Eke A C, Saccone G, Berghella V
Division of Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of Neuroscience, Reproductive Sciences and Dentistry, School of Medicine, University of Naples Federico II, Naples, Italy.
BJOG. 2016 Nov;123(12):1900-1907. doi: 10.1111/1471-0528.14144. Epub 2016 May 30.
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.
To evaluate the risk of preterm birth (PTB) in cases of exposure to SSRIs during pregnancy.
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'.
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.
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.
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 1.10-1.25) in the SSRI group was found compared with controls (i.e. depressed women treated with psychotherapy alone).
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.
Selective serotonin reuptake inhibitors may be associated with preterm birth.
抑郁症在孕期很常见,约10%的女性受其影响。母亲患抑郁症与早产、低出生体重、胎儿生长受限及产后并发症增多有关。抑郁症的现有治疗方法包括心理治疗干预和抗抑郁药物,其中包括选择性5-羟色胺再摄取抑制剂(SSRI)。孕期使用SSRI与多种胎儿及新生儿并发症有关;然而,目前孕期使用SSRI的女性发生早产的风险仍存在争议。
评估孕期暴露于SSRI的情况下早产(PTB)的风险。
检索电子数据库(MEDLINE、Scopus、ClinicalTrials.gov、PROSPERO国际前瞻性系统评价注册库、EMBASE和Cochrane对照试验中央注册库),检索时间从建库起至2015年5月,使用以下文本词的组合:“抑郁症”“妊娠”“暴露”“抗抑郁药”“SSRI”“选择性5-羟色胺再摄取抑制剂”“早产”“小于胎龄儿”和“早产”。
我们纳入了评估子宫内暴露于SSRI及其妊娠结局影响的研究。所有队列研究和病例对照研究,只要报告了任何暴露于SSRI后的PTB发病率,且有未暴露孕妇的对照组,均符合纳入标准。无对照组的研究被排除。
主要结局为孕周<37周的PTB发病率。计划对将对照组定义为孕期患抑郁症但未暴露于SSRI的女性的研究进行亚组分析。
纳入8项研究(1237669名女性):暴露组93982名,对照组1143687名。校正混杂因素后,与对照组(即患抑郁症但未暴露于SSRI的女性和未患抑郁症的女性)相比,接受SSRI治疗的女性组PTB发病率显著更高(校正比值比(aOR)1.24,95%置信区间1.09 - 1.41)。在将对照组定义为孕期患抑郁症但未暴露于SSRI的女性的研究亚组分析中,与对照组(即仅接受心理治疗的抑郁症女性)相比,SSRI组PTB风险增加(6.8%对5.8%;OR 1.17,95%置信区间1.10 - 1.25)。
与对照组相比,孕期接受SSRI治疗的女性发生PTB的风险显著更高。即使将使用SSRI的抑郁症女性与未使用SSRI的女性进行比较,这种较高风险仍然显著。
选择性5-羟色胺再摄取抑制剂可能与早产有关。