4.6 Article

Home treatment in pulmonary embolism

Journal

THROMBOSIS RESEARCH
Volume 126, Issue 1, Pages E1-E5

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.thromres.2009.09.026

Keywords

Early discharge; low molecular weight heparin; pulmonary embolism; anticoagulants; home treatment; disease management

Funding

  1. Ministry of Health and Consumer Affairs, Instituto de Salud Carlos III [PI03/0192]
  2. Sociedad Espanola de Neumologia y Cirugia Toracica (SEPAR)

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Background: Limited data exist on the feasibility of providing outpatient care to patients with acute pulmonary embolism (PE). Methods: We conducted a multicenter randomized clinical trial in acute symptomatic PE to compare the efficacy and safety of early discharge versus standard hospitalization. A clinical prediction rule was used to identify low-risk patients. All patients were followed for three months. The primary outcomes were venous thromboembolic recurrences, major and minor bleeding, and overall mortality. Results: One hundred and thirty two low-risk patients with acute symptomatic PE were randomized to early discharge (n=72) or standard hospitalization (n=60). Overall mortality was 4.2% (95% CI, 0.5-8.9) in the early discharge group and 8.3% (95% CI, 1.1-15) in the standard hospitalization group (Relative Risk (RR) 0.5; 95% confidence interval [CI], 0.12-2.01). Non-fatal recurrences were 2.8% (95% CI, 1.1-6.6) in the early discharge group and 3.3% (95% CI, 1.3-8%) in the standard hospitalization group (RR 0.8; 95% CI, 0.12-5.74). The rates of clinically relevant bleeding were 5.5% in the early discharge group and 5% in the standard hospitalization group (P=0.60). Short-term mortality was 2.8% (95% CI, 0.8-9.6%) in the early discharge group as compared with 0% in the standard hospitalization group. Based on the rate of short-term death in a carefully selected population, the study was suspended. Conclusions: In spite of the number of complications in patients with acute symptomatic PE randomized to standard hospitalization or early discharge did not differ significantly. The rate of short-term mortality was unexpectedly high in a (a priori) low-risk group of patients with acute PE. The accuracy of clinical prediction scores needs to be validated in well designed clinical trials. (ClinicalTrials.govnumber, NCT00214929.) (C) 2009 Elsevier Ltd. All rights reserved.

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