TY - JOUR
T1 - Incomplete echocardiographic recovery at 6 months predicts long-term sequelae after intermediate-risk pulmonary embolism. A post-hoc analysis of the Pulmonary Embolism Thrombolysis (PEITHO) trial
AU - Barco, Stefano
AU - Russo, Mariaconcetta
AU - Vicaut, Eric
AU - Becattini, Cecilia
AU - Bertoletti, Laurent
AU - Beyer-Westendorf, Jan
AU - Bouvaist, Hélène
AU - Couturaud, Francis
AU - Danays, Thierry
AU - Dellas, Claudia
AU - Duerschmied, Daniel
AU - Empen, Klaus
AU - Ferrari, Emile
AU - Galiè, Nazzareno
AU - Jiménez, David
AU - Klok, Frederikus A.
AU - Kostrubiec, Maciej
AU - Kozak, Matija
AU - Kupatt, Christian
AU - Lang, Irene M.
AU - Lankeit, Mareike
AU - Meneveau, Nicolas
AU - Palazzini, Massimiliano
AU - Pruszczyk, Piotr
AU - Rugolotto, Matteo
AU - Salvi, Aldo
AU - Sanchez, Olivier
AU - Schellong, Sebastian
AU - Sobkowicz, Bozena
AU - Meyer, Guy
AU - Konstantinides, Stavros V.
PY - 2019/7/1
Y1 - 2019/7/1
N2 - Introduction: Symptoms and functional limitation are frequently reported by survivors of acute pulmonary embolism (PE). However, current guidelines provide no specific recommendations on which patients should be followed after acute PE, when follow-up should be performed, and which tests it should include. Definition and classification of late PE sequelae are evolving, and their predictors remain to be determined. Methods: In a post hoc analysis of the Pulmonary Embolism Thrombolysis (PEITHO) trial, we focused on 219 survivors of acute intermediate-risk PE with clinical and echocardiographic follow-up 6 months after randomisation as well as over the long term (median, 3 years after acute PE). The primary outcome was a composite of (1) confirmed chronic thromboembolic pulmonary hypertension (CTEPH) or (2) ‘post-PE impairment’ (PPEI), defined by echocardiographic findings indicating an intermediate or high probability of pulmonary hypertension along with New York Heart Association functional class II–IV. Results: Confirmed CTEPH or PPEI occurred in 29 (13.2%) patients, (6 with CTEPH and 23 with PPEI). A history of chronic heart failure at baseline and incomplete or absent recovery of echocardiographic parameters at 6 months predicted CTEPH or PPEI at long-term follow-up. Conclusions: CTEPH or PPEI occurs in almost one out of seven patients after acute intermediate-risk PE. Six-month echocardiographic follow-up may be useful for timely detection of late sequelae.
AB - Introduction: Symptoms and functional limitation are frequently reported by survivors of acute pulmonary embolism (PE). However, current guidelines provide no specific recommendations on which patients should be followed after acute PE, when follow-up should be performed, and which tests it should include. Definition and classification of late PE sequelae are evolving, and their predictors remain to be determined. Methods: In a post hoc analysis of the Pulmonary Embolism Thrombolysis (PEITHO) trial, we focused on 219 survivors of acute intermediate-risk PE with clinical and echocardiographic follow-up 6 months after randomisation as well as over the long term (median, 3 years after acute PE). The primary outcome was a composite of (1) confirmed chronic thromboembolic pulmonary hypertension (CTEPH) or (2) ‘post-PE impairment’ (PPEI), defined by echocardiographic findings indicating an intermediate or high probability of pulmonary hypertension along with New York Heart Association functional class II–IV. Results: Confirmed CTEPH or PPEI occurred in 29 (13.2%) patients, (6 with CTEPH and 23 with PPEI). A history of chronic heart failure at baseline and incomplete or absent recovery of echocardiographic parameters at 6 months predicted CTEPH or PPEI at long-term follow-up. Conclusions: CTEPH or PPEI occurs in almost one out of seven patients after acute intermediate-risk PE. Six-month echocardiographic follow-up may be useful for timely detection of late sequelae.
KW - Chronic thromboembolic pulmonary hypertension
KW - Post-PE impairment
KW - Pulmonary embolism
KW - Right ventricular dysfunction
KW - Risk stratification
UR - http://www.scopus.com/inward/record.url?scp=85065387903&partnerID=8YFLogxK
U2 - 10.1007/s00392-018-1405-1
DO - 10.1007/s00392-018-1405-1
M3 - Article
C2 - 30564950
AN - SCOPUS:85065387903
SN - 1861-0684
VL - 108
SP - 772
EP - 778
JO - Clinical Research In Cardiology
JF - Clinical Research In Cardiology
IS - 7
ER -