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PAH-CHD predominantly Lt-Rt shunt with borderline PVR and ES

Completed
Conditions
Data of outcomes in patients who had PAH-CHD (confirmed by dignostic cardiac catheterization) with borderline pulmonary vascular resistance (PVR) and recieved directed targeted therapy prior to surgic
Pulmonary arterial hypertension, Congenital heart disease, treat and repair
Registration Number
TCTR20200420004
Lead Sponsor
Faculty of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
432
Inclusion Criteria

1.Patients who underwent cardiac catheterization to assess hemodynamic data or transcatheter closure of the defects in Siriraj Hospital between January 1st, 1995 and December 31st, 2021
2.All patients who had evidence of PAH-CHD on the cardiac catheterization including mPAP >20 mmHg, PAWP < 15 mmHg and calculated PVR > 3 WU based on a current definition of PAH
3.Patients who were classified in Eisenmenger syndrome and PAH-CHD with prevalent left to right shunt

Exclusion Criteria

1.Patients who had age < 3 months,
2.Patients with single ventricle following surgery
3.Patients who were classified in PAH with small defect and PAH following defect correction

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Survival rate/mortality End of 2023 Survival rate
Secondary Outcome Measures
NameTimeMethod
WHO Functional class end of 2023 Declined of functional class to III-IV
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