Patient Outcomes after Acute Pulmonary Embolism: A Pooled Survival Analysis of Different Adverse Events

There is a lack of information on the long-term prognosis of patients with acute pulmonary embolism (PE). To assess the long-term risk for adverse events after PE. Consecutive patients diagnosed with PE between January 2001 and July 2007, and patients in whom PE was ruled out from a previous study w...

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Veröffentlicht in:American journal of respiratory and critical care medicine 2010-03, Vol.181 (5), p.501-506
Hauptverfasser: Klok, Frederikus A, Zondag, Wendy, van Kralingen, Klaas W, van Dijk, Arie P. J, Tamsma, Jouke T, Heyning, Fenna H, Vliegen, Hubert W, Huisman, Menno V
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container_end_page 506
container_issue 5
container_start_page 501
container_title American journal of respiratory and critical care medicine
container_volume 181
creator Klok, Frederikus A
Zondag, Wendy
van Kralingen, Klaas W
van Dijk, Arie P. J
Tamsma, Jouke T
Heyning, Fenna H
Vliegen, Hubert W
Huisman, Menno V
description There is a lack of information on the long-term prognosis of patients with acute pulmonary embolism (PE). To assess the long-term risk for adverse events after PE. Consecutive patients diagnosed with PE between January 2001 and July 2007, and patients in whom PE was ruled out from a previous study were followed until July 2008 for the occurrence of adverse clinical events: mortality, symptomatic recurrent venous thromboembolism, cancer, arterial cardiovascular events and chronic thromboembolic pulmonary hypertension. Hazard ratios (HR) for all endpoints and a combined endpoint were calculated and adjusted for potential confounders. Three hundred eight patients with unprovoked, 558 with provoked, and 334 without PE were studied with a median follow-up period of 3.3 years. Patients with unprovoked PE had a lower overall risk for mortality than patients with provoked PE (HR, 0.59; 95% confidence interval [CI], 0.43-0.82), but a higher risk for nonmalignancy-related mortality (HR, 1.8; 95% CI, 1.3-2.5), recurrent venous thromboembolism (HR, 2.1; 95% CI, 1.3-3.1), cancer (HR, 4.4; 95% CI, 2.0-10), cardiovascular events (HR, 2.6; 95% CI, 1.5-3.8) and chronic thromboembolic pulmonary hypertension (1.5 vs. 0%). The risk for the combined endpoint did not differ between both groups (HR, 0.98; 95% CI, 0.82-1.1). Patients without PE had similar risks for malignancy and cardiovascular events than patients with provoked PE, but lower risks for the remaining outcomes. The fraction of both patients with provoked and unprovoked PE without events after 1 year was only 70% and decreased to fewer than 60% after 2 years and fewer than 50% after 4 years, whereas this latter was 84% for the control patients. The clinical course of acute PE is complicated by high rates of serious adverse events, which occur in half of the patients within 4 years.
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The fraction of both patients with provoked and unprovoked PE without events after 1 year was only 70% and decreased to fewer than 60% after 2 years and fewer than 50% after 4 years, whereas this latter was 84% for the control patients. The clinical course of acute PE is complicated by high rates of serious adverse events, which occur in half of the patients within 4 years.</description><identifier>ISSN: 1073-449X</identifier><identifier>EISSN: 1535-4970</identifier><identifier>DOI: 10.1164/rccm.200907-1141OC</identifier><identifier>PMID: 19965808</identifier><language>eng</language><publisher>New York, NY: Am Thoracic Soc</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. 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Hazard ratios (HR) for all endpoints and a combined endpoint were calculated and adjusted for potential confounders. Three hundred eight patients with unprovoked, 558 with provoked, and 334 without PE were studied with a median follow-up period of 3.3 years. Patients with unprovoked PE had a lower overall risk for mortality than patients with provoked PE (HR, 0.59; 95% confidence interval [CI], 0.43-0.82), but a higher risk for nonmalignancy-related mortality (HR, 1.8; 95% CI, 1.3-2.5), recurrent venous thromboembolism (HR, 2.1; 95% CI, 1.3-3.1), cancer (HR, 4.4; 95% CI, 2.0-10), cardiovascular events (HR, 2.6; 95% CI, 1.5-3.8) and chronic thromboembolic pulmonary hypertension (1.5 vs. 0%). The risk for the combined endpoint did not differ between both groups (HR, 0.98; 95% CI, 0.82-1.1). Patients without PE had similar risks for malignancy and cardiovascular events than patients with provoked PE, but lower risks for the remaining outcomes. 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Consecutive patients diagnosed with PE between January 2001 and July 2007, and patients in whom PE was ruled out from a previous study were followed until July 2008 for the occurrence of adverse clinical events: mortality, symptomatic recurrent venous thromboembolism, cancer, arterial cardiovascular events and chronic thromboembolic pulmonary hypertension. Hazard ratios (HR) for all endpoints and a combined endpoint were calculated and adjusted for potential confounders. Three hundred eight patients with unprovoked, 558 with provoked, and 334 without PE were studied with a median follow-up period of 3.3 years. Patients with unprovoked PE had a lower overall risk for mortality than patients with provoked PE (HR, 0.59; 95% confidence interval [CI], 0.43-0.82), but a higher risk for nonmalignancy-related mortality (HR, 1.8; 95% CI, 1.3-2.5), recurrent venous thromboembolism (HR, 2.1; 95% CI, 1.3-3.1), cancer (HR, 4.4; 95% CI, 2.0-10), cardiovascular events (HR, 2.6; 95% CI, 1.5-3.8) and chronic thromboembolic pulmonary hypertension (1.5 vs. 0%). The risk for the combined endpoint did not differ between both groups (HR, 0.98; 95% CI, 0.82-1.1). Patients without PE had similar risks for malignancy and cardiovascular events than patients with provoked PE, but lower risks for the remaining outcomes. The fraction of both patients with provoked and unprovoked PE without events after 1 year was only 70% and decreased to fewer than 60% after 2 years and fewer than 50% after 4 years, whereas this latter was 84% for the control patients. The clinical course of acute PE is complicated by high rates of serious adverse events, which occur in half of the patients within 4 years.</abstract><cop>New York, NY</cop><pub>Am Thoracic Soc</pub><pmid>19965808</pmid><doi>10.1164/rccm.200907-1141OC</doi><tpages>6</tpages></addata></record>
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subjects Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Anticoagulants
Biological and medical sciences
Cancer
Cardiovascular Diseases - epidemiology
Cohort analysis
Female
Hemodynamics
Hormone replacement therapy
Humans
Intensive care medicine
Kaplan-Meier Estimate
Lung Neoplasms - epidemiology
Male
Medical imaging
Medical prognosis
Medical sciences
Middle Aged
Mortality
Patients
Pneumology
Prognosis
Proportional Hazards Models
Pulmonary arteries
Pulmonary Embolism - complications
Pulmonary Embolism - mortality
Pulmonary embolisms
Pulmonary hypertension
Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases
Recurrence
Risk Factors
Survival Analysis
Thromboembolism
Thrombosis
Time Factors
Treatment Outcome
title Patient Outcomes after Acute Pulmonary Embolism: A Pooled Survival Analysis of Different Adverse Events
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