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首页> 外文期刊>International Journal of Cardiology >Acute effect of sildenafil on hypoxemic patients (excluding those with Eisenmenger syndrome) with incurable congenital heart disease and disturbed pulmonary vasculature in the mid-term follow-up.
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Acute effect of sildenafil on hypoxemic patients (excluding those with Eisenmenger syndrome) with incurable congenital heart disease and disturbed pulmonary vasculature in the mid-term follow-up.

机译:西地那非对中期随访中的低氧血症患者(不包括艾森曼格综合征的患者)的先天性心脏病和肺血管疾病的治疗。

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摘要

Cyanotic patients associated with complex heart disease, which is incurable due to disturbed pulmonary vasculature, are complicated with functional impairment and various systemic disorders in the long-term [1]. Phosphodiesterase (PDE) type 5 inhibitors improve oxygen saturation in patients with Eisenmenger syndrome or in patients with interstitial lung fibrosis [2,3]- Management ofhypox-emic CHD patients, who were not indicated for further corrective surgery due to inappropriate pulmonary vasculature other than typical pulmonary arterial hypertension, is an evolving issue in developed countries with few new cases of Eisenmenger syndrome. We hereby report our initial observations regarding the acute effects of sildenafil on oxygen saturation in hypoxemic CHD patients, excluding those with Eisenmenger syndrome, who are accompanied by inappropriate pulmonary vascular bed in univentricular physiology after cavopulmonary connection or severely hypoplastic pulmonary artery in tetralogy-like biventricular physiology, in the early and mid-term follow-up period.
机译:长期因伴发复杂心血管疾病而无法治愈的青紫病患者因肺血管系统紊乱而无法治愈,其并发功能受损和各种全身性疾病[1]。磷酸二酯酶(PDE)5型抑制剂可改善艾森曼格综合征或间质性肺纤维化患者的血氧饱和度[2,3]-低氧血症型CHD患者的治疗,由于除肺血管异常外,其他患者均不宜进行进一步的矫正手术在发达国家,艾森曼格综合征新病例很少,典型的肺动脉高压是一个正在发展的问题。我们在此报告关于西地那非对低氧性CHD患者(包括艾森曼格综合征的患者)的氧饱和度的急性影响的初步观察结果,艾森曼格综合征不伴有心肺连接后单心室生理性肺血管床不适或四联征状双室严重肺发育不良生理学,在早期和中期的随访期。

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