Left and right ventricle assessment with Cardiac CT: validation study vs. Cardiac MR

Abstract

Objectives

To compare Magnetic Resonance (MR) and Computed Tomography (CT) for the assessment of left (LV) and right (RV) ventricular functional parameters.

Methods

Seventy nine patients underwent both Cardiac CT and Cardiac MR. Images were acquired using short axis (SAX) reconstructions for CT and 2D cine b-SSFP (balanced-steady state free precession) SAX sequence for MR, and evaluated using dedicated software.

Results

CT and MR images showed good agreement: LV EF (Ejection Fraction) (52 ± 14% for CT vs. 52 ± 14% for MR; r = 0.73; p > 0.05); RV EF (47 ± 12% for CT vs. 47 ± 12% for MR; r = 0.74; p > 0.05); LV EDV (End Diastolic Volume) (74 ± 21 ml/m² for CT vs. 76 ± 25 ml/m² for MR; r = 0.59; p > 0.05); RV EDV (84 ± 25 ml/m² for CT vs. 80 ± 23 ml/m² for MR; r = 0.58; p > 0.05); LV ESV (End Systolic Volume)(37 ± 19 ml/m² for CT vs. 38 ± 23 ml/m² for MR; r = 0.76; p > 0.05); RV ESV (46 ± 21 ml/m² for CT vs. 43 ± 18 ml/m² for MR; r = 0.70; p > 0.05). Intra- and inter-observer variability were good, and the performance of CT was maintained for different EF subgroups.

Conclusions

Cardiac CT provides accurate and reproducible LV and RV volume parameters compared with MR, and can be considered as a reliable alternative for patients who are not suitable to undergo MR.

Key Points

• Cardiac-CT is able to provide Left and Right Ventricular function.

• Cardiac-CT is accurate as MR for LV and RV volume assessment.

• Cardiac-CT can provide accurate evaluation of coronary arteries and LV and RV function.

Electronic supplementary material

The online version of this article (doi:10.1007/s00330-011-2345-6) contains supplementary material, which is available to authorized users.

Introduction

Correct and reproducible evaluation of left (LV) and right ventricular (RV) functional parameters underly appropriate decision making in cardiac and pulmonary diseases [1–7]. Owing to high temporal, spatial and contrast resolution the Magnetic Resonance (MR) 2D-b-SSFP (balanced-Steady State Free Precession) sequence guarantees the excellent results in terms of accuracy of LV and RV volume assessment and is nowadays regarded as the in vivo reference standard for this purpose [8–13]. Recently, as a result of improved temporal resolution, numerous studies have explored the role of cardiac CT in providing LV and RV functional parameters [14–32]; in fact it is important to have alternative tools to evaluate an important parameter, such as for example EF, when other techniques cannot be used. CT has some drawbacks in respect of Echo and MRI, such as radiation dose and contrast medium administration, but it is important to demonstrate that in particular situations, like in patients with poor echocardiographic compliance, and contra-indications to MR, CT can offer a reliable alternative to assess ventricular function in a fast way and with contemporary information on the coronary artery tree status.

The importance of an alternative functional imaging investigation is even more evident for the RV, which has a complex shape that lends itself poorly for echocardiographic functional assessment. Our results suggest that CT could be a reliable second option to MR, for instance in patients with (corrected) grown-up congenital heart disease.

The majority of studies explored singularly the possibility of performing LV and RV analysis with CT and so far the feasibility and reproducibility of concurrent left and right ventricular volume assessment by CT has not been compared with MR in a large sample size. We think it is really important to test the accuracy of contemporary LV and RV analysis because LV abnormalities can frequently involve RV function and vice versa and because concurrent assessment can speed up the acquisition of important information especially when there is no time to lose.

We report our experience in 79 patients who underwent CT for evaluation of coronary artery disease.

Material and methods

Patients

Between April 2007 and October 2009 we prospectively enrolled 100 patients who underwent CT for evaluation of coronary artery disease. For bi-ventricular volume assessment, patients were also scheduled for an MR within one week after CT. We adhered to the exclusion criteria reported in literature [33–35]: for CT, we excluded patients with a) an heart rate >65 bpm (beats per minute) not responding to beta-blockers; b) atrial fibrillation and concomitant high ventricular response; c) known reactions to contrast medium; d) renal insufficiency (creatinine > 1.5 mg/dL); e) impaired pulmonary function (unable to perform a 12-s breath-hold); for MR, we excluded patients with a) claustrophobia; b) pacemaker/other non MR compatible devices [34]. Twenty-one patients were excluded because of unsuitability to undergo MR (11 for claustrophobia; 3 for increasing dyspnoea during acquisition; 4 for ICD; 2 for pacemaker; 1 for a Starr-Edwards mitral valve); within our cohort no patient needed exclusion from CT. Complete CT and MR datasets could be acquired in 79 patients (mean age: 58; 46 male) (Table 1).

