scholarly journals Monotherapy in patients with pulmonary arterial hypertension at four German PH centres

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Beate Stubbe ◽  
Hans-Jürgen Seyfarth ◽  
Janina Kleymann ◽  
Michael Halank ◽  
Hussam Al Ghorani ◽  
...  

Abstract Background Although combination therapy is the gold standard for patients with pulmonary arterial hypertension (PAH), some of these patients are still being treated with monotherapy. Methods We conducted a retrospective analysis at four German PH centres to describe the prevalence and characteristics of patients receiving monotherapy. Results We identified 131 incident PAH patients, with a mean age of 64 ± 13.8 years and a varying prevalence of comorbidities, cardiovascular risk factors and targeted therapy. As in other studies, the extent of prescribed PAH therapy varied with age and coexisting diseases, and younger, so-called “typical” PAH patients were more commonly treated early with combination therapy (48% at 4–8 months). In contrast, patients with multiple comorbidities or cardiovascular risk factors were more often treated with monotherapy (69% at 4–8 months). Survival at 12 months was not significantly associated with the number of PAH drugs used (single, dual, triple therapy) and was not different between “atypical” and “typical” PAH patients (89% vs. 85%). Conclusion Although “atypical” PAH patients with comorbidities or a more advanced age are less aggressively treated with respect to combination therapy, the outcome of monotherapy in these patients appears to be comparable to that of dual or triple therapy in “typical” PAH patients.

2021 ◽  
pp. 1-2
Author(s):  
Simon-Dominik Herkenrath

<b>Background:</b> Background: Although combination therapy is the gold standard for patients with pulmonary arterial hypertension (PAH), some of these patients are still being treated with monotherapy. <b>Methods:</b> We conducted a retrospective analysis at four German PH centres to describe the prevalence and characteristics of patients receiving monotherapy. <b>Results:</b> We identified 131 incident PAH patients, with a mean age of 64 ± 13.8 years and a varying prevalence of comorbidities, cardiovascular risk factors and targeted therapy. As in other studies, the extent of prescribed PAH therapy varied with age and coexisting diseases, and younger, so-called «typical» PAH patients were more commonly treated early with combination therapy (48% at 4–8 months). In contrast, patients with multiple comorbidities or cardiovascular risk factors were more often treated with monotherapy (69% at 4–8 months). Survival at 12 months was not significantly associated with the number of PAH drugs used (single, dual, triple therapy) and was not different between «atypical» and «typical» PAH patients (89% vs. 85%). <b>Conclusion:</b> Although «atypical» PAH patients with comorbidities or a more advanced age are less aggressively treated with respect to combination therapy, the outcome of monotherapy in these patients appears to be comparable to that of dual or triple therapy in «typical» PAH patients.


2019 ◽  
Vol 38 (12) ◽  
pp. 1286-1295 ◽  
Author(s):  
Vallerie V. McLaughlin ◽  
Jean-Luc Vachiery ◽  
Ronald J. Oudiz ◽  
Stephan Rosenkranz ◽  
Nazzareno Galiè ◽  
...  

2013 ◽  
Vol 34 (suppl 1) ◽  
pp. P309-P309
Author(s):  
A. C. Charalampopoulos ◽  
I. Tzoulaki ◽  
L. S. Howard ◽  
R. Davies ◽  
W. Gin-Sing ◽  
...  

2014 ◽  
Vol 4 (4) ◽  
pp. 669-678 ◽  
Author(s):  
Athanasios Charalampopoulos ◽  
Luke S. Howard ◽  
Ioanna Tzoulaki ◽  
Wendy Gin-Sing ◽  
Julia Grapsa ◽  
...  

2016 ◽  
Vol 25 (142) ◽  
pp. 408-417 ◽  
Author(s):  
Olivier Sitbon ◽  
Sean Gaine

There is a strong rationale for combining therapies to simultaneously target three of the key pathways implicated in the pathogenesis of pulmonary arterial hypertension (PAH). Evidence to support this strategy is growing, and a number of studies have demonstrated that combination therapy, administered as either a sequential or an initial regimen, can improve long-term outcomes in PAH. Dual combination therapy with a phosphodiesterase-5 inhibitor and an endothelin receptor antagonist is the most widely utilised combination regimen. However, some patients fail to achieve their treatment goals on dual therapy and may benefit from the addition of a third drug. The use of triple therapy in clinical practice was previously reserved for patients with severe disease due to the need for parenteral administration of prostanoids. Although triple therapy with parenteral prostanoids plays a key role in the management of severe PAH, the approval of oral therapies that target the prostacyclin pathway means that all three pathways can now be targeted with oral drugs at an earlier disease stage. Furthermore, there is evidence demonstrating that this approach can delay disease progression. Based on the evidence available, it is becoming increasingly clear that all PAH patients should be offered the benefits of combination therapy.


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