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阿达木单抗上市后 PYRAMID 注册研究中接受治疗的妊娠克罗恩病患者的观察性数据:一项事后分析。

Observational data from the adalimumab post-marketing PYRAMID registry of patients with Crohn's disease who became pregnant: A post hoc analysis.

机构信息

IBD Unit, St Mark's Hospital, London, UK.

Department of Gastroenterology and Hepatology, Amsterdam University Medical Center, Amsterdam, The Netherlands.

出版信息

United European Gastroenterol J. 2022 Jun;10(5):485-495. doi: 10.1002/ueg2.12236. Epub 2022 May 13.

Abstract

BACKGROUND

PYRAMID was an international post-marketing registry that aimed to collect data on the long-term safety and effectiveness of adalimumab treatment per local standard of care in patients with moderately to severely active Crohn's disease (CD). Here, we present post hoc analyses of observational data from patients who became pregnant while participating in this registry and receiving adalimumab.

METHODS

From the subpopulation of patients receiving adalimumab who became pregnant while taking part in PYRAMID, data on patient characteristics, pregnancy outcomes, and complications of pregnancy were analysed retrospectively.

RESULTS

Across the PYRAMID registry, 293 pregnancies occurred in patients who had gestational adalimumab exposure (average disease duration at last menstrual period: 8.6 years), resulting in 300 pregnancy outcomes. A total of 197 pregnancies (67.2%) were exposed to adalimumab in all trimesters per physician's decision. Of the known reported outcomes (96.3%), 81.7% (236/289) were live births, 10.4% (30/289) were spontaneous abortions, 4.8% (14/289) elective terminations, 2.8% (8/289) ectopic pregnancies, and 0.3% (1/289) was a stillbirth. Congenital malformations (pulmonary valve stenosis and tricuspid valve incompetence) were reported in one infant. In addition to the pregnancy outcomes described above, 23 complications of pregnancy were reported in 20 patients.

CONCLUSIONS

This analysis showed that adalimumab treatment in patients with CD, who became pregnant whilst participating in the PYRAMID registry, contributed no additional adverse effects during the pregnancy course or on pregnancy outcomes.

摘要

背景

PYRAMID 是一项国际上市后注册研究,旨在按照当地的标准护理收集接受阿达木单抗治疗的中重度活动期克罗恩病(CD)患者的长期安全性和有效性数据。在此,我们报告了参与该注册研究并接受阿达木单抗治疗的患者在妊娠期间的观察性数据的事后分析结果。

方法

从接受阿达木单抗治疗并在 PYRAMID 注册研究期间妊娠的患者亚人群中,回顾性分析了患者特征、妊娠结局和妊娠并发症的数据。

结果

在整个 PYRAMID 注册研究中,293 名患者在妊娠期间接受了阿达木单抗治疗(末次月经前的平均疾病病程:8.6 年),导致 300 次妊娠结局。197 次妊娠(67.2%)是根据医生的决定在所有孕期都接受了阿达木单抗治疗。在已知报告的结局中(96.3%),81.7%(236/289)为活产,10.4%(30/289)为自然流产,4.8%(14/289)为选择性终止妊娠,2.8%(8/289)为异位妊娠,0.3%(1/289)为死胎。1 例婴儿报告有先天性畸形(肺动脉瓣狭窄和三尖瓣关闭不全)。除上述妊娠结局外,20 例患者还报告了 23 例妊娠并发症。

结论

这项分析表明,在参与 PYRAMID 注册研究的 CD 患者中,阿达木单抗治疗并未在妊娠期间或对妊娠结局产生额外的不良影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a42/9189454/896d796ceaba/UEG2-10-485-g001.jpg

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