The assessment of global left ventricular (LV) function and volumes is important in patients with coronary artery disease (CAD) and serves as a valuable diagnostic and prognostic marker.1,2 There are several noninvasive imaging modalities to analyze cardiac function, which include two-dimensional (2D)-echocardiography,3 single photon emission computed tomography (SPECT),4 and cardiac magnetic resonance imaging (MRI).5
In recent years, multidetector computed tomography (MDCT) has emerged as a rapidly advancing imaging modality for the noninvasive assessment of CAD. Since the introduction of MDCT in the early 1990s, acquisition times, spatial and temporal resolution have continuously improved resulting in excellent image quality and diagnostic accuracy in the detection of CAD.6 Furthermore, various studies have shown that accurate simultaneous assessment of CAD and LV function is feasible.7-13 Accurate evaluation of cardiac function and volumes with MDCT, in addition to noninvasive assessment of the coronary arteries is likely to optimize the clinical evaluation of patients with CAD.14
Previous 4-, 16- and 64-row MDCT systems used a helical scanning technique with retrospective ECG gating. These systems covered the entire heart in multiple heartbeats, which involved a considerable risk of motion artifacts due to arrhythmias and breathing. With the recent introduction of 320-row MDCT, a cylindrical volumetric dataset covering the entire heart is acquired within a single rotation or heartbeat. This technology, in combination with prospective ECG gating, markedly reduces scan time and contrast administration, while at the same time reducing motion artifacts. In addition, 320-row MDCT has a reduced gantry rotation time with improved temporal resolution.
The accuracy of 320-row MDCT for the evaluation of LV function and volumes has not been reported. The purpose of this study therefore was to evaluate the accuracy of 320-row MDCT in the assessment of global LV function compared to 2D-echocardiography as the standard of reference.
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Number of patients |
114 |
|
Age (years) |
62 ± 13 |
|
Men/women |
68/46 |
|
Body mass index (kg/m2) |
27 ± 4 |
|
Family history of coronary artery disease |
40 (35%) |
|
Diabetes |
28 (25%) |
|
Hypertension |
78 (68%) |
|
Hypercholesterolemia |
54 (47%) |
|
Current smoker |
17 (15%) |
|
Previous myocardial infarction |
9 (8%) |
|
Location |
|
|
Anterior |
2 (2%) |
|
Inferior |
7 (6%) |
|
Previous percutaneous coronary intervention |
16 (14%) |
|
Previous coronary artery bypass grafting |
9 (8%) |
|
Pacemaker or implantable cardioverter defibrillator |
6 (5%) |
Data acquisition
MDCT studies were performed using a 320-row MDCT scanner (Aquilion ONE, Toshiba Medical Systems, Otawara, Japan) with 320 detector rows (each .5 mm wide) and a rotation time of 350 ms (with a temporal resolution of 175 ms for half reconstruction). Unless contraindicated, beta-blocker was administered orally (50-100 mg metoprolol depending on heart rate) 1 hour before data acquisition to patients with a heart rate exceeding 65 beats per minute (bpm) to reduce cardiac motion artifacts. During the MDCT examination, the average heart rate ± standard deviation (SD) was 57 ± 9 bpm.
