Aortic Dissection Clinical Trial
Official title:
Aortic Dissection Detection Risk Score Plus D-dimer in the Diagnostic Workup of Suspected Acute Aortic Dissection: a Prospective Multicenter Study
Acute aortic dissection (AD) is a deadly, difficult to diagnose disease presenting with an
array of common and unspecific symptoms. Aortic dissection detection (ADD) risk score is a
bedside clinical tool to estimate the risk of AD. D-dimer has been evaluated in several
studies as a biomarker of AD and has showed a pooled diagnostic sensitivity of 97%. However,
considering the severe morbidity and mortality of AD, a negative d-dimer per se is considered
insufficient to rule-out AD in unselected patients.
The aim of the present study is to evaluate whether the diagnostic performance of d-dimer
differs in patients at different clinical risk of AD, and in particular whether a negative
d-dimer test may allow safe rule-out of AD in any patient subgroup without necessity to
perform urgent aortic imaging.
Consecutive adult patients with suspected AD presenting to Emergency Department will be
enrolled before the establishment of a final diagnosis; a standardized clinical form
comprehensive of presence/absence of 12 risk markers allowing ADD risk score fulfilled and
d-dimer levels measured at presentation.
The aortic imaging exam used to confirm or refuse of AD will be computed tomography
angiography or transesophageal echocardiography and final diagnosis established after
reviewing of all available data.
The accuracy, failure rate and efficiency of a diagnostic strategy combining standardized
clinical stratification via the ADD risk score with d-dimer testing will therefore be
assessed.
Acute AD will include the following etiological entities, also known as acute aortic
syndromes: acute aortic dissection, intramural aortic hematoma, penetrating aortic ulcer and
spontaneous aortic rupture.
A pre-specified secondary sub-analysis will evaluate the diagnostic accuracy of focus cardiac
ultrasound (FoCUS) and chest x ray for suspected AD.
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