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Published on: August 25, 2014
Neurodevelopmental outcomes in infants exposed in utero to antipsychotics: a systematic review of published data
Salvatore Gentile1, Maria Luigia Fusco2
11Department of Mental Health ASL Salerno,Cava de' Tirreni,Salerno,Italy.
Insights
Limited research exists on the neurobehavioral effects of antipsychotic medications during pregnancy. Current evidence quality is low, making it impossible to determine long-term neurodevelopmental outcomes in children exposed to second-generation antipsychotics (SGAs) or first-generation antipsychotics (FGAs) in utero.
Area of Science:
- Neuroscience
- Pharmacology
- Developmental Pediatrics
Background:
- Antipsychotic medication use during pregnancy is common, with 0.3%-2% of pregnancies exposed to either second-generation antipsychotics (SGAs) or first-generation antipsychotics (FGAs).
- The potential for these medications to cause neurobehavioral harm (teratogenicity) in developing fetuses is largely unknown.
Purpose of the Study:
- To systematically review existing literature on the neurodevelopmental outcomes of children exposed to SGAs or FGAs in utero.
- To assess the quality of evidence regarding the long-term neurobehavioral safety of antenatal antipsychotic exposure.
Main Methods:
- A comprehensive literature search was conducted across PubMed, Scopus, and Google Scholar for studies published up to May 2016.
- Inclusion criteria required original data on neurodevelopmental outcomes in offspring older than 4 months, regardless of study design.
- A total of 9,250 articles were screened, with 29 meeting the final selection criteria.
Main Results:
- Published data on the neurodevelopmental teratogenicity of SGAs primarily consists of case reports and small case-series.
- Even findings from larger study designs (case-control, prospective/retrospective) are limited by small sample sizes.
- Data on FGAs is also scarce, and the overall quality of retrieved evidence is low to very low.
Conclusions:
- The long-term neurodevelopmental outcomes for children exposed to antipsychotics in utero remain unclear.
- The low quality of available evidence prevents confirmation or exclusion of potential long-lasting adverse effects on infant neurocognitive development associated with antenatal exposure to SGAs or FGAs.
Abstract:
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.
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