| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
CMAJ
Reason for posting: Major depressive disorders affect one in 10 women of reproductive age, and selective serotonin reuptake inhibitors (SSRIs), with their generally favourable efficacy and safety profiles, are the most common medications used to treat these conditions. However, the results of a recent case control study suggest that women taking the drugs in the latter half of their pregnancy may have an increased risk of their offspring developing persistent pulmonary hypertension of the newborn (PPHN).1
|
|
The potential mechanism of this adverse effect is not certain, but SSRIs, which pool in the fetal lungs, may inihibit nitric oxide synthesis.1 Alternatively, increased serotonin levels may vasoconstrict pulmonary vessels, or cause pulmonary smooth muscle cell proliferation and increased pulmonary vascular resistance.1
What to do: These findings add to previously described problems of congenital malformations and neonatal adaptation syndrome seen in some pregnant women using SSRIs.2,3 Although it is important to acknowledge the limitations of casecontrol studies (including their inability to establish causation and possible confounding by unmeasured variables) and a possible recall bias, the relative risk increase (6-fold) seen here is dramatic. Nevertheless, the absolute risks of having a child with PPHN still remain low. Women taking SSRIs in the second half of their pregnancy will see their baseline risk of having a child with PPHN increase from 0.1% to 0.6%, an absolute increase of 0.5%. Although there is a 99.5% chance that such a woman's child would be unaffected, the number needed to harm is only 200. Women should be made aware of this potential adverse effect and the benefits and risks of treatment considered on a patient-by-patient basis. Infants born to women using the drugs should be monitored closely postpartum. It's not clear whether lower SSRI doses were protective. Alternate antidepressants had a similar but slightly lower risk of PPHN relative to controls (adjusted OR 3.2, 95% CI 1.37.4).
| REFERENCES |
|---|
|
|
|---|
This article has been cited by other articles:
![]() |
E. Ferreira, A. M. Carceller, C. Agogue, B. Z. Martin, M. St-Andre, D. Francoeur, and A. Berard Effects of Selective Serotonin Reuptake Inhibitors and Venlafaxine During Pregnancy in Term and Preterm Neonates Pediatrics, January 1, 2007; 119(1): 52 - 59. [Abstract] [Full Text] [PDF] |
||||
Read all eLetters
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||