Ll. Altshuler et al., PHARMACOLOGICAL MANAGEMENT OF PSYCHIATRIC-ILLNESS DURING PREGNANCY - DILEMMAS AND GUIDELINES, The American journal of psychiatry, 153(5), 1996, pp. 592-606
Objective: Given concerns about use of psychotropic medication during
pregnancy, the authors reviewed the literature regarding the effects o
f prenatal exposure to psychotropic medications on fetal outcome. Meth
od: A MEDLINE search of all articles written in English from 1966 to 1
995 was performed to review information on the effects of psychotropic
drug use during pregnancy on fetal outcome. Where sufficient data wer
e available and when methodologically appropriate, meta-analyses were
performed to assess risk of fetal exposure by psychotropic medication
class. Results: Three primary effects are associated with medication u
se during pregnancy: 1) teratogenicity, 2) perinatal syndromes (neonat
al toxicity), and 3) postnatal behavioral sequelae. For many drug clas
ses there are substantial data regarding risk for teratogenicity. Tric
yclic antidepressants do not seem to confer increased risk for organ d
ysgenesis. The available data indicate that first-trimester exposure t
o low-potency phenothiazines, lithium, certain anticonvulsants, and be
nzodiazepines may increase the relative risk for congenital anomalies.
However, the absolute risk of congenital malformations following pren
atal exposure to most psychotropics is low. Conclusions: Exposure to c
ertain psychotropic drugs in utero may increase the risk for some spec
ific congenital anomalies, but the rate of occurrence of these anomali
es even with the increased risk remains low. Use of psychotropic medic
ations during pregnancy is appropriate in many clinical situations and
should include thoughtful weighing of risk of prenatal exposure versu
s risk of relapse following drug discontinuation. The authors present
disorder-based guidelines for psychotropic drug use during pregnancy a
nd for psychiatrically ill women who wish to conceive.