Key result
Rest-to-exercise changes in heart rate (HR 0.92; 95% CI 0.86-0.99) and systolic pulmonary artery pressure (HR 0.93; 95% CI 0.88-0.99) were significant predictors of survival in patients with PAH.
Why the study?
Assessment of prognosis is essential when determining therapeutic strategies in pulmonary arterial hypertension, but the prognostic value of exercise hemodynamics needed investigation.
Do rest-to-exercise changes in pulmonary hemodynamics predict survival in patients with pulmonary arterial hypertension?
Cohort (n=49)
Do rest-to-exercise changes in pulmonary hemodynamics predict survival in patients with pulmonary arterial hypertension?
Hazard Ratio: 0.92 (95% CI 0.86–0.99)
Rest-to-exercise changes in heart rate and systolic pulmonary artery pressure measured during right heart catheterization are significant predictors of survival in patients with PAH.
May aid PAH risk stratification; hypothesis-generating and should not yet change practice.
BACKGROUND: Assessment of prognosis is of major importance when deciding on a therapeutic strategy in patients with pulmonary arterial hypertension (PAH). OBJECTIVES: The aim of this study was to investigate the prognostic value of pulmonary hemodynamics during exercise and changes during treatment in patients with PAH. METHODS: Consecutive incident patients (n = 49) with PAH undergoing right heart catheterization at rest and during a constant workload cycle exercise in supine position were included. Predictors of survival were identified at baseline using Cox proportional hazard regression models in a univariate analysis unadjusted and adjusted for age and gender. RESULTS: During a median follow-up period of 42 months, 13 (27%) of the 49 patients studied died. Two predictors of death were found: rest-to-exercise changes in heart rate and systolic pulmonary artery pressure. Adjusted hazard ratios were 0.92 (95% CI 0.86-0.99) and 0.93 (95% CI 0.88-0.99), respectively. These 2 variables were correlated with each other (r = 0.55, p < 0.001). CONCLUSIONS: Rest-to-exercise changes in heart rate and systolic pulmonary artery pressure measured at diagnosis are predictors of survival in patients with PAH. These measurements taken from an exercise test reflect right ventricular function.
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Faure et al. (2020) conducted a cohort in pulmonary arterial hypertension (PAH) (n=49). Rest-to-exercise changes in heart rate and systolic pulmonary artery pressure was evaluated on death (HR 0.92, 95% CI 0.86-0.99). Rest-to-exercise changes in heart rate (HR 0.92; 95% CI 0.86-0.99) and systolic pulmonary artery pressure (HR 0.93; 95% CI 0.88-0.99) were significant predictors of survival in patients with PAH.
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