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Published on: February 20, 2017
Diagnostic accuracy of echocardiography combined with chest CT in pulmonary hypertension
Adil Shujaat1, Abubakr A Bajwa2, Farah Al-Saffar3
1Division of Pulmonary, Critical Care and Sleep Medicine, University at Buffalo, SUNY, Buffalo, NY, USA.
Insights
Combining transthoracic echocardiography (TTE) and computerized axial tomography (CT) improves pulmonary hypertension (PH) diagnosis. This combined approach offers better accuracy than individual imaging techniques for identifying PH.
Area of Science:
- Cardiology
- Radiology
- Pulmonary Medicine
Background:
- Transthoracic echocardiography (TTE) and computerized axial tomography (CT) are established imaging modalities.
- Their complementary roles in diagnosing pulmonary hypertension (PH) warrant investigation.
Purpose of the Study:
- To assess the diagnostic accuracy of combining TTE and chest CT for identifying PH.
- To compare the combined diagnostic performance against individual imaging techniques.
Main Methods:
- Retrospective review of 87 patients who underwent TTE, CT, and right heart catheterization (RHC).
- PH defined by specific criteria on TTE (systolic pulmonary artery pressure >40 mm Hg or TR jet velocity >2.8m/s), CT (rPA >1 or dPA >30 mm), and RHC (mPAP >25 mm Hg).
Main Results:
- A total of 87 patients were analyzed, with 75% prevalence of PH.
- The combination of TTE's TR jet velocity and CT's rPA demonstrated high sensitivity (98%) and specificity (70%), with an ROC area under the curve of 0.84.
Conclusions:
- The combined use of TTE and chest CT is superior to either modality alone for PH identification.
- This integrated imaging strategy can aid in the diagnosis and exclusion of PH in diverse patient populations.
Background:
Transthoracic echocardiography (TTE) and computerized axial tomography (CT) are complementary imaging techniques. It is possible that a combination of the two may offer a better way of identifying pulmonary hypertension (PH) than either one alone.
Objectives:
To determine the diagnostic accuracy of TTE combined with chest CT in pulmonary hypertension.
Methods:
We performed a retrospective review of consecutive patients who had undergone TTE, CT and right heart catheterization (RHC) between 7/1/2008 and 6/30/2012. PH was defined as systolic pulmonary artery pressure >40 mm Hg or tricuspid regurgitant (TR) jet velocity >2.8m/s on TTE, ratio of diameter of pulmonary artery to ascending aorta (rPA) >1 or diameter of PA (dPA) >30 mm on CT, and mean PAP (mPAP) >25 mm Hg on RHC.
Results:
There was a total of 87 patients. The mean ± SD age was 54.3 ± 15.9 years and 69 (79%) were female. The prevalence of PH was 75%. The mean ± SD mPAP was 35.8 ± 14.2 mm Hg. The majority of the patients belonged to World Health Organization group I PH. Fifty per cent of the CT scans were done with intravenous contrast dye. The combination of TR jet velocity and rPA provided the best combination of sensitivity (98%) and specificity (70%) with an ROC area under the curve of 0.84.
Conclusion:
The combination of TTE and chest CT is better than either imaging technique alone in identifying patients with PH in a heterogeneous population and may exclude PH.
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