Table 1.

Demographics

Population	Total
Number	79
Age (mean±SD; median; range)	58±17 (58; 24–89)
Male/Female	46/33
Cardiovascular Risk Factors
Hypertension (%)	35 (44.3)
Dyslipidaemia (%)	15 (18.9)
Diabetes mellitus (%)	12 (15.2)
Nicotine abuse (%)	23 (29.1)
Family history of cardiovascular disease (%)	18 (22.8)
BSA (m2; mean±SD)	1.9±0.2

The Table shows demographics of the study population

Abbreviations: SD Standard Deviation, BSA Body Surface Area (according to Mosteller’s formula)

Written informed consent was obtained from all patients, and the study was approved by the Ethics Review Board of our hospital.

CT protocol

Upon arrival, blood pressure and heart rate (HR) were measured and 5–20 mg of intra-venous atenolol were administered if the HR exceeded 65 bpm, in order to reach a HR below 65 bpm. Twenty-five patients required treatment with β-blockers before CT; the others had no necessity (40 patients) or had contraindications (14 patients). ECG-gated 64-slice spiral CT (Sensation 64, Siemens, Forchheim, Germany) was performed without ECG-triggered tube modulation: detector collimation: 32 × 0.6 mm, Z-axis focal spot alternation resulting in simultaneous acquisition of 64 slices; gantry rotation: 330 ms; effective temporal resolution 165 ms; table feed per rotation: 3.84 mm; tube voltage 120 kVp; tube current 800–950 mAs; direction in which data acquisition proceeded : cranio-caudal. Just before the CT data acquisition 0.3 mg of sublingual nitroglycerin was administered in the absence of contraindications. For contrast enhancement, 110 mL of contrast medium (Iomeprol, Iomeron 400, Bracco, Milan, Italy) was administered intravenously at 5 mL/s (2 g iodine/s) flow rate, followed by 40 mL of saline chaser at same flow rate [17]. A bolus tracking technique for contrast bolus arrival and data acquisition synchronisation was used. The anatomical coverage extended from the tracheal bifurcation to the diaphragm. In patients who previously underwent bypass graft surgery, the start was positioned just at clavicle level to include internal mammary artery origin. Using a partial reconstruction algorithm (requiring 180° of projections) thin-slice images were reconstructed for the coronary evaluation. In addition functional MPR (multiplanar reconstruction) images were reconstructed using dedicated CT software (Syngo CT-2007A; Siemens, Forchheim, Germany). Using the standard cardiac planes for orientation, 8-mm MPR thick with a 2-mm gap images of the ventricles, extending from the base to the apex, were reconstructed throughout the cardiac cycle at 5% intervals (Fig. 1).

Fig. 1.

Short Axis views of the Left and Right Ventricle by MR and CT. End-diastolic Short Axis views of the Left and Right Ventricle by MR and CT (MPR 8 mm thick reconstructions). Example of the same patient imaged with MR (on the left) and CT (on the right). Short axis views for left and right ventricular volume calculation. Abbreviations: MR Magnetic Resonance, CT Computed Tomography

MR protocol

MR was performed at 1.5T (Achieva, Philips Medical Systems, Best, The Netherlands) with the following acquisition parameters: maximum gradient strength of 66 mT/m, maximum slew rate 180 mT/m × ms, maximum gradient strength during Cine-Cardiac MR acquisition 33 mT/m, and maximum slew rate during Cine-Cardiac MR acquisition 180 mT/m × ms. Five-element synergy cardiac coil and vector electrocardiography were used for signal detection and cardiac gating. One experienced operator (4 years’ Cardiac MR) performed all examinations. After initial scout imaging and reference acquisition, short-axis cine images covering the entire left and right ventricles from base to apex were acquired during repeated end-expiratory breath holds using a 2D b-SSFP (2D-cine) sequence (Fig. 1). All acquisitions were performed holding the breath at end expiration to avoid slice misalignment [36, 37]. The imaging parameters for 2D-cine were as follows: TR (repertition time) 3.1 ms; TE (echo time) 1.53 ms; flip angle 60°; bandwidth 1249.7 HZ/pixel; in plane resolution 2 × 2.3 mm; slice thickness 8 mm; slice gap 2 mm; temporal resolution 32 ± 6 ms (depending on heart rate); cardiac phase 30; SENSE: off; half scan: Yes.

