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妊娠期炎症性肠病:疾病发作或缓解期的管理

Inflammatory bowel disease during pregnancy: management of a disease flare or remission.

作者信息

Afzali Anita

机构信息

aThe Ohio State University Inflammatory Bowel Disease Center bDivision of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.

出版信息

Curr Opin Gastroenterol. 2019 Jul;35(4):281-287. doi: 10.1097/MOG.0000000000000541.

Abstract

PURPOSE OF REVIEW

Roughly half of the nearly 1.6 million people with inflammatory bowel disease (IBD) are women of reproductive age. Caring for women with IBD who are also pregnant can be challenging, particularly if with a disease flare or in remission, as there are special considerations needed.

RECENT FINDINGS

Despite older studies concluding potential risks associated with IBD medical therapies, more recent literature reports healthier maternal and birth outcomes associated with disease control and reduction in the inflammatory burden. Most IBD therapies should generally be continued throughout all three trimesters without interruption as this is associated with better outcomes.

SUMMARY

Active IBD increases risk of pregnancy complications and adverse pregnancy outcomes. Most medications have a favorable safety profile for use during pregnancy, regardless if in disease flare or remission. Short course corticosteroids for induction and management of flare is permitted. Thiopurines should not be started during pregnancy for a disease flare, but may be continued during pregnancy if previously on monotherapy. Biologics should be continued throughout pregnancy without interruption and timing of third trimester dosing made based on drug levels and estimated date of delivery. Risks/benefit assessment of therapies and disease control is important and should be individualized.

摘要

综述目的

在近160万炎症性肠病(IBD)患者中,约有一半是育龄妇女。照顾患有IBD且怀孕的女性可能具有挑战性,尤其是在疾病发作或缓解期,因为需要特殊考虑。

最新研究发现

尽管早期研究得出IBD药物治疗存在潜在风险,但最近的文献报道,疾病得到控制且炎症负担减轻与更健康的孕产妇和分娩结局相关。大多数IBD治疗通常应在整个孕期持续进行,不间断,因为这与更好的结局相关。

总结

活动性IBD会增加妊娠并发症和不良妊娠结局的风险。大多数药物在孕期使用具有良好的安全性,无论疾病处于发作期还是缓解期。允许短期使用皮质类固醇诱导和控制发作。硫唑嘌呤在孕期发作时不应开始使用,但如果之前是单药治疗,孕期可继续使用。生物制剂应在整个孕期持续使用,不间断,孕晚期给药时间应根据药物水平和预计分娩日期确定。评估治疗的风险/获益以及疾病控制情况很重要,且应因人而异。

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