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经皮封堵严重右位脊柱侧弯患儿的大型房间隔缺损:一例报告。

Percutaneous closure of a large atrial septal defect in a child with severe dextroscoliosis: A case report.

作者信息

Linte Adrian, Balanescu Andra Rodica, Onorato Eustaquio, Balanescu Dinu Valentin, Bojinca Violeta Claudia, Drakonaki Elena, Bojinca Mihai, Balanescu Serban Mihai

机构信息

Department of Cardiology, Elias Emergency University Hospital, 'Carol Davila' University of Medicine and Pharmacy, 011461 Bucharest, Romania.

Department of Internal Medicine and Rheumatology, 'Sfanta Maria' Hospital, 'Carol Davila' University of Medicine and Pharmacy, 011172 Bucharest, Romania.

出版信息

Exp Ther Med. 2019 Aug;18(2):972-975. doi: 10.3892/etm.2018.6991. Epub 2018 Nov 19.

Abstract

In this study, we present the case of an 11-year-old child with cachexia, severe dextroscoliosis, pectus carinatum, secondary restrictive pulmonary disease, and an incidental finding of a large ostium secundum atrial septal defect (ASD) that was identified on preoperative assessment for surgical correction of the spinal deformity. Transthoracic and transesophageal echocardiography confirmed significant left-to-right shunting with a pulmonary blood flow to systemic blood flow ratio (Qp/Qs) of 3.18 through a 14 mm defect with good circumferential rims, larger than 5 mm. Despite significant left-to-right shunting, the defect was found prior to the development of pulmonary hypertension or right heart enlargement. The decision to close the atrial septal defect by percutaneous intervention was preferred over surgical closure, due to the restrictive pulmonary physiology and low body mass index (12.6 kg/m). Percutaneous closure of the ASD was successfully performed under general anesthesia using an Occlutech Figulla Flex II ASD device, with no residual shunt. Surgical correction of the dextroscoliosis was subsequently performed with good results. A comprehensive clinical and echocardiographic evaluation is needed in patients with skeletal abnormalities in order to rule out associated congenital heart defects, which may impose therapeutic challenges.

摘要

在本研究中,我们报告了一例11岁儿童的病例,该患儿患有恶病质、严重右旋脊柱侧弯、鸡胸、继发性限制性肺病,在术前评估脊柱畸形手术矫正时偶然发现一个大型继发孔房间隔缺损(ASD)。经胸和经食管超声心动图证实存在显著的左向右分流,通过一个14毫米的缺损,肺血流量与体循环血流量之比(Qp/Qs)为3.18,缺损边缘良好,大于5毫米。尽管存在显著的左向右分流,但在肺动脉高压或右心扩大之前就发现了该缺损。由于存在限制性肺生理和低体重指数(12.6 kg/m²),经皮介入关闭房间隔缺损的决定优于手术关闭。在全身麻醉下使用Occlutech Figulla Flex II ASD装置成功进行了经皮ASD封堵,无残余分流。随后进行了右旋脊柱侧弯的手术矫正,效果良好。对于骨骼异常的患者,需要进行全面的临床和超声心动图评估,以排除相关的先天性心脏缺陷,因为这些缺陷可能带来治疗挑战。

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1
Current Concepts - Congenital Scoliosis.当前概念——先天性脊柱侧凸
Open Orthop J. 2017 Apr 28;11:337-345. doi: 10.2174/1874325001711010337. eCollection 2017.
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Atrial septal defect closure.房间隔缺损封堵术。
Cardiol Clin. 2013 Aug;31(3):385-400. doi: 10.1016/j.ccl.2013.05.003.
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Congenital spinal deformity: a comprehensive assessment at presentation.先天性脊柱畸形:就诊时的综合评估
Spine (Phila Pa 1976). 2002 Oct 15;27(20):2255-9. doi: 10.1097/00007632-200210150-00014.

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