Evidence map›Paper›PMID 40519511›Full record

ArticleBMJ medicine2024

Use of sodium valproate and other antiseizure drug treatments in England and Wales: quantitative analysis of nationwide linked electronic health records.

Caroline E Dale, Rohan Takhar, Yat Yi Fan, Fatemeh Torabi, Michail Katsoulis, Samuel Kim, Andrew Lambarth, Christopher Tomlinson, Tim Wilkinson, Tanja Mueller and 12 more

Abstract read
In one paragraph

Article in BMJ medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

Caroline E Dale *Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.ORCID 0000-0002-3889-8974
Rohan Takhar *Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
Yat Yi FanDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
Fatemeh TorabiSwansea University Medical School, Swansea, UK.ORCID 0000-0002-5853-4625
Michail KatsoulisMedical Research Council (MRC) Unit for Lifelong Health and Ageing, London, London, UK.
Samuel KimRoyal Free London NHS Foundation Trust, London, UK.
Andrew LambarthSt George's University Hospitals NHS Foundation Trust, London, UK.
Christopher TomlinsonUniversity College London Institute of Health Informatics, London, UK.ORCID 0000-0002-0903-5395
Tim WilkinsonUniversity of Edinburgh Centre for Clinical Brain Sciences, Edinburgh, UK.ORCID 0000-0001-8952-0982
Tanja MuellerStrathclyde Institute of Pharmacy and Biomedical Sciences, Glasgow, UK.ORCID 0000-0002-0418-4789
Amanj KurdiStrathclyde Institute of Pharmacy and Biomedical Sciences, Glasgow, UK.ORCID 0000-0001-5036-1988
Mark AshworthKing's College London School of Life Course and Population Sciences, London, UK.
Mamas A MamasKeele University Faculty of Medicine and Health Sciences, Keele, UK.
Kamlesh KhuntiUniversity of Leicester Diabetes Research Centre, Leicester, UK.
Ashley AkbariSwansea University Medical School, Swansea, UK.ORCID 0000-0003-0814-0801
Andrew D MorrisHealth Data Research UK, London, UK.
Munir PirmohamedDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.ORCID 0000-0002-7534-7266
Anthony G MarsonDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
David WilliamsUniversity College London Elizabeth Garrett Anderson (UCL EGA) Institute for Women's Health, London, UK.ORCID 0000-0002-8186-9124
David HuntUniversity of Edinburgh Centre for Clinical Brain Sciences, Edinburgh, UK.
Cathie SudlowHealth Data Research UK, London, UK.ORCID 0000-0002-7725-7520
Reecha SofatDepartment of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Objective: To investigate the use of sodium valproate in England and Wales, including during pregnancy, compared with other antiseizure drug treatments, based on national level electronic health records. Design: Quantitative analysis of nationwide linked electronic health records. Setting: Individual level, population scale data from NHS England's Secure Data Environment, from the British Heart Foundation Data Science Centre's CVD-COVID-UK/COVID-IMPACT Consortium (for England), and the Secure Anonymised Information Linkage Databank (for Wales), 1 January 2019 to 31 December 2023. Participants: 1 200 000 individuals dispensed any selected antiseizure drug treatment (ie, sodium valproate, lamotrigine, levetiracetam, carbamazepine, or topiramate); 304 000 women, aged 15-49 years, dispensed any selected antiseizure drug treatment and 28 400 women, aged 15-49 years, dispensed sodium valproate. Main outcome measures: Prevalent (current) and incident (new) uses of sodium valproate and other antiseizure drug treatments before and during the covid-19 pandemic (1 January 2019 to 31 December 2023), grouped by age and sex. Pregnancy rates per 1000 women, aged 15-49 years, who used antiseizure drug treatments, and timing and dose of sodium valproate dispensed during pregnancy. Geographical variation in use of sodium valproate and disease indications (epilepsy and bipolar affective disorder). Trends in deaths related to epilepsy for 2015-22. Results: Prevalent use of sodium valproate in women of childbearing potential decreased and use of most other antiseizure drug treatments increased between 2019 and 2023. Incident use of sodium valproate per 100 000 women decreased from seven to five in women aged 15-19 years, from 11 to seven in women aged 20-29 years, and from 14 to seven in women aged 30-39 years between 2019 and 2022. Incident use also decreased in men of the same age but remained at much higher levels (from 53 to 43 in men aged 15-19 years, 59 to 47 in men aged 20-29 years, and 57 to 42 in men aged 30-39 years, per 100 000 men). Pregnancy rates decreased from 6.0 to 5.2 per 1000 women of childbearing potential who were dispensed sodium valproate over the same period. The number of pregnant women who used sodium valproate during pregnancy decreased from 140 in 2019 to 85 in 2023. Epilepsy was the most common indication, followed by bipolar affective disorder (751 and 193 per 1000 women of childbearing potential dispensed sodium valproate, respectively, in 2023). No clear evidence was found that deaths related to epilepsy increased in women aged 15-49 during 2015-22, but a slight increase was found in men aged 15-49 during the later period between April 2018 and December 2022. Conclusions: Based on comprehensive national records, changes in the dispensing of antiseizure drug treatments in response to regulatory actions were tracked. Rates for use of sodium valproate by women, including during pregnancy, decreased before and continued to slowly decrease during the covid-19 pandemic. Incident use was also reduced in men but remained at much higher levels than in women. This approach, linking national dispensing data to health records at the individual level, could help monitor changes to medicines affected by regulatory changes, including in specific population groups, such as pregnant individuals, and their potential effect on health outcomes.

Indexed as

Medical informaticsNeurologyPharmacologyPrenatal care

Identifiers

PMID40519511
PMCPMC12164316

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.