Department of Obstetrics and Gynaecology, Jawaharlal Institute of Post Graduate Medical Education and Research (JIPMER), Puducherry, India.
Department of Cardiology, JIPMER, Puducherry, India.
J Obstet Gynaecol. 2022 May;42(4):594-596. doi: 10.1080/01443615.2021.1932777. Epub 2021 Aug 18.
Pregnancy complicated with uncorrected Ebstein's anomaly is uncommon and may pose a serious threat to maternal and foetal life in the clinical setting of altered hemodynamics of pregnancy. Data of eight pregnancies in four women with Ebstein's anomaly who delivered in a tertiary care institute was analysed. Among the four women, one had associated atrial septal defect, one had pulmonary hypertension and three had right bundle branch block. There were two miscarriages and six successful pregnancies resulting in live births. Three of the pregnancies were delivered by caesarean section. There was one pregnancy complicated by severe preeclampsia, no preterm births or maternal cardiac complications. There was one neonate with congenital ostium secundum atrial septal defect. All patients were managed by a multidisciplinary team involving Obstetrician, Cardiologist, Anaesthesiologist and Neonatologist.IMPACT STATEMENT Ebstein's anomaly is a rare congenital anomaly with apical displacement of the septal tricuspid leaflet in association with leaflet dysplasia. It may cause varied presentation in pregnancy depending on the severity of the lesion. Ebstein's anomaly may become symptomatic for the first-time during pregnancy. Patients with NYHA class II symptoms and no cyanosis generally tolerate pregnancy well. Miscarriages and intrauterine growth restriction may occur in the presence of this condition. Vaginal delivery is advised and caesarean is done only for obstetric indications. The management of pregnancy with uncorrected Ebstein's anomaly is highly challenging especially in a low resource setting and requires tertiary centre care. Multidisciplinary team involvement can help to improve the outcomes in such pregnancies.
妊娠合并未经矫正的埃布斯坦畸形并不常见,但在妊娠血液动力学改变的临床情况下,可能对母婴生命构成严重威胁。分析了在一家三级保健机构分娩的 4 名女性中的 8 例埃布斯坦畸形妊娠的数据。在这 4 名女性中,1 名合并房间隔缺损,1 名患有肺动脉高压,3 名患有右束支传导阻滞。有 2 例流产和 6 例成功妊娠导致活产。其中 3 例经剖宫产分娩。有 1 例妊娠合并严重子痫前期,无早产或母体心脏并发症。有 1 例新生儿患有先天性继发孔房间隔缺损。所有患者均由产科医生、心脏病专家、麻醉师和新生儿科医生组成的多学科团队管理。
埃布斯坦畸形是一种罕见的先天性畸形,三尖瓣隔瓣的顶端移位与瓣叶发育不良有关。它可能会根据病变的严重程度在妊娠期间引起不同的表现。埃布斯坦畸形可能会在妊娠期间首次出现症状。NYHA 心功能分级 II 级且无发绀的患者一般能很好地耐受妊娠。这种情况下可能会发生流产和宫内生长受限。建议阴道分娩,仅在产科指征下行剖宫产。未经矫正的埃布斯坦畸形妊娠的管理极具挑战性,特别是在资源匮乏的环境中,需要三级中心护理。多学科团队的参与可以帮助改善此类妊娠的结局。