选择性5 -羟色胺再摄取抑制剂在妊娠和产后出血的风险。

C. Andrade
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引用次数: 2

摘要

选择性5 -羟色胺再摄取抑制剂(SSRIs)可能通过干扰血小板介导的止血和5 -羟色胺介导的子宫肌收缩性而诱发产后出血(PPH)。一项对8项观察性研究的荟萃分析发现,无论药物类别如何,妊娠期接触抗抑郁药与PPH风险增加的相关性很小(优势比为1.25),但在统计学上具有显著性;然而,这一发现仅在抗抑郁药物暴露接近分娩日期时才成立。最近一项中等规模、具有全国代表性的瑞典观察性研究也发现,妊娠期暴露于SSRIs与PPH风险显著增加相关;需要伤害的粗略数字是48。由于所采用的方法相关的原因,本研究可能低估了风险。为了帮助读者理解如何批判性地阅读和解释该领域的研究文献,对meta分析和观察性研究的结果进行了检验。一个合理的观点是,与妊娠期暴露于SSRIs相关的PPH风险增加小于与PPH产科风险因素相关的风险增加;然而,采取预防措施是明智的。这些措施包括在分娩前一个月内接受过5 -羟色胺再摄取抑制剂治疗的所有妇女,在分娩后立即常规给予子宫强直剂;子宫扩张剂的选择取决于当地医院的治疗方案。还应密切监测有风险的妇女在分娩后24小时内是否继续失血。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Selective Serotonin Reuptake Inhibitor Use in Pregnancy and Risk of Postpartum Hemorrhage.
Selective serotonin reuptake inhibitors (SSRIs) may predispose to postpartum hemorrhage (PPH) by interfering with platelet-mediated hemostasis and serotonin-mediated myometrial contractility. A meta-analysis of 8 observational studies found that, regardless of drug class, gestational exposure to antidepressants was associated with a small (odds ratio, 1.25) but statistically significantly increased risk of PPH; however, this finding was true only when antidepressant exposure was proximal to the date of delivery. A recent, moderately large, nationally representative, Swedish observational study also found that gestational exposure to SSRIs was associated with a significantly increased risk of PPH; the crude number needed to harm was 48. For reasons related to the methodology employed, it is possible that the risk was underestimated in this study. The findings of the meta-analysis and of the observational study are examined with a view to help readers understand how to critically read and interpret the research literature in the field. A reasonable viewpoint is that the increase in risk of PPH associated with gestational exposure to SSRIs is smaller than the increase in risk associated with obstetric risk factors for PPH; nevertheless, following precautionary measures would be wise. Such measures would include the routine administration of a uterotonic agent immediately after delivery to all women who have received serotonin reuptake inhibitor treatment during the month preceding delivery; the choice of uterotonic agent would depend on local hospital protocols. Women at risk should also be closely monitored for continued blood loss during the first 24 hours after delivery.
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