Tosato Sarah, Albert Umberto, Tomassi Simona, Iasevoli Felice, Carmassi Claudia, Ferrari Silvia, Nanni Maria Giulia, Nivoli Alessandra, Volpe Umberto, Atti Anna Rita, Fiorillo Andrea
Section of Psychiatry, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Policlinico GB Rossi, Ple LA Scuro 10, 37134 Verona (VR), Italy.
Section of Psychiatry, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Italy.
J Clin Psychiatry. 2017 May;78(5):e477-e489. doi: 10.4088/JCP.15r10483.
To summarize risks related to (1) illness and (2) second-generation antipsychotic (SGA) treatment in pregnant women and their offspring. Concerning illness-related risks, we focused on bipolar disorder and schizophrenia, psychiatric disorders for which SGAs are preferentially prescribed.
PubMed, Ovid, Scopus, PsycINFO, and Cochrane Library were searched from the date of the first available article to October 2015 using the following key terms: pregnancy OR gestation OR bipolar disorder OR schizophrenia. We also included cross-references from identified articles.
We included 49 English-language articles regarding illness-related and SGA-related risks in bipolar disorder and schizophrenia. First, searches were done for epidemiologic or experimental studies (from January 2000 to October 2015), then for systematic reviews and meta-analyses.
Data were extracted independently, after removing duplicates and studies that were not relevant or not pertinent.
Abrupt discontinuation of treatment-exposed mothers with bipolar disorder or schizophrenia led to a high risk of relapses during pregnancy. Both bipolar disorder and schizophrenia were linked to a slightly increased risk of obstetric complications for mothers (schizophrenia) and the newborn (bipolar disorder and schizophrenia), although data on drug exposure during pregnancy were not given in the majority of studies. Maternal morbidity (schizophrenia but not bipolar disorder) may be associated with the worst neonatal outcomes (stillbirth, neonatal or infant deaths, and intellectual disability). Untreated bipolar disorder and schizophrenia may be considered independent risk factors for congenital malformations, while SGAs were not associated with increased recurring defects in fetuses. Evidence regarding the potential effects of SGAs on child neurodevelopment remains reassuring.
After taking into account the parents' will and after they provide informed consent, the most reasonable and less harmful choice for treating future mothers with bipolar disorder or schizophrenia appears to be maintaining them at the safest minimum dosage.
总结与(1)疾病以及(2)孕妇及其后代使用第二代抗精神病药物(SGA)治疗相关的风险。关于疾病相关风险,我们重点关注双相情感障碍和精神分裂症,这两种精神疾病是优先使用SGA治疗的。
从第一篇可用文章发表之日至2015年10月,使用以下关键词在PubMed、Ovid、Scopus、PsycINFO和Cochrane图书馆进行检索:妊娠或孕期或双相情感障碍或精神分裂症。我们还纳入了已识别文章的交叉参考文献。
我们纳入了49篇关于双相情感障碍和精神分裂症中疾病相关及SGA相关风险的英文文章。首先,检索了流行病学或实验研究(2000年1月至2015年10月),然后检索了系统评价和荟萃分析。
在去除重复项以及不相关或不切题的研究后,独立提取数据。
患有双相情感障碍或精神分裂症且接受治疗的母亲突然停药会导致孕期复发风险很高。双相情感障碍和精神分裂症均与母亲(精神分裂症)和新生儿(双相情感障碍和精神分裂症)产科并发症风险略有增加有关,尽管大多数研究未给出孕期药物暴露数据。母亲发病(精神分裂症而非双相情感障碍)可能与最差的新生儿结局(死产、新生儿或婴儿死亡以及智力残疾)相关。未经治疗的双相情感障碍和精神分裂症可能被视为先天性畸形的独立危险因素,而SGA与胎儿反复出现缺陷增加无关。关于SGA对儿童神经发育潜在影响的证据仍然令人放心。
在考虑父母意愿并获得他们的知情同意后,对于患有双相情感障碍或精神分裂症的未来母亲,最合理且危害较小的治疗选择似乎是将她们维持在最安全的最低剂量。