PedAM
Pediatric Disease Annotations & Medicines
| Disease | pulmonary hypertension |
| Phenotype | C0034069|pulmonary fibrosis |
| Sentences | 23 |
| PubMedID- 25055292 | Conclusion: the relative ct volume of any single lesion was of limited value in predicting pulmonary hypertension in patients with pulmonary fibrosis and emphysema. |
| PubMedID- 23527830 | Aim: pulmonary fibrosis is often complicated by pulmonary hypertension. |
| PubMedID- 22428220 | Failure of noninvasive prediction of pulmonary hypertension in patients with idiopathic pulmonary fibrosis. |
| PubMedID- 26096076 | Right ventricular structure and function in idiopathic pulmonary fibrosis with or without pulmonary hypertension. |
| PubMedID- 19643948 | pulmonary hypertension in patients with combined pulmonary fibrosis and emphysema syndrome. |
| PubMedID- 21835902 | Background: pulmonary hypertension (ph) associated with pulmonary fibrosis (pf) is a severe condition with poor outcome. |
| PubMedID- 26113671 | Furthermore, chymase inhibition prevented big endothelin-1-induced vasoconstriction of the pulmonary arteries.therefore, chymase plays a role in the pathogenesis of pulmonary hypertension associated with pulmonary fibrosis and may represent a promising therapeutic target. |
| PubMedID- 21660584 | Prevalence of pulmonary hypertension in patients with idiopathic pulmonary fibrosis: correlation with physiological parameters. |
| PubMedID- 26029570 | This report describes a case of successful treatment with bosentan for severe pulmonary hypertension in a patient with idiopathic pulmonary fibrosis. |
| PubMedID- 20946337 | Heart rate recovery after six-minute walk test predicts pulmonary hypertension in patients with idiopathic pulmonary fibrosis. |
| PubMedID- 25473528 | Broad and heterogeneous vasculopathy in pulmonary fibrosis and emphysema with pulmonary hypertension. |
| PubMedID- 23928001 | pulmonary hypertension (ph) associated with pulmonary fibrosis (pf) considerably worsens prognosis of interstitial lung diseases (ild). |
| PubMedID- 26075134 | A 64-year-old male underwent bilateral lung transplantation at an outside hospital in 2011 for idiopathic pulmonary fibrosis with pulmonary hypertension. |
| PubMedID- 25444371 | Effect of pulmonary hypertension on survival in patients with idiopathic pulmonary fibrosis after lung transplantation: an analysis of the united network of organ sharing registry. |
| PubMedID- 23840349 | pulmonary hypertension in patients with idiopathic pulmonary fibrosis - the predictive value of exercise capacity and gas exchange efficiency. |
| PubMedID- 23372927 | The degree of pressure overload is usually mild when pulmonary hypertension develops in patients with idiopathic pulmonary fibrosis, and angioproliferative lesions are rarely seen in these patients. |
| PubMedID- 24918967 | Rationale: the development of pulmonary hypertension (ph) in patients with idiopathic pulmonary fibrosis (ipf) or chronic obstructive pulmonary disease (copd) is associated with increased morbidity. |
| PubMedID- 23605508 | Clinical, radiologic, and laboratory findings suggested a diagnosis of chronic hypoxemic, type 1 respiratory failure, due to combined pulmonary fibrosis and emphysema, complicated by severe, precapillary pulmonary hypertension. |
| PubMedID- 25836609 | Incidence and clinical characteristics of pulmonary hypertension in patients with idiopathic pulmonary fibrosis. |
| PubMedID- 23734851 | Clinical case: combined pulmonary fibrosis and emphysema with pulmonary hypertension--clinical management. |
| PubMedID- 26319484 | Influence of pulmonary hypertension on patients with idiopathic pulmonary fibrosis awaiting lung transplantation. |
| PubMedID- 26099567 | As progressive pulmonary fibrosis can lead to pulmonary hypertension (rockey et al., 2015), it will be of considerable interest to ask whether endmt participates in the regulatory network of human ph and, if so, what is the exact role of endmt in the development of ph? |
| PubMedID- 22054725 | We describe a 76-year-old former smoker with a diagnosis of combined pulmonary fibrosis and emphysema associated with pulmonary hypertension and rapidly progressive right heart failure, in whom combined treatment with sitaxsentan and sildenafil resulted in sustained improvement of his clinical condition and exercise performance, without any relevant adverse events. |
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