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1064 名挪威妇女妊娠剧吐的止吐治疗及欧洲警示对甲氧氯普胺的影响:一项 2002-2019 年的回顾性队列研究。

Antiemetic treatment of hyperemesis gravidarum in 1,064 Norwegian women and the impact of European warning on metoclopramide: a retrospective cohort study 2002-2019.

机构信息

Centre for Pharmacy, Department of Global Public Health and Primary Care, Faculty of Medicine, University of Bergen, Årstadveien 17, 5009, Bergen, Norway.

Regional Medicines Information and Pharmacovigilance Centre, Department of Clinical Biochemistry and Pharmacology, Haukeland University Hospital, Bergen, Norway.

出版信息

BMC Pregnancy Childbirth. 2022 Jun 2;22(1):464. doi: 10.1186/s12884-022-04777-x.

Abstract

BACKGROUND

Women suffering from severe nausea and vomiting during pregnancy, hyperemesis gravidarum, have poor quality of life and increased risk of potentially fatal maternal and fetal complications. There is increasing and reassuring knowledge about safety of antiemetics in pregnancy. In 2013, the European Medical Agency (EMA) issued a warning on metoclopramide limiting treatment to maximum five days. Metoclopramide was the most used antiemetic in pregnancy at the time the warning was implemented in the Norwegian hyperemesis guidelines (2014). We aimed at describing changes in the treatment of hyperemesis over time, including changes associated with the EMA warning.

METHODS

Retrospective chart review of all women hospitalized for hyperemesis gravidarum with metabolic disturbances between 01/Jan/2002 and 31/Dec/2019 at a university hospital serving nearly 10% of the pregnant population in Norway. Time-series analysis described changes over time and interrupted time series analysis quantified changes in treatment and clinical outcomes related to the EMA warning.

RESULTS

In total, 1,064 women (1.2% of the birthing population) were included. The use of meclizine, prochlorperazine, and ondansetron increased during 2002-2019. This led to a yearly increase in the percentage of women using any antiemetic of 1.5% (95%CI 0.6; 2.4) pre-hospital, 0.6% (95%CI 0.2; 1.1) during hospitalization, and 2.6% (95%CI 1.3; 3.8) at discharge. Overall, only 50% of the women received antiemetics pre-hospital. Following the EMA warning, prehospital use of metoclopramide dropped by 30% (95%CI 25; 36), while use of any antiemetic pre-hospital dropped by 20% (95%CI 5.7; 34). In timely association, we observed a decrease in gestational age (-3.8 days, 98.75%CI 0.6; 7.1) at first admission, as well as indication of increased rate of termination of pregnancy with an absolute increase of 4.8% (98.75%CI 0.9; 8.7) in 2014.

CONCLUSION

During 2002-2019, the overall use of antiemetics in treatment of hyperemesis increased. The EMA-warning on metoclopramide in 2013 temporarily limited pre-hospital antiemetic provision associated with hospitalization at lower gestational length and indication of an increase in termination of pregnancy.

摘要

背景

患有妊娠剧吐(严重恶心和呕吐的孕妇)的女性生活质量较差,且存在潜在致命的母婴并发症风险增加。关于妊娠期间止吐药安全性的知识不断增加且令人安心。2013 年,欧洲药品管理局(EMA)发布了一项关于限制多潘立酮治疗时间最长为 5 天的警告。在挪威妊娠剧吐指南(2014 年)实施时,多潘立酮是当时最常用的妊娠止吐药。我们旨在描述随着时间的推移,妊娠剧吐治疗的变化,包括与 EMA 警告相关的变化。

方法

对 2002 年 1 月 1 日至 2019 年 12 月 31 日期间在一家为挪威近 10%孕妇人群服务的大学医院因代谢紊乱住院的所有妊娠剧吐女性的病历进行回顾性图表审查。时间序列分析描述了随时间的变化,中断时间序列分析量化了与 EMA 警告相关的治疗和临床结局的变化。

结果

共纳入 1064 名女性(分娩人群的 1.2%)。2002-2019 年间,苯海拉明、丙氯拉嗪和昂丹司琼的使用有所增加。这导致住院前使用任何止吐药的女性比例每年增加 1.5%(95%CI 0.6; 2.4),住院期间增加 0.6%(95%CI 0.2; 1.1),出院时增加 2.6%(95%CI 1.3; 3.8)。总体而言,只有 50%的女性在住院前接受了止吐药治疗。EMA 警告发布后,住院前多潘立酮的使用减少了 30%(95%CI 25; 36),而住院前使用任何止吐药的比例减少了 20%(95%CI 5.7; 34)。在及时关联中,我们观察到首次入院时的孕龄(-3.8 天,98.75%CI 0.6; 7.1)降低,以及终止妊娠率增加的迹象,2014 年绝对增加了 4.8%(98.75%CI 0.9; 8.7)。

结论

2002-2019 年期间,妊娠剧吐治疗中抗呕吐药物的总体使用有所增加。2013 年 EMA 对多潘立酮的警告暂时限制了住院前止吐药的供应,与住院时的妊娠周数较短有关,并表明终止妊娠的数量有所增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f19b/9161510/8db82659fef7/12884_2022_4777_Fig1_HTML.jpg

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