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Bolus tenecteplase for right ventricle dysfunction in hemodynamically stable patients with pulmonary embolism.
- Source :
-
Thrombosis research [Thromb Res] 2010 Mar; Vol. 125 (3), pp. e82-6. Date of Electronic Publication: 2009 Oct 14. - Publication Year :
- 2010
-
Abstract
- Introduction: The clinical benefit of thrombolytic treatment over heparin in patients with pulmonary embolism without hemodynamic compromise remains controversial. In these patients bolus tenecteplase has the potential to provide an effective and safe thrombolysis.<br />Methods: We evaluated the effect of tenecteplase on right ventricle dysfunction (RVD) assessed by echocardiography in hemodynamically stable patients with PE in a multicenter, randomized, double-blind, placebo-controlled study. RVD was defined as right/left ventricle end-diastolic dimension ratio >1 in the apical 4-chamber view. Patients were randomized to receive weight-adjusted single-bolus tenecteplase or placebo. All patients received unfractionated heparin. Reduction of RVD at 24 hours was the primary efficacy end-point and was evaluated by an independent committee unaware of treatment allocation.<br />Results: Overall, 58 patients were randomized. Echocardiograms were adequate for efficacy analysis in 51 patients, 23 randomized to tenecteplase and 28 to placebo. The reduction of right to left ventricle end-diastolic dimension ratio at 24 hours was 0.31+/-0.08 in patients randomized to tenecteplase as compared to 0.10+/-0.07 in patients randomized to placebo (p=0.04). One patient randomized to tenecteplase suffered a clinical event (recurrent pulmonary embolism) in comparison to three patients randomized to placebo (1 recurrent pulmonary embolism; 1 clinical deterioration and 1 non pulmonary embolism-related death). Two non fatal major bleedings occurred with tenecteplase (1 intracranial) and one with placebo.<br />Conclusion: In hemodynamically stable patients with PE, treatment with single bolus tenecteplase is feasible at the same dosages used for acute myocardial infarction and is associated with reduction of RVD at 24 hours. Whether this benefit is associated with an improved clinical outcome without excessive bleeding is currently explored in a large clinical trial.<br /> ((c) 2009 Elsevier Ltd. All rights reserved.)
- Subjects :
- Aged
Anticoagulants therapeutic use
Dosage Forms
Double-Blind Method
Drug Administration Schedule
Drug Therapy, Combination
Echocardiography
Feasibility Studies
Female
Fibrinolytic Agents administration & dosage
Hemorrhage complications
Heparin therapeutic use
Humans
Male
Middle Aged
Pilot Projects
Pulmonary Embolism diagnostic imaging
Tenecteplase
Tissue Plasminogen Activator administration & dosage
Treatment Outcome
Ventricular Dysfunction, Right diagnostic imaging
Fibrinolytic Agents therapeutic use
Pulmonary Embolism complications
Tissue Plasminogen Activator therapeutic use
Ventricular Dysfunction, Right drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1879-2472
- Volume :
- 125
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Thrombosis research
- Publication Type :
- Academic Journal
- Accession number :
- 19833379
- Full Text :
- https://doi.org/10.1016/j.thromres.2009.09.017