Data analysis

A total of 158 short axis datasets, 79 obtained by MR acquisition and 79 by CT multiphasic reconstruction, were transferred to a dedicated workstation (Syngo MMWP – Siemens, Forchheim, Germany) equipped with ARGUS Va60c analysis software (ARGUS, Va60c, Siemens, Forchheim, Germany), which is able to process DICOM images from images obtained using different techniques. One experienced observer (>5 years in Cardiac MR and CT) blindly and randomly analyzed all MR and CT images to measure the end-diastolic volume (EDV) and end-systolic volume (ESV), and calculate the stroke volume (SV) and ejection fraction (EF) of left and right ventricle, as well as the end-diastolic wall mass (ED Wall Mass) on the left ventricle. [38]. Images acquired at the time of the R-wave of the ECG were considered to represent end-diastole (ED), while images showing the smallest detectable left ventricular cavity were considered as end-systolic (ES) [18]. Endocardial and epicardial contours were manually traced on the end-diastolic SAX images. Endocardial borders were automatically “propagated” on end-systolic phase images, and manually corrected when deemed necessary. Papillary muscles and trabeculations of the LV and RV cavities were included in the LV and RV cavity volumes as previously described [39–41]. The most apical section with visible cavity was considered as apex and the most basal section with at least 50% surrounding myocardium was regarded as base [23]. EDV and ESV were calculated without geometric assumptions, using the Simpson’s rule. All parameters were indexed for body surface area (BSA). For calculation of intra-observer and inter-observer variability tracing of myocardial borders was repeated after at least 1 month by the same investigator, and in addition by a second investigator (4 years’ Cardiac CT and Cardiac MR), who was unaware of previous results.

Statistical analysis

We hypothesized that CT can measure right and left ventricular volumes, and left myocardial mass with acceptable accuracy and reproducibility; thus we directly compared right and left ventricular measurements obtained by CT with the results of MR as the currently accepted reference standard for cardiac chamber volume measurement. For data analysis we used commercially available software (MedCalc v9.2.1.0, Mariakerke, Belgium). The correlation between CT and MR was tested by two-variable linear regression analysis including calculation of Pearson’s correlation coefficient. To further examine the agreement between CT and MRI , Bland-Altman method was used [42] (Fig. 2). The agreement between CT and MR was determined as the mean difference, the standard error of estimation for the mean difference, the 95% confidence interval of the mean difference, and the limits of agreement for both investigations (mean ± SD). Differences were investigated with Student’s T test (2 tails) for paired samples and a p < 0.05 was considered as significant. The comparison of the intra-observer and inter-observer variability between CT and MR was assessed by calculating the coefficient of variability equal to the standard deviation of the difference between two measurements over the mean of the two measurements and expressed as percentage [16, 43]. Three patient subgroups were created according to EF value: <35%, 35% ≤ EF ≤ 50%, >50% and analyzed with Student’s T Test, Pearson’s correlation and Bland Altman analysis.

Fig. 2.

Bland-Altman plots. Bland-Altman plots show good agreement for Left and Right Ventricular EF and for Left Ventricular ED wall Mass. Abbreviations: LV Left Ventricle, RV Right Ventricle, EF Ejection Fraction, EDV End Diastolic Volume, ED mass End Diastolic wall mass, MR Magnetic Resonance, CT Computed Tomography, SD standard deviation

Results

No complications occurred during CT and MR imaging. No patient was excluded due to ECG triggering artifacts. All patients had a regular sinus rhythm with a mean HR of 62 ± 10 bpm (range: 53-76 bpm) during MSCT and 64 ± 11 bpm (range: 54-78 bpm) during MR (p > 0.05). The time needed to acquire CT datasets was 12 ± 3 s and a complete CT examination took about 5 ± 3 min; the time needed to acquire MR datasets was 5 ± 2 min and a complete MR examination took about 30 ± 10 min (p < 0.05). LV and RV cavities had good visual quality on all CT and MR images, with sufficient cavity enhancement. We therefore obtained 79 analyzable datasets for CT and 79 analyzable datasets for MR. Delineation of both left and right ventricular borders took 13 ± 5 min for CT datasets and 25 ± 7 min for MR datasets (p < 0.05). The mean values and standard deviation for LV and RV volumes and the analysis of the respective differences between CT and MR are given in Table 2. Student’s paired T test showed no significant differences between CT and MR for any of the measurements. The limits of agreement between CT and MR were in a good range for all measurements (Fig. 2). Calculation of Pearson’s correlation coefficient (r) revealed a good association between CT and MR (Fig. 3). The intra-observer and inter-observer variability for both left and right ventricular volumes for CT and MR were calculated with Deming regression and are summarized in Table 3. Reproducibility of CT was significantly higher on an intra-observer level for LV SV and ED Wall Mass, and between readers for the LV ED Wall Mass and RV EDV assessment. Results from the subgroup analysis are listed in Table 4 demonstrating good limits of agreement and an acceptable mean bias for the clinical practice.

