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Reduced-Dose Intravenous Thrombolysis for Acute Intermediate–High-risk Pulmonary Embolism: Rationale and Design of the Pulmonary Embolism International THrOmbolysis (PEITHO)-3 trial

Intermediate–high-risk pulmonary embolism (PE) is characterized by right ventricular (RV) dysfunction and elevated circulating cardiac troponin levels despite apparent hemodynamic stability at presentation. In these patients, full-dose systemic thrombolysis reduced the risk of hemodynamic decompensa...

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Autores principales: Sanchez, Olivier, Charles-Nelson, Anaïs, Ageno, Walter, Barco, Stefano, Binder, Harald, Chatellier, Gilles, Duerschmied, Daniel, Empen, Klaus, Ferreira, Melanie, Girard, Philippe, Huisman, Menno V., Jiménez, David, Katsahian, Sandrine, Kozak, Matija, Lankeit, Mareike, Meneveau, Nicolas, Pruszczyk, Piotr, Petris, Antoniu, Righini, Marc, Rosenkranz, Stephan, Schellong, Sebastian, Stefanovic, Branislav, Verhamme, Peter, de Wit, Kerstin, Vicaut, Eric, Zirlik, Andreas, Konstantinides, Stavros V., Meyer, Guy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9197594/
https://www.ncbi.nlm.nih.gov/pubmed/34560806
http://dx.doi.org/10.1055/a-1653-4699
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author Sanchez, Olivier
Charles-Nelson, Anaïs
Ageno, Walter
Barco, Stefano
Binder, Harald
Chatellier, Gilles
Duerschmied, Daniel
Empen, Klaus
Ferreira, Melanie
Girard, Philippe
Huisman, Menno V.
Jiménez, David
Katsahian, Sandrine
Kozak, Matija
Lankeit, Mareike
Meneveau, Nicolas
Pruszczyk, Piotr
Petris, Antoniu
Righini, Marc
Rosenkranz, Stephan
Schellong, Sebastian
Stefanovic, Branislav
Verhamme, Peter
de Wit, Kerstin
Vicaut, Eric
Zirlik, Andreas
Konstantinides, Stavros V.
Meyer, Guy
author_facet Sanchez, Olivier
Charles-Nelson, Anaïs
Ageno, Walter
Barco, Stefano
Binder, Harald
Chatellier, Gilles
Duerschmied, Daniel
Empen, Klaus
Ferreira, Melanie
Girard, Philippe
Huisman, Menno V.
Jiménez, David
Katsahian, Sandrine
Kozak, Matija
Lankeit, Mareike
Meneveau, Nicolas
Pruszczyk, Piotr
Petris, Antoniu
Righini, Marc
Rosenkranz, Stephan
Schellong, Sebastian
Stefanovic, Branislav
Verhamme, Peter
de Wit, Kerstin
Vicaut, Eric
Zirlik, Andreas
Konstantinides, Stavros V.
Meyer, Guy
author_sort Sanchez, Olivier
collection PubMed
description Intermediate–high-risk pulmonary embolism (PE) is characterized by right ventricular (RV) dysfunction and elevated circulating cardiac troponin levels despite apparent hemodynamic stability at presentation. In these patients, full-dose systemic thrombolysis reduced the risk of hemodynamic decompensation or death but increased the risk of life-threatening bleeding. Reduced-dose thrombolysis may be capable of improving safety while maintaining reperfusion efficacy. The Pulmonary Embolism International THrOmbolysis (PEITHO)-3 study (ClinicalTrials.gov Identifier: NCT04430569) is a randomized, placebo-controlled, double-blind, multicenter, multinational trial with long-term follow-up. We will compare the efficacy and safety of a reduced-dose alteplase regimen with standard heparin anticoagulation. Patients with intermediate–high-risk PE will also fulfill at least one clinical criterion of severity: systolic blood pressure ≤110 mm Hg, respiratory rate >20 breaths/min, or history of heart failure. The primary efficacy outcome is the composite of all-cause death, hemodynamic decompensation, or PE recurrence within 30 days of randomization. Key secondary outcomes, to be included in hierarchical analysis, are fatal or GUSTO severe or life-threatening bleeding; net clinical benefit (primary efficacy outcome plus severe or life-threatening bleeding); and all-cause death, all within 30 days. All outcomes will be adjudicated by an independent committee. Further outcomes include PE-related death, hemodynamic decompensation, or stroke within 30 days; dyspnea, functional limitation, or RV dysfunction at 6 months and 2 years; and utilization of health care resources within 30 days and 2 years. The study is planned to enroll 650 patients. The results are expected to have a major impact on risk-adjusted treatment of acute PE and inform guideline recommendations.
