PedAM
Pediatric Disease Annotations & Medicines
| Disease | idiopathic pulmonary hypertension |
| Phenotype | C1619734|pulmonary arterial hypertension |
| Sentences | 4 |
| PubMedID- 25583377 | Background and objective: in this study, we evaluated survival in rheumatoid arthritis-associated pulmonary arterial hypertension (ra-pah) compared with idiopathic pulmonary arterial hypertension (ipah) patients, and evaluate differences in disease severity and treatment. |
| PubMedID- 22110770 | Table legend: yr, years; f, female; m, male; bmi, body mass index; kg, kilogram; rap, right atrial pressure; mpap, mean pulmonary artery pressure; pcwp, pulmonary capillary wedge pressure; ci, cardiac index; pvri, pulmonary vascular resistance index; wu, wood units; nyha, new york heart association; 6mwt, six-minute walk test; m, meters; % pred, percentage of predicted value; ctrl, healthy control subjects; ipah, patients with idiopathic pulmonary arterial hypertension; ssc, subjects with limited systemic sclerosis without pah; pah-ssc, patients with pulmonary arterial hypertension associated with limited systemic sclerosis. |
| PubMedID- 22545094 | Phenotype labels: interstitial lung disease (ssc-ph-ild), idiopathic arterial hypertension (ipah), scleroderma with pulmonary arterial hypertension (ssc-pah), scleroderma (ssc), pulmonary arterial hypertension only (pah), idiopathic pulmonary fibrosis with pulmonary hypertension (ipf-ph), and human cord blood versus human adult blood (cbvab). |
| PubMedID- 21329286 | We sought to investigate observed vs expected mortality among geriatric ipah patients treated with specific pulmonary arterial hypertension (pah) therapy. |
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