Use of selective serotonin-reuptake inhibitors in pregnancy and the risk of birth defects

被引:336
作者
Alwan, Sura
Reefhuis, Jennita
Rasmussen, Sonja A.
Olney, Richard S.
Friedman, Jan M.
机构
[1] Ctr Dis Control & Prevent, Natl Ctr Birth Defects & Dev Disabil, Atlanta, GA 30333 USA
[2] Univ British Columbia, Dept Med Genet, Vancouver, BC, Canada
关键词
D O I
10.1056/NEJMoa066584
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Information regarding the safety of selective serotonin-reuptake inhibitors (SSRIs) in human pregnancy is sparse. Concern has been raised about the risk of congenital heart defects associated with the use of SSRIs in pregnancy. METHODS: We obtained data on 9622 case infants with major birth defects and 4092 control infants born from 1997 through 2002 from the National Birth Defects Prevention Study. Case infants were ascertained through birth-defects surveillance systems in eight U.S. states; controls were selected randomly from the same geographic areas. Mothers completed a standardized telephone interview regarding exposure to potential risk factors, including medications, before and during pregnancy. Exposure to SSRIs was defined as treatment with any SSRI from 1 month before to 3 months after conception. Birth defects were assigned to 26 categories and subcategories. RESULTS: There were no significant associations between maternal use of SSRIs overall during early pregnancy and congenital heart defects or most other categories or subcategories of birth defects. Maternal SSRI use was associated with anencephaly (214 infants, 9 exposed; adjusted odds ratio, 2.4; 95% confidence interval [CI], 1.1 to 5.1), craniosynostosis (432 infants, 24 exposed; adjusted odds ratio, 2.5; 95% CI, 1.5 to 4.0), and omphalocele (181 infants, 11 exposed; adjusted odds ratio, 2.8; 95% CI, 1.3 to 5.7). CONCLUSIONS: Maternal use of SSRIs during early pregnancy was not associated with significantly increased risks of congenital heart defects or of most other categories of birth defects. Associations were observed between SSRI use and three types of birth defects, but the absolute risks were small, and these observations require confirmation by other studies.
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页码:2684 / 2692
页数:9
相关论文
共 34 条
  • [1] The effects of maternal depression on fetal heart rate response to vibroacoustic stimulation
    Allister, L
    Lester, BM
    Carr, S
    Liu, J
    [J]. DEVELOPMENTAL NEUROPSYCHOLOGY, 2001, 20 (03) : 639 - 651
  • [2] Maternal obesity, gestational diabetes, and central nervous system birth defects
    Anderson, JL
    Waller, DK
    Canfield, MA
    Shaw, GM
    Watkins, ML
    Werler, MM
    [J]. EPIDEMIOLOGY, 2005, 16 (01) : 87 - 92
  • [3] First trimester exposure to paroxetine and risk of cardiac malformations in infants:: The importance of dosage
    Berard, Anick
    Ramos, Elodie
    Rey, Evelyne
    Blais, Lucie
    St. Andre, Martin
    Oraichi, Driss
    [J]. BIRTH DEFECTS RESEARCH PART B-DEVELOPMENTAL AND REPRODUCTIVE TOXICOLOGY, 2007, 80 (01) : 18 - 27
  • [4] DEVELOPMENTAL TOXICOLOGY STUDIES OF FLUOXETINE HYDROCHLORIDE ADMINISTERED ORALLY TO RATS AND RABBITS
    BYRD, RA
    MARKHAM, JK
    [J]. FUNDAMENTAL AND APPLIED TOXICOLOGY, 1994, 22 (04): : 511 - 518
  • [5] Carey J C, 1978, Birth Defects Orig Artic Ser, V14, P253
  • [6] Birth outcomes in pregnant women taking fluoxetine
    Chambers, CD
    Johnson, KA
    Dick, LM
    Felix, RJ
    Jones, KL
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (14) : 1010 - 1015
  • [7] Mechanisms of cellular distribution of psychotropic, drugs. Significance for drug action and interactions
    Daniel, WA
    [J]. PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2003, 27 (01) : 65 - 73
  • [8] Delivery outcome after the use of antidepressants in early pregnancy
    Ericson, A
    Källén, B
    Wiholm, BE
    [J]. EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1999, 55 (07) : 503 - 508
  • [9] Pregnancy outcome after exposure to ranitidine and other H2-blockers - A collaborative study of the European Network of Teratology Information Services
    Garbis, H
    Elefant, E
    Diav-Citrin, O
    Mastroiacovo, P
    Schaefer, C
    Vial, T
    Clementi, M
    Valti, E
    McElhatton, P
    Smorles, C
    Rodriguez, EP
    Robert-Gnansia, E
    Merlob, P
    Peiker, G
    Pexieder, T
    Schueler, L
    Ritvanen, A
    Mathieu-Nolf, M
    [J]. REPRODUCTIVE TOXICOLOGY, 2005, 19 (04) : 453 - 458
  • [10] *GLAXOSMITHKLINE, EP STUD PREL REP BUP