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spelling pubmed-91975942022-06-15 Reduced-Dose Intravenous Thrombolysis for Acute Intermediate–High-risk Pulmonary Embolism: Rationale and Design of the Pulmonary Embolism International THrOmbolysis (PEITHO)-3 trial Sanchez, Olivier Charles-Nelson, Anaïs Ageno, Walter Barco, Stefano Binder, Harald Chatellier, Gilles Duerschmied, Daniel Empen, Klaus Ferreira, Melanie Girard, Philippe Huisman, Menno V. Jiménez, David Katsahian, Sandrine Kozak, Matija Lankeit, Mareike Meneveau, Nicolas Pruszczyk, Piotr Petris, Antoniu Righini, Marc Rosenkranz, Stephan Schellong, Sebastian Stefanovic, Branislav Verhamme, Peter de Wit, Kerstin Vicaut, Eric Zirlik, Andreas Konstantinides, Stavros V. Meyer, Guy Thromb Haemost Intermediate–high-risk pulmonary embolism (PE) is characterized by right ventricular (RV) dysfunction and elevated circulating cardiac troponin levels despite apparent hemodynamic stability at presentation. In these patients, full-dose systemic thrombolysis reduced the risk of hemodynamic decompensation or death but increased the risk of life-threatening bleeding. Reduced-dose thrombolysis may be capable of improving safety while maintaining reperfusion efficacy. The Pulmonary Embolism International THrOmbolysis (PEITHO)-3 study (ClinicalTrials.gov Identifier: NCT04430569) is a randomized, placebo-controlled, double-blind, multicenter, multinational trial with long-term follow-up. We will compare the efficacy and safety of a reduced-dose alteplase regimen with standard heparin anticoagulation. Patients with intermediate–high-risk PE will also fulfill at least one clinical criterion of severity: systolic blood pressure ≤110 mm Hg, respiratory rate >20 breaths/min, or history of heart failure. The primary efficacy outcome is the composite of all-cause death, hemodynamic decompensation, or PE recurrence within 30 days of randomization. Key secondary outcomes, to be included in hierarchical analysis, are fatal or GUSTO severe or life-threatening bleeding; net clinical benefit (primary efficacy outcome plus severe or life-threatening bleeding); and all-cause death, all within 30 days. All outcomes will be adjudicated by an independent committee. Further outcomes include PE-related death, hemodynamic decompensation, or stroke within 30 days; dyspnea, functional limitation, or RV dysfunction at 6 months and 2 years; and utilization of health care resources within 30 days and 2 years. The study is planned to enroll 650 patients. The results are expected to have a major impact on risk-adjusted treatment of acute PE and inform guideline recommendations. Georg Thieme Verlag KG 2021-10-31 /pmc/articles/PMC9197594/ /pubmed/34560806 http://dx.doi.org/10.1055/a-1653-4699 Text en The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. ( https://creativecommons.org/licenses/by-nc-nd/4.0/ ) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited.
spellingShingle Sanchez, Olivier
Charles-Nelson, Anaïs
Ageno, Walter
Barco, Stefano
Binder, Harald
Chatellier, Gilles
Duerschmied, Daniel
Empen, Klaus
Ferreira, Melanie
Girard, Philippe
Huisman, Menno V.
Jiménez, David
Katsahian, Sandrine
Kozak, Matija
Lankeit, Mareike
Meneveau, Nicolas
Pruszczyk, Piotr
Petris, Antoniu
Righini, Marc
Rosenkranz, Stephan
Schellong, Sebastian
Stefanovic, Branislav
Verhamme, Peter
de Wit, Kerstin
Vicaut, Eric
Zirlik, Andreas
Konstantinides, Stavros V.
Meyer, Guy
Reduced-Dose Intravenous Thrombolysis for Acute Intermediate–High-risk Pulmonary Embolism: Rationale and Design of the Pulmonary Embolism International THrOmbolysis (PEITHO)-3 trial
title Reduced-Dose Intravenous Thrombolysis for Acute Intermediate–High-risk Pulmonary Embolism: Rationale and Design of the Pulmonary Embolism International THrOmbolysis (PEITHO)-3 trial
title_full Reduced-Dose Intravenous Thrombolysis for Acute Intermediate–High-risk Pulmonary Embolism: Rationale and Design of the Pulmonary Embolism International THrOmbolysis (PEITHO)-3 trial
title_fullStr Reduced-Dose Intravenous Thrombolysis for Acute Intermediate–High-risk Pulmonary Embolism: Rationale and Design of the Pulmonary Embolism International THrOmbolysis (PEITHO)-3 trial
title_full_unstemmed Reduced-Dose Intravenous Thrombolysis for Acute Intermediate–High-risk Pulmonary Embolism: Rationale and Design of the Pulmonary Embolism International THrOmbolysis (PEITHO)-3 trial
title_short Reduced-Dose Intravenous Thrombolysis for Acute Intermediate–High-risk Pulmonary Embolism: Rationale and Design of the Pulmonary Embolism International THrOmbolysis (PEITHO)-3 trial
title_sort reduced-dose intravenous thrombolysis for acute intermediate–high-risk pulmonary embolism: rationale and design of the pulmonary embolism international thrombolysis (peitho)-3 trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9197594/
https://www.ncbi.nlm.nih.gov/pubmed/34560806
http://dx.doi.org/10.1055/a-1653-4699
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