2011
DOI: 10.1016/j.jvs.2011.05.114
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Effects of age on the risk of dying from pulmonary embolism or bleeding during treatment of deep vein thrombosis

Abstract: During the first week of treatment, the risk of fatal bleeding and fatal PE were similar. Then, particularly in patients who were aged ≥ 60 years, the risk of dying from bleeding exceeded the risk of dying from PE.

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Cited by 55 publications
(29 citation statements)
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References 19 publications
(13 reference statements)
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“…However, clinical care should be based on a broader set of medical outcomes than just mortality, and only half of PE patients dying within the first 30 days had a PE-related death. [10][11][12][13] In the current analysis, we tried to identify characteristics associated with the occurrence of the composite outcome of recurrent PE, major bleeding or death within the first 10 days of therapy. 9 Therefore, improvements in the risk stratification of patients with PE are still needed.…”
mentioning
confidence: 99%
“…However, clinical care should be based on a broader set of medical outcomes than just mortality, and only half of PE patients dying within the first 30 days had a PE-related death. [10][11][12][13] In the current analysis, we tried to identify characteristics associated with the occurrence of the composite outcome of recurrent PE, major bleeding or death within the first 10 days of therapy. 9 Therefore, improvements in the risk stratification of patients with PE are still needed.…”
mentioning
confidence: 99%
“…On multivariate analysis, fatal PE was significantly more common in patients with recent immobility. Finally, we assessed the risk of fatal PE and fatal bleeding in 16,199 patients with lower limb DVT (without symptomatic PE at the time of inclusion), with patients categorized according to age 6. During the first 3 months of treatment, there were 31 fatal PE (0.19%) and 83 fatal bleeds (0.51%).…”
Section: Study Supportmentioning
confidence: 99%
“…The RIETE (Registro Informatizado de Enfermedad TromboEmbólica) Registry is an ongoing, multicenter, international (Spain, Italy, France, Israel, Portugal, Germany, Switzerland, Czech Republic, Republic of Macedonia, Greece, Canada and Ecuador), observational registry of patients with symptomatic, objectively confirmed, acute VTE (ClinicalTrials.gov identifier: NCT02832245). Data from this registry have been used to evaluate outcomes after acute VTE, such as the frequency of recurrent VTE, bleeding and mortality, and risk factors for these outcomes . In the current analysis, we compared the effectiveness and safety of the two different dosing strategies of enoxaparin (once vs. twice daily) in the initial therapy of patients with acute VTE.…”
Section: Introductionmentioning
confidence: 99%