Post-capillary pulmonary hypertension in heart failure: impact of current definition in the PH-HF multicentre study

Charles Fauvel1,2,3, Thibaud Damy4, Emmanuelle Berthelot5,6

  • 1Cardiology Department, Rouen University Hospital, F-76000 Rouen, France.

PubMed

Insights

The new 2022 European guidelines for post-capillary pulmonary hypertension (pcPH) in heart failure (HF) increase prevalence and identify combined pcPH (CpcPH) as a worse prognostic indicator. Elevated mean pulmonary artery pressure (mPAP) and pulmonary vascular resistance (PVR) predict outcomes.

Area of Science:

  • Cardiology
  • Pulmonary Hypertension
  • Heart Failure Research

Background:

  • The 2022 European guidelines revised post-capillary pulmonary hypertension (pcPH) definitions in heart failure (HF) by lowering mean pulmonary artery pressure (mPAP) and pulmonary vascular resistance (PVR) thresholds.
  • The clinical impact and prognostic value of these revised pcPH definitions have not been prospectively evaluated.

Purpose of the Study:

  • To prospectively evaluate the impact of the successive pcPH definitions on pcPH prevalence and its subgroups (isolated vs. combined pcPH) in stable left HF patients.
  • To assess the prognostic value of mPAP and PVR on all-cause death or HF hospitalization using multivariable Cox regression analysis.

Main Methods:

  • A multicentre study enrolled 662 stable left HF patients requiring right heart catheterization between 2010 and 2018.
  • Patients were prospectively followed up to evaluate the impact of successive pcPH definitions on prevalence and subgroup analysis (IpcPH vs. CpcPH).
  • Multivariable Cox regression was used to determine the prognostic significance of mPAP and PVR for the primary outcome (all-cause death or HF hospitalization).

Main Results:

  • Lowering mPAP from 25 to 20 mmHg increased pcPH prevalence by 10%; lowering PVR from 3 to 2 WU increased combined pcPH (CpcPH) prevalence by 60%, showing significant net reclassification improvement.
  • Both mPAP and PVR remained significant predictors of the primary outcome (HR 1.02, P=.01 for mPAP; HR 1.07, P=.03 for PVR).
  • The optimal PVR threshold for predicting the primary outcome was approximately 2.2 WU. Patients classified with pcPH using the 2022 definition had worse survival, with CpcPH showing significantly worse outcomes than isolated pcPH (IpcPH).

Conclusions:

  • This study is the first to highlight the impact of the new pcPH definition on CpcPH prevalence in HF patients.
  • The findings validate the prognostic value of mPAP > 20 mmHg and PVR > 2 WU for predicting adverse outcomes in HF patients.
  • The revised definition and identified thresholds are crucial for risk stratification and management of HF patients with pulmonary hypertension.
Abstract

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