Related Experiment Video
Updated: Jan 17, 2026

The Left Pneumonectomy Combined with Monocrotaline or Sugen as a Model of Pulmonary Hypertension in Rats
Published on: March 8, 2019
TAPSE/sPAP Ratio to Improve Risk Assessment in Pulmonary Arterial Hypertension.
Roberto Badagliacca1, Khodr Tello2, Michele D'Alto3
1Department of Cardiovascular and Respiratory Sciences-Sapienza University of Rome, Italy (R.B., D.F., G.M., A.M., S.P., T.R., C.D.V.).
Assessing right ventricular-pulmonary artery coupling using the tricuspid annular plane systolic excursion to systolic pulmonary artery pressure (TAPSE/sPAP) ratio enhances risk prediction in pulmonary arterial hypertension (PAH) patients. This ratio improves survival prediction, particularly in intermediate-risk groups.
Area of Science:
- Cardiology
- Pulmonary Medicine
- Echocardiography
Background:
- Right ventricular (RV) function is crucial for outcomes in pulmonary arterial hypertension (PAH).
- RV-PA coupling, assessed by TAPSE/sPAP, may refine risk stratification.
Purpose of the Study:
- To evaluate if the TAPSE/sPAP ratio improves risk assessment for survival prediction in PAH patients on targeted therapies.
Main Methods:
- Prospective enrollment of 677 PAH patients across 11 Italian centers.
- Collection of baseline and follow-up clinical, echocardiographic, and right heart catheterization data.
- Comparison of European Society of Cardiology/European Respiratory Society and REVEAL 2.0 risk scores with and without the TAPSE/sPAP ratio, validated in a German cohort.
Main Results:
- Increased TAPSE/sPAP ratio correlated with low-risk status at long-term follow-up (OR 1.78 for ESC/ERS, OR 1.43 for REVEAL 2.0).
- TAPSE/sPAP ratio enhanced prognostic information for both risk scores, especially in intermediate-risk strata (cutoffs 0.5, 0.35, 0.30 mm/mmHg for ESC/ERS; 0.35 mm/mmHg for REVEAL 2.0).
- Findings were confirmed in a retrospective German validation cohort.
Conclusions:
- The TAPSE/sPAP ratio improves risk stratification in PAH patients.
- This ratio adds prognostic value to existing risk scores, except in the very low or very high disease stages.
More Related Videos
09:23Shunt Surgery, Right Heart Catheterization, and Vascular Morphometry in a Rat Model for Flow-induced Pulmonary Arterial Hypertension
Published on: February 11, 2017
10:03Evaluation of Right Ventricular Function in Experimental Models of Pulmonary Arterial Hypertension
Published on: June 27, 2025
Related Concept Videos
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
Treatment for Pulmonary Arterial Hypertension: Oxygen Therapy for Respiratory Failure
Oxygen therapy is vital in increasing and maintaining blood oxygen levels in PAH patients. As a result, it aids in reducing fatigue,...
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...
Treatment for Pulmonary Arterial Hypertension: Phosphodiesterase Inhibitors
Among the PDE5 inhibitors, sildenafil (Revatio) stands out as a competitive and selective inhibitor. It operates by elevating cellular levels of cGMP and augmenting signaling through the cGMP-PKG pathway, promoting vasodilation. Upon oral...
Pulmonary Hypertension: Classification and Pathogenesis
There are various classifications for PH, each relating to different underlying causes and also...
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme...