To treat or not to treat: maternal depression, SSRI use in pregnancy and adverse neonatal effects

被引:39
作者
Austin, Marie-Paule
机构
[1] Prince Wales Hosp, Dept Liaison Psychiat, Black Dog Inst, Randwick, NSW 2031, Australia
[2] Univ New S Wales, Sch Psychiat, Kensington, NSW 2033, Australia
关键词
D O I
10.1017/S003329170600835X
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Recent pharmaceutical company and regulatory body circulars warning against the use of selective serotonin reuptake inhibitors (SSRIs) in late pregnancy have left clinicians in somewhat of a quandary as to how to manage their more severely depressed patients in pregnancy. Conversely, Lip to 75% of depressed women ceasing their antidepressants periconceptually will relapse. Studies reporting on adverse neonatal outcomes following exposure to SSRIs in the latter half of pregnancy suggest that the fetus is exposed to significant concentrations of these medications during this time. Adverse neonatal effects affecting the respiratory, gastrointestinal and neurological systems are, however, predominantly mild and self-limiting. One small retrospective case study Suggests that SSRI exposure in the latter half of pregnancy may be associated with an increased risk of persistent pulmonary hypertension of the neonate (PPHN), however, the absolute risk of developing PPHN remains very small and these findings will require replication with a prospective study. While the studies to date suggest the need to closely monitor SSRI-exposed neonates in the immediate postnatal period, preferably with a neonatal withdrawal scale and access to neonatology services, there is currently no clear argument for women to be weaned off their SSRI in late pregnancy. The decision to use SSRIs at this time will have to be made on a case-by-case basis in close consultation with the mother and her partner.
引用
收藏
页码:1663 / 1670
页数:8
相关论文
共 44 条
[1]  
Administration US Food and Drug Administration, 2004, FDA MEDW DRUG AL EFF
[2]   Maternal stress and obstetric and infant outcomes: epidemiological findings and neuroendocrine mechanisms [J].
Austin, MP ;
Leader, L .
AUSTRALIAN & NEW ZEALAND JOURNAL OF OBSTETRICS & GYNAECOLOGY, 2000, 40 (03) :331-337
[3]   Clinical issues in perinatal mental health: new developments in the detection and treatment of perinatal mood and anxiety disorders [J].
Austin, MP ;
Priest, SR .
ACTA PSYCHIATRICA SCANDINAVICA, 2005, 112 (02) :97-104
[4]  
Bayley N., 1993, Bayley scales of infant and toddler development, VSecond
[5]  
Brazelton TB., 1984, NEONATAL BEHAV ASSES
[6]   Follow-up of children of depressed mothers exposed or not exposed to antidepressant drugs during pregnancy [J].
Casper, RC ;
Fleisher, BE ;
Lee-Ancajas, JC ;
Gilles, A ;
Gaylor, E ;
DeBattista, A ;
Hoyme, HE .
JOURNAL OF PEDIATRICS, 2003, 142 (04) :402-408
[7]   Selective serotonin-reuptake inhibitors and risk of persistent pulmonary hypertension of the newborn [J].
Chambers, CD ;
Hernandez-Diaz, S ;
Van Marter, LJ ;
Werler, MM ;
Louik, C ;
Jones, KL ;
Mitchell, AA .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (06) :579-587
[8]   Birth outcomes in pregnant women taking fluoxetine [J].
Chambers, CD ;
Johnson, KA ;
Dick, LM ;
Felix, RJ ;
Jones, KL .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (14) :1010-1015
[9]   Birth outcomes following prenatal exposure to fluoxetine [J].
Cohen, LS ;
Heller, VL ;
Bailey, JW ;
Grush, L ;
Ablon, JS ;
Bouffard, SM .
BIOLOGICAL PSYCHIATRY, 2000, 48 (10) :996-1000
[10]   Relapse of major depression during pregnancy in women who maintain or discontinue antidepressant treatment [J].
Cohen, LS ;
Altshuler, LL ;
Harlow, BL ;
Nonacs, R ;
Newport, DJ ;
Viguera, AC ;
Suri, R ;
Burt, VK ;
Hendrick, V ;
Reminick, AM ;
Loughead, A ;
Vitonis, AF ;
Stowe, ZN .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (05) :499-507