Zobrazeno 1 - 10
of 512
pro vyhledávání: '"Idiopathic pulmonary hypertension"'
Idiopathic Pulmonary Hypertension and in Situ Thromboembolism: A Difficult Case in Clinical Practice
Autor:
M. A. Us, Ju. Ju. Karpenko
Publikováno v:
Архивъ внутренней медицины, Vol 13, Iss 6, Pp 466-477 (2024)
Pulmonary hypertension is a complex syndrome for differential diagnosis, which is the outcome of various pathological conditions. With the exclusion of the two most common causes of pulmonary hypertension, such as pathology of the left heart chambers
Externí odkaz:
https://doaj.org/article/ffe77a4ff456401d864efbae24b89b70
Publikováno v:
BMC Cardiovascular Disorders, Vol 23, Iss 1, Pp 1-10 (2023)
Abstract Background Pulmonary hypertension (PH) is considered to increase maternal and fetal risk, and we attempt to explore pregnancy outcomes in women with different types of PH. Methods We retrospectively analyzed the clinical data of pregnant wom
Externí odkaz:
https://doaj.org/article/4828865e65ab4713b49ed68c8152188a
Autor:
Wenzhang Lu, Jiayi Xu, Yanrong Chen, Jinbo Huang, Qin Shen, Fei Sun, Yan Zhang, Daojun Ji, Bijuan Xue, Jun Li
Publikováno v:
Experimental Gerontology, Vol 182, Iss , Pp 112303- (2023)
Background: Idiopathic pulmonary hypertension (IPAH) is a rare and severe disease that affects the pulmonary vasculature. As the diagnosis of IPAH requires invasive right heart catheterization surgery, early detection of this condition is notoriously
Externí odkaz:
https://doaj.org/article/96746303afda4492b271941516bfc1a7
Autor:
Sergei N. Ivanov, Alexander G. Edemskiy, Oksana Ya. Vasiltseva, Aleksandr M. Chernyavskiy, Maria V. Kalashnikova, Svetlana V. Seletskaya
Publikováno v:
Consilium Medicum, Vol 24, Iss 12, Pp 876-881 (2023)
The manuscript presents a clinical case of treatment of a patient with idiopathic pulmonary hypertension and a rare complication left main coronary artery stenosis caused due to compression by the dilated pulmonary artery. This complication was clini
Externí odkaz:
https://doaj.org/article/70f1166f6ae449f78d76ebd076f3db01
Autor:
Ashfaq Ahmad, Peng Zhang, Lingling Li, Xiaoyu Wang, Ahmed Ali Mohsen, Yousen Wang, Fenling Fan
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
Externí odkaz:
https://doaj.org/article/128a8be1ce4a45e1b85de8ed52314ade
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:
Евразийский Кардиологический Журнал, Vol 0, Iss 4, Pp 80-86 (2021)
Our observation demonstrates a case of a 40-year-old female with idiopathic pulmonary arterial hypertension World Health Organization functional class III, who was admitted to NMRC of Cardiology repeatedly due to disease progression including dyspnea
Externí odkaz:
https://doaj.org/article/809d97d91a7a40e49bbeff638f8aa6dd
Autor:
Irina N. Taran, Zarina S. Valieva, Anna A. Belevskaya, Marina A. Saidova, Tamila V. Martynyuk, Irina E. Chazova
Publikováno v:
Терапевтический архив, Vol 93, Iss 3, Pp 283-289 (2021)
Aim. To assess the clinical course of the disease and the features of the treatment goals achievement in patients with IPAH and inoperable CTEPH depending on gender and age at the time of diagnosis verification. Materials and methods. The study in
Externí odkaz:
https://doaj.org/article/ca17bf291d5a4bb388a9094660ec901f
Autor:
Alexandra Arvanitaki, George Giannakoulas, Eva Triantafyllidou, Christos Feloukidis, Afroditi K. Boutou, Alexandros Garyfallos, Haralambos Karvounis, Theodoros Dimitroulas
Publikováno v:
Respiratory Research, Vol 22, Iss 1, Pp 1-9 (2021)
Abstract Background Although pulmonary vascular bed has been the main subject of research for many years in pulmonary hypertension (PH), interest has recently started to divert towards the possibility of a co-existing peripheral microangiopathy. The
Externí odkaz:
https://doaj.org/article/fc75ab55943e45d6a9c31ff6322fd43c
Autor:
Prashant Bobhate, Sandeep Garg, Anuj Sharma, Diptiman Roy, Abhijeet Raut, Ravindra Pawar, Tanuja Karande, Snehal Kulkarni
Publikováno v:
Indian Heart Journal, Vol 73, Iss 1, Pp 99-103 (2021)
Objective: Abernethy malformation (congenital extrahepatic portosystemic shunt) is a rare anomaly of the splanchnic venous system. Though rare, it is an important cause of pulmonary artery hypertension (PAH) which is often missed. All patients with P
Externí odkaz:
https://doaj.org/article/4f2370bbc2734343bc190b05fb3e17be