Key result
Monotherapy is linked to comparable survival versus dual or triple therapy in atypical PAH patients.
Why the study?
Although combination therapy is the gold standard for pulmonary arterial hypertension, some patients are still treated with monotherapy.
Does monotherapy result in comparable survival to combination therapy in patients with pulmonary arterial hypertension?
Cohort (n=131)
Yes
Does monotherapy result in comparable survival to combination therapy in patients with pulmonary arterial hypertension?
In older PAH patients with comorbidities, monotherapy appears to yield comparable 12-month survival to the combination therapy typically used in younger, 'typical' PAH patients.
Answers are grounded in this paper and cite their sources.
May support monotherapy in atypical PAH; hypothesis-generating and requires RCT confirmation before practice change.
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.
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Stubbe et al. (2021) conducted a cohort in Pulmonary arterial hypertension (PAH) (n=131). Monotherapy vs. Dual or triple combination therapy was evaluated on Survival (p=0.411). Monotherapy in 'atypical' pulmonary arterial hypertension patients with comorbidities or advanced age resulted in comparable survival to dual or triple therapy.
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