Factor Information
Data ID 707
Factor mean pulmonary arterial pressure(mPAP)
Description N/A
Biomarker NA
Classification E11 (physiological factor - physical sign)
Association
Application prognosis
Objective APAH-CHD
p Value 0.015
Conclusion Patients with Eisenmenger syndrome showed higher mPAP.
Risk Factor unknown
CHD Type
ID 477
CHD Type isolated CHD
CHD Subtype CHD with PAH/EA
Reference
PMID 28966315
Year 2017
Title Prognostic Value of Pulmonary Artery Compliance in Patients with Pulmonary Arterial Hypertension Associated with Adult Congenital Heart Disease
Sample
Population adult
Source data
Region China, Beijing
Method T-test and analysis of variance
Race Asian
Disease History N/A
Treatment History cardiac operation
Group Eisenmenger syndrome(Treatment) PAH with small defects; PAH after defect correction(Control)
Number 112 20(PAH with small defects), 43(PAH after defect correction)
Age 29±9 years 32±11 years(PAH with small defects), 26±9 years(PAH after defect correction)
Gender (Male: Female) 33:79 4:16(PAH with small defects); '9:34(PAH after defect correction)
Marker Level 79±18 mmHg 64±20 mmHg (PAH with small defects), 75±27 mmHg (PAH after defect correction)

All rights reserved: Center for Systems Biology, Soochow University