TY - JOUR
T1 - Pulmonale Hypertonie bei Linksherzerkrankungen
AU - Schmidt, Kai Helge
AU - Adler, Joana
AU - Bikou, Olympia
AU - Felgendreher, Ralf
AU - Hohenforst-Schmidt, Wolfgang
AU - Holt, Stephan
AU - Kleber, Franz X.
AU - Ladage, Dennis
AU - Lichtblau, Mona
AU - Pfeuffer-Jovic, Elena
AU - Pott, Julian
AU - Rieth, Andreas
AU - Schmeisser, Alexander
AU - Schnitzler, Katharina
AU - Stadler, Stefan
AU - Kuebler, Wolfgang M.
AU - Blindt, Rüdiger
AU - Opitz, Christian
N1 - Publisher Copyright:
© 2025 Georg Thieme Verlag. All rights reserved.
PY - 2025/10/1
Y1 - 2025/10/1
N2 - Left heart disease (LHD) is the most common cause of pulmonary hypertension (PH), which is further categorised into isolated post-capillary PH (IpcPH) and combined pre- and post-capillary PH (CpcPH). With the aim of developing treatment strategies, the PH-LHD working group of the 7 thWorld Symposium on Pulmonary Hypertension placed a stronger focus on phenotyping, subtyping and a more differentiated approach to the broad spectrum of PH-LHD. With this intention, a four-stage PH-LHD system was developed in which each stage (A=risk, B=structural heart disease, C=symptomatic heart disease, D=advanced) is characterised by specific pathophysiological, haemodynamic, clinical and ultimately therapeutic strategies. In this context, attention is also paid to cardiac diseases leading to PH-LHD with specific therapeutic approaches, such as mitral and aortic valve stenosis and selected cardiomyopathies. The overlap with other PH groups such as CTEPH and PH in lung diseases is also emphasised and specified. The therapeutic use of PAH drugs that have a pulmonary vascular approach can still not be recommended outside of clinical trials.
AB - Left heart disease (LHD) is the most common cause of pulmonary hypertension (PH), which is further categorised into isolated post-capillary PH (IpcPH) and combined pre- and post-capillary PH (CpcPH). With the aim of developing treatment strategies, the PH-LHD working group of the 7 thWorld Symposium on Pulmonary Hypertension placed a stronger focus on phenotyping, subtyping and a more differentiated approach to the broad spectrum of PH-LHD. With this intention, a four-stage PH-LHD system was developed in which each stage (A=risk, B=structural heart disease, C=symptomatic heart disease, D=advanced) is characterised by specific pathophysiological, haemodynamic, clinical and ultimately therapeutic strategies. In this context, attention is also paid to cardiac diseases leading to PH-LHD with specific therapeutic approaches, such as mitral and aortic valve stenosis and selected cardiomyopathies. The overlap with other PH groups such as CTEPH and PH in lung diseases is also emphasised and specified. The therapeutic use of PAH drugs that have a pulmonary vascular approach can still not be recommended outside of clinical trials.
KW - ejection fraction
KW - left heart disease
KW - postcapillary pulmonary hypertension
KW - stenosis
UR - https://www.scopus.com/pages/publications/105017931718
U2 - 10.1055/a-2625-4920
DO - 10.1055/a-2625-4920
M3 - Article
C2 - 41052532
AN - SCOPUS:105017931718
SN - 0934-8387
VL - 79
SP - 787
EP - 796
JO - Pneumologie
JF - Pneumologie
IS - 10
ER -