Evidence map›Paper›PMID 37294532›Full record

ArticleDrug safety2023

Impact of 2018 EU Risk Minimisation Measures and Revised Pregnancy Prevention Programme on Utilisation and Prescribing Trends of Medicinal Products Containing Valproate: An Interrupted Time Series Study.

Shahab Abtahi, Romin Pajouheshnia, Carlos E Durán, Judit Riera-Arnau, Magdalena Gamba, Ema Alsina, Vjola Hoxhaj, Morten Andersen, Claudia Bartolini, Sarah Brøgger Kristiansen and 18 more

Abstract read
In one paragraph

Article in Drug safety, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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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

28 authors.

Shahab AbtahiDivision of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University (UU), David de Wiedgebouw, Universiteitsweg 99, 3584 CG, Utrecht, The Netherlands.ORCID 0000-0003-0482-5563
Romin PajouheshniaDivision of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University (UU), David de Wiedgebouw, Universiteitsweg 99, 3584 CG, Utrecht, The Netherlands.
Carlos E DuránJulius Global Health, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.
Judit Riera-ArnauJulius Global Health, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.
Magdalena GambaDivision of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University (UU), David de Wiedgebouw, Universiteitsweg 99, 3584 CG, Utrecht, The Netherlands.
Ema AlsinaJulius Global Health, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.
Vjola HoxhajJulius Global Health, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.
Morten AndersenPharmacovigilance Research Center, Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Claudia BartoliniAgenzia Regionale di Sanità della Toscana (ARS), Firenze, Italy.
Sarah Brøgger KristiansenPharmacovigilance Research Center, Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Jeremy BrownLondon School of Hygiene & Tropical Medicine (LSHTM), London, UK.
Christine Erikstrup HallgreenCopenhagen Centre for Regulatory Science, Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Patricia Garcia-PozaAgencia Espanola de Medicamentos y Productos Sanitarios (AEMPS), Madrid, Spain.
Helga GardarsdottirDivision of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University (UU), David de Wiedgebouw, Universiteitsweg 99, 3584 CG, Utrecht, The Netherlands.
Rosa GiniAgenzia Regionale di Sanità della Toscana (ARS), Firenze, Italy.
Anna GirardiAgenzia Regionale di Sanità della Toscana (ARS), Firenze, Italy.
Emily HolthuisPHARMO Institute for Drug Outcomes Research, Utrecht, The Netherlands.
Consuelo HuertaDepartment of Public Health, Maternal and Child Health, Faculty of Medicine, Universidad Complutense de Madrid, Madrid, Spain.
Luisa IbánezClinical Pharmacology Department, Hospital Universitari de la Vall d'Hebron, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
Giorgio LimoncellaAgenzia Regionale di Sanità della Toscana (ARS), Firenze, Italy.
Mar Martín-PérezAgencia Espanola de Medicamentos y Productos Sanitarios (AEMPS), Madrid, Spain.
Olga PaolettiAgenzia Regionale di Sanità della Toscana (ARS), Firenze, Italy.
Giuseppe RobertoAgenzia Regionale di Sanità della Toscana (ARS), Firenze, Italy.
Patrick SouvereinDivision of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University (UU), David de Wiedgebouw, Universiteitsweg 99, 3584 CG, Utrecht, The Netherlands.
Karin M A SwartPHARMO Institute for Drug Outcomes Research, Utrecht, The Netherlands.
Kevin WingLondon School of Hygiene & Tropical Medicine (LSHTM), London, UK.
Miriam SturkenboomJulius Global Health, University Medical Center Utrecht (UMCU), Utrecht, The Netherlands.
Olaf KlungelDivision of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University (UU), David de Wiedgebouw, Universiteitsweg 99, 3584 CG, Utrecht, The Netherlands. o.h.klungel@uu.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDue to established teratogenicity of valproates, the EU risk minimisation measures (RMMs) with a pregnancy prevention programme (PPP) for valproate were updated in March 2018.

objectivesTo investigate the effectiveness of the 2018 EU RMMs on valproate utilisation in five European countries/regions.

methodsA multi-database, times series study of females of childbearing potential (12-55 years) was conducted using electronic medical records from five countries/regions (01.01.2010-31.12.2020): Denmark, Tuscany (Italy), Spain, the Netherlands, and the UK. Clinical and demographic information from each database was transformed to the ConcePTION Common Data Model, quality checks were conducted and a distributed analysis was performed using common scripts. Incident and prevalent use of valproate, proportion of discontinuers and switchers to alternative medicine, frequency of contraception coverage during valproate use, and occurrence of pregnancies during valproate exposure were estimated per month. Interrupted time series analyses were conducted to estimate the level or trend change in the outcome measures.

resultsWe included 69,533 valproate users from 9,699,371 females of childbearing potential from the five participating centres. A significant decline in prevalent use of valproates was observed in Tuscany, Italy (mean difference post-intervention -7.7%), Spain (-11.3%), and UK (-5.9%) and a non-significant decline in the Netherlands (-3.3%), but no decline in incident use after the 2018 RMMs compared to the period before. The monthly proportion of compliant valproate prescriptions/dispensings with a contraceptive coverage was low (<25%), with an increase after the 2018 RMMs only in the Netherlands (mean difference post-intervention 12%). There was no significant increase in switching rates from valproates to alternative medicine after the 2018 intervention in any of the countries/regions. We observed a substantial number of concurrent pregnancies during valproate exposure, but with a declining rate after the 2018 RMMs in Tuscany, Italy (0.70 per 1000 valproate users pre- and 0.27 post-intervention), Spain (0.48 and 0.13), the Netherlands (0.34 and 0.00), and an increasing rate in UK (1.13 and 5.07).

conclusionThere was a small impact of the 2018 RMMs on valproate use in the studied European countries/regions. The substantial number of concurrent pregnancies with valproate exposure warrants a careful monitoring of implementation of the existing PPP for valproate in clinical practice in Europe, to see if there is any need for additional measures in the future.

Indexed as

ContraceptionValproic AcidEuropeFemaleHumansInterrupted Time Series AnalysisItalyPregnancyValproic Acid

Identifiers

PMID37294532
PMCPMC10252161

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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.