Effects of sildenafil on pulmonary hypertension and exercise tolerance in severe cystic fibrosis-related lung disease

被引:14
作者
Montgomery, GS
Sagel, SD
Taylor, AL
Abman, SH
机构
[1] Indiana Univ, Med Ctr, Div Pediat Pulmonol, Indianapolis, IN USA
[2] Univ Colorado, Denver Hlth Sci Ctr, Dept Pediat, Sect Pulm Med, Denver, CO 80202 USA
[3] Univ Colorado, Denver Hlth Sci Ctr, Dept Pediat, Cardiol Sect, Denver, CO 80202 USA
[4] Univ Colorado, Denver Hlth Sci Ctr, Dept Pediat, Pediat Heart Lung Ctr, Denver, CO 80202 USA
关键词
cystic fibrosis; exercise; pulmonary hypertension; sildenafil; 6-min walk test; phosphodiesterase inhibitor; echocardiogram;
D O I
10.1002/ppul.20393
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Cystic fibrosis (CF) patients with advanced lung disease are at risk for developing pulmonary vascular disease and pulmonary hypertension, characterized by progressive exercise intolerance beyond the exercise-limiting effects of airways disease in CF We report on a patient with severe CF lung disease who experienced clinically significant improvements in exercise tolerance and pulmonary hypertension without changing lung function during sildenafil therapy.
引用
收藏
页码:383 / 385
页数:3
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