Background: Pulmonary artery thrombosis is common in Eisenmenger syndrome, although its underlying pathophysiology is poorly understood.
背景：肺动脉血栓形成在艾森·曼格综合征中很常见，但其病理生理机制目前还不十分清楚。
Tardive cyanosis caused by some congenital heart diseases must be carefully diagnosed for the similarity to that of Eisenmenger syndrome.
某些迟发性紫绀的先天性心脏病与艾森·门格综合征较难鉴别，诊断务必谨慎。
All CHD patients were divided into the following five subgroups: normal pulmonary pressure, mild dynamic PH, moderate dynamic PH, severe dynamic PH and Eisenmenger syndrome.
先心组分为正常肺压、动力型轻度PH、动力型中度PH、动力型重度PH及梗阻型PH五个亚组。
Objective To evaluate the operative technique, perioperative management and ontcome of single lung transplantation and ventricular septal defect repair for Eisenmenger syndrome.
目的探讨同种异体单肺移植同期行心内缺损修补治疗先天性心脏病室间隔缺损并艾森曼格综合征的可行性及围手术期的处理。
Objective To evaluate the operative technique, perioperative management and ontcome of single lung transplantation and ventricular septal defect repair for Eisenmenger syndrome.
目的探讨同种异体单肺移植同期行心内缺损修补治疗先天性心脏病室间隔缺损并艾森曼格综合征的可行性及围手术期的处理。
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