The entire heart was imaged in a single heartbeat, using prospective dose modulation attaining maximal tube current during 65-85% of R-R interval (in patients with a heart rate ≥ 60 bpm), or during 75% of R-R interval (in patients with stable heart rate < 60 bpm). Outside the predefined interval, tube current was 25% of the maximal tube current. In addition, at the start of the R-R interval image acquisition was performed at maximal tube current. Six patients had a heart rate > 65 bpm and in these patients images were acquired during multiple heartbeats (typically two). Tube voltage and tube current were adapted to body weight and thoracic anatomy. Tube voltage was 100 kV (n = 4), 120 kV (n = 109), or 135 kV (n = 1). Tube voltage was adapted to 135 kV in patients with a body mass index > 35 kg/m2. Maximal tube current was 400 mA (n = 5), 450 mA (n = 7), 480 mA (n = 2), 500 mA (n = 61), 550 mA (n = 3), or 580 mA (n = 36). A tri-phasic injection of intravenous contrast was used and the total amount of nonionic contrast media (Iomeron 400; Bracco, Milan, Italy) injected into the antecubital vein was 60-70 mL (depending on body weight). First, 50-60 mL of contrast media was administered at a flow rate of 5.0 or 6.0 mL/s, followed by 20 mL of 50% contrast/saline. Subsequently a saline flush of 25 mL was administered at a flow rate of 3.0 mL/s. In order to synchronize the arrival of the contrast media and the scan, bolus arrival was detected using automated peak enhancement detection in the LV. After the preset contrast enhancement threshold of baseline Hounsfield units (HU) + 100 HU was reached, the MDCT examination was automatically initiated. After a two second delay, images were acquired during an inspiratory breath hold of approximately 5 seconds. During the scan, the ECG was registered simultaneously for prospective gating of the data. Average estimated radiation exposure (±SD) during a single examination was 11.5 ± 2.1 mSv. Radiation dose was quantified with a dose-length product conversion factor of .014 mSv/(mGy × cm) as described.15 MDCT was performed successfully in all patients without complications. The average investigation time for the MDCT acquisitions was approximately 20 minutes.
Data analysis
To assess LV function and LV volumes, 10 series of 2.0-mm slices were reconstructed in the short-axis orientation at every 10% throughout the cardiac cycle, starting at early systole (0% of cardiac cycle) to end-diastole (90% of cardiac cycle). Subsequently, images were transferred to a remote workstation with dedicated cardiac function analysis software (Vitrea FX 1.0, Vital Images, Minnetonka, MN, USA). To acquire the appropriate phases for LV end-systolic volume (LVESV) and LV end-diastolic volume (LVEDV), the smallest and largest cross-sectional LV cavity areas were selected, respectively. Upper limit of the LV was determined at the basal level of the mitral valve and the start of the LV outflow tract. Endocardial borders were semi-automatically outlined from the base to the apex on the short-axis cine images by an independent observer. Papillary muscles were excluded from the ventricular cavity. The LVEDV and LVESV volumes were calculated, and the LVEF was derived by subtracting the LVESV from the LVEDV and dividing the result by the LVEDV. Time to reconstruct the required image sets and calculate LV volumes and LVEF was approximately 10 minutes. Inter-observer agreement of LV volume and function analyses was analyzed with repeated measurements of a second experienced independent observer in 13 randomly selected patients.
2D-echocardiography
For comparison of LVEF and LV volumes, 2D-echocardiography was performed to serve as the standard of reference. All patients were imaged in left lateral decubital position with a commercially available system (Vivid 7 Dimension, GE Healthcare, Horten, Norway) equipped with a 3.5-MHz transducer. Images were obtained in the standard 4- and 2-chamber apical views and were saved in cine-loop format. Analyses were subsequently performed offline using EchoPAC version 7.0.0 (GE Healthcare, Horten, Norway) by a cardiologist, with 10 years of experience, blinded to MDCT data. LVEDV and LVESV volumes were measured according to the Simpson’s biplane method16 and LVEF was derived.
Statistical analysis
Continuous data were expressed as mean ± SD and compared using the paired two-tailed Student’s t test. Agreement for the LV volumes and function by MDCT and echocardiography were determined by Pearson’s correlation coefficient for linear regression and Bland-Altman analysis. The 95% limits of agreement were defined as the range of values ± 2 SDs from the mean value of the differences. A P value < .05 was considered statistically significant. To determine inter-observer agreement, intra-class correlation coefficients were used as indicators of reproducibility. Good agreement was defined as intra-class correlation coefficients >.80.
The inter-observer agreement for LVEDV, LVESV, and LVEF, measured by intra-class correlation, were .98, .97, and .92, respectively.