Table 2.

Ventricular function parameters

	MR	CT	p-value	r-value	95% LA (mean)
Left Ventricle
EDV (ml/m2)	76 ± 25	74 ± 21	>0.05	0.59	−47.3;53.9 (3.3)
ESV (ml/m2)	38 ± 23	37 ± 19	>0.05	0.76	−66.2;71.4 (2.6)
SV (ml/m2)	38 ± 11	37 ± 13	>0.05	0.44	−57.7;65.6 (3.9)
EF (%)	52 ± 14	52 ± 14	>0.05	0.73	−40.9;42.0 (0.6)
ED wall mass (g/m2)	59 ± 18	57 ± 18	>0.05	0.76	−37.9;46.3 (4.2)
Right Ventricle
EDV (ml/m2)	80 ± 23	84 ± 25	>0.05	0.58	−50.2;39.9 (−5.2)
ESV (ml/m2)	43 ± 18	46 ± 21	>0.05	0.70	−65.7;53.3 (−6.2)
SV (ml/m2)	37 ± 12	38 ± 12	>0.05	0.55	−58.3;51.8 (−3.2)
EF (%)	47 ± 12	47 ± 12	>0.05	0.74	−38.4;42.2 (1.9)

The Table shows global ventricular parameters (Right and Left Ventricle) calculated with MR and CT. Parameters are expressed as mean ± SD

Abbreviations: MR Magnetic Resonance, CT Computed Tomography, EDV End Diastolic Volume, ESV End Systolic Volume, SV Stroke Volume, EF Ejection Fraction, ED wall mass End Diastolic wall mass, p-Value Student’s paired test, r-value Pearson’s correlation, 95% LA Limits of agreement with Bland-Altman analysis (mean in parenthesis)

Fig. 3.

Scatter plots. Correlation of ejection fraction (EF) values in LV and RV and of ED Mass in LV. The graphs show minimal dispersion of the data and moderate/good correlation (r > 0.7) for all displayed parameters. Abbreviations: EF Ejection Fraction, ED mass End Diastolic wall mass, MR magnetic resonance, CT computed tomography, SD standard deviation

Table 3.

Intra/inter-observer variability

	Intra-observer variability			Inter-observer variability
Left Ventricle	MR	CT	p-value	MR	CT	p-value
EDV (%)	1.2	1.0	>0.05	1.3	2.3	>0.05
ESV (%)	1.8	1.3	>0.05	2.1	3.8	>0.05
SV (%)	2.7	2.1	<0.05	3.4	6.4	>0.05
EF (%)	2.0	1.3	>0.05	2.5	4.4	>0.05
ED wall mass (%)	4.8	1.1	<0.05	2.9	1.6	<0.05
Right Ventricle
EDV (%)	0.7	0.8	>0.05	1.7	1.0	<0.05
ESV (%)	1.2	0.9	>0.05	2.6	1.8	>0.05
SV (%)	2.0	1.8	>0.05	4.3	3.1	>0.05
EF (%)	1.2	1.2	>0.05	2.9	2.4	>0.05

The Table shows the Coefficient of Variation of ventricular parameters calculated with Deming Regression. Parameters are expressed as percentage variability

Abbreviations: MR Magnetic Resonance, CT Computed Tomography, EDV End Diastolic Volume, ESV End Systolic Volume, SV Stroke Volume, EF Ejection Fraction, ED wall mass End Diastolic wall mass, p-Value Student’s paired test

Table 4.

