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dc.contributorIDIAP Jordi Gol
dc.contributor.authorBellas, Lucía
dc.contributor.authorGiner-Soriano, Maria
dc.contributor.authorPrats Uribe, Albert
dc.contributor.authorVedia Urgell, Cristina
dc.contributor.authorAgustí, Antònia
dc.contributor.authorCamacho-Arteaga, Lina
dc.contributor.authorAguilera, Cristina
dc.date.accessioned2024-09-05T08:22:44Z
dc.date.available2024-09-05T08:22:44Z
dc.date.issued2024-08-12
dc.identifier.citationBellas L, Camacho-Arteaga L, Giner-Soriano M, Prats-Uribe A, Aguilera C, Vedia C, et al. Women’s health in focus: Real-world data on valproate prescriptions during pregnancy - a cohort study in Catalonia, Spain. BMJ Open 2024;14(8):e085167.
dc.identifier.issn2044-6055
dc.identifier.urihttps://hdl.handle.net/11351/11901
dc.descriptionValproic acid (VPA); Pregnancy outcomes; electronic health records (EHR)
dc.description.abstractObjectives To characterise the exposure to valproate within a cohort of pregnant women using electronic health records (EHRs) from Catalonia (System for the Development of Research in Primary Care, SIDIAP). Design Drug-utilisation cohort study covering the period from January 2011 to June 2020. The study included pregnancy episodes of women from Catalonia identified by the algorithm. Setting Data were sourced from SIDIAP, a comprehensive EHR repository that includes information from various data sources: recorded prescriptions (both hospital and primary care), diagnoses and sociodemographic characteristics identified by primary care physicians, and sexual and reproductive health data from ASSIR (used by gynaecologists and midwives). Participants Women aged 12–50 with at least one pregnancy episode occurred during January 2011–June 2020 and at least a prescription of valproate during pregnancy. Primary and secondary outcomes Primary outcomes included valproate exposure, measured through prevalence and cumulative incidence in pregnancy episodes and by trimester. The impact of regulatory measures (risk mitigation measures, RMMs) was assessed, and prescriptions over time were analysed using interrupted time series analysis. Secondary outcomes included health issues, pregnancy outcomes, smoking habits and socioeconomic characteristics. Results A total of 99 605 pregnancies were identified, with at least 3.03‰ (95% CI 2.69‰ to 3.39‰) exposed to valproate at some point (302 pregnancies, 276 women). The median pregnancy duration was 38.30 weeks (IQR 12.6–40.1), and the median age at pregnancy was 32.37 years (IQR 27.20–36.56). Epilepsy was the most frequent health issue. The prevalence and cumulative incidence of valproate prescriptions decreased during pregnancy and increased postpregnancy. The RMMs implemented in 2014 led to a reduction in monthly valproate prescriptions during pregnancy in this cohort. Conclusions The study highlights the decline in valproate prescriptions during pregnancy due to RMMs and underscores the need for standardised methodologies in future studies to ensure the safety of pregnant patients and optimise scientific evidence.
dc.format.mimetypepdf
dc.language.isoeng
dc.publisherBMJ Publishing Group
dc.relation.isreferencedbyhttps://doi.org/10.1136/bmjopen-2024-085167
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectÀcid valproic
dc.subjectAnticonvulsius
dc.subjectEmbaràs - Complicacions
dc.subject.meshValproic Acid
dc.subject.mesh/therapeutic use
dc.subject.meshAnticonvulsants
dc.subject.mesh/adverse effects
dc.subject.meshPregnancy Complications
dc.subject.mesh/epidemiology
dc.titleWomen’s health in focus: Real-world data on valproate prescriptions during pregnancy – a cohort study in Catalonia (Spain)
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1136/bmjopen-2024-085167
dc.identifier.doi10.1136/bmjopen-2024-085167
dc.subject.decsácido valproico
dc.subject.decs/uso terapéutico
dc.subject.decsanticonvulsivantes
dc.subject.decs/efectos adversos
dc.subject.decscomplicaciones del embarazo
dc.subject.decs/epidemiología
dc.relation.publishversionhttps://bmjopen.bmj.com/content/14/8/e085167
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.authoraffiliation[Bellas L, Camacho-Arteaga L, Aguilera C, Agustí A] Servei de Farmacologia Clínica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Departament de Farmacologia, Terapèutica i Toxicologia, Universitat Autònoma de Barcelona, Bellaterra, Spain. [Giner-Soriano M] Fundació Institut Universitari per a la Recerca a l'Atenció Primària de Salut Jordi Gol i Gurina (IDIAPJGol), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. [Prats-Uribe A] Nuffield Department of Orthopaedics Rheumatology and Musculoskeletal Science, University of Oxford, Oxford, UK. [Vedia Urgell C] Unitat de farmàcia, Servei d’Atenció Primària Barcelonès Nord i Maresme, Institut Català de la Salut, Badalona, Spain. Departament de Farmacologia, Terapèutica i Toxicologia, Universitat Autònoma de Barcelona, Bellaterra, Spain
dc.identifier.pmid39134441
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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