| A
recent analysis of all the published data on antidepressants
used in breastfeeding mothers suggests that the transfer of fluoxetine
is the highest and citalopram is next highest of this family.
Fluoxetine produces the highest proportion (22%) of infant levels
that are elevated above 10% of the average maternal level. Based
on smaller numbers, the data on citalopram indicate that it produces
elevated levels in 17% of infants.
They concluded
that Nortriptyline, paroxetine, and sertraline may be preferred
choices in breast-feeding women. Minimizing the maternal dose
may be helpful with citalopram.(1)
A
new case of fluoxetine toxicity has been reported
in a preterm infant. They describe a preterm infant with marked
motor automatism and skin manifestations after being exposed to
fluoxetine in utero. The fluoxetine level drawn at 96 hours of
age was 92 ng/ml, which was in adult therapeutic range. The neurologic
symptoms resolved by 7 days and follow-up at 4 months revealed
normal neurodevelopmental examination.(2)
I've received
a number of queries around the world about Ultravist
(iopromide)
Its just another of the hundreds of ?iodinated? radiocontrast
agents used from CT scans. Its initial phase half-life is 0.24
hours, and its terminal phase half-life is about 2 hours. As with
all the other radiocontrast agents, Ultravist levels in milk are
unknown, but are likely to be extremely low and virtually non-bioavailable
orally in the infant.
I've recently
come across some old data on prostaglandin
E2 suggesting that in some patients it could suppress
milk production. In two papers, it was suggested that prostaglandin
E2 given orally for several days significantly suppressed milk
production. One other paper found no change. At this time, some
caution is recommended in exposing breastfeeding mothers to prolonged
oral ingestion of prostaglandin E2. The acute use for cervical
ripening used in thousands of deliveries, is unlikely to be a
problem.(3-5)
Neonatal
Withdrawal Syndrome:
For a good review of neonatal withdrawal syndrome from Selective
Serotonin Reuptake inhibitors used in pregnant women, see the
review by Nordeng et.al. They conclude: Neonatal withdrawal syndrome
can occur after third trimester in utero SSRI exposure. Further
research should focus on whether it is safe to use SSRIs during
the last trimester. All neonates exposed to SSRIs during the last
trimester should be followed-up closely for withdrawal symptoms
after birth.(6) |