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Web site: September 2010
Prescriber Update 2010;31(3):23
In 2008 Medsafe provided advice on the use of Selective Serotonin Reuptake Inhibitors (SSRIs) in pregnancy.1
Since that time further epidemiological studies have been published.2-5 The Medicines Adverse Reactions Committee (MARC) has reviewed these studies investigating the association between SSRI or serotonin noradrenaline reuptake inhibitor (SNRI) treatment and congenital anomalies. The MARC concluded that there is a small increased risk of congenital cardiac defects associated with fluoxetine, similar to that seen with paroxetine.6 The possibility of a class effect for all SSRIs or a similar effect with SNRIs could not be excluded.
In addition to the risk of congenital anomalies SSRIs and SNRIs have been associated with an increase in risk of pre-term birth, persistent pulmonary hypertension of the newborn (PPHN) and neonatal withdrawal symptoms when the mother is treated until the birth of the baby. There is less information on the use of tricyclic antidepressants (TCA) in pregnancy. However, a recent epidemiological study indicated that TCAs may also be associated with an increased risk of congenital anomalies, pre-term birth and neonatal withdrawal symptoms.7
It is important to remember that untreated antenatal depression has also been associated with adverse outcomes for both mother and foetus. The decision to treat a pregnant woman with antidepressant medicines can only be made on an individual basis in collaboration with the patient. The risks associated with ineffective treatment need to be balanced with the small increase in risk of congenital abnormalities, pre-term birth and neonatal withdrawal symptoms.
Healthcare professionals should be aware of the use of antidepressants in pregnancy and should closely observe neonates exposed to antidepressants for signs of withdrawal symptoms or PPHN.
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