgroundValproate is a known teratogen. In April 2018, the Medicines and Healthcare products Regulatory Agency (MHRA) restricted its use in women and banned use in pregnancy, except for epilepsy with no other effective treatment. To date, there is limited information on valproate prescribing within primary care.AimTo characterise valproate prescribing to women of childbearing age, recorded advice or GP prescribed contraception, and recorded pregnancies.Design & settingA cross-sectional study of patients from all 141 general practices across three clinical commissioning groups (CCGs) in East London.MethodWomen aged 15–44 years prescribed valproate between 1 October 2017 and 1 January 2020 were included. Exclusion criteria were early menopause, sterilisation procedures, or hysterectomy. Pseudonymised data on valproate indication, pregnancy, pre-conception, and contraception advice were retrospectively extracted from general practice consultation data. Data were analysed by quarter using univariate statistics.ResultsOf the total 1 042 463 registered patients, 344 women aged 15–44 years were prescribed valproate during the study period; 14 were excluded. There were 10 pregnancies during possible valproate exposure; one was terminated. During the study period, the number of women prescribed valproate significantly decreased (P = 0.003). The pregnancy rate decreased from 9.9/1000 on valproate before the MHRA April 2018 warning, to an average of 2.8/1000 afterwards. Recorded pre-conception and contraception advice increased by 79%, from 24% to 43%, of women prescribed valproate.ConclusionWith continued pregnancies in women aged 15–44 years prescribed valproate, patient education and foetal outcomes remain ongoing concerns. Further improvements are needed to ensure women make informed reproductive choices and safeguard future pregnancies from valproate exposure.

Highlights

  • Valproate is an anti-epileptic drug (AED) and mood stabiliser licensed in the UK for use in the treatment of all forms of epilepsy, mania in bipolar affective disorder and migraine prophylaxis.[1]

  • Based on two major meta-analyses of data from studies worldwide, the rate of major congenital malformations in babies born to mothers taking valproate monotherapy during pregnancy has been estimated to be 11% compared to 3% in women without epilepsy.[2 3]

  • This study aimed to characterise: valproate prescribing to women of childbearing age, recorded advice or contraception prescribed by general practitioners and recorded pregnancies between 2017 and 2020 across three Clinical Commissioning Groups (CCG) areas of East London

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Summary

Introduction

Valproate is an anti-epileptic drug (AED) and mood stabiliser licensed in the UK for use in the treatment of all forms of epilepsy, mania in bipolar affective disorder and migraine prophylaxis.[1]. Of the anti-epileptic drugs (AEDs), valproate has been consistently highlighted as having the highest rate of congenital malformations.[2 4] Based on two major meta-analyses of data from studies worldwide, the rate of major congenital malformations in babies born to mothers taking valproate monotherapy during pregnancy has been estimated to be 11% compared to 3% in women without epilepsy.[2 3]. Method: Women aged 15-44 years prescribed valproate between 1/10/2017-1/1/2020 were included. Results: Of the total 1,042,463 registered patients, 344 women aged 15-44 years were prescribed valproate during the study period; 14 were excluded. Recorded pre-conception/contraception advice increased by 79%, from 24% to 43%, of women prescribed valproate. Conclusion: With continued pregnancies in women aged 15-44 years prescribed valproate, patient education and foetal outcomes remain ongoing concerns. Further improvements are needed to ensure women make informed reproductive choices and safeguard future pregnancies from valproate exposure

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