Psychiatric Times.
No. 6
Psychopharmacologic Therapy in Pregnancy: Effects on Newborns
By Emilio J. Sanz, MD, PhD and Carlos De las Cuevas, MD, PhD |
May 1, 2006
Antiepileptic drugs (AEDs)
A mother's use of AEDs is linked to
the immediate withdrawal effects of the
newborn and to long-term neurologic
dysfunctions. Valproate(Drug information on valproate) was shown to
be associated with immediate NWS symptoms, such as hyperexcitability,
causing neurologic deficits, seizures,
and jitteriness.32,33 Furthermore, in a
retrospective study based on hospital
records, Dean and associates34 found
significant NWS symptoms, including
jitteriness, hypotonia, seizures, apneic
episodes, hypoglycemia, and feeding
disorder, after exposure in utero to
valproate, phenytoin(Drug information on phenytoin), or combination
therapy.
Long-term effects of AEDs have
also been demonstrated. In the study by
Koch and associates,32 when children
were examined 6 years later, they
continued to have long-term neurologic
dysfunctions, which are more congruent
with drug toxicity than withdrawal
effects. Similar results are reported in
the study by Moore and associates33 of
57 children prenatally exposed to AEDs:
77% had learning difficulties, 81% had
speech delay, 60% had gross motor
delay, and 42% had fine motor delay.
Eighty percent of these children had
prenatal exposure to valproate alone or
in combination with another AED.
Seventy-four percent of school-aged
children were enrolled in special education
classes or were receiving learning
support, and 81% had some type of
behavioral dysfunction; of these, 60%
had some autistic features and 39% had
hyperactivity, but autism or Asperger
syndrome had actually been diagnosed
in only a few. The developmental effects
seem to be associated not only with
valproate but also with carbamazepine(Drug information on carbamazepine),
phenytoin, and polypharmacy.34
Although these investigators did not find
a link between NWS and cognitive
dysfunction, this is a topic in which
further research is badly needed.
Conclusions
Pregnant women with psychiatric conditions
must be adequately treated.
Pharmacologic treatment should be initiated or maintained when the disorder is
severe and the efficacy of the psychopharmacologic
approach has been
demonstrated, giving attention to nonpharmacologic
alternatives in order to
prevent the relapse of the disease in the
mother. Psychiatric clinical practice
shows that most pregnant women with
psychiatric conditions are treated with
polypharmacy,35 making it even more
complex to identify the effects of these
drugs on the newborn. Psychopharmacologic
agents can induce direct
effects on the newborn, as well as withdrawal
symptoms associated with their
suppression. The clinical picture of both
cases is often similar and confounding.
Nevertheless, NWS has clearly been
associated with TCAs, SSRIs, and
AEDs. However, with the exception of
AEDs, the clinical picture for most of
these drugs appears to be self-limited
and moderate, most frequently needing
only supportive therapy.
Dr Sanz is associate professor in clinical pharmacology
at the University of La Laguna in
Tenerife, Canary Islands, Spain, and a member
of the Review Panel of Experts of the WHO
Collaborating Centre for International Drug
Monitoring. He reports that he has no conflicts
of interest concerning the subject matter
of this article.
Dr De las Cuevas is associate professor of
psychiatry at the University of La Laguna in
Tenerife, Canary Islands, Spain, a specialist in
psychiatry with clinical responsibilities, and a
senior member of the Educational Liaisons
Network of the World Psychiatric Association.
He reports that he has no conflicts of interest
concerning the subject matter of this article.
Drugs Mentioned in This Article
Alprazolam (Xanax)
Carbamazepine (Carbatrol, Tegretol, others)
Citalopram (Celexa)
Diazepam (Valium)
Fluoxetine (Prozac)
Paroxetine (Paxil)
Pentylenetetriazol (Metrazol)
Phenytoin (Dilantin)
Valproate/Valproic acid (Depakote, others)
References
1. Altshuler LL, Hendrick V, Cohen LS. An update on
mood and anxiety disorders during pregnancy and
the postpartum period. Prim Care Companion J Clin
Psychiatry. 2000;2:217-222.
2. Andersson L, Sundstrom-Poromaa I, Bixo M, et
al. Point prevalence of psychiatric disorders during
the second trimester of pregnancy: a population based
study. Am J Obstet Gynecol. 2003;189:148-154.
3. Bennett HA, Einarson A, Taddio A, et al. Prevalence
of depression during pregnancy: systematic review.
Obstet Gynecol. 2004;103:698-709.
4. Goldstein DJ, Sundell K. A review of the safety of
selective serotonin reuptake inhibitors during pregnancy.
Hum Psychopharmacol Clin Exp. 1999;14:
319-324.
5. Kohen D. Psychotropic medication in pregnancy.
Adv Psychiatric Treat. 2004;10:59-66.
6. Ward RK, Zamorski MA. Benefits and risks of
psychiatric medications during pregnancy. Am Fam
Physician. 2002;66:629-636.
7. NSW Health. Neonatal Abstinence Syndrome Guidelines.
Available at: http://www.health.nsw.gov.au/policies/
pd/2005/PD2005_494.html. Accessed March 23, 2006.
8. American Academy of Pediatrics: Committee on Drugs. Neonatal drug withdrawal. Pediatrics. 1998;
101:1079-1088.
