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房室(AV)管缺损患儿肺动脉高压风险的对比分析:一项多中心研究。

A comparative analysis on risk of pulmonary hypertension in children with Atrio-ventricular (AV) canal defect: a multi-centre study.

机构信息

College of Medicine, Department of pediatrics, University of Nigeria/ University of Nigeria Teaching Hospital (UNTH), Ituku- Ozalla, Enugu State, Nigeria.

Senior Lecturer, Department of Paediatrics and Child health.

出版信息

Afr Health Sci. 2022 Mar;22(1):220-226. doi: 10.4314/ahs.v22i1.28.

DOI:10.4314/ahs.v22i1.28
PMID:36032495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9382489/
Abstract

OBJECTIVES

This study is aimed at determining the risk of pulmonary hypertension in children with AV canal defect when compared with children with other congenital heart disease.

METHODS

A descriptive study carried out in three institutions over a six-year period among children who presented with AV canal defect and their controls who presented with other congenital heart defects.

RESULTS

A large proportion of the children with AV canal (77.5%) had pulmonary hypertension. Among the patients with pulmonary hypertension, 45.2% were males compared 54.8% females (χ2 = 3.2, p = 0.2). There was a positive correlation between pulmonary hypertension and size of VSD and ASD, although the correlation was not significant (Pearson correlation coefficient = 0.01 and 0.4, p = 0.9 and 0.1 respectively). Children with AV canal defect had higher odds of developing most clinical symptoms and pulmonary hypertension than children with other congenital heart disease and this is statistically significant.

CONCLUSION

Majority of children with AV canal defect presented with pulmonary hypertension. These children present with higher odds of having pulmonary hypertension and clinical symptoms than children with other types of congenital heart disease.

摘要

目的

本研究旨在比较房室管缺损与其他先天性心脏病患儿的肺动脉高压风险。

方法

这是一项为期六年在三家机构进行的描述性研究,研究对象为患有房室管缺损的儿童及其对照组(患有其他先天性心脏病的儿童)。

结果

很大一部分房室管缺损(77.5%)的儿童存在肺动脉高压。在肺动脉高压患者中,男性占 45.2%,女性占 54.8%(χ2 = 3.2,p = 0.02)。尽管相关性不显著(Pearson 相关系数分别为 0.01 和 0.4,p 值分别为 0.9 和 0.1),但肺动脉高压与 VSD 和 ASD 的大小呈正相关。与其他先天性心脏病患儿相比,房室管缺损患儿出现大多数临床症状和肺动脉高压的可能性更高,这具有统计学意义。

结论

大多数房室管缺损患儿存在肺动脉高压。与其他类型的先天性心脏病患儿相比,这些患儿出现肺动脉高压和临床症状的可能性更高。

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A comparative analysis on risk of pulmonary hypertension in children with Atrio-ventricular (AV) canal defect: a multi-centre study.房室(AV)管缺损患儿肺动脉高压风险的对比分析:一项多中心研究。
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本文引用的文献

1
Diagnosis of pulmonary hypertension.肺动脉高压的诊断。
Eur Respir J. 2019 Jan 24;53(1). doi: 10.1183/13993003.01904-2018. Print 2019 Jan.
2
Atrial septal defects and pulmonary arterial hypertension.房间隔缺损与肺动脉高压。
J Thorac Dis. 2018 Sep;10(Suppl 24):S2953-S2965. doi: 10.21037/jtd.2018.08.92.
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Pulmonary Hypertension and Congenital Heart Disease.肺动脉高压与先天性心脏病
Cardiol Clin. 2016 Aug;34(3):391-400. doi: 10.1016/j.ccl.2016.04.002.
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Shape of the Pulmonary Artery Doppler-Flow Profile Predicts the Hemodynamics of Pulmonary Hypertension Caused by Left-Sided Heart Disease.肺动脉多普勒血流频谱形态可预测左心疾病所致肺动脉高压的血流动力学情况。
Clin Cardiol. 2016 Mar;39(3):150-6. doi: 10.1002/clc.22493.
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Nutritional status of congenital heart disease (CHD) patients: Burden and determinant of malnutrition at university of Nigeria teaching hospital Ituku - Ozalla, Enugu.先天性心脏病(CHD)患者的营养状况:尼日利亚大学教学医院(位于埃努古伊图库-奥扎拉)营养不良的负担及决定因素
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The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome.唐氏综合征先天性心脏缺陷风险增加的复杂 SNP 和 CNV 遗传结构。
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Survival in childhood pulmonary arterial hypertension: insights from the registry to evaluate early and long-term pulmonary arterial hypertension disease management.儿童肺动脉高压的生存状况:来自登记处评估早期和长期肺动脉高压疾病管理的见解。
Circulation. 2012 Jan 3;125(1):113-22. doi: 10.1161/CIRCULATIONAHA.111.026591. Epub 2011 Nov 15.
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Failure to thrive: an update.发育不良:最新研究进展。
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Updated clinical classification of pulmonary hypertension.肺动脉高压的更新临床分类。
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