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[不同类型先天性心脏病相关艾森曼格综合征成年患者的临床特征]

[Clinical features of adult patients with Eisenmenger syndrome associated with different types of congenital heart disease].

作者信息

Chen Guo, He Jian-guo, Liu Zhi-hong, Gu Qing, Ni Xin-hai, Zhao Zhi-hui, Xiong Chang-ming

机构信息

Chinese Academy of Medical Sciences, Beijing, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2013 May 28;93(20):1546-9.

PMID:24028720
Abstract

OBJECTIVE

To explore the clinical features and hemodynamics of adult patients with Eisenmenger syndrome in different types of congenital heart diseases (CHD).

METHODS

Patients with Eisenmenger syndrome with different types of CHD diagnosed by right heart catheterization were enrolled from 31 clinical centers in China during the period from May 2007 to October 2010. Age, gender, body mass index (BMI), symptoms and signs, World Health Organization functional class (WHO-FC) of pulmonary hypertension, six-minute walk distance (6MWD) and hemodynamics were recorded. All the above indices were analyzed and compared.

RESULTS

A total of 224 patients with Eisenmenger syndrome with 3 kinds of CHD were enrolled, including atrial septal defect (n = 67), ventricular septal defect (n = 104) and patent ductus arteriosus (n = 53). Among them, there were 67 males (29.9%) and 157 females (70.1%) with a mean age of (29.6 ± 9.9) years (range: 15-63). Mean BMI was (19.9 ± 4.0) kg/m(2) and mean 6MWD (371 ± 75) m. The majority of patients were in WHO-FC II (n = 158, 70.5%) and III (n = 64, 28.6%). Electrocardiogram of 77.2% of them indicated hypertrophic right ventricle. Mean right atrial pressure was (8.9 ± 5.7) mm Hg (1 mm Hg = 0.133 kPa), mean pulmonary arterial pressure (mPAP) (77.2 ± 19.1) mm Hg, cardiac index (3.03 ± 1.35) L·min(-1) · m(-2) and pulmonary vascular resistance (PVR) (1621 ± 887) dyn · s · cm(-5).

CONCLUSIONS

The majority of patients with Eisenmenger syndrome with different types of CHD are young females and ventricular septal defect is the most frequent underlying cause. The deterioration of heart function in patients with Eisenmenger syndrome is non-parallel to mPAP and PVR in CHD.

摘要

目的

探讨不同类型先天性心脏病(CHD)成人艾森曼格综合征患者的临床特征及血流动力学情况。

方法

选取2007年5月至2010年10月期间来自中国31个临床中心的经右心导管检查确诊为不同类型CHD的艾森曼格综合征患者,并记录其年龄、性别、体重指数(BMI)、症状和体征、世界卫生组织肺动脉高压功能分级(WHO-FC)、6分钟步行距离(6MWD)及血流动力学指标。对上述所有指标进行分析比较。

结果

共纳入224例患有3种CHD的艾森曼格综合征患者,包括房间隔缺损(n = 67)、室间隔缺损(n = 104)和动脉导管未闭(n = 53)。其中男性67例(29.9%) ,女性157例(70.1%) ;平均年龄为(29.6±9.9)岁(范围:15 - 63岁) 。平均BMI为(199±4.0)kg/m²,平均6MWD为(371±75)m ;大多数患者处于WHO-FCⅡ级(n = 158,70.5%)和Ⅲ级(n = 64 ,286%) 。772%患者的心电图显示右心室肥厚。平均右心房压力(89±57)mmHg(1 mmHg = 0133 kPa) ,平均肺动脉压(mPAP)(772±191)mmHg ,心脏指数(303±135)L·min⁻¹·m⁻² ,肺血管阻力(PVR)(1621±887)dyn·s·cm⁻⁵ :

结论

不同类型CHD的艾森曼格综合征患者以年轻女性为主,室间隔缺损是最常见病因。艾森曼格综合征患者的心功能恶化情况与CHD中的mPAP和PVR不平行。

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