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Updated: Jun 4, 2025

Increasing Pulmonary Artery Pulsatile Flow Improves Hypoxic Pulmonary Hypertension in Piglets
Published on: May 11, 2015
Pulmonary hypertension as a prognostic marker in low-flow low-gradient aortic stenosis: Insights from invasive
Arif Albulushi1, Usama Al-Abri2, Nadya Al Matrooshi3
1Division of Adult Cardiology, National Heart Center, The Royal Hospital, Muscat, Oman; Division of Cardiovascular Medicine, University of Nebraska Medical Center, NE, USA.
Introduction:
Pulmonary hypertension (PH) is a common and significant comorbidity in patients with low-flow low-gradient (LF-LG) aortic stenosis, impacting prognosis after transcatheter aortic valve replacement (TAVR). Non-invasive tools often fail to capture PH's full clinical impact due to inherent limitations. This study evaluates the prognostic significance of PH measured invasively and explores its implications on post-TAVR outcomes.
Methods:
This retrospective study analyzed 90 patients with symptomatic LF-LG aortic stenosis who underwent TAVR. Pulmonary artery systolic pressure (PASP) was categorized as mild (<35 mmHg), moderate (35-50 mmHg), or severe (>50 mmHg) using invasive right heart catheterization. Key endpoints included 12-month all-cause mortality and heart failure rehospitalization, assessed via Kaplan-Meier survival analysis and Cox proportional hazards modeling.
Results:
PH was present in 50% of patients, with moderate-to-severe cases showing higher mortality (25% vs. 8%, p < 0.001) and rehospitalization rates (20% vs. 6%, p = 0.02). Baseline PASP emerged as an independent predictor of mortality (HR 1.07 per mmHg, p < 0.001) and rehospitalization (HR 1.04 per mmHg, p = 0.01). Subgroup analyses revealed that patients with concomitant COPD or advanced diastolic dysfunction exhibited worse outcomes, underscoring the role of systemic disease burden.
Conclusion:
Invasive hemodynamic assessment provides superior prognostic insight for PH in LF-LG aortic stenosis patients. The findings advocate for targeted PH management strategies to improve post-TAVR outcomes and challenge the sole reliance on non-invasive methods in high-risk cohorts.
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