AI Article Synopsis

  • Intermediate-high-risk pulmonary embolism (PE) involves right ventricular dysfunction and elevated troponin levels, even if patients appear stable initially.
  • The PEITHO-3 study will assess the safety and efficacy of a reduced-dose alteplase treatment compared to standard heparin anticoagulation in patients who meet certain severity criteria.
  • With a goal of enrolling 650 participants, the study aims to evaluate critical outcomes related to death, hemodynamic stability, and bleeding risks within 30 days, potentially influencing future treatment guidelines for acute PE.

Article Abstract

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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9197594PMC
http://dx.doi.org/10.1055/a-1653-4699DOI Listing

Publication Analysis

Top Keywords

pulmonary embolism
16
hemodynamic decompensation
12
life-threatening bleeding
12
intermediate-high-risk pulmonary
8
embolism international
8
international thrombolysis
8
thrombolysis peitho-3
8
primary efficacy
8
efficacy outcome
8
all-cause death
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!