Psychiatric Drugs, Pregnancy and Lactation: Eating Disorders
January 1, 2003 from
ObGynNews
By Lee S. Cohen, M.D.
Eating disorders are highly prevalent in the general population, certainly
more so in women, appearing to peak during the
childbearing years. While we tend
not to see pregnant women with
anorexia nervosa because they have secondary
reproductive endocrine dysfunction, we do see those who have been successfully
treated and are contemplating pregnancy or who are pregnant. Far more often, we
see patients with bulimia or other
binge-eating disorders on the less severe end
of the spectrum.
There is very little information in the literature on the course of these
disorders as women try to conceive or in pregnancy--and even less on the
treatment of symptomatic women during pregnancy or the postpartum period.
The few data that are available include studies reported in the last several
years suggesting that pregnancy is associated with improvements in eating
disorders followed by postpartum exacerbation of symptoms. A limitation of these
studies was that there were very few women included in the samples with active
illness who were on medication.
The two drug classes used most frequently in patients with eating disorders
are
selective serotonin reuptake inhibitors (SSRIs), most commonly
fluoxetine
and sertraline, and
antianxiety agents, typically lorazepam and clonazepam. In
our experience, many women have a recurrence of symptoms of the eating disorder
when they stop their medication while trying to conceive or while
pregnant-consistent with what we see when women with mood and anxiety disorders
stop their medications.
So what is the best way to manage patients? There are two avenues of
treatment, group- and individual-based cognitive-behavioral therapy and
pharmacologic interventions. We have found that patients who have been on
pharmacologic therapy may be able to successfully switch from medication to
cognitive-behavioral therapy in conjunction with state-of-the-art nutritional
counseling while trying to conceive or during pregnancy.
Patients who do well using this approach are on the less severe ends of the
spectrum, for example those who engage in some binge-eating behaviors, followed
by some restrictivelike behavior (calorie restriction), or who have intermittent
bulimic symptoms when they experience anxiety. Cognitive-behavioral
interventions can help these patients justify the need to consume calories and
gain weight to sustain a healthy pregnancy.
SSRI doses used to treat eating disorders are frequently higher than those
used to treat depression, but the risk of adverse fetal effects, including fetal
malformations, is not dose related. Patients who decide to stay on medication
therefore should remain on the most effective dose, because reducing the dose
increases the risk of relapse.
We frequently prescribe benzodiazepines during pregnancy and post partum in
combination with antidepressants to modulate the anxiety symptoms that are
frequently associated with eating disorders. A benzodiazepine can often break a
cycle of behavior during pregnancy but is particularly effective during the
postpartum period. A recent metaanalysis on prenatal exposure to benzodiazepines
suggested that if these agents are linked to an increased risk for
malformations, that risk is not for overall congenital anomalies, but only for
cleft lip or palate. And this risk is less than 0.5% over the normal background
risk. The risk of neonatal complications with exposure to benzodiazepines is
extremely small.
Postpartum worsening of psychiatric disorders is the rule. In the postpartum
period women may demonstrate reemergence of rituals practiced before pregnancy,
and comorbid depression and anxiety are common. While prophylaxis with
medication is not necessarily indicated, these women should be considered at
high risk for postpartum psychiatric disturbance. Women who have been
successfully treated with cognitive therapy and nutritional counseling during
pregnancy may need to resume or start pharmacologic treatment. For example, it
would not be unusual for a patient with mild to moderate symptoms before
pregnancy, who managed well during pregnancy with cognitive interventions and
nutritional counseling, to experience a reemergence of the eating disorder with
major depression post partum. These patients can become ill relatively quickly,
so prompt reintroduction of a medication can be extremely important.
The incidence of treatment-emergent side effects in nursing babies whose
mothers are taking a benzodiazepine or an SSRI is exceedingly low, and these
drugs are not contraindicated during breast-feeding.
Dr. Lee Cohen is a psychiatrist and director of the
perinatal psychiatry program at Massachusetts General Hospital, Boston. He is a
consultant for and has received research support from manufacturers of several
SSRIs. He is also a consultant to Astra Zeneca, Lilly and Jannsen -
manufacturers of atypical antipsychotics.
continue: Psychiatric Disorders
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