About this trial
Multicenter longitudinal observational ambispective (retrospective cases from 2014 and prospective from 2018 onwards) cohort study. The registry recruits a series of consecutive patients admitted for moderate-high risk or high-risk pulmonary embolism (according to 2019 European Society of Cardiology guidelines) treated invasively. This study aims to describe the acute management of the safety and effectiveness of different percutaneous interventions for acute pulmonary embolism.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
adult patients (aged 18 years old or older)
confirmed diagnosis of acute PE (on computed tomography or echocardiogram plus pulmonary angiography)
high-risk PE or intermediate-high risk according to ESC risk stratification in the 2019 guidelines (briefly, elevated cardiac biomarkers [troponin or N-terminal pro-B-type natriuretic peptide], and right ventricle to left ventricle ratio > 0.9 [on computed tomography or echocardiogram], and PE severity index III to IV or simplified PE severity index=1
eligibility for catheter-directed intervention
Disqualifiers
unconfirmed diagnosis of PE
undefined risk stratification, and
PE with uncertain chronology or beyond seven days of symptom initiation.
Trial population
Consecutive patients admitted for moderate-high risk or high-risk PE and treated invasively with any kind of catheter-directed intervention.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
All cause-death
Secondary outcomes
all cause-death
all cause-death
all cause-death
procedural success
defined as technical procedure completed without procedural complications or 48-hour death
Sponsors and contacts
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Hospital San Carlos, Madrid
Lead sponsor
Asociación de Cardiología Intervencionista de la Sociedad Española de Cardiología
Collaborator