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A comprehensive echocardiographic method for risk stratification in pulmonary arterial hypertension.
Ghio, Stefano; Mercurio, Valentina; Fortuni, Federico; Forfia, Paul R; Gall, Henning; Ghofrani, Ardeschir; Mathai, Stephen C; Mazurek, Jeremy A; Mukherjee, Monica; Richter, Manuel; Scelsi, Laura; Hassoun, Paul M; Tello, Khodr.
Affiliation
  • Ghio S; Division of Cardiology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy s.ghio@smatteo.pv.it.
  • Mercurio V; These authors contributed equally as co-first authors.
  • Fortuni F; Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Forfia PR; Dept of Translational Medical Sciences, Federico II University, Naples, Italy.
  • Gall H; These authors contributed equally as co-first authors.
  • Ghofrani A; Division of Cardiology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Mathai SC; Dept of Molecular Medicine, Unit of Cardiology, University of Pavia, Pavia, Italy.
  • Mazurek JA; These authors contributed equally as co-first authors.
  • Mukherjee M; Pulmonary Hypertension, Right Heart Failure and Pulmonary Thromboendarterectomy Program, Temple University Hospital, Philadelphia, PA, USA.
  • Richter M; University Hospital Giessen und Marburg GmbH, Pulmonary Hypertension Division, Medical Clinic II, Giessen, Germany.
  • Scelsi L; University Hospital Giessen und Marburg GmbH, Pulmonary Hypertension Division, Medical Clinic II, Giessen, Germany.
  • Hassoun PM; Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Tello K; Dept of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Eur Respir J ; 56(3)2020 09.
Article in En | MEDLINE | ID: mdl-32430422
ABSTRACT
QUESTION ADDRESSED Echocardiography is not currently considered as providing sufficient prognostic information to serve as an integral part of treatment goals in pulmonary arterial hypertension (PAH). We tested the hypothesis that incorporation of multiple parameters reflecting right heart function would improve the prognostic value of this imaging modality. METHODS AND MAIN

RESULTS:

We pooled individual patient data from a total of 517 patients (mean age 52±15 years, 64.8% females) included in seven observational studies conducted at five European and United States academic centres. Patients were subdivided into three groups representing progressive degrees of right ventricular dysfunction based on a combination of echocardiographic measurements, as follows. Group 1 (low risk) normal tricuspid annular plane systolic excursion (TAPSE) and nonsignificant tricuspid regurgitation (TR) (n=129); group 2 (intermediate risk) normal TAPSE and significant TR or impaired TAPSE and nondilated inferior vena cava (IVC) (n=256); group 3 (high risk) impaired TAPSE and dilated IVC (n=132). The 5-year cumulative survival rate was 82% in group 1, 63% in group 2 and 43% in group 3. Low-risk patients had better survival rates than intermediate-risk patients (log-rank Chi-squared 12.25; p<0.001) and intermediate-risk patients had better survival rates than high-risk patients (log-rank Chi-squared 26.25; p<0.001). Inclusion of other parameters such as right atrial area and pericardial effusion did not provide added prognostic value. ANSWER TO THE QUESTION The proposed echocardiographic approach integrating the evaluation of TAPSE, TR grade and IVC is effective in stratifying the risk for all-cause mortality in PAH patients, outperforming the prognostic parameters suggested by current guidelines.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Ventricular Dysfunction, Right / Pulmonary Arterial Hypertension Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Year: 2020 Type: Article

Full text: 1 Database: MEDLINE Main subject: Ventricular Dysfunction, Right / Pulmonary Arterial Hypertension Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Year: 2020 Type: Article