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慢性西地那非对艾森曼格综合征患者与特发性肺动脉高压患者的影响。

Effects of chronic sildenafil in patients with Eisenmenger syndrome versus idiopathic pulmonary arterial hypertension.

作者信息

Chau Elaine M C, Fan Katherine Y Y, Chow W H

机构信息

Department of Cardiology, Grantham Hospital, 125 Wong Chuk Hang Road, Hong Kong.

出版信息

Int J Cardiol. 2007 Sep 3;120(3):301-5. doi: 10.1016/j.ijcard.2006.10.018. Epub 2006 Dec 14.

Abstract

BACKGROUND

To test the hypothesis that chronic sildenafil treatment has similar functional and hemodynamic effects in patients with severe pulmonary arterial hypertension due to Eisenmenger syndrome as those due to idiopathic pulmonary arterial hypertension without intracardiac shunts.

METHODS

A prospective open-label study was carried out to compare the effects of sildenafil on the pulmonary hemodynamics between two groups of patients with severe pulmonary hypertension and similar baseline functional capacity--Eisenmenger syndrome (ES group) (n=7) versus idiopathic pulmonary arterial hypertension (IPAH group) (n=6).

RESULTS

After 6 months of sildenafil, there was a significant improvement in the functional capacity, the arterial saturation and the pulmonary hemodynamics in the ES group, as shown by significant reduction in the systolic and mean pulmonary artery pressures and the pulmonary vascular resistance.

CONCLUSION

Sildenafil increases pulmonary blood flow and improves cyanosis in patients with Eisenmenger syndrome. Efficacy of sildenafil as treatment for idiopathic pulmonary arterial hypertension may be extended to patients with Eisenmenger syndrome.

摘要

背景

为验证以下假设:对于因艾森曼格综合征导致的重度肺动脉高压患者,慢性使用西地那非治疗所产生的功能和血流动力学效应,与无心脏内分流的特发性肺动脉高压患者相似。

方法

开展一项前瞻性开放标签研究,比较西地那非对两组重度肺动脉高压且基线功能能力相似的患者的肺血流动力学的影响——艾森曼格综合征组(ES组)(n = 7)与特发性肺动脉高压组(IPAH组)(n = 6)。

结果

西地那非治疗6个月后,ES组的功能能力、动脉血氧饱和度和肺血流动力学有显著改善,表现为收缩压和平均肺动脉压以及肺血管阻力显著降低。

结论

西地那非可增加艾森曼格综合征患者的肺血流量并改善紫绀。西地那非作为特发性肺动脉高压治疗药物的疗效可能可扩展至艾森曼格综合征患者。

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