Zobrazeno 1 - 10
of 662
pro vyhledávání: '"pulmonary vasodilators"'
Publikováno v:
Respiratory Medicine Case Reports, Vol 49, Iss , Pp 102006- (2024)
Fibrosing mediastinitis (FM) is a heterogeneous disease characterized by sclerosing fibrosis of mediastinal structures. Pulmonary hypertension (PH) may complicate the course of the disease and can contribute significantly to the morbidity of FM. Due
Externí odkaz:
https://doaj.org/article/fc68d1ea651f4e60a868319acf282192
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-9 (2023)
Abstract Background Persistent pulmonary hypertension of the newborn (PPHN) is a common neonatal condition associated with significant morbidity and mortality. First-line diagnostic and treatment options such as echocardiography and inhaled nitric ox
Externí odkaz:
https://doaj.org/article/6b5a146b976146ce8217c8c660d20e57
Publikováno v:
Journal of the Practice of Cardiovascular Sciences, Vol 9, Iss 2, Pp 148-151 (2023)
Total anomalous pulmonary venous connection (TAPVC) is a rare congenital heart disease with an incidence of 1%–3% of all congenital heart disease patients. The pulmonary veins returning oxygenated blood from the lungs are draining into the right si
Externí odkaz:
https://doaj.org/article/1059169885104b1aaf95b18b8566efef
Akademický článek
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Akademický článek
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Publikováno v:
Journal of Indian College of Cardiology, Vol 13, Iss 1, Pp 40-42 (2023)
Pulmonary arterial hypertension secondary to congenital heart diseases is a subset of patients who need pulmonary vasodilators (PVDs). We are reporting an adult female who continued to have severe pulmonary hypertension after corrective surgery for t
Externí odkaz:
https://doaj.org/article/933d6a3424c44c969eb8b00e222288c1
Publikováno v:
Pulmonary Circulation, Vol 13, Iss 2, Pp n/a-n/a (2023)
Abstract Multiple myeloma (MM) is a common hematological malignancy resulting from clonal proliferation of plasma cells and is defined by criteria set forth by the international myeloma working group. Pulmonary hypertension (PH) is defined by an elev
Externí odkaz:
https://doaj.org/article/f98c40c19fa644b29a38fb82142e1bbb
Publikováno v:
Pulmonary Circulation, Vol 13, Iss 1, Pp n/a-n/a (2023)
Abstract We evaluated pressure‐based right ventricular ejection fraction (RVEF) and diastolic isovolumetric relaxation time constant (Tau) from continuously (up to 30 days) invasive measured right ventricular pressures in mechanically ventilated pa
Externí odkaz:
https://doaj.org/article/7720b041a29444cbb455f1fc99f72b56
Autor:
Filip Baszkowski, Weronika Pelczar-Płachta, Nikola Pempera, Sylwia Sławek-Szmyt, Marta Kałużna-Oleksy, Maciej Lesiak, Waldemar Bobkowski
Publikováno v:
Diagnostics, Vol 13, Iss 20, p 3185 (2023)
Pulmonary arterial hypertension (PAH) is a rare heterogeneous disorder in the paediatric population which is mostly associated with congenital heart disease. The management of paediatric idiopathic PAH (IPAH) is difficult due to insufficient comparat
Externí odkaz:
https://doaj.org/article/a2edac54dccb412383d0b91edb8e0e00
Publikováno v:
Pulmonary Circulation, Vol 11, Iss 4, Pp 1-5 (2021)
There are limited data regarding the feasibility of transitioning from intravenous prostacyclins to selexipag in pulmonary arterial hypertension patients. We present a case series of successful transitions from intravenous prostacyclins to selexipag
Externí odkaz:
https://doaj.org/article/64c2238a361e404e8a5c02385f2a096e