Abstract
Background
Multidetector computed tomography (MDCT) has been demonstrated as a feasible imaging modality for noninvasive assessment of coronary artery disease and left ventricular (LV) function. Recently, 320-row systems have become available with 16 cm anatomical coverage allowing image acquisition of the entire heart within a single heartbeat. The purpose of this study was to evaluate the accuracy of 320-row MDCT in the assessment of global LV function compared to two-dimensional (2D) echocardiography as the standard of reference.
Methods and Results
A head-to-head comparison between 320-row MDCT and 2D-echocardiography was performed in 114 patients (68 men; mean age 62 ± 13 years) who were clinically referred for MDCT coronary angiography. The entire heart was imaged in a single heartbeat, using prospective dose modulation. LV end-diastolic volumes (LVEDV) and LV end-systolic volumes (LVESV) were determined and the LV ejection fraction (LVEF) was derived. Average LVEF was 60 ± 10% (range 26-78%) as determined on MDCT, compared with 59 ± 10% (range 25-77%) on 2D-echocardiography. Evaluation of LVEF by linear regression analysis showed a good correlation between MDCT and 2D-echocardiography (r 2 = .87; P < .001). Good correlations between MDCT and 2D-echocardiography were demonstrated for the assessment of LVEDV (r 2 = .91; P < .001) and LVESV (r 2 = .94; P < .001). At Bland-Altman analysis, mean differences (±SD) of 7.3 ± 12.1 mL (P < .05) and 1.8 ± 7.4 mL (P < .05) were observed between MDCT and 2D-echocardiography for LVEDV and LVESV, respectively. LVEF was slightly overestimated with MDCT (.9 ± 3.6%; P < .05).
Conclusions
Accurate assessment of LV function and volumes is feasible with single heartbeat 320-row MDCT in patients referred for MDCT coronary angiography.
Keywords: Multidetector computed tomography, left ventricular function, cardiac imaging
Introduction
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.
Materials and Methods
Patients and Study Protocol
The study group consisted of 114 patients who were clinically referred for MDCT coronary angiography to evaluate the presence and extent of CAD. All patients were consecutively enrolled and prospectively included in the study. All patients underwent 320-row cardiac MDCT. Exclusion criteria were: (1) (supra)ventricular arrhythmias, (2) renal insufficiency (glomerular filtration rate < 30 mL/min), (3) known allergy to iodine contrast material, (4) severe claustrophobia, and (5) pregnancy. The study population consisted of 68 men and 46 women, with a mean age of 62 ± 13 years. The main clinical characteristics of the study population are listed in Table 1. LV volumes and LV ejection fraction (LVEF) were assessed and compared with 2D-echocardiography. MDCT and 2D-echocardiography were performed within 3 months of each other. In 21 patients, both examinations were performed on the same day. No cardiac events occurred between examinations.
Table 1.
Clinical characteristics of the study population
| 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%) |
MDCT
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.
Results
LVEDV
Average LVEDV was 146 ± 40 mL (range 78-278 mL) on MDCT, as compared with 139 ± 40 mL (range 72-269 mL) on 2D-echocardiography. Linear regression analysis showed a good correlation between MDCT and 2D-echocardiography for the assessment of LVEDV (r 2 = .91; P < .001) (Figure 1A). At Bland-Altman analysis, mean differences (±SD) of 7.3 ± 12.1 mL (P < .05) were observed between MDCT and 2D-echocardiography, with 95% limits of agreement ranging from −16.5 to 31.1 (Figure 1B).
Figure 1.
Comparison of MDCT and 2D-echocardiography in the assessment of LVEDV. Linear regression plot shows the correlation between LVEDV as measured by MDCT and 2D-echocardiography (A). Bland-Altman plot of LVEDV shows the difference between each pair plotted against the average value of the same pair (solid line, mean value of difference; dotted line, mean value of differences ± 2 SDs) (B). LVEDV, Left ventricular end-diastolic volume; MDCT, multidetector computed tomography
LVESV
On MDCT, average LVESV was 61 ± 30 mL (range 17-195 mL), as compared with 59 ± 29 mL (range 18-183 mL) on 2D-echocardiography. The correlation coefficient between the two modalities for the assessment of LVESV was good (r 2 = .94; P < .001) (Figure 2A). Bland-Altman analysis showed a mean value of difference (±SD) of 1.8 ± 7.4 mL (P < .05) between MDCT and 2D-echocardiography. The 95% limits of agreement ranged from −12.7 to 16.2 (Figure 2B).
Figure 2.