In this study, the accuracy of single heartbeat 320-row MDCT in the assessment of global cardiac function was evaluated in patients clinically referred for MDCT coronary angiography. 2D-echocardiography served as the standard of reference.
This study demonstrates that evaluation of LV volumes and global LV function is feasible with single heartbeat 320-row MDCT in patients clinically referred for MDCT coronary angiography. Excellent correlations were observed between MDCT and 2D-echocardiography for LVEDV (r 2 = .91; P < .001) and LVESV (r 2 = .94; P < .001). Minor overestimations for LVESV and LVEDV of 1.8 and 7.3 mL, respectively, were observed on MDCT. Consequently, LVEF measured by MDCT yielded a slight overestimation of .9% compared with 2D-echocardiography.
The results of this study are in-line with results of previous MDCT studies.7-13 In a prior study conducted by Kim et al,9 a good agreement was demonstrated for LVEF, as determined by 16-row MDCT and 2D-echocardiography (r = .86; P < .001). Similar to our study, a slight overestimation of 2.9% using MDCT was shown. More recently, global LV function was investigated by Wu et al13 using 64-row MDCT and 2D-echocardiography. The investigators showed a good correlation between the two imaging modalities for the assessment of LVEF (r = .87, P < .001). However, also with 64-row MDCT, systematic overestimation of LVEF has been reported.12 Accordingly, the results of this study using 320-row MDCT technology appear to be in agreement with prior results using 16- and 64-row MDCT. Possibly, assessment with 320-row MDCT may even be more closely related to 2D-echocardiography as compared to older MDCT generations due to the fact that data are acquired in a single heartbeat rather than during multiple heartbeats.
Although assessment of cardiac function is feasible with 320-row MDCT, several limitations should be addressed. First, the main limitation of the current study is the lack of a true gold standard such as cardiac MRI. Cardiac MRI has long been regarded as the gold standard in noninvasive analysis of LV function.18 Importantly, many studies have previously shown excellent correlations between MDCT and MRI in the assessment of LVEF and LV volumes.17,19,20 Accordingly, in order to further validate the performance of 320-row MDCT for the assessment of LV volumes and function, a direct comparison between 320-row MDCT and MRI is desirable. Second, in patients with a heart rate > 65 bpm additional beta-blocking medication was administered prior to MDCT investigation, but not before 2D-echocardiography. A potential bias may have been introduced by the administration of beta-blockade immediately prior to MDCT examination,21 as well as the use of contrast agents at the time of MDCT, as these pharmacological interventions may have affected LV volumes and LVEF. Third, a disadvantage of MDCT in general is the radiation exposure to the patient. Previously, information for LV function analysis could be derived retrospectively from the dataset acquired for the noninvasive evaluation of the coronary arteries.12 Recently, prospective ECG gating has become possible, allowing data-acquisition for MDCT coronary angiography during only a small proportion of the cardiac cycle. Since assessment of LV function requires data-acquisition during an entire cardiac cycle, in systems employing prospective ECG gating, including 320-row MDCT, functional analysis extends total exposure time. Consequently, the assessment of LV function by MDCT increases the radiation dose when compared to MDCT analysis for the purpose of coronary angiography alone. The necessity for LV function analysis should therefore be carefully considered for each individual patient. Importantly, lower mean radiation doses may be achieved with more optimal heart rate reduction, e.g., by using intravenous beta-blockade, which allows scanning at 75% of R-R interval in a larger proportion of patients. Furthermore, although the current population was scanned at 16 cm cranio-caudal scan-range, 320-row MDCT allows scanning of smaller ranges, which also decreases radiation exposure. In addition, only few patients with an LVEF lower than 50% were included. As a result, the study is limited by the inclusion of a relatively homogeneous population with predominantly normal LV function. Further research is warranted to determine the accuracy of this technique in patients with low LVEF. Additionally, the time difference between 2D-echocardiography and MDCT may limit accurate comparison. Finally, as almost all patients were scanned during a single heartbeat, the current results predominantly reflect the evaluation of LV function using half-scan reconstructions.
