Otis Anne-Sophie, Brochet Marie-Sophie, Tremblay Zoë, Balayla Jacques, Dahdouh Elias M
Department of Pharmacy, CHU Sainte-Justine, Montreal, Quebec, Canada.
Faculty of Pharmacy, Université de Montréal, Montreal, Quebec, Canada.
Birth Defects Res. 2025 Mar;117(3):e2464. doi: 10.1002/bdr2.2464.
Lack of available expert guidelines leads clinicians to interrupt cabergoline treatment upon confirmation of pregnancy and consider switching to bromocriptine, which is more commonly used during pregnancy but is poorly tolerated.
The objective of this review was to evaluate pregnancy outcomes, primarily major malformations and spontaneous abortions, after pregnancy exposure to cabergoline during the first trimester compared to pregnancy exposure to other comparators or no treatment.
An Embase, Pubmed, Google Scholar, and ClinicalTrials.gov search was performed. Full articles published before October 27, 2022, and evaluating the effect of cabergoline on major malformations and spontaneous abortions were considered for inclusion in the review. Search results were manually screened and selected by two independent reviewers.
Totally, 2186 records were identified. After removal of duplicates and screening of abstracts, 65 full-text articles were consulted. Thirty articles corresponded to our selection criteria and were included in the systematic review. This review identified 1662 pregnancies exposed to cabergoline. Most studies did not find an increased risk of congenital malformations or spontaneous abortions with cabergoline compared to other comparators or no treatment. Overall study quality was low, and there was high heterogeneity between studies.
This review revealed no negative impact on major malformations and spontaneous abortions of cabergoline use in pregnancy compared to other comparators or no treatment. However, additional high-quality studies are needed to further study the safety of cabergoline use during pregnancy.
PROSPERO, CRD42021256219 (October 19, 2021).
由于缺乏可用的专家指南,临床医生在确认妊娠后会中断卡麦角林治疗,并考虑改用溴隐亭,溴隐亭在孕期使用更为普遍,但耐受性较差。
本综述的目的是评估与孕期暴露于其他对照药物或未接受治疗相比,孕早期暴露于卡麦角林后的妊娠结局,主要是严重畸形和自然流产。
进行了Embase、Pubmed、谷歌学术和ClinicalTrials.gov搜索。纳入综述的文章需为2022年10月27日前发表的全文文章,且评估了卡麦角林对严重畸形和自然流产的影响。两名独立评审员对搜索结果进行人工筛选和选择。
共识别出2186条记录。在去除重复记录并筛选摘要后,查阅了65篇全文文章。30篇文章符合我们的选择标准,被纳入系统评价。本综述确定了1662例暴露于卡麦角林的妊娠。大多数研究未发现与其他对照药物或未接受治疗相比,卡麦角林会增加先天性畸形或自然流产的风险。总体研究质量较低,研究之间存在高度异质性。
本综述显示,与其他对照药物或未接受治疗相比,孕期使用卡麦角林对严重畸形和自然流产没有负面影响。然而,需要更多高质量的研究来进一步探讨孕期使用卡麦角林的安全性。
PROSPERO,CRD42021256219(2021年10月19日)。