Gentile Salvatore, Fusco Maria Luigia
1Department of Mental Health ASL Salerno,Cava de' Tirreni,Salerno,Italy.
3Developmental Psychologist,Mental Health Institute,Torre Annunziata,Naples,Italy.
CNS Spectr. 2017 Jun;22(3):273-281. doi: 10.1017/S1092852916000699. Epub 2016 Nov 21.
The proportion of pregnancies exposed to either second-generation antipsychotics (SGAs) or first-generation antipsychotics (FGAs) varies between 0.3%-2% of all pregnancies, but, until now, little is known about the potential neurobehavioral teratogenicity of antipsychotics. Assessing this safety facet is the aim of this article. PubMed, Scopus, and Google Scholar were searched for eligible articles. PubMed (1954 to May 2016) was searched using several medical subject headings, variously combined. PubMed search results were also limited using the search filter for human studies published in English. Scopus and Google Scholar searches were filtered for article title (antipsychotics/neuroleptics, pregnancy). After excluding duplicates, 9,250 articles were identified and 29 met the following inclusion criteria: only articles that provided original/primary data on neurodevelopmental outcome in human offspring older than 4 months of age, independently of the study design, were selected for review. Indeed, some relevant neurodevelopmental milestones are achieved at this time. Length of study and neurodevelopmental assessment methodology did not influence the study selection. Unfortunately, published data on neurodevelopmental teratogenicity of SGAs mainly derive from case reports and small case-series studies. Even findings emerging from case-control and prospective/retrospective studies are of limited clinical relevance because of their small sample sizes. Limited data are also available on FGAs. Hence, we have to conclude that the long-term neurodevelopmental outcomes for children exposed in utero remain unclear. Low to very low quality evidence of retrieved data makes impossible to confirm or exclude potential long-lasting untoward effects on infant neurocognitive development associate with antenatal exposure to either SGAs or FGAs.
在所有妊娠中,暴露于第二代抗精神病药物(SGA)或第一代抗精神病药物(FGA)的妊娠比例在0.3%至2%之间,但迄今为止,人们对抗精神病药物潜在的神经行为致畸性知之甚少。评估这一安全性方面是本文的目的。我们在PubMed、Scopus和谷歌学术中搜索符合条件的文章。使用多个医学主题词对PubMed(1954年至2016年5月)进行搜索,并进行各种组合。PubMed搜索结果也使用英文发表的人类研究搜索过滤器进行了限制。对Scopus和谷歌学术搜索的文章标题进行了筛选(抗精神病药物/神经阻滞剂、妊娠)。在排除重复项后,共识别出9250篇文章,其中29篇符合以下纳入标准:仅选择那些提供4个月以上人类后代神经发育结果的原始/主要数据的文章进行综述,而不考虑研究设计。事实上,此时会达到一些相关的神经发育里程碑。研究时长和神经发育评估方法不影响研究选择。不幸的是,关于SGA神经发育致畸性的已发表数据主要来自病例报告和小型病例系列研究。由于样本量小,即使是病例对照研究和前瞻性/回顾性研究得出的结果,其临床相关性也有限。关于FGA的数据也有限。因此,我们不得不得出结论,子宫内暴露儿童的长期神经发育结果仍不清楚。检索到的数据质量低至极低,无法证实或排除产前暴露于SGA或FGA与婴儿神经认知发育潜在的长期不良影响之间的关联。