Women with epilepsy: Evidence‐based counseling across the lifespan

社会心理的 多学科方法 癫痫 医学 生育率 生殖健康 怀孕 精神科 医疗保健 梅德林 重症监护医学 产妇护理 心理学 更年期 生殖医学 家庭医学 生命历程法 老年学 母乳喂养 母乳喂养 发达国家 产前护理 年轻人
作者
Barbara Tettenborn,Georgia Ramantani,Dominique Flügel,Verena Gaus,Susanne Schubert‐Bast,Elisabeth Sellitto,Jennifer Bausch,B. Schmitz
出处
期刊:Epilepsia [Wiley]
标识
DOI:10.1002/epi.70202
摘要

Women with epilepsy (WWE) encounter distinct and evolving challenges across the lifespan that require clinical management extending beyond seizure control alone. Although awareness of sex-specific aspects of epilepsy has increased, important gaps remain in their integration into routine care. This review synthesizes current evidence on epilepsy management across key life stages, including adolescence and transition to adult care, reproductive health, contraception, fertility and pregnancy, lactation, menopause, and bone health. It integrates recent literature with expert interpretation in alignment with contemporary clinical guidelines, with the aim of enhancing clinical applicability. Hormonal changes, bidirectional interactions between antiseizure medications (ASMs), and reproductive physiology as well as shifting psychosocial demands influence seizure patterns, treatment efficacy, and long-term health outcomes in WWE. Particular focus is placed on interactions between epilepsy, endocrine regulation, and ASM therapy, and on teratogenic and neurodevelopmental risks associated with specific ASMs. Effective care for WWE requires continuous, individualized counseling that adapts to changing priorities and risks over time. Structured transition processes, evidence-based counseling on contraception and pregnancy, therapeutic drug monitoring during pregnancy, and transparent communication regarding fetal risks of ASMs are essential components of high-quality care. Beyond the reproductive years, seizure changes during menopause and the cumulative impact of long-term ASM exposure, particularly on bone health, require surveillance and prevention. Despite advances in pregnancy registries and treatment recommendations, participation in registries is low, and evidence outside pregnancy remains limited. Awareness of sex-specific epilepsy issues continues to be insufficient among both WWE and health care professionals. Addressing these gaps will require improved education, coordinated multidisciplinary care, and expanded research efforts to support patient-centered, lifelong care for WWE.
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