Einarson Adrienne, Boskovic Rada
Motherisk Program, Division of Clinical Pharmacology, The Hospital for Sick Children, University of Toronto, Canada.
J Psychiatr Pract. 2009 May;15(3):183-92. doi: 10.1097/01.pra.0000351878.45260.94.
The incidence of schizophrenia in the general population ranges from about 1% to 2%. Schizophrenia affects men and women equally, occurring in all cultures and socioeconomic classes. The peak age of onset in women is 25 to 35 years, which are also the peak childbearing years, and women with psychotic illnesses are likely to have more unplanned pregnancies than women without a psychotic illness. Not only are antipsychotic medications prescribed for schizophrenia, but, especially since the introduction of the second-generation (atypical) antipsychotics, these drugs are also used to treat other psychiatric illnesses such as bipolar disorder. As a result, there is an increase in the number of women requiring antipsychotic drug therapy who are likely to become pregnant. It is important to evaluate the safety of these drugs in pregnancy, as most women with a serious psychiatric illness cannot stop taking their medication, as this would interfere with their activities of daily living, especially taking care of an infant. In this review, we describe available up-to-date, evidence-based information regarding the safety of antipsychotic drugs that are currently used in pregnancy. These include first-generation (conventional) antipsychotics (eg, promethazine, chlorpromazine, prochlorperazine, haloperidol, perphenazine, trifluoperazine, loxapine, thioridazine, flupenthixol, fluphenazine) and second-generation antipsychotics (eg, clozapine, risperidone, olanzapine, quetiapine, ziprasidone, aripiprazole, paliperidone). To date, no definitive association has been found between use of antipsychotics during pregnancy and an increased risk of birth defects or other adverse outcomes. However, there is a paucity of information, with a lack of large, well designed, prospective comparative studies. The information presented here should therefore not be interpreted as conclusive with regard to the safety of these drugs, as more research is needed. Women who require treatment should always discuss the risks and benefits of pharmacotherapy with their physician and, if it is felt that treatment should be continued during pregnancy, the evidenced-based information presented here will be of help in this important decision.
普通人群中精神分裂症的发病率约为1%至2%。精神分裂症对男性和女性的影响相同,在所有文化和社会经济阶层中都有发生。女性发病的高峰年龄为25至35岁,这也是生育的高峰期,患有精神病的女性比没有精神病的女性更有可能意外怀孕。不仅抗精神病药物用于治疗精神分裂症,而且特别是自第二代(非典型)抗精神病药物问世以来,这些药物还用于治疗其他精神疾病,如双相情感障碍。因此,需要抗精神病药物治疗且可能怀孕的女性数量有所增加。评估这些药物在孕期的安全性很重要,因为大多数患有严重精神疾病的女性不能停药,因为这会干扰她们的日常生活,尤其是照顾婴儿。在本综述中,我们描述了有关目前孕期使用的抗精神病药物安全性的最新、基于证据的信息。这些药物包括第一代(传统)抗精神病药物(如异丙嗪、氯丙嗪、丙氯拉嗪、氟哌啶醇、奋乃静、三氟拉嗪、洛沙平、硫利达嗪、氟奋乃静、氟哌噻吨)和第二代抗精神病药物(如氯氮平、利培酮、奥氮平、喹硫平、齐拉西酮、阿立哌唑、帕利哌酮)。迄今为止,尚未发现孕期使用抗精神病药物与出生缺陷或其他不良后果风险增加之间存在明确关联。然而,信息匮乏,缺乏大型、设计良好的前瞻性对照研究。因此,此处提供的信息不应被解释为关于这些药物安全性的定论,因为还需要更多研究。需要治疗的女性应始终与医生讨论药物治疗的风险和益处,如果认为孕期应继续治疗,此处提供的基于证据的信息将有助于做出这一重要决定。