Key result
Polyvascular atherosclerotic disease in patients with acute pulmonary embolism was associated with a significantly increased risk of recurrent PE compared to those without atherosclerosis (HR 3.2).
Why the study?
The prognostic role of atherosclerosis in pulmonary embolism remained uncertain.
Does the presence and extent of atherosclerotic disease increase the risk of recurrent PE, VTE, and adverse outcomes in patients with acute pulmonary embolism?
Observational (n=47,578)
Yes
Does the presence and extent of atherosclerotic disease increase the risk of recurrent PE, VTE, and adverse outcomes in patients with acute pulmonary embolism?
Atherosclerosis in acute PE patients is associated with a dose-dependent increased risk of recurrent PE and all-cause death, highlighting the importance of cardiovascular risk stratification.
Answers are grounded in this paper and cite their sources.
May inform CV risk stratification in acute PE; leaves open whether atherosclerosis modification reduces recurrence.
BACKGROUND: The role of atherosclerosis in pulmonary embolism (PE) prognosis remains uncertain. Our study assesses characteristics and outcomes of acute PE patients according to the presence and extent of atherosclerotic disease. METHODS: Using data from the RIETE registry, acute PE patients were classified into three groups based on personal history: (1) polyvascular atherosclerosis, (2) single vascular atherosclerosis, and (3) no symptomatic atherosclerosis. Primary outcomes included recurrent PE and venous thromboembolism (VTE), arterial events, major bleeding, and all-cause death. Hazard ratios (HR) and Kaplan-Meier curves for clinical outcomes were estimated using Cox regression models. RESULTS: Among 47,578 acute PE patients, 1,040 had polyvascular, 6,191 single-vascular, and 40,347 no atherosclerosis. During a median follow-up of 331 days, Adverse outcomes were more frequent in patients with atherosclerosis (vs. no atherosclerosis), rising with the number of affected vascular territories. Recurrent PE rates were 2.8, 1.6, and 1.2 per 100 patient-years in the polyvascular, single-vascular, and no atherosclerosis groups. Multivariable analysis showed a dose-dependent relationship between atherosclerosis and recurrent PE risk, with HRs of 3.2 (95% CI 1.7-5.9) and 1.6 (95% CI 1.1-2.3) for polyvascular and single-vascular disease (vs. no atherosclerosis). The risk of all-cause death followed a similar trend, with HRs of 1.3 (95% CI 1.1-1.6) and 1.2 (95% CI 1.1-1.4), respectively. Major bleeding appeared to be influenced by overall health status and antithrombotic therapy intensity. CONCLUSION: Atherosclerosis in acute PE patients may serve as a marker of disease severity and lead independently to adverse outcomes, highlighting the importance of cardiovascular risk stratification.
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Cardi et al. (2025) conducted an observational in Acute pulmonary embolism (n=47,578). Polyvascular atherosclerotic disease vs. No symptomatic atherosclerotic disease was evaluated on Recurrent pulmonary embolism (HR 3.2, 95% CI 1.7-5.9). Polyvascular atherosclerotic disease in patients with acute pulmonary embolism was associated with a significantly increased risk of recurrent PE compared to those without atherosclerosis (HR 3.2).
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