Functional subgroups and ventricular function parameters

Groups	Parameter	MR	CT	p-value	r-value	95% LA (mean)
All (n. 79)	LV EF (%)	52 ± 14	52 ± 14	>0.05	0.73	−40.9;42.0 (0.6)
	RV EF (%)	47 ± 12	47 ± 12	>0.05	0.74	−38.4;42.2 (1.9)
EF < 35% (n. 11)	LV EF (%)	25 ± 5	27 ± 5	>0.05	0.90	−22.9;15.6 (−3.6)
	RV EF (%)	36 ± 12	37 ± 14	>0.05	0.78	−61.2;58.1 (−1.6)
35% ≤ EF ≤ 50% (n. 18)	LV EF (%)	44 ± 4	46 ± 10	>0.05	0.52	−38.1;30.6 (3.8)
	RV EF (%)	44 ± 9	43 ± 10	>0.05	0.74	−32.9;41.0 (4.1)
EF > 50% (n. 50)	LV EF (%)	61 ± 7	58 ± 11	<0.05	0.52	−38.1;30.6 (−3.8)
	RV EF (%)	51 ± 10	50 ± 11	>0.05	0.74	−32.9;41.0 (4.1)

The Table shows the comparison of Ejection Fraction (Right and Left Ventricle) calculated with MR and CT for the entire population and for ventricular functional subgroups (EF < 35%; 35% ≤ EF ≤ 50%; EF > 50%). Parameters are expressed as mean ± SD

Abbreviations: MR Magnetic Resonance, CT Computed Tomography, n. number of patients, EF Ejection Fraction, p-Value Student’s paired test, r-value Pearson’s correlation, 95% LA Limits of agreement with Bland-Altman analysis (mean in parenthesis)

Discussion

Diagnostic and therapeutic decision making in many areas of cardiovascular medicine, including valvular heart disease, ischemic heart disease, ventricular arrhythmias, congenital heart disease, and surgical ventricular restoration planning, requires assessment of coronary artery status and concurrent bi-ventricular volumes and function [17]. Currently, MR is considered the standard of reference in LV and RV volume assessment with better accuracy and reproducibility as compared with echocardiography [22]. Recent publications demonstrated excellent agreement between CT and MR in LV and RV volume calculation, and the superiority of CT compared with echocardiography [14, 15, 21, 44]. So far, few data are available on concurrent RV and LV volume assessment with CT as compared with MR . Our results show a good agreement between CT and MR. Only slight differences with no clinical impact were found between analyzed parameters. In particular, LV EDV by CT was lower as compared with MR and RV EDV by CT was higher than MR. This finding further confirm our previous hypothesis that these differences may be caused by different respiratory phases related to different acquisition techniques [14]. The lower temporal resolution of CT is unlikely to be responsible for underestimation of the LV EDV compared with MR, since it is not associated with a consensual overestimation of the LV ESV.

Although we cannot exclude an effect of ß-blockers in patients examined with CT, the expected increase in EDV was not observed in our study. Differences may to some extend be explained by the fact that MR images were acquired during expiration, while CT was performed during an inspiratory breath hold. In maximum inspiration LV venous return is decreased, resulting in EDV reduction and consensual ESV reduction preserving SV and EF. Just the opposite happens for RV venous return, with increased EDV and consensual ESV increment but preserved SV and EF.

Despite good agreement with MR, CT is unlikely to become the preferred imaging investigation for LV and RV functional assessment because of the radiation exposure and administration of contrast material. However, for patients with poor echocardiographic compliance, and contra-indications to MR, CT can offer a reliable alternative to assess ventricular function. The importance of an alternative functional imaging investigation is even more evident for the RV, which has a complex shape that lends itself poorly for echocardiographic functional assessment. Our results suggest that CT could be a reliable second option to MR, for instance in patients with (corrected) grown-up congenital heart disease.

The lower intra- and inter-observer variability for LV ED Wall mass by CT may be related to better definition of contours as a result of higher spatial resolution, which improves evaluation of the base slice. Good limits of agreement were maintained after dividing patients in varying EF subgroups, which confirms that cardiac CT can be a reliable tool independently of impaired ventricular function.

CT datasets were analyzed in shorter time compared with MR despite the higher number of images, which may be related to more efficient, semi-automated contours definition on the CT images.

It is important to underline that 21 patients were excluded because of unsuitability for an MR environment, while no patient were excluded because of CT contraindications.

Limitations

Although the exact radiation dose was not evaluated in this population, it should be mentioned that ECG-gated 64-slice CT without ECG-triggered tube modulation is associated with an exposure between 12–18mSv [45–47]. More modern CT equipment implements different techniques able to acquire datasets useful for coronary tree and LV and RV function evaluation at lower radiation dose [48, 49].

Conclusions

Using MR as reference, we demonstrated that ECG-gated cardiac CT accurately assesses both left and right ventricular function, with excellent reproducibility of the functional parameters. Thereby it may be regarded as a reliable alternative to echocardiography and magnetic resonance imaging taking into account the potential risks of radiation and iodinated contrast medium.

Electronic supplementary material

Below is the link to the electronic supplementary material.