Navigating Tx of bipolar disorder in pregnancy.
"Pregnancy, and particularly the post-partum period, is associated with a high risk of disease recurrence for women with bipolar disorder." said Dr. Viguera, director of the perinatal and reproductive psychiatry program at Massachusetts General Hospital in Boston. Although mood-stabilizing drugs can reduce this risk, most are associated with some degree of teratogenicity, she said.
Limited data exist to support the use in pregnancy of the mood stabilizers most commonly used to treat bipolar disorder. In addition, mood stabilizers have been shown to increase the risk of certain types of birth defects or congenital malformations in infants exposed in utero, Dr. Viguera said during a meeting on bipolar disorder sponsored by Harvard Medical School.
To minimize the possibility of fetal damage, some women choose to discontinue their mood-stabilizing regimen, which itself markedly increases the risk of disease recurrence during pregnancy as well as postpartum illness. "More than half of women who discontinue treatment before or during pregnancy relapse, most frequently in the first trimester," Dr. Viguera said.
The risks associated with treatment and treatment cessation vary co isiderably, depending on the nature and degree of illness and the agents used to treat it. "There is no single optimal management approach," Dr. Viguera said. "Clinical management requires ongoing assessment of maternal and fetal status, risks, and benefits."
Further complicating management is the fact that the Food and Drug Administration has not approved for use during pregnancy any of the psychotropic medications used to treat bipolar disease, because these agents diffuse across the placenta. The risk of birth defects depends on the drug used, when exposure occurs, and the duration of the exposure. It is generally understood that the highest risk to the fetus is during the first trimester, "but later exposure can also lead to malformations, behavioral effects, low birth weight, and preterm delivery," Dr. Viguera said.
Women with bipolar disorder who have been stable for many years may be able to slowly decrease their medication dosage and stop the medication before conception. If symptoms emerge during the first trimester, these women may be able to avoid using a mood stabilizer by treating some of the more troubling symptoms, such as irritability, insomnia, and hypomania, with an antipsychotic agent such as haloperidol or perphenazine. If symptoms appear after the first trimester, the mood stabilizer can be reintroduced with less risk of congenital malformation, she suggested.
Among women who choose to continue a mood stabilizer during pregnancy to minimize the risk of recurrence, lithium appears to be the safest option. However, it is associated with a relatively small increased risk of a serious cardiac malformation. Valproic acid, on the other hand, is associated with a 3%-5% risk of a neural tube defect and an 8.9% risk for all anomalies, compared with a baseline rate of 2%-4%.
The risk of bipolar relapse during the postpartum period is very high, as is the risk for postpartum psychosis among women with bipolar disorder. Conse-quently, medication prophylaxis generally is recommended, although there is some debate on timing, Dr. Viguera said. "The goal is to maintain euthymia by reintroducing the mood stabilizer early," she said. Some studies have shown benefits to rein-troducing the drug in the third trimester, and others have suggested 24-48 hours post partum. In any case, Dr. Viguera said, "the postpartum treatment plan should be addressed in advance."
RELATED ARTICLE: Drugs Often Used As Treatment
Following are some drugs commonly used to treat the symptoms of bipolar disorder during pregnancy:
* Lithium. Recent studies have shown the teratogenicity rates are much lower than previously reported. The most common effects of fetal exposure are high birth weight and "floppy-baby" syndrome.
* Valproate and carbamazepine. These anticonvulsants are associated with major congenital malformations and carry a greater risk of birth defects than lithium. They have been linked to neural tube defects, craniofacial anomalies, urogenital problems, growth retardation, microcephaly, and heart defects.
Late last year, the American Epilepsy Society's pregnancy out-comes forum panel recommended that valproate not be prescribed as firstline therapy for any indication in women of childbearing age, (See article on p. 56.)
* Lamotrigine. This anticonvulsant is associated with a low overall rate of fetal malformations, but it carries a higher rate of miscarriages and stillbirths than seen in unmedicated women, Dr. Viguera said.
* Chlorpromazine. This first-generation antipsychotic is often used to treat mania during pregnancy. It is among the best-studied of the antipsychotics in pregnancy, and the data support its relative safety in this population. Related compounds, such as trifluoperazine and perphenazine, also may have low teratogenic risk.
* Lorazepam and clonazepam. These benzodiazepines have not been associated with significant increases in malformation rates, she said, although the chronic use of benzodiazepines by pregnant women has been linked to withdrawal symptoms in babies.
* Olanzapine. Olanzapine is used for acute mania and for prophylaxis against recurrent mania; however, data on this and the other atypical antipsychotics in pregnancy are still too sparse to make conclusions regarding their reproductive safety, according to Dr. Viguera.
BY DIANA MAHONEY
New England Bureau
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|Title Annotation:||Adult Psychiatry|
|Publication:||Clinical Psychiatry News|
|Date:||Feb 1, 2005|
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