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孕期异维甲酸暴露:荷兰一项基于人群的研究。

Isotretinoin exposure during pregnancy: a population-based study in The Netherlands.

作者信息

Zomerdijk Ingeborg M, Ruiter Rikje, Houweling Leanne M A, Herings Ron M C, Sturkenboom Miriam C J M, Straus Sabine M J M, Stricker Bruno H

机构信息

Department of Medical Informatics, Erasmus University Medical Center, Rotterdam, The Netherlands Department of pharmacovigilance, Dutch Medicines Evaluation Board, Utrecht, The Netherlands.

Department of Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands Department of Internal Medicine, Groene Hart Hospital, Gouda, The Netherlands.

出版信息

BMJ Open. 2014 Nov 12;4(11):e005602. doi: 10.1136/bmjopen-2014-005602.

Abstract

OBJECTIVE

To estimate isotretinoin exposure in Dutch pregnant women despite the implemented pregnancy prevention programme (PPP) and second, to analyse the occurrence of adverse fetal or neonatal outcomes in these isotretinoin exposed pregnancies.

DESIGN

Population-based study.

SETTING

The Netherlands.

PARTICIPANTS

A cohort of 203,962 pregnancies with onset between 1 January 1999 and 1 September 2007 consisting of 208,161 fetuses or neonates.

MAIN OUTCOME MEASURES

Isotretinoin exposure in the 30 days before or during pregnancy. Proportions of adverse fetal or neonatal outcomes, defined as intrauterine deaths ≥16 week of gestation and neonates with major congenital anomalies. ORs with 95% CIs adjusted for maternal age were calculated to estimate the risk of adverse fetal or neonatal outcome after maternal isotretinoin exposure.

RESULTS

51 pregnancies, 2.5 (95% CI 1.9 to 3.3) per 10,000 pregnancies, were exposed to isotretinoin despite the pregnancy prevention programme. Forty-five of these pregnancies, 2.2 (95% CI 1.6 to 2.9) per 10,000 pregnancies, were exposed to isotretinoin during pregnancy and six additional women became pregnant within 30 days after isotretinoin discontinuation. In 60% of isotretinoin exposed pregnancies, women started isotretinoin while already pregnant. In five out of the 51 isotretinoin exposed pregnancies (53 fetuses), 9.4% (95% CI 1.3% to 17.6%), had an adverse fetal or neonatal outcome. The OR for adverse fetal or neonatal outcomes after isotretinoin exposure in 30 days before or during pregnancy was 2.3 (95% CI 0.9 to 5.7) after adjustment for maternal age.

CONCLUSIONS

Although a PPP was already implemented in 1988, we showed that isotretinoin exposed pregnancies and adverse fetal and neonatal events potentially related to the exposure still occur. These findings from the Netherlands add to the evidence that there is no full compliance to the isotretinoin PPP in many Western countries. Given the limited success of iPLEDGE, the question is which further measures are able to improve compliance.

摘要

目的

评估荷兰孕妇中异维A酸的暴露情况,尽管已实施了预防妊娠计划(PPP);其次,分析这些暴露于异维A酸的妊娠中不良胎儿或新生儿结局的发生情况。

设计

基于人群的研究。

地点

荷兰。

参与者

一组203,962例妊娠,妊娠开始时间在1999年1月1日至2007年9月1日之间,包括208,161例胎儿或新生儿。

主要观察指标

妊娠前或妊娠期间30天内异维A酸的暴露情况。不良胎儿或新生儿结局的比例,定义为妊娠≥16周的宫内死亡和患有重大先天性异常的新生儿。计算调整产妇年龄后的95%置信区间的比值比,以估计产妇暴露于异维A酸后不良胎儿或新生儿结局的风险。

结果

尽管实施了预防妊娠计划,但仍有51例妊娠(每10,000例妊娠中有2.5例,95%置信区间为1.9至3.3)暴露于异维A酸。其中45例妊娠(每10,000例妊娠中有2.2例,95%置信区间为1.6至2.9)在妊娠期间暴露于异维A酸,另外6名妇女在停用异维A酸后30天内怀孕。在60%暴露于异维A酸的妊娠中,妇女在已怀孕时开始服用异维A酸。在51例暴露于异维A酸的妊娠中的5例(53例胎儿)中,9.4%(95%置信区间为1.3%至17.6%)有不良胎儿或新生儿结局。在调整产妇年龄后,妊娠前或妊娠期间30天内暴露于异维A酸后不良胎儿或新生儿结局的比值比为2.3(95%置信区间为0.9至5.7)。

结论

尽管1988年就已实施了预防妊娠计划,但我们发现仍有暴露于异维A酸的妊娠以及可能与该暴露相关的不良胎儿和新生儿事件发生。荷兰的这些研究结果进一步证明,许多西方国家并未完全遵守异维A酸预防妊娠计划。鉴于iPLEDGE计划成效有限,问题在于还需要采取哪些进一步措施来提高依从性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c416/4244495/275c889bad45/bmjopen2014005602f01.jpg

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