Dilated cardiomyopathy CT: Difference between revisions
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== CT scan == | == CT scan == | ||
Cardiac CT scanning with angiography (CTA) can be | Cardiac CT scanning with angiography (CTA) can be useful to: | ||
* Diagnose heart failure: by calculating the biventricular volume and ejection fraction with good correlation to echocardiography. | |||
* Assessing the regional wall motion (with cine-loop formatting) | |||
* Excluding ischemia as a cause for DCM (Cardiac CTA has a 98% diagnostic sensitivity and 97% specificity in excluding ischemic cardiomyopathy). Also, Myocardial perfusion analysis of the coronary arteries is also beneficial. | |||
* Differential diagnosis of DCM from hypertrophic cardiomyopathy, arrhythmogenic right ventricular dysplasia, and left ventricular noncompaction. | |||
==References== | ==References== |
Revision as of 17:15, 12 December 2019
Dilated cardiomyopathy Microchapters |
Diagnosis |
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Treatment |
Case Studies |
Dilated cardiomyopathy CT On the Web |
American Roentgen Ray Society Images of Dilated cardiomyopathy CT |
Risk calculators and risk factors for Dilated cardiomyopathy CT |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Abdelrahman Ibrahim Abushouk, MD[2]
Overview
Cardiac CT scanning with angiography (CTA) can be helpful in detecting the complication of heart failure, as well excluding ischemia as a cause of dilated cardiomyopathy (calcium coronary score and myocardial perfusion analysis).
CT scan
Cardiac CT scanning with angiography (CTA) can be useful to:
- Diagnose heart failure: by calculating the biventricular volume and ejection fraction with good correlation to echocardiography.
- Assessing the regional wall motion (with cine-loop formatting)
- Excluding ischemia as a cause for DCM (Cardiac CTA has a 98% diagnostic sensitivity and 97% specificity in excluding ischemic cardiomyopathy). Also, Myocardial perfusion analysis of the coronary arteries is also beneficial.
- Differential diagnosis of DCM from hypertrophic cardiomyopathy, arrhythmogenic right ventricular dysplasia, and left ventricular noncompaction.