PedAM
Pediatric Disease Annotations & Medicines
| Disease | eisenmenger syndrome |
| Phenotype | C0020538|hypertension |
| Sentences | 7 |
| PubMedID- 22762976 | The perioperative management of pulmonary hypertension in a patient with eisenmenger syndrome, the most advanced form of associated pulmonary artery hypertension (pah), who required a sigmoidectomy is presented. |
| PubMedID- 22291842 | Large shunts lead to pulmonary hypertension and the development of eisenmenger syndrome. |
| PubMedID- 26457208 | Right heart catheterization and aortic root injection showed a large apw and eisenmenger syndrome with severe pulmonary hypertension with a pulmonary artery pressure of 131/32/97 mmhg and increased pulmonary vascular resistance of 9 wood units/m2 (figures 2(a), 2(b), and 2(c)). |
| PubMedID- 20864788 | Transthoracic and transesophageal echo revealed a large ventricular septal defect (vsd) with pulmonary arterial hypertension, which was suggestive of eisenmenger syndrome. |
| PubMedID- 25787798 | Previous studies examining the use of pulmonary arterial hypertension (pah) drugs in patients with eisenmenger syndrome (es) have shown that it may have beneficial effects in some patients with es; however, experience with additional cases is necessary to confirm its efficacy and appropriate clinical use. |
| PubMedID- 21943933 | The dual endothelin receptor antagonist, bosentan, has been shown to be well tolerated and effective in improving pulmonary arterial hypertension (pah) symptoms in patients with eisenmenger syndrome but data from longer-term studies are lacking. |
| PubMedID- 20026774 | Background: advanced therapy (at) for pulmonary arterial hypertension in the context of congenital heart disease (eisenmenger syndrome) improves pulmonary hemodynamics, functional class, and the 6-minute walk test. |
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