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Fibrinolysis for patients with intermediate-risk pulmonary embolism

Authors :
UCL - (SLuc) Service des urgences
UCL - SSS/IREC/MEDA - Pôle de médecine aiguë
Meyer, Guy
Vicaut, Eric
Danays, Thierry
Agnelli, Giancarlo
Becattini, Cecilia
Beyer-Westendorf, Jan
Bluhmki, Erich
Bouvaist, Helene
Brenner, Benjamin
Couturaud, Francis
Dellas, Claudia
Empen, Klaus
Franca, Ana
Galiè, Nazzareno
Geibel, Annette
Goldhaber, Samuel Z
Jimenez, David
Kozak, Matija
Kupatt, Christian
Kucher, Nils
Lang, Irene M
Lankeit, Mareike
Meneveau, Nicolas
Pacouret, Gerard
Palazzini, Massimiliano
Petris, Antoniu
Pruszczyk, Piotr
Rugolotto, Matteo
Salvi, Aldo
Schellong, Sebastian
Sebbane, Mustapha
Sobkowicz, Bozena
Stefanovic, Branislav S
Thiele, Holger
Torbicki, Adam
Verschuren, Franck
Konstantinides, Stavros V
PEITHO Investigators
UCL - (SLuc) Service des urgences
UCL - SSS/IREC/MEDA - Pôle de médecine aiguë
Meyer, Guy
Vicaut, Eric
Danays, Thierry
Agnelli, Giancarlo
Becattini, Cecilia
Beyer-Westendorf, Jan
Bluhmki, Erich
Bouvaist, Helene
Brenner, Benjamin
Couturaud, Francis
Dellas, Claudia
Empen, Klaus
Franca, Ana
Galiè, Nazzareno
Geibel, Annette
Goldhaber, Samuel Z
Jimenez, David
Kozak, Matija
Kupatt, Christian
Kucher, Nils
Lang, Irene M
Lankeit, Mareike
Meneveau, Nicolas
Pacouret, Gerard
Palazzini, Massimiliano
Petris, Antoniu
Pruszczyk, Piotr
Rugolotto, Matteo
Salvi, Aldo
Schellong, Sebastian
Sebbane, Mustapha
Sobkowicz, Bozena
Stefanovic, Branislav S
Thiele, Holger
Torbicki, Adam
Verschuren, Franck
Konstantinides, Stavros V
PEITHO Investigators
Source :
New England Journal of Medicine, Vol. 370, no. 15, p. 1402-1411 (2014)
Publication Year :
2014

Abstract

BACKGROUND: The role of fibrinolytic therapy in patients with intermediate-risk pulmonary embolism is controversial. METHODS: In a randomized, double-blind trial, we compared tenecteplase plus heparin with placebo plus heparin in normotensive patients with intermediate-risk pulmonary embolism. Eligible patients had right ventricular dysfunction on echocardiography or computed tomography, as well as myocardial injury as indicated by a positive test for cardiac troponin I or troponin T. The primary outcome was death or hemodynamic decompensation (or collapse) within 7 days after randomization. The main safety outcomes were major extracranial bleeding and ischemic or hemorrhagic stroke within 7 days after randomization. RESULTS: Of 1006 patients who underwent randomization, 1005 were included in the intention-to-treat analysis. Death or hemodynamic decompensation occurred in 13 of 506 patients (2.6%) in the tenecteplase group as compared with 28 of 499 (5.6%) in the placebo group (odds ratio, 0.44; 95% confidence interval, 0.23 to 0.87; P=0.02). Between randomization and day 7, a total of 6 patients (1.2%) in the tenecteplase group and 9 (1.8%) in the placebo group died (P=0.42). Extracranial bleeding occurred in 32 patients (6.3%) in the tenecteplase group and 6 patients (1.2%) in the placebo group (P<0.001). Stroke occurred in 12 patients (2.4%) in the tenecteplase group and was hemorrhagic in 10 patients; 1 patient (0.2%) in the placebo group had a stroke, which was hemorrhagic (P=0.003). By day 30, a total of 12 patients (2.4%) in the tenecteplase group and 16 patients (3.2%) in the placebo group had died (P=0.42). CONCLUSIONS: In patients with intermediate-risk pulmonary embolism, fibrinolytic therapy prevented hemodynamic decompensation but increased the risk of major hemorrhage and stroke. (Funded by the Programme Hospitalier de Recherche Clinique in France and others; PEITHO EudraCT number, 2006-005328-18; ClinicalTrials.gov number, NCT00639743.).

Details

Database :
OAIster
Journal :
New England Journal of Medicine, Vol. 370, no. 15, p. 1402-1411 (2014)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1130479176
Document Type :
Electronic Resource