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经导管封堵遗传性球形红细胞增多症患儿的房间隔缺损

Transcatheter Closing Atrial Septal Defect in a Child With Hereditary Spherocytosis.

作者信息

Ji Zhixian, Liu Na, Du Zhanhui, Luo Gang, Bing Zhen, Xing Quansheng, Pan Silin

机构信息

Heart Center, Qingdao Women and Children's Hospital, Qingdao University, Qingdao, China.

出版信息

Front Pediatr. 2019 Dec 17;7:506. doi: 10.3389/fped.2019.00506. eCollection 2019.

DOI:10.3389/fped.2019.00506
PMID:31921720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6929411/
Abstract

A 3-year-old girl was admitted to our hospital for the correction of atrial septal defect (ASD). Open heart operation with cardiopulmonary bypass is dangerous because the patient also had hereditary spherocytosis, which put her at risk for hemolytic anemia. Therefore, percutaneous transcatheter closure for ASD was chosen and performed successfully, which avoided the erythrocyte damage caused by cardiopulmonary bypass. This is the first time such a case has been reported, and we present an alternative approach for ASD with hereditary spherocytosis.

摘要

一名3岁女孩因房间隔缺损(ASD)矫正术入住我院。由于该患者还患有遗传性球形红细胞增多症,存在溶血性贫血风险,因此在体外循环下进行心脏直视手术具有危险性。所以,选择并成功实施了经皮导管封堵术治疗房间隔缺损,避免了体外循环造成的红细胞损伤。这是首次报道此类病例,我们为患有遗传性球形红细胞增多症的房间隔缺损患者提供了一种替代治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdd/6929411/2442d8a06151/fped-07-00506-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdd/6929411/2c53231d77a6/fped-07-00506-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdd/6929411/2442d8a06151/fped-07-00506-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdd/6929411/2c53231d77a6/fped-07-00506-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdd/6929411/2442d8a06151/fped-07-00506-g0002.jpg

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BMC Pediatr. 2021 Jun 28;21(1):291. doi: 10.1186/s12887-021-02771-4.

本文引用的文献

1
Atrial Septal Defects Accelerate Pulmonary Hypertension Diagnoses in Premature Infants.房间隔缺损会加速早产儿肺动脉高压的诊断。
Front Pediatr. 2018 Nov 23;6:342. doi: 10.3389/fped.2018.00342. eCollection 2018.
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Echocardiography guidance of atrial septal defect closure.超声心动图引导下房间隔缺损封堵术
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Open-heart surgery using a centrifugal pump: a case of hereditary spherocytosis.使用离心泵的心脏直视手术:一例遗传性球形红细胞增多症病例
J Cardiothorac Surg. 2016 Aug 26;11(1):138. doi: 10.1186/s13019-016-0534-8.
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Hereditary spherocytosis in children: profile and post-splenectomy outcome.儿童遗传性球形红细胞增多症:概况及脾切除术后结局
Indian Pediatr. 2014 Feb;51(2):139-41. doi: 10.1007/s13312-014-0348-5.
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Transcatheter Atrial Septal Defect Closure under Transthorasic Echocardiography in Children.经胸超声心动图引导下儿童房间隔缺损封堵术
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Hereditary spherocytosis.遗传性球形红细胞增多症
Lancet. 2008 Oct 18;372(9647):1411-26. doi: 10.1016/S0140-6736(08)61588-3.
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Non-compaction cardiomyopathy in an adult with hereditary spherocytosis.一名患有遗传性球形红细胞增多症的成年人的致密化不全型心肌病。
Eur J Heart Fail. 2007 Jan;9(1):98-9. doi: 10.1016/j.ejheart.2006.03.008. Epub 2006 May 30.
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Guidelines for the diagnosis and management of hereditary spherocytosis.遗传性球形红细胞增多症的诊断与管理指南。
Br J Haematol. 2004 Aug;126(4):455-74. doi: 10.1111/j.1365-2141.2004.05052.x.
9
Transcatheter closure of atrial septal defect in young children: results and follow-up.小儿房间隔缺损的经导管封堵术:结果与随访
J Am Coll Cardiol. 2003 Jul 16;42(2):241-5. doi: 10.1016/s0735-1097(03)00589-8.
10
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