Department of Clinical Epidemiology, Leibniz Institute for Prevention Research and Epidemiology-BIPS, Achterstraße 30, 28359, Bremen, Germany.
Department of Biometry and Data Management, Leibniz Institute for Prevention Research and Epidemiology-BIPS, Achterstraße 30, 28359, Bremen, Germany.
Clin Drug Investig. 2023 Nov;43(11):865-872. doi: 10.1007/s40261-023-01314-2. Epub 2023 Oct 31.
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.
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.
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).
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.
阿维 A 酯具有持久的致畸性。因此,在阿维 A 酯治疗期间和治疗结束后 3 年内必须避免怀孕。我们旨在描述:(i)德国生育年龄女性中阿维 A 酯的使用情况;(ii)阿维 A 酯暴露妊娠的发生情况;(iii)子宫内暴露儿童的畸形情况。
利用德国 Pharmacoepidemiological Research Database(2004-2019 年期间的 GePaRD-索赔数据,覆盖德国约 20%的人口)2004-2019 年的数据,我们确定了年龄标准化的 13-49 岁女孩和女性中阿维 A 酯使用的年度患病率。在纵向分析中,我们通过评估最后一次配药(配药覆盖天数加上 3 年)的暴露窗口是否与妊娠开始重叠,或者在妊娠的前 8 周是否有配药,来估计暴露妊娠的数量。审查子宫内暴露于阿维 A 酯的活产儿童的数据,以评估是否存在先天性畸形。
2019 年,每 1000 名女孩和女性中阿维 A 酯使用的年龄标准化患病率为 0.04。我们发现了 35 例阿维 A 酯暴露妊娠;其中 94.3%的妊娠被归类为暴露,因为它们发生在停止阿维 A 酯治疗后 3 年内。在 18 例与母亲相关的活产儿童中,有 4 名儿童(22.2%)患有先天性畸形(3 名儿童有重大畸形)。
我们观察到的 35 例阿维 A 酯暴露妊娠主要是因为妊娠前停药太晚。这些妊娠中大约有五分之一的儿童有畸形,这突显了对这种药物持久致畸性的重视。