Selective serotonin reuptake inhibitor (SSRI) use during pregnancy and risk of preterm birth: a systematic review and meta-analysis

被引:84
|
作者
Eke, A. C. [1 ]
Saccone, G. [2 ]
Berghella, V. [3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Obstet & Gynecol, Div Maternal Fetal Med, Baltimore, MD 21205 USA
[2] Univ Naples Federico II, Sch Med, Dept Neurosci Reprod Sci & Dent, Naples, Italy
[3] Thomas Jefferson Univ Hosp, Dept Obstet & Gynecol, Div Maternal Fetal Med, Philadelphia, PA 19107 USA
关键词
Depression; drug; malformation; prematurity; preterm birth; PRENATAL EXPOSURE; 3RD TRIMESTER; DEPRESSION; ANTIDEPRESSANTS; OUTCOMES; EPIDEMIOLOGY;
D O I
10.1111/1471-0528.14144
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background Depression is a prevalent condition in pregnancy affecting about 10% of women. Maternal depression has been associated with an increase in preterm births (PTB), low birthweight and fetal growth restriction, and postnatal complications. Available treatments for depressive disorders are psychotherapeutic interventions and antidepressant medications including selective serotonin inhibitors (SSRIs). SSRI use during pregnancy has been associated with several fetal and neonatal complications; so far, however, the risk of PTB in women using SSRIs during pregnancy is still a subject of debate. Objective To evaluate the risk of preterm birth (PTB) in cases of exposure to SSRIs during pregnancy. Search strategy Electronic databases (MEDLINE, Scopus, ClinicalTrials.gov, the PROSPERO International Prospective Register of Systematic Reviews, EMBASE and the Cochrane Central Register of Controlled Trials) were searched from their inception until May 2015 with the use of a combination of the following text words 'depression', 'pregnancy', 'exposure', 'antidepressant', 'SSRI', 'selective serotonin reuptake inhibitor', 'preterm birth', 'small for gestational age' and 'prematurity'. Selection criteria We included studies evaluating the effect of SSRIs exposure in utero and pregnancy outcomes. All cohort and case-control studies were eligible to be included if they reported the incidence of PTB after any exposure to SSRIs and had a comparison group of unexposed pregnant women. Studies without a control group were excluded. Data collection and analysis The primary outcome was the incidence of PTB < 37 weeks. Subgroup analysis of studies in which controls were defined as women with depression but without SSRI exposure during pregnancy were planned. Main results Eight studies (1 237 669 women) were included: 93 982 in the exposure group and 1 143 687 in the control group. After adjusting for confounders, the incidence of PTB was significantly higher in the group of women treated with SSRIs compared with controls (i.e. both women with depression but without SSRI exposure and women without depression) (adjusted OR (aOR) 1.24, 95% CI 1.09-1.41). In the subgroup analysis of studies in which controls were defined as women with depression but without SSRI exposure during pregnancy, an increased risk of PTB (6.8 versus 5.8%; OR 1.17, 95% CI 1.101.25) in the SSRI group was found compared with controls (i.e. depressed women treated with psychotherapy alone). Conclusions Women who received SSRIs during pregnancy had a significantly higher risk of developing PTB compared with controls. This higher risk remained significant even when comparing depressed women on SSRI with women not on SSRI.
引用
收藏
页码:1900 / 1907
页数:8
相关论文
共 50 条
  • [31] SELECTIVE SEROTONIN REUPTAKE INHIBITORS FOR STROKE RECOVERY: A SYSTEMATIC REVIEW AND META-ANALYSIS
    Mead, G.
    Legg, L.
    Hua, X.
    Wu, S.
    Hackett, M.
    Hsieh, C. -F.
    Barugh, A.
    Lundstrom, E.
    Lindgren, L.
    Rudberg, A. S.
    Kutlubaev, M.
    Tilney, R.
    Dennis, M.
    Hankey, G.
    INTERNATIONAL JOURNAL OF STROKE, 2021, 16 (3_SUPPL) : 15 - 15
  • [32] Selective Serotonin Reuptake Inhibitor Use in Pregnancy and Risk of Postpartum Hemorrhage
    Andrade, Chittaranjan
    JOURNAL OF CLINICAL PSYCHIATRY, 2022, 83 (02)
  • [33] Selective Serotonin Reuptake Inhibitors for Stroke Recovery A Systematic Review and Meta-analysis
    Mead, Gillian E.
    Hsieh, Cheng-Fang
    Lee, Rebecca
    Kutlubaev, Mansur
    Claxton, Anne
    Hankey, Graeme J.
    Hackett, Maree
    STROKE, 2013, 44 (03) : 844 - +
  • [35] Systematic meta-analysis of individual selective serotonin reuptake inhibitor medications and congenital malformations
    Myles, Nicholas
    Newall, Hannah
    Ward, Harvey
    Large, Matthew
    AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY, 2013, 47 (11): : 1002 - 1012
  • [36] Ozone exposure during early pregnancy and preterm birth: A systematic review and meta-analysis
    Rappazzo, Kristen M.
    Nichols, Jennifer L.
    Rice, R. Byron
    Luben, Thomas J.
    ENVIRONMENTAL RESEARCH, 2021, 198
  • [37] Selective serotonin reuptake inhibitor discontinuation during pregnancy At what risk?
    Ejaz, Resham
    Leibson, Tom
    Koren, Gideon
    CANADIAN FAMILY PHYSICIAN, 2014, 60 (12) : 1105 - 1106
  • [38] Alliance between selective serotonin reuptake inhibitors and fracture risk: an updated systematic review and meta-analysis
    Manoj Kumar
    Ram Bajpai
    Abdul Rahaman Shaik
    Swati Srivastava
    Divya Vohora
    European Journal of Clinical Pharmacology, 2020, 76 : 1373 - 1392
  • [39] ALLIANCE BETWEEN SELECTIVE SEROTONIN REUPTAKE INHIBITORS AND FRACTURE RISK: AN UPDATED SYSTEMATIC REVIEW AND META-ANALYSIS
    Kumar, M.
    Bajpai, R.
    Shaik, A. R.
    Vohora, D.
    OSTEOPOROSIS INTERNATIONAL, 2020, 31 (SUPPL 1) : S142 - S143
  • [40] Alliance between selective serotonin reuptake inhibitors and fracture risk: an updated systematic review and meta-analysis
    Kumar, Manoj
    Bajpai, Ram
    Shaik, Abdul Rahaman
    Srivastava, Swati
    Vohora, Divya
    EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2020, 76 (10) : 1373 - 1392