An integrated approach to the treatment of pulmonary hypertension related to hypoxic lung diseases

2011 ◽  
pp. 479-488
Author(s):  
Ari Chaouat ◽  
Emmanuel Gomez ◽  
Matthieu Canuet ◽  
Christine Selton-Suty ◽  
François Chabot ◽  
...  
2021 ◽  
Vol 8 ◽  
Author(s):  
Christopher A. Thomas ◽  
Justin Lee ◽  
Roberto J. Bernardo ◽  
Ryan J. Anderson ◽  
Vladimir Glinskii ◽  
...  

Background: Pulmonary hypertension is a complication of chronic lung diseases (PH-CLD) associated with significant morbidity and mortality. Management guidelines for PH-CLD emphasize the treatment of the underlying lung disease, but the role of PH-targeted therapy remains controversial. We hypothesized that treatment approaches for PH-CLD would be variable across physicians depending on the type of CLD and the severity of PH.Methods and Results: Between May and July 2020, we conducted an online survey of PH experts asking for their preferred treatment approach in seven hypothetical cases of PH-CLD of varying severity. We assessed agreement amongst clinicians for initial therapy choice using Fleiss' kappa calculations. Over 90% of respondents agreed that they would treat cases of severe PH in the context of mild lung disease with some form of PH-targeted therapy. For cases of severe PH in the context of severe lung disease, over 70% of respondents agreed to use PH-targeted therapy. For mild PH and mild lung disease cases, <50% of respondents chose to start PH-specific therapy. There was overall poor agreement between respondents in the choice to use mono-, double or triple combination therapy with PH-specific agents in all cases.Conclusion: Although management guidelines discourage the routine use of PH-targeted therapies to treat PH-CLD patients, most physicians choose to treat patients with some form of PH-targeted therapy. The choice of therapy and treatment approach are variable and appear to be influenced by the severity of the PH and the underlying lung disease.


Author(s):  
Dimitar Sajkov ◽  
Bliegh Mupunga ◽  
Jeffrey J. ◽  
Nikolai Petrovsky

2018 ◽  
Vol 272 ◽  
pp. 63-68 ◽  
Author(s):  
Horst Olschewski ◽  
Jürgen Behr ◽  
Hinrich Bremer ◽  
Martin Claussen ◽  
Philipp Douschan ◽  
...  

2014 ◽  
pp. 529-539
Author(s):  
David Montani ◽  
Barbara Girerd ◽  
Andrei Seferian ◽  
Laurent Godinas ◽  
Marc Humbert

2021 ◽  
Vol 8 (2) ◽  
Author(s):  
Adele VALENTINI ◽  
Giovanni SAVIETTO ◽  
Federica MELONI ◽  
Roberto DORE ◽  
Andrea BORGHESI ◽  
...  

Asthma ◽  
2014 ◽  
pp. 215-228
Author(s):  
Aaron B. Waxman ◽  
Kerri Akaya Smith

Pulmonary hypertension (PH) is a spectrum of diseases involving the pulmonary vascular circuit and is defined as an elevation in pulmonary arterial pressures. PH is an uncommon disorder that presents with nonspecific complaints. There remains a significant delay in the diagnosis of PH and initiation of appropriate therapy because often patients are misdiagnosed with more common causes of dyspnea such as obstructive lung diseases like asthma. The diagnosis of PH should be considered in patients who do not fit the usual profile of patients presenting with dyspnea and asthma, especially if they do not respond to therapy. The finding of PH foreshadows a poor outcome if not discovered early and treated aggressively.


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