Use of Acitretin Among Girls and Women of Childbearing Age and Occurrence of Acitretin-Exposed Pregnancies in Germany.

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Clinical Drug Investigation Pub Date : 2023-11-01 Epub Date: 2023-10-31 DOI:10.1007/s40261-023-01314-2
Jonas Reinold, Bianca Kollhorst, Hellen L Temme, Nadine Wentzell, Ulrike Haug
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Abstract

Background and objective: Acitretin has long-lasting teratogenic properties. Therefore, pregnancies must be avoided during and within 3 years after acitretin treatment. We aimed to describe (i) acitretin use in women of childbearing age in Germany, (ii) the occurrence of acitretin-exposed pregnancies, and (iii) malformations among children exposed in utero.

Methods: Using 2004-2019 data from the German Pharmacoepidemiological Research Database (GePaRD-claims data from ~ 20% of the German population), we determined annual age-standardized prevalence of acitretin use among girls and women aged 13-49 years. In longitudinal analyses, we estimated the number of exposed pregnancies by assessing whether the exposure window assigned to the last dispensation before pregnancy (days covered by dispensation plus 3 years) overlapped the onset of pregnancy or whether there was a dispensation in the first eight weeks of pregnancy. Data of live-born children with in utero exposure to acitretin were reviewed to assess the presence of congenital malformations.

Results: The age-standardized prevalence of acitretin use per 1000 girls and women was 0.04 in 2019. We identified 35 acitretin-exposed pregnancies; 94.3% of these pregnancies were classified as exposed because they occurred within 3 years after stopping acitretin treatment. Among 18 live-born children linked to their mother, four children (22.2%) had congenital malformations (three children with a major malformation).

Conclusions: We observed 35 acitretin-exposed pregnancies mainly because treatment ended too late before pregnancy. Approximately one in five children born from these pregnancies had malformations, highlighting the importance of drawing more attention to the long-lasting teratogenicity of this drug.

Abstract Image

德国育龄女孩和妇女使用阿曲素与阿曲素暴露妊娠的发生率。
背景和目的:阿曲汀具有长期的致畸特性。因此,在阿曲汀治疗期间和治疗后3年内必须避免怀孕。我们的目的是描述(i)德国育龄妇女使用阿曲汀,(ii)暴露于阿曲汀的妊娠发生率,以及(iii)暴露于子宫内的儿童畸形。方法:使用德国药物流行病学研究数据库2004-2019年的数据(GePaRD声称数据来自~ 20%的德国人口),我们确定了13-49岁女孩和妇女使用阿曲汀的年度年龄标准化流行率。在纵向分析中,我们通过评估妊娠前最后一次给药的暴露窗口(给药天数加3年)是否与妊娠期重叠,或者在妊娠的前八周是否有给药,来估计暴露妊娠的数量。回顾了子宫内接触阿曲汀的活产儿童的数据,以评估先天畸形的存在。结果:2019年,每1000名女孩和妇女使用阿曲汀的年龄标准化患病率为0.04。我们确定了35例暴露于阿曲汀的妊娠;94.3%的妊娠被归类为暴露妊娠,因为它们发生在停止阿曲汀治疗后的3年内。在与母亲有联系的18名活产儿童中,有4名儿童(22.2%)患有先天性畸形(3名儿童患有严重畸形)。结论:我们观察到35例接触阿曲汀的妊娠,主要是因为治疗在妊娠前结束得太晚。大约五分之一的这些妊娠期出生的儿童患有畸形,这突出了引起人们更多关注这种药物长期致畸性的重要性。
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来源期刊
CiteScore
5.90
自引率
3.10%
发文量
108
审稿时长
6-12 weeks
期刊介绍: Clinical Drug Investigation provides rapid publication of original research covering all phases of clinical drug development and therapeutic use of drugs. The Journal includes: -Clinical trials, outcomes research, clinical pharmacoeconomic studies and pharmacoepidemiology studies with a strong link to optimum prescribing practice for a drug or group of drugs. -Clinical pharmacodynamic and clinical pharmacokinetic studies with a strong link to clinical practice. -Pharmacodynamic and pharmacokinetic studies in healthy volunteers in which significant implications for clinical prescribing are discussed. -Studies focusing on the application of drug delivery technology in healthcare. -Short communications and case study reports that meet the above criteria will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Clinical Drug Investigation may be accompanied by plain language summaries to assist readers who have some knowledge, but non in-depth expertise in, the area to understand important medical advances.
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