Winterfeld Ursula, Klinger Gil, Panchaud Alice, Stephens Sally, Arnon Judy, Malm Heli, Te Winkel Bernke, Clementi Maurizio, Pistelli Alessandra, Maňáková Eva, Eleftheriou Georgios, Merlob Paul, Kaplan Yusuf C, Buclin Thierry, Rothuizen Laura E
From the *STIS and Division of Clinical Pharmacology, University Hospital, Lausanne, Switzerland; †BELTIS Rabin Medical Center and Sackler School of Medicine, University of Tel-Aviv, Tel-Aviv, Israel; ‡School of Pharmaceutical Sciences, University of Geneva and Lausanne, Geneva, Switzerland; §UKTIS, Regional Drug and Therapeutics Centre, Newcastle-Upon-Tyne, United Kingdom; ∥The Israeli Teratology Information Service, Israel Ministry of Health, Jerusalem, Israel; ¶Teratology Information Service, Helsinki University Central Hospital and HUSLAB, Helsinki, Finland; #TIS, Netherlands Pharmacovigilance Centre Lareb, Den Bosch, The Netherlands; **Servizio di Informazione Teratologica, Padova; ††Centro di Riferimento Regionale di Tossicologia Perinatale, Azienda Ospedaliero Universitaria Careggi, Florence, Italy; ‡‡CZTIS, 3rd Faculty of Medicine, Charles University, Prague, Czech Republic; §§Poison Control, Bergamo, Italy; and ∥∥Terafar-Izmir Katip Celebi University Teratology Information, Training and Research Center, Izmir, Turkey.
J Clin Psychopharmacol. 2015 Jun;35(3):250-9. doi: 10.1097/JCP.0000000000000309.
This multicenter, observational prospective cohort study addresses the risk associated with exposure to mirtazapine during pregnancy. Pregnancy outcomes after exposure to mirtazapine were compared with 2 matched control groups: (1) exposure to any selective serotonin reuptake inhibitor (SSRI, control subjects with a psychiatric condition) and (2) no exposure to medication known to be teratogenic or any antidepressant (general control subjects). Data were collected by members of the European Network of Teratology Information Services between 1995 and 2011. Observations from 357 exposed pregnancies were compared with 357 pregnancies from each control group. The rate of major birth defects between the mirtazapine and the SSRI group did not differ significantly (4.5% vs 4.2%; odds ratio [OR], 1.1; 95% confidence interval [95% CI], 0.5-2.3; P = 0.9). A trend toward a higher rate of birth defects in the mirtazapine group compared with general control subjects (4.5% vs 1.9%; OR, 2.4; 95% CI, 0.9-6.3; P = 0.08) reached statistical significance after exclusion of chromosomal or genetic anomalies (4.1% vs 1.3%; OR, 3.3; 95% CI, 1.04-10.3; P = 0.03), but this difference became again nonsignificant if cases of exposure not comprising the first trimester were excluded from the analysis (3.4% vs 1.9%; OR, 1.8; 95% CI, 0.6-5.0; P = 0.26). The crude miscarriage rate did not differ significantly between the mirtazapine, the SSRI, and the general control groups (12.1% vs 12.0% vs 9.3%; P = 0.44). However, a higher rate of elective pregnancy termination was observed in the mirtazapine group compared with SSRI and general control subjects (7.8% vs 3.4% vs 5.6%; P = 0.03). This study did not observe a statistically significant difference in the rate of major birth defects after first-trimester exposure between mirtazapine, SSRI-exposed, and nonexposed pregnancies. A marginally higher rate of birth defects was, however, observed in the mirtazapine and SSRI groups compared with the low rate of birth defects in our general control subjects. Overall pregnancy outcome after mirtazapine exposure was similar to that of the SSRI-exposed control group.
这项多中心、前瞻性观察性队列研究探讨了孕期暴露于米氮平的相关风险。将暴露于米氮平后的妊娠结局与两个匹配的对照组进行比较:(1)暴露于任何选择性5-羟色胺再摄取抑制剂(SSRI,患有精神疾病的对照受试者)和(2)未暴露于已知致畸药物或任何抗抑郁药(一般对照受试者)。数据由欧洲畸形学信息服务网络成员在1995年至2011年期间收集。将357例暴露妊娠的观察结果与每个对照组的357例妊娠进行比较。米氮平组与SSRI组之间的主要出生缺陷发生率无显著差异(4.5%对4.2%;优势比[OR],1.1;95%置信区间[95%CI],0.5 - 2.3;P = 0.9)。与一般对照受试者相比,米氮平组出生缺陷发生率有升高趋势(4.5%对1.9%;OR,2.4;95%CI,0.9 - 6.3;P = 0.08),在排除染色体或基因异常后达到统计学显著性(4.1%对1.3%;OR,3.3;95%CI,1.04 - 10.3;P = 0.03),但如果将非孕早期暴露病例排除在分析之外,这种差异再次变得不显著(3.4%对1.9%;OR,1.8;95%CI,0.6 - 5.0;P = 0.26)。米氮平组、SSRI组和一般对照组之间的自然流产率无显著差异(12.1%对12.0%对9.3%;P = 0.44)。然而,与SSRI组和一般对照受试者相比,米氮平组观察到更高的选择性妊娠终止率(7.8%对3.4%对5.6%;P = 0.03)。本研究未观察到孕早期暴露后米氮平组、暴露于SSRI组和未暴露组之间主要出生缺陷发生率的统计学显著差异。然而,与我们一般对照受试者的低出生缺陷率相比,米氮平组和SSRI组观察到略高的出生缺陷率。米氮平暴露后的总体妊娠结局与暴露于SSRI的对照组相似。