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本文引用的文献

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Sex Hormones across the Menstrual Cycle in Pulmonary Arterial Hypertension: Adding a New Layer of Complexity.肺动脉高压患者月经周期中的性激素:增添新的复杂层面
Ann Am Thorac Soc. 2021 Feb;18(2):209-211. doi: 10.1513/AnnalsATS.202011-1379ED.
2
Gender differences in pulmonary arterial hypertension patients with BMPR2 mutation: a meta-analysis.BMPR2 基因突变的肺动脉高压患者的性别差异:一项荟萃分析。
Respir Res. 2020 Feb 6;21(1):44. doi: 10.1186/s12931-020-1309-2.
3
The revised definition of pulmonary hypertension: exploring the impact on patient management.肺动脉高压的修订定义:探索对患者管理的影响。
Eur Heart J Suppl. 2019 Dec;21(Suppl K):K4-K8. doi: 10.1093/eurheartj/suz211. Epub 2019 Dec 17.
4
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.
5
Atrial septal defect with pulmonary hypertension: when/how can we consider closure?房间隔缺损合并肺动脉高压:我们何时/如何考虑封堵治疗?
J Thorac Dis. 2018 Sep;10(Suppl 24):S2890-S2898. doi: 10.21037/jtd.2018.07.112.
6
Pulmonary Arterial Hypertension Complicating Congenital Heart Disease: Advances in Therapy.先天性心脏病合并肺动脉高压:治疗进展
Semin Respir Crit Care Med. 2017 Oct;38(5):636-650. doi: 10.1055/s-0037-1606222. Epub 2017 Oct 15.
7
2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: The Joint Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT).2015年欧洲心脏病学会(ESC)/欧洲呼吸学会(ERS)肺动脉高压诊断和治疗指南:欧洲心脏病学会(ESC)和欧洲呼吸学会(ERS)肺动脉高压诊断和治疗联合工作组:得到以下组织认可:欧洲儿科和先天性心脏病协会(AEPC)、国际心肺移植学会(ISHLT)。
Eur Heart J. 2016 Jan 1;37(1):67-119. doi: 10.1093/eurheartj/ehv317. Epub 2015 Aug 29.
8
Guidelines for the Echocardiographic Assessment of Atrial Septal Defect and Patent Foramen Ovale: From the American Society of Echocardiography and Society for Cardiac Angiography and Interventions.房间隔缺损和卵圆孔未闭的超声心动图评估指南:来自美国超声心动图学会和心血管造影与介入学会。
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9
Systolic and mean pulmonary artery pressures: are they interchangeable in patients with pulmonary hypertension?收缩压和肺动脉平均压:在肺动脉高压患者中两者可以互换吗?
Chest. 2015 Apr;147(4):943-950. doi: 10.1378/chest.14-1755.
10
A different view on predictors of pulmonary hypertension in secundum atrial septal defect.继发孔型房间隔缺损肺动脉高压预测因素的不同观点。
Int J Cardiol. 2014 Oct 20;176(3):833-40. doi: 10.1016/j.ijcard.2014.08.009. Epub 2014 Aug 8.

预测房间隔缺损(ASD)患儿肺动脉高压的因素。

Predictors of pulmonary hypertension among children with atrial septal defects (ASD).

机构信息

Professor and Pediatric Cardiologist, 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, Niger Delta University Teaching Hospital, Nigeria.

出版信息

Libyan J Med. 2022 Dec;17(1):2007603. doi: 10.1080/19932820.2021.2007603.

DOI:10.1080/19932820.2021.2007603
PMID:34813403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8635614/
Abstract

INTRODUCTION

Atrial septal defect (ASD) is a common congenital heart disease in children that uncommonly presents with pulmonary hypertension. Much is not known about the exact predictor of PAH in children with ASD.

OBJECTIVES

This study aimed to determine the predictors of pulmonary hypertension in children with ASD.

PATIENTS AND METHODS

This was a descriptive analysis of children with ASD carried out in three different institutions over a five-year period. Data entry and analysis were done using IBM Statistical Package for Social Sciences (SPSS) statistical software, version 25.

RESULTS

The majority of the participants, 52.2%, had pulmonary hypertension and 62.5% of them occurred as mild pulmonary hypertension. There was a very weak positive correlation between pulmonary hypertension and the size of atrial septal defect, increases in size of atrial septal defect correlate with increases in pulmonary hypertension and this was found not to be statistically significant (n = 67, r = 0.193, p = 0.118). There was a positive correlation between the size of atrial septal defect and the age of participants in months, increases in age correlate with increases in size of atrial septal defect and this was found to be statistically significant (n = 67, r = 0.357, p = 0.003).The highest proportion of respondents who had pulmonary hypertension, 64.7%, was seen among children less than 1 year old while the least proportion, 27.3%, was within 1-5 years, and the difference in proportions was found to be statistically significant (χ = 8.187, p = 0.017).

CONCLUSION

Pulmonary hypertension in children with ASD occur usually in the mild form. Age is the only strong predictor of PAH in children with isolated ASD.

摘要

引言

房间隔缺损(ASD)是儿童常见的先天性心脏病,不常见于肺动脉高压。关于 ASD 患儿肺动脉高压的确切预测因素知之甚少。

目的

本研究旨在确定 ASD 患儿肺动脉高压的预测因素。

患者和方法

这是一项在五年内在三个不同机构进行的 ASD 患儿描述性分析。数据录入和分析使用 IBM 统计软件包(SPSS)统计软件,版本 25。

结果

大多数参与者(52.2%)患有肺动脉高压,其中 62.5%为轻度肺动脉高压。肺动脉高压与房间隔缺损大小之间存在非常弱的正相关,房间隔缺损大小的增加与肺动脉高压的增加相关,但无统计学意义(n=67,r=0.193,p=0.118)。房间隔缺损大小与参与者年龄呈正相关,年龄的增加与房间隔缺损大小的增加相关,这具有统计学意义(n=67,r=0.357,p=0.003)。肺动脉高压比例最高的是年龄小于 1 岁的儿童,占 64.7%,而比例最低的是 1-5 岁的儿童,占 27.3%,差异具有统计学意义(χ=8.187,p=0.017)。

结论

ASD 患儿的肺动脉高压通常呈轻度。年龄是 ASD 患儿唯一的肺动脉高压强预测因素。