Cs. Birnbaum et al., Serum concentrations of antidepressants and benzodiazepines in nursing infants: A case series, PEDIATRICS, 104(1), 1999, pp. E111-E116
Objective. The relative risk of psychotropic medication use in women with p
uerperal psychiatric illness who are breastfeeding has yet to be quantified
adequately. Although the emotional and medical benefits of breastfeeding a
nd adverse effects of maternal depression on infant development are well de
scribed, how these absolute benefits weigh against the potential effects of
psychotropic drug use during lactation to ultimately guide clinical decisi
ons is still unclear. The objective of this report was to evaluate the exte
nt that psychotropic medications were present in the serum of infants breas
tfed by mothers treated with antidepressants and benzodiazepines.
Design. Serum samples were obtained from 35 nursing infants whose mothers w
ere treated with psychotropic medications while breastfeeding. When a detec
table concentration of medication was reported, information regarding infan
t behavior was obtained by maternal report.
Setting. The Perinatal and Reproductive Psychiatry Program at Massachusetts
General Hospital serves as a regional consultation center for the treatmen
t of psychiatric disorders during pregnancy;md the postpartum period.
Patients. Subjects were mothers referred to the Perinatal Psychiatry Progra
m for consultation regarding the relative safety of psychotropic medication
use while breastfeeding. Primary Outcome Measures. Presence of detectable
levels of medication in infants whose mothers breastfed while taking psycho
tropic medications during pregnancy and/or during the puerperium and the we
ll-being (based on maternal report) of infants who had detectable serum con
centrations of medication.
Results. Seventy-four percent (n = 26) of infants had serum medication conc
entrations below the laboratory limit of detection (assay sensitivity 5-50
ng/mL). In the remaining 26% of the sample (n = 9), serum concentrations of
psychotropic medications and/or active metabolites were detected. In each
of these cases, infants had been exposed to the medication during pregnancy
. Medications were not detected in infant serum when mothers had taken thes
e agents solely during the postpartum period. No readily apparent difficult
ies with the infants were reported by mothers.
Conclusions. These data support the low incidence of infant toxicity and ad
verse effects associated with antidepressant and benzodiazepine use during
breastfeeding. These data also suggest that infant serum monitoring is help
ful in the assessment of medication exposure in children of mothers who bre
astfeed while using psychotropic medications. Given the limited accumulated
data regarding serum concentrations of psychotropic medications in breastf
eeding infants, no single agent seems to be safer than another. Therefore,
choice of pharmacologic treatment should be guided by the likelihood that i
t will result in restoration of maternal psychiatric well-being.