Pulmonary hypertension experience in an expert university hospital
Tarih
2018Yazar
Kucukoglu, Mehmet Serdar
Demir, Rengin
Palabiyik, Mert
Sinan, Umit Yasar
Kaya, Aysem
Canbolat, Ismail Polat
Üst veri
Tüm öğe kaydını gösterÖzet
Objective: Pulmonary artery hypertension (PAH) is characterized by remodeling of the small pulmonary arteries, leading to a progressive increase in pulmonary vascular resistance and right ventricular failure. In this study, we aimed to share our 10 years of experience dealing with pulmonary hypertension (PH) and provide information in real-life settings in terms of demographics, clinical course, PH subgroup distribution, and treatment patterns in patients with PAH in a tertiary center.
Bağlantı
http://hdl.handle.net/20.500.12627/67101https://doi.org/10.14744/anatoljcardiol.2018.60252
Koleksiyonlar
- Makale [92796]