Comparison of MDCT and 2D-echocardiography in the assessment of LVESV. Linear regression plot shows the correlation between LVESV as measured by MDCT and 2D-echocardiography (A). In a Bland-Altman plot of LVESV, the difference between each pair plotted against the average value of the same pair is shown (solid line, mean value of difference; dotted line, mean value of differences ± 2 SDs) (B). LVESV, Left ventricular end-systolic volume; MDCT, multidetector computed tomography
LVEF
Average LVEF was 60 ± 10% (range 26-78%) as determined on MDCT, compared with 59 ± 10% (range 25-77%) on 2D-echocardiography. Evaluation of LVEF by linear regression analysis demonstrated a good correlation between MDCT and 2D-echocardiography (r 2 = .87; P < .001) (Figure 3A). At Bland-Altman analysis, LVEF was slightly overestimated with MDCT (.9 ± 3.6%; P < .05) (Figure 3B).
Figure 3.
Comparison of MDCT and 2D-echocardiography in the assessment of LVEF. Linear regression plot comparing MDCT and 2D-echocardiography in the assessment of LVEF (A). Bland-Altman plot of LVEF shows the difference between each pair plotted against the average value of the same pair (solid line, mean value of difference; dotted line, mean value of differences ± 2 SDs) (B). LVEF, Left ventricular ejection fraction; MDCT, multidetector computed tomography
The inter-observer agreement for LVEDV, LVESV, and LVEF, measured by intra-class correlation, were .98, .97, and .92, respectively.
Discussion
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.
Comparison with Previous Studies
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.
Overestimation LV Volumes by MDCT
In this study, a slight overestimation of LV volumes by MDCT was observed as compared with 2D-echocardiography. A factor that might contribute to the overestimation in LV volumes by 320-row MDCT is the use of dose modulation. While this feature has become available as a means to reduce radiation exposure to the patient as compared to full-dose scanning, it is associated with a slight decrease in image quality in images acquired during decreased tube current (Figure 4). However, it is unlikely that this minor decrease in image quality would have affected global LV volume measurements. Second, discrepancies may be explained by differences in the definition of the upper limits of the ventricle, which can be set at different levels depending on the technique used. Currently, there are no clear guidelines on the systematic analysis of MDCT data for the purpose of cardiac function assessment. Finally, the minor overestimation of LV volumes by MDCT as compared to 2D-echocardiography may be explained by the different approach of LV volume calculation between the two techniques. While 2D-echocardiography is most routinely used to measure cardiac function in daily clinical practice, its main limitation remains that measurements are based on a geometric assumption of 2D images. As a result, inaccuracies in volumetric calculations may occur. In contrast, MDCT allows endocardial border definition with high-resolution using true 3D reconstructions. Yamamuro et al recently showed that measurements between MDCT and MRI, the current gold standard for LV function assessment, were more closely related as compared to measurements between 2D-echocardiography and MRI.17 MDCT may therefore be a more accurate tool for LV function analysis than 2D-echocardiography, and this may explain the small differences in LV volumes between the two techniques.
Figure 4.
Example of 320-row MDCT image acquisition using dose modulation. Short-axis view of the left ventricle during end-diastolic phase (A) and end-systolic phase (B), acquired with 320-row MDCT using dose modulation. To reduce radiation dose, image acquisition was performed using dose modulation, attaining maximal tube current at 75% of the R-R interval. Of note, at the start of the R-R interval image acquisition was still performed at maximal tube current. Outside the predefined interval and the first portion of the R-R interval, tube current was 25% of the maximal tube current. As a result, the end-diastolic phase (typically 0%) still has good image quality whereas an increase in image noise in the end-systolic phase was observed. Additional scan parameters were: 120 kV and 580 mA at maximal tube current. MDCT, Multidetector computed tomography
Study Limitations
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.
Open Access
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
Footnotes
Dr. de Graaf is co-supported by the Dutch Technology Foundation STW (Utrecht, the Netherlands), applied science division of NWO and the Technology Program of the Ministry of Economic Affairs, grant nr. 10084. Dr. van Velzen is supported by the Netherlands Heart Foundation (The Hague, The Netherlands), grant nr. 2007B223. Dr. Nucifora is supported by a grant from the European Association of Percutaneous Cardiovascular Interventions. Dr. Schalij has research grants from Boston Scientific (Natick, United States), Medtronic (Minneapolis, United States) and Biotronik (Berlin, Germany). Dr. Bax has research grants from Medtronic (Minneapolis, United States), Boston Scientific (Natick, United States), BMS medical imaging (New York, United States), St. Jude Medical (St. Paul, United States), GE Healthcare (Chalfont St. Giles, United Kingdom), Biotronik (Berlin, Germany), and Edwards Lifesciences (Irvine, United States).
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