Prognostic value of systolic pulmonary artery pressure change at exercise in pulmonary arterial hypertension

Author(s):  
Morgane Faure ◽  
Ari Chaouat ◽  
Emmanuel Gomez ◽  
Magalie Mercy ◽  
Anne Guillaumot ◽  
...  
2021 ◽  
Vol 10 (13) ◽  
pp. 2995
Author(s):  
Remigiusz Kazimierczyk ◽  
Ewelina Kazimierczyk ◽  
Malgorzata Knapp ◽  
Bozena Sobkowicz ◽  
Lukasz A. Malek ◽  
...  

In response to an increased afterload in pulmonary arterial hypertension (PAH), the right ventricle (RV) adapts by remodeling and increasing contractility. The idea of coupling refers to maintaining a relatively constant relationship between ventricular contractility and afterload. Twenty-eight stable PAH patients (mean age 49.5 ± 15.5 years) were enrolled into the study. The follow-up time of this study was 58 months, and the combined endpoint (CEP) was defined as death or clinical deterioration. We used echo TAPSE as a surrogate of RV contractility and estimated systolic pulmonary artery pressure (sPAP) reflecting RV afterload. Ventricular–arterial coupling was evaluated by the ratio between these two parameters (TAPSE/sPAP). In the PAH group, the mean pulmonary artery pressure (mPAP) was 47.29 ± 15.3 mmHg. The mean echo-estimated TAPSE/sPAP was 0.34 ± 0.19 mm/mmHg and was comparable in value and prognostic usefulness to the parameter derived from magnetic resonance and catheterization (ROC analysis). Patients who had CEP (n = 21) had a significantly higher mPAP (53.11 ± 17.11 mmHg vs. 34.86 ± 8.49 mmHg, p = 0.03) and lower TAPSE/sPAP (0.30 ± 0.21 vs. 0.43 ± 0.23, p = 0.04). Patients with a TAPSE/sPAP lower than 0.25 mm/mmHg had worse prognosis, with log-rank test p = 0.001. the echocardiographic estimation of TAPSE/sPAP offers an easy, reliable, non-invasive prognostic parameter for the comprehensive assessment of hemodynamic adaptation in PAH patients.


Author(s):  
George K Istaphanous ◽  
Andreas W Loepke

Pediatric pulmonary arterial hypertension (PAH) is characterized by a pathologically elevated pulmonary artery pressure in children. The etiology of PAH is multifactorial, and while its prognosis is closely related to the reversibility of the underlying disease process, much progress has recently been made in its diagnosis and treatment, significantly decreasing the associated morbidity and mortality.


Medicine ◽  
2017 ◽  
Vol 96 (43) ◽  
pp. e8349 ◽  
Author(s):  
Hiroyuki Nakamura ◽  
Masaru Kato ◽  
Toshitaka Nakaya ◽  
Michihiro Kono ◽  
Shun Tanimura ◽  
...  

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