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d-Dimer With the Aortic Dissection Detection Risk Score May Improve Patient Selection for Acute Aortic Syndrome
Sameer Bhat1,2, Shreya Bhat3, Franco Schreve4
1Department of Surgery, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.
Insights
A negative d-dimer test effectively rules out acute aortic syndrome (AAS) in low-risk patients. This finding supports using d-dimer to avoid unnecessary computerised tomographic aortography (CTA) scans for suspected AAS.
Area of Science:
- Cardiovascular Medicine
- Diagnostic Imaging
- Emergency Medicine
Background:
- Acute aortic syndrome (AAS) is a life-threatening condition requiring definitive diagnosis via computerised tomographic aortography (CTA).
- Current risk-stratification tools for AAS, like the aortic dissection detection risk score (ADD-RS), lack validation in low-to-intermediate risk populations.
- There is a need for effective methods to identify patients who do not require advanced imaging for suspected AAS.
Purpose of the Study:
- To evaluate the diagnostic efficacy of d-dimer testing in identifying AAS in patients with low or intermediate pre-test probability.
- To determine the sensitivity and negative predictive value (NPV) of a negative d-dimer result in ruling out AAS.
- To analyze trends in d-dimer test utilization for suspected AAS over time.
Main Methods:
- Retrospective analysis of atraumatic thoracic CTAs in adults suspected of AAS presenting to the emergency department.
- Aortic dissection detection risk score (ADD-RS) was used to stratify patients into low/intermediate (ADD-RS ≤ 1) and high-risk groups.
- Calculation of sensitivity and NPV for d-dimer (< 500 ng/mL) in the low/intermediate risk group.
Main Results:
- In 181 low/intermediate risk patients, a negative d-dimer (< 500 ng/mL) demonstrated 100% sensitivity and 100% NPV for ruling out AAS.
- A significant increase in annual d-dimer requests for patients undergoing CTA for suspected AAS was observed (p=0.0059).
- The proportion of negative d-dimer results increased significantly (p=0.0036), while positive results remained stable.
Conclusions:
- A d-dimer level below 500 ng/mL can reliably exclude AAS in low-to-intermediate risk patients.
- This biomarker may help clinicians avoid unnecessary computerised tomographic aortography (CTA) scans in this patient cohort.
- The findings support the judicious use of d-dimer as a rule-out test for AAS in selected emergency department presentations.
Objective:
Acute aortic syndrome (AAS) refers to a group of life-threatening cardiovascular emergencies that require computerised tomographic aortography (CTA) for definitive diagnosis. However, there is currently no validated risk-stratification tool for AAS in low or intermediate risk patients using the aortic dissection detection risk score (ADD-RS). This study evaluated the efficacy of d-dimer in low or intermediate risk patients who underwent CTA for suspected AAS.
Methods:
This retrospective, cross-sectional study included all atraumatic thoracic CTAs performed at Auckland City Hospital (Aotearoa New Zealand) between 2009 and 2019 for adults with suspected AAS presenting to the emergency department (ED). Pre-test probability for AAS was determined using the ADD-RS. The sensitivity and negative predictive value (NPV) of a negative d-dimer (< 500 ng/mL) for ruling out AAS in low or intermediate risk patients (ADD-RS ≤ 1) were calculated. Trends in d-dimer requests over time were also analysed.
Results:
d-dimers were assessed in 181 low or intermediate risk patients with thoracic CTAs. Negative d-dimer had a sensitivity of 100% (95% CI: 66%-100%) and NPV of 100% (95% CI: 97%-100%) for ruling out AAS. There was a significant rise in the annual number of d-dimer requests among patients who underwent CTA scans (p = 0.0059). Significantly more of these requests returned negative values (p = 0.0036), while the number of positive results (≥ 500 ng/mL) remained unchanged (p = 0.15).
Conclusions:
Our findings suggest that d-dimer < 500 ng/mL may be used to forgo unfavourable CTA scans in low or intermediate risk patients within our small AoNZ cohort in whom AAS is suspected.
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