Pharmacologic treatment of
depression during pregnancy
by
Wisner KL, Gelenberg AJ, Leonard H, Zarin D, Frank E
Case Western Reserve University School of Medicine,
Cleveland, Ohio 44106,
USA.
klw6@po.cwru.edu
JAMA 1999 Oct 6; 282(13):1264-9
ABSTRACT
CONTEXT: Despite the frequency of depression in women of childbearing age,
information to guide patients and physicians through a consideration of
treatment during pregnancy is limited. OBJECTIVE: To identify risk factors
associated with treatment of major depression during pregnancy to help
physicians develop treatment plans that optimize clinical care. DATA SOURCES:
Reports of prospective controlled trials in English were identified from MEDLINE
and Health STAR using the search terms antidepressant during pregnancy and
depression during pregnancy, by manually searching bibliographies of review
articles, and through discussions with investigators for 1989-1999. STUDY
SELECTION: We selected studies in which maternal and infant health outcomes
associated with antidepressant exposure were compared with those of
non-teratogen-exposed controls. Four studies published since 1993 were
identified and included in the analysis. DATA EXTRACTION: We abstracted
information about identification of subjects, comparison groups, pregnancy, and
birth outcomes. We organized the data along 5 domains of reproductive toxicity:
intrauterine fetal death, morphologic teratogenicity, growth impairment,
behavioral teratogenicity, and neonatal toxicity. DATA SYNTHESIS: Data were
available for tricyclic antidepressants (collectively), fluoxetine, and newer
selective serotonin reuptake inhibitors (collectively). Exposure to these agents
did not increase risk for intrauterine death or major birth defects. Decreased
birth weights of infants exposed to fluoxetine in the third trimester were
identified in 1 study. The development of children whose mothers took tricyclics
or fluoxetine during gestation did not differ from that of controls. Direct drug
effects and withdrawal syndromes occurred in some neonates whose mothers were
treated with antidepressants near term. CONCLUSIONS: Although few in number, new
information from prospective studies provides a welcome change from decision
making based on nonprospective data. Monitoring and interventions for patients
with identified risks (eg, poor weight gain) are recommended.
TCAs
SSRIs
Options
Estrogen
Fluoxetine
Imidazoline
Cortisol blues
SSRIs and PMT
Sertraline and PMT
Fluoxetine and PMT
Tryptophan and PMT
Alpha2 adrenoreceptors
Pregnancy and depression
Genetic conflicts in pregnancy
Antidepressants and breast milk
The newer antidepressants and pregnancy
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