Risk Stratification in Pulmonary Arterial Hypertension, Update and Perspectives

Author:

Vraka Argyro1,Diamanti Eleni1,Kularatne Mithum2ORCID,Yerly Patrick3ORCID,Lador Frédéric4,Aubert John-David1ORCID,Lechartier Benoit1

Affiliation:

1. Pulmonary Division, Lausanne University Hospital, University of Lausanne, 1011 Lausanne, Switzerland

2. Division of Respiratory Medicine, Department of Medicine, University of Calgary, Calgary, AB T2N 1N4, Canada

3. Division of Cardiology, Cardiovascular Department, Lausanne University Hospital, University of Lausanne, 1011 Lausanne, Switzerland

4. Pulmonary Division, Geneva University Hospital, 1211 Geneva, Switzerland

Abstract

Risk stratification in pulmonary arterial hypertension (PAH) is crucial in assessing patient prognosis. It serves a prominent role in everyday patient care and can be determined using several validated risk assessment scores worldwide. The recently published 2022 European Society of Cardiology (ESC)/European Respiratory Society (ERS) guidelines underline the importance of risk stratification not only at baseline but also during follow-up. Achieving a low-risk status has now become the therapeutic goal, emphasising the importance of personalised therapy. The application of these guidelines is also important in determining the timing for lung transplantation referral. In this review, we summarise the most relevant prognostic factors of PAH as well as the parameters used in PAH risk scores and their evolution in the guidelines over the last decade. Finally, we describe the central role that risk stratification plays in the current guidelines not only in European countries but also in Asian countries.

Publisher

MDPI AG

Subject

General Medicine

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