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孤立性卵圆孔限制的胎儿临床特征及超声心动图表现。

Clinical features and echocardiographic findings of isolated foramen ovale restriction in foetuses.

机构信息

Faculty of Medicine, Deparment of Pediatric Cardiology, Çukurova University, Adana, Turkey.

Faculty of Medicine, Deparment of Neonatology, Çukurova University, Adana, Turkey.

出版信息

J Obstet Gynaecol. 2022 Jul;42(5):946-950. doi: 10.1080/01443615.2021.1962822. Epub 2021 Oct 27.

Abstract

Isolated restrictive foramen ovale (rFO) without complex heart defects is a rare pathology. There may be difficulties in managing this situation, which can lead to right heart enlargement, tricuspid regurgitation and hydrops findings in the foetus. We conducted a retrospective analysis of 8451 foetuses. 7883 (93.2%) had a structurally normal heart or minor heart disease, 18 (0.22%) of which had a diagnosis of isolated rFO. Nine patients with neonatal echocardiographic examination were included in the study. In 8 (88.8%) patients, it was stated that a decision to give birth should be made at the time of presentation. Evaluating postpartum echocardiographic examinations, 7 (77.7%) patients had normal or minor defects. The decision of delivery made at the right time during follow-up is critical to determine the prognosis.IMPACT STATEMENT The data about the prenatal diagnosis of isolated rFO is limited. We conducted a retrospective analysis of 8451 foetuses. 7883 (93.2%) foetuses had a structurally normal heart or minor heart disease, 18 (0.22%) of which had a diagnosis of rFO. Nıne patients with foetal and postnatal follow-up and echocardiographic findings were examined in the study. The group's median gestational age at admission was 35.0 weeks (range: 27.0-39.0 weeks). The delivery decision was made in 8 (88.8%) patients at the time of admission. Evaluating postpartum echocardiographic examinations, 7 (77.7%) patients had normal or minor defects. Additionally, one patient was diagnosed with cardiomyopathy, and the other patient was diagnosed with functional pulmonary atresia. No death occurred in any foetus during follow-up. Isolated rFO, a rare condition in the foetus, is generally well-tolerated in foetal life. However, the right heart enlargement, tricuspid regurgitation, or hydrops findings can be seen in patients. The decision of delivery made at the right time during follow-up is critical to determine the prognosis.

摘要

孤立性房间隔缺损(rFO)而无复杂心脏缺陷是一种罕见的病理情况。处理这种情况可能存在困难,可能导致胎儿右心增大、三尖瓣反流和水肿。我们对 8451 例胎儿进行了回顾性分析。7883 例(93.2%)心脏结构正常或存在轻微心脏病,其中 18 例(0.22%)诊断为孤立性 rFO。本研究纳入了 18 例新生儿超声心动图检查的患者。其中 9 例患者进行了研究。在 8 例(88.8%)患者中,认为在就诊时应做出分娩决定。评估产后超声心动图检查,7 例(77.7%)患者心脏正常或存在轻微缺陷。在随访过程中及时做出分娩决定对确定预后至关重要。

孤立性房间隔缺损(rFO)在胎儿中是一种罕见的疾病,通常在胎儿期可以耐受。然而,在患者中可能会出现右心增大、三尖瓣反流或水肿。在随访过程中及时做出分娩决定对确定预后至关重要。

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