Collen, Jacob Lettieri, Christopher Wickwire, Emerson Holley, Aaron
Published in
Sleep & breathing = Schlaf & Atmung
Obstructive sleep apnea (OSA) syndrome is increasingly common among middle aged and older adults and is frequently linked to most cardiovascular diseases (CVD). Sleep-disordered breathing and CVD share a number of common risk factors and comorbid conditions including obesity, male gender, advancing age, metabolic syndrome, and hypertension. OSA app...
Lin, Jie-Long Chen, Hai-Ming Lin, Feng-Cheng Li, Jie-Ying Xie, Cheng-Xin Guo, Wen-Liang Huang, Xiu-Fen Hong, Cheng
Published in
European radiology
To investigate the feasibility and accuracy of balloon pulmonary angioplasty (BPA) using DynaCT angiographic reconstruction guidance. Thirty-four BPAs (23 CTEPH patients) targeting 175 pulmonary arteries were included. Eleven BPAs (2D group) were guided by DSA two-dimensional angiography. Another twenty-three BPAs (3D group) were guided using DynaC...
Husain-Syed, Faeq Gröne, Hermann-Josef Assmus, Birgit Bauer, Pascal Gall, Henning Seeger, Werner Ghofrani, Ardeschir Ronco, Claudio Birk, Horst-Walter
Published in
ESC heart failure
Venous congestion has emerged as an important cause of renal dysfunction in patients with cardiorenal syndrome. However, only limited progress has been made in differentiating this haemodynamic phenotype of renal dysfunction, because of a significant overlap with pre-existing renal impairment due to long-term hypertension, diabetes, and renovascula...
Mayeux, Jennalyn D. Pan, Irene Z. Dechand, John Jacobs, Joshua A. Jones, Tara L. McKellar, Stephen H. Beck, Emily Hatton, Nathan D. Ryan, John J.
Published in
Current Cardiovascular Risk Reports
Purpose of ReviewThis review focuses on the therapeutic management and individualized approach to Group 1 pulmonary arterial hypertension (PAH), utilizing Food and Drug Administration-approved PAH-specific therapies and various interventional and surgical options for PAH.Recent FindingsThe paradigm for the optimal management of PAH has shifted in r...
Haller, Christoph Friedberg, Mark K. Laflamme, Michael A.
Published in
Stem Cell Research & Therapy
Right ventricular (RV) failure is a commonly encountered problem in patients with congenital heart disease but can also be a consequence of left ventricular disease, primary pulmonary hypertension, or RV-specific cardiomyopathies. Improved survival of the aforementioned pathologies has led to increasing numbers of patients suffering from RV dysfunc...
Girsberger, Michael Chan, Christopher T.
Published in
BMC Nephrology
BackgroundIncreased right ventricular systolic pressure (RVSP), a surrogate marker for pulmonary hypertension, is common in patients with end-stage kidney disease. Limited data suggest improvement of RVSP with intensive dialysis, but it is unknown whether these improvements translate to better clinical outcomes.MethodsWe conducted a retrospective s...
Grünig, Ekkehard; MacKenzie, Alison; Peacock, Andrew J; Eichstaedt, Christina A; Benjamin, Nicola; Nechwatal, Robert; Ulrich, Silvia; Saxer, Stéphanie; Bussotti, Maurizio; Sommaruga, Marinella;
...
AIMS: This prospective, randomized, controlled, multicentre study aimed to evaluate efficacy and safety of exercise training in patients with pulmonary arterial (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH). METHODS AND RESULTS: For the first time a specialized PAH/CTEPH rehabilitation programme was implemented in 11 centres acros...
Swaminathan, Aparna C. Zhu, Hongmei Tapson, Victor Lokhnygina, Yuliya Poms, Abby Kelleher, Zach Gaspard, Elijah Kennedy, Karla Fee, Brian E. Fortin, Terry
...
Published in
Respiratory Research
BackgroundMultiple classes of oral therapy are available for the treatment of pulmonary arterial hypertension (PAH), but there is little to guide clinicians in choosing a specific regimen or therapeutic class. We aimed to investigate whether treatment-relevant blood biomarkers can predict therapy response in prevalent PAH patients.MethodsThis prosp...
Ruffenach, Grégoire Hong, Jason Vaillancourt, Mylène Medzikovic, Lejla Eghbali, Mansoureh
Pulmonary hypertension (PH) developing secondarily in pulmonary fibrosis (PF) patients (PF-PH) is a frequent co-morbidity. The high prevalence of PH in PF patients is very concerning since the presence of PH is a strong predictor of mortality in PF patients. Until recently, PH was thought to arise solely from fibrotic destruction of the lung parenc...
Ruffenach, Grégoire Hong, Jason Vaillancourt, Mylène Medzikovic, Lejla Eghbali, Mansoureh
Published in
Respiratory Research
Pulmonary hypertension (PH) developing secondarily in pulmonary fibrosis (PF) patients (PF-PH) is a frequent co-morbidity. The high prevalence of PH in PF patients is very concerning since the presence of PH is a strong predictor of mortality in PF patients. Until recently, PH was thought to arise solely from fibrotic destruction of the lung parenc...