9. Desmond MM, Rudolph AJ, Hill RM, et al.
Behavioral alterations in infants born to mothers on
psychoactive medication during pregnancy. In: Farrell
G, ed. Congenital Mental Retardation. Austin, Tex:
University of Texas Press; 1967:235-245.
10. Auerbach JG, Hans SL, Marcus J, Maeir S.
Maternal psychotropic medication and neonatal
behavior. Neurotoxicol Teratol. 1992;14:399-406.
11. Lee A, Inch S, Finnigan D. Therapeutics in Pregnancy
and Lactation. Oxfordshire, UK: Radcliffe
Medical Press Ltd; 2000.
12. Haddad PM. Antidepressant discontinuation
syndromes. Drug Saf. 2001;24:183-197.
13. Musa AB, Smith CS. Neonatal effects of maternal
clomipramine therapy. Arch Dis Child. 1979;54:405.
14. Cowe L, Lloyd DJ, Dawling S. Neonatal convulsions
caused by withdrawal from maternal
clomipramine. Br Med J (Clin Res Ed). 1982;284:
1837-1838.
15. Singh S, Gulati S, Narang A, Bhakoo ON. Nonnarcotic
withdrawal syndrome in a neonate due to
maternal clomipramine therapy. J Paediatr Child
Health. 1990;26:110.
16. Schimmell MS, Katz EZ, Shaag Y, et al. Toxic
neonatal effects following maternal clomipramine
therapy. J Toxicol Clin Toxicol. 1991;29:479-484.
17. Levinson-Castiel R, Merlob P, Linder N, et al.
Neonatal abstinence syndrome after in utero exposure
to selective serotonin reuptake inhibitors in term
infants. Arch Pediatr Adolesc Med. 2006;160:173-176.
18. Chambers CD, Johnson KA, Dick LM, et al. Birth
outcomes in pregnant women taking fluoxetine. N
Engl J Med. 1996;335:1010-1015.
19. Nordeng H, Lindemann R, Perminov KV, Reikvam
A. Neonatal withdrawal syndrome after in utero exposure
to selective serotonin reuptake inhibitors. Acta
Paediatr. 2001;90:288-291.
20. Sanz EJ, De las Cuevas C, Kiuru A, et al. Selective
serotonin reuptake inhibitors in pregnant women and
neonatal withdrawal syndrome: a database analysis.
Lancet. 2005;365:482-487.
21. Simon GE, Cunningham ML, Davis RL. Outcomes
of prenatal antidepressant exposure. Am J Psychiatry.
2002;159:2055-2061.
22. Costei AM, Kozer E, Ho T, et al. Perinatal outcome
following third trimester exposure to paroxetine. Arch
Pediat Adolesc Med. 2002;156:1129-1132.
23. Laine K, Heikkinen T, Ekblad U, Kero P. Effects
of exposure to selective serotonin reuptake inhibitors
during pregnancy on serotonergic symptoms in
newborns and cord blood monoamine and prolactin
concentrations. Arch Gen Psychiatry. 2003;60:
720-726.
24. Laegreid L, Hagberg G, Lundberg A. The effect
of benzodiazepines on the fetus and the newborn.
Neuropediatrics. 1992;23:18-23.
25. Gilstrap LC, Little BB. Drugs and Pregnancy.
Toronto: Chapman and Hall; 1998.
26. Iqbal MM, Sobhan T, Ryals T. Effects of commonly
used benzodiazepines on the fetus, the neonate, and
the nursing infant. Psychiatric Serv. 2002;53:39-49.
27. Bertilsson L, Henthorn T, Sanz E, et al. Importance
of genetic factors in the regulation of diazepam metabolism:
relationship to S-mephenytoin, but not debrisoquin,
hydroxylation phenotype. Clin Pharmacol Ther.
1989;45:348-355.
28. Jaiswal AK, Bhattacharya SK. Effects of gestational
undernutrition, stress and diazepam treatment
on spatial discrimination learning and retention in
young rats. Indian J Exp Biol. 1993;31:353-359.
29. Christensen HD, Gonzalez CL, Rayburn WF.
Effects from prenatal exposure to alprazolam on the
social behaviour of mice offspring. Am J Obstet
Gynecol. 2003;189:1452-1457.
30. Jaiswal AK. Effects of prenatal alprazolam exposure
on anxiety patterns in rat offspring. Indian J
Exp Biol. 2002;40:35-39.
31. Nicosia A, Giardina L, Di Leo F, et al. Long-lasting
behavioral changes induced by pre- or neonatal
exposure to diazepam in rats. Eur J Pharmacol.
2003;469:103-109.
32. Koch S, Jager-Roman E, Losche G, et al.
Antiepileptic drug treatment in pregnancy: drug side
effects in the neonate and neurological outcome. Acta
Paediatr. 1996;85:739-746.
33. Moore SJ, Turnpenny P, Quinn A, et al. A clinical
study of 57 children with fetal anticonvulsant
syndromes. J Med Genet. 2000;37:489-497.
34. Dean JC, Hailey H, Moore SJ, et al. Long term
health and neurodevelopment in children exposed
to antiepileptic drugs before birth. J Med Genet.
2002;39:251-259.
35. De las Cuevas C, Sanz EJ. Polypharmacy in psychiatric
practice in the Canary Islands.BMC Psychiatry.
2004;4:18.