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Management of Pregnancy in Patients With Complex Congenital Heart Disease: A Scientific Statement for Healthcare Professionals From the American Heart Association.患有复杂先天性心脏病的孕妇管理:美国心脏协会为医疗保健专业人员提供的科学声明。
Circulation. 2017 Feb 21;135(8):e50-e87. doi: 10.1161/CIR.0000000000000458. Epub 2017 Jan 12.
2
Echocardiographic Follow-Up of Patent Foramen Ovale and the Factors Affecting Spontaneous Closure.卵圆孔未闭的超声心动图随访及影响自然闭合的因素
Acta Cardiol Sin. 2016 Nov;32(6):731-737. doi: 10.6515/acs20160205a.
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A review of spontaneous closure of ventricular septal defect.室间隔缺损自然闭合的综述。
Proc (Bayl Univ Med Cent). 2015 Oct;28(4):516-20. doi: 10.1080/08998280.2015.11929329.
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Factors influencing the spontaneous closure of ventricular septal defect in infants.影响婴儿室间隔缺损自然闭合的因素。
Int J Clin Exp Pathol. 2015 May 1;8(5):5614-23. eCollection 2015.
5
Diagnostic yield of pelvic magnetic resonance venography in patients with cryptogenic stroke and patent foramen ovale.隐匿性卒中伴卵圆孔未闭患者行盆腔磁共振静脉血管成像的诊断率。
Stroke. 2014 Aug;45(8):2324-9. doi: 10.1161/STROKEAHA.114.005539. Epub 2014 Jun 17.
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Temporal trends in survival among infants with critical congenital heart defects.危重新生儿先天性心脏病患者的生存时间趋势。
Pediatrics. 2013 May;131(5):e1502-8. doi: 10.1542/peds.2012-3435. Epub 2013 Apr 22.
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Patterns of cardiac and extracardiac anomalies in adults with tetralogy of fallot.法洛四联症成年患者的心脏和心脏外畸形模式。
Am Heart J. 2011 Jan;161(1):131-7. doi: 10.1016/j.ahj.2010.09.015.
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20-year survival of children born with congenital anomalies: a population-based study.先天性畸形患儿 20 年生存状况:一项基于人群的研究。
Lancet. 2010 Feb 20;375(9715):649-56. doi: 10.1016/S0140-6736(09)61922-X. Epub 2010 Jan 19.
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Atrial and ventricular septal defects - epidemiology and spontaneous closure.房间隔和室间隔缺损——流行病学与自然闭合
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Patent foramen ovale: current pathology, pathophysiology, and clinical status.卵圆孔未闭:当前的病理学、病理生理学及临床状况
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探讨中国新生儿持续性卵圆孔未闭或动脉导管未闭的超声心动图特征及预测因素。

Investigation of echocardiographic characteristics and predictors for persistent defects of patent foramen ovale or patent ductus arteriosus in Chinese newborns.

机构信息

Department of Cardiology, Xiamen ChangGung Hospital, Xiamen, Fujian, China.

Division of Cardiology, Department of Pediatrics, Chang Gung Memorial Hospital at Linkou, Taoyuan, Taiwan; College of Medicine, Chang Gung University, Taoyuan, Taiwan.

出版信息

Biomed J. 2021 Apr;44(2):209-216. doi: 10.1016/j.bj.2019.12.007. Epub 2021 Apr 15.

DOI:10.1016/j.bj.2019.12.007
PMID:33867286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8178580/
Abstract

BACKGROUND

Persistent patent foramen ovale (PFO) and patent ductus arteriosus (PDA) increase the adult risk of cryptogenic embolic stroke and chronic pulmonary hypertension. To understand the characteristics of PFO and PDA in newborns, we investigated the spontaneous closure rate and derived the determinants for residual defects.

METHODS

We utilized the database of congenital heart disease (CHD) in Xiamen ChangGung Memorial Hospital from 2015 to 2017 and allocated 2523 eligible newborns into four groups according to PDA, PFO, both or neither at birth. A total of 574, 1229, 202 and 518 newborns were assigned into the group of PFO and PDA, PFO alone, PDA alone and non-PFO/non-PDA, respectively. Regular echocardiographic follow-ups at baseline, 6, 12 and 24 months after birth were performed for evaluating the spontaneous closure rate in the subjects. Regression analysis was carried out to study the risk factors of residual congenital defects.

RESULTS

Newborns with PFO alone had the youngest birth age and lowest birth weight among the four groups. About one in four PDA-alone newborns had concomitant small ASD, i.e., <5 mm in diameter. Echocardiographic study showed that 71.3% and 30.8% of CHD newborns had PFO and PDA, respectively, compared to less than 10% of them having ASD or VSD. However, more than 95% of newborns with PFO or PDA closed spontaneously at 6 months, in contrast to about 30% of newborns with ASD or VSD had persistent existence of the intracardiac defects. Complex CHD significantly linked to persistent PFO or PDA at 6 and 12 months, with an adjusted hazard ratio of 9.03 (95% CI 1.97-41.46) and 12.11 (95% CI 2.11-69.72), respectively.

CONCLUSIONS

Chinese newborns with PFO or PDA expressed differences in characteristics and concomitant congenital defects. Additionally, persistent PFO or PDA is strongly associated with complex CHD and requires long-term regular monitoring for future associated complications.

摘要

背景

持续性卵圆孔未闭(PFO)和动脉导管未闭(PDA)会增加成人隐源性栓塞性中风和慢性肺动脉高压的风险。为了了解新生儿 PFO 和 PDA 的特征,我们研究了其自然闭合率,并得出了残余缺陷的决定因素。

方法

我们利用 2015 年至 2017 年厦门长庚纪念医院先天性心脏病(CHD)数据库,根据出生时是否存在 PDA、PFO、两者或两者均无,将 2523 名符合条件的新生儿分为四组。共有 574、1229、202 和 518 名新生儿分别被分配到 PFO 和 PDA 组、PFO 组、PDA 组和非 PFO/非 PDA 组。在出生后基线、6、12 和 24 个月时进行常规超声心动图随访,以评估受试者的自然闭合率。回归分析用于研究残余先天性缺陷的危险因素。

结果

单独存在 PFO 的新生儿在四组中出生年龄最小,出生体重最低。大约四分之一的单独存在 PDA 的新生儿同时存在小的 ASD,即直径<5mm。超声心动图研究显示,71.3%和 30.8%的 CHD 新生儿存在 PFO 和 PDA,而 ASD 或 VSD 的比例不到 10%。然而,超过 95%的 PFO 或 PDA 新生儿在 6 个月时自然闭合,而大约 30%的 ASD 或 VSD 新生儿存在持续性心脏内缺陷。复杂的 CHD 与 6 个月和 12 个月时持续存在的 PFO 或 PDA 显著相关,调整后的危险比分别为 9.03(95%CI 1.97-41.46)和 12.11(95%CI 2.11-69.72)。

结论

中国新生儿的 PFO 或 PDA 在特征和伴发先天性缺陷方面存在差异。此外,持续性 PFO 或 PDA 与复杂的 CHD 密切相关,需要长期定期监测以预防未来的相关并发症。