TCTR20200420004
已完成
不适用
Current era survival of treat and repair congenital systemic to pulmonary shunt with borderline pulmonary vascular disease
Faculty of Medicine0 个研究点目标入组 432 人2020年4月20日
概览
- 阶段
- 不适用
- 干预措施
- 未指定
- 疾病 / 适应症
- 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
- 发起方
- Faculty of Medicine
- 入组人数
- 432
- 状态
- 已完成
- 最后更新
- 去年
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •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
排除标准
- •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
结局指标
主要结局
未指定
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