Antidepressiva
slecht voor ongeboren baby.*
Zwangere
vrouwen die tijdens de laatste vier maanden van de zwangerschap bepaalde
antidepressiva, de SSRI’s, gebruiken geven hun baby een duidelijk verhoogde
kans op het ontwikkelen van een blijvende hoge bloeddruk in de longen (PPHN).
Gebruik tijdens de eerste 4 maanden gaf volgens de studie geen aanwijzing voor
PPHN. Andere soorten antidepressiva geven geen verhoogde kans op PPHN.
Alhoewel de kans op het krijgen van een baby met PPHN bij SSRI’s laag is is
het toch verstandig de resultaten van deze studie bij een mogelijk beslissing
over het gebruik van antidepressiva te betrekken.
Late
Pregnancy Use Of SSRI Antidepressant Medication May Affect Fetus
A
University of California , San Diego (UCSD) School of Medicine collaborative
study with Boston University ’s Slone Epidemiology Center found an increased
risk of persistent pulmonary hypertension (PPHN)
in newborns of mothers who used certain commonly prescribed antidepressants
in late pregnancy. The results of the study will
be published in the February 9 issue of the New England Journal of Medicine.
According to the
study authors, PPHN is a serious condition that typically involves severe
respiratory failure in a newborn infant and requires immediate treatment. The
condition occurs in about one to two per thousand babies. The new study findings indicate that pregnant women who take one of the antidepressants known as selective
serotonin reuptake inhibitors or SSRIs, such as Prozac ® ,
Paxil ® or Zoloft ® , in the second half of pregnancy have a small but
significantly increased chance of delivering an infant who develops PPHN. The
study found that exposure to antidepressants other than SSRIs did not pose a
risk for PPHN. In addition, women who discontinued use of SSRIs in the first
half of pregnancy did not have an increased risk of delivering a child with
the condition.
These
findings may be important for pregnant women and clinicians when making
decisions about the most appropriate treatments for depression late in
pregnancy.
Lead
author on the study, Christina Chambers, Ph.D., M.P.H., of the Departments of
Pediatrics and Family and Preventive Medicine at UCSD, worked with a team of
investigators who identified at birth 377 infants with PPHN and 836 normal
newborns from 97 delivery hospitals in four metropolitan centers in the U.S.
and Canada between 1998 and 2003. The study was part of the ongoing Birth
Defects Surveillance Program being conducted by the Slone Epidemiology Center
with the collaboration of 17 San Diego County hospitals including UCSD Medical
Center.
Within
six months after birth, the researchers examined the records and carefully
interviewed the mothers of children with PPHN and the mothers of the matched
control infants selected from the same hospitals. The mothers in both groups
were asked specifically about the use of any antidepressant medications during
pregnancy, the names of products used, and the timing in gestation when the
mother used the medication. Mothers were also queried about a wide variety of
other maternal exposures, medical history, pregnancy history, and lifestyle
factors.
“Based
on our findings, we estimate that six to twelve mothers per thousand who use
an SSRI after 20 weeks’ gestation, are likely to deliver a child with PPHN,”
said Chambers. “Put in practical terms, the risk is relatively low -- about
99 percent of women exposed to one of these medications during the latter half
of pregnancy will deliver an infant unaffected by PPHN.”
“Our
findings suggest that prenatal exposure to SSRIs might contribute to the
pathological origin of this disorder,” says Chambers. She adds that although
the study cannot establish cause, several possible mechanisms suggesting an
association between the use of the SSRIs and PPHN are plausible.
Although
the researchers noted an increased risk of PPHN in infants whose mothers took
SSRIs late in pregnancy, the research team points out that mothers may need to
continue SSRI treatment during pregnancy in order to care for themselves
appropriately. The findings of this study might be factored into decisions
about continuing treatment with SSRIs into late pregnancy.
The
research team consisted of Chambers, Sonia Hernandez-Diaz, M.D. Dr.P.H of
Slone Epidemiology Center at Boston University School of Public Health, Linda
J. Van Marter, M.D., Ph.D of Boston Children’s Hospital, Brigham and Women’s
Hospital, and Harvard Medical School, Martha M. Werler, Sc.D, and Allen A.
Mitchell, M.D. of Slone Epidemiology Center, and Kenneth Lyons Jones, M.D. of
the UCSD Department of Pediatrics.
Chambers
is Program Director of the California Teratogen Information Service (CTIS).
CTIS operates a statewide telephone service and a clinical research program
from the Department of Pediatrics at UCSD with satellite offices at UCLA, Los
Angeles Children’s Hospital and Stanford University. Founded in 1979, this
program provides no-cost, confidential information regarding the fetal safety
of medications, chemicals, or other agents when used in pregnancy. The CTIS
Pregnancy Risk Information line provides information to over 8,000 callers per
year including pregnant or pre-pregnant women and health care providers
located throughout the state of California. The CTIS program also conducts
pregnancy outcome research studies so that evidence-based information can be
developed for women with similar questions in the future.
Pregnant women and health care providers can reach CTIS specialists by calling toll free at 800-532-3749 or by contacting CTIS through their website at http://www.ctispregnancy.org. For people outside of California, information on exposures in pregnancy can be obtained by calling the Organization of Teratology Information Specialists (OTIS) national toll-free number 866-626-6847 or visiting the OTIS website at http://www.otispregnancy.org. (Februari 2006)