Alejandro Narváez Orozco, Alberto Navarro Navajas, Carolina Cardona Buitrago, Emilio Herrera Céspedes, Juan Camilo Ortiz Uribe, Juan Andrés Delgado Restrepo, Juan Manuel Senior Sánchez, Jairo Alfonso Gándara Ricardo, Edison Muñoz Ortiz
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引用次数: 0
摘要
目标孕妇可能患有先天性心脏病(CHD)。尽管在导管室进行心脏介入治疗被认为是安全有效的,但最好在分娩后 3-6 个月再进行简单、无并发症的先天性心脏病矫治;然而,这可能会导致随访损失。本文旨在介绍我们在产后早期(EP)矫正先天性心脏病的经验:收集2017-2023年间所有在产褥期接受经皮缺损矫治的CHD孕妇病例,包括房间隔缺损(ASD)、动脉导管未闭(PDA)和主动脉瓣狭窄(CoA):共纳入15名孕妇,诊断为ASD(5名)、PDA(6名)和CoA(4名)。5名患者(33.3%)被列为WHO IV级风险;80%的病例手术成功,只有1名患者出现并发症:根据我们的经验,在 EP 期间闭合无并发症的先天性缺陷不会出现重大并发症,可以作为一种治疗策略,防止患有先天性心脏病的孕妇在分娩后出现随访损失。
[Percutaneous correction of structural congenital heart diseases during the early puerperium. Experience of a center].
Objetive: Congenital heart diseases (CHD) can be found in pregnant women. Although cardiac interventions in the catheterization laboratory are considered safe and effective, it is preferable to wait 3-6 months after delivery to correct simple, uncomplicated CHD; however, this may result in follow-up losses. The objective is to present our experience in correcting CHD during the early puerperium (EP).
Materials and methods: All cases of pregnant women with CHD, including atrial septal defect (ASD), patent ductus arteriosus (PDA), and aortic coarctation (CoA) between 2017-2023, who underwent percutaneous defect correction during the EP were collected.
Results: Fifteen pregnant women were included, diagnosed with ASD (5), PDA (6), and CoA (4). Five patients (33.3%) were classified as WHO risk class IV; the procedure was successful in 80% of the cases, and only 1 patient presented complications.
Conclusions: In our experience, the closure of uncomplicated congenital defects during the EP did not present major complications and could be a treatment strategy to prevent follow-up losses after delivery in pregnant women with CHD.