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Article

60-S Retrogated Compressed Sensing 2D Cine of the Heart: Sharper Borders and Accurate Quantification

1
University of Lille, Inserm, CHU Lille, Institut Pasteur Lille, U1011—European Genomic Institute for Diabetes (EGID), F-59000 Lille, France
2
CHU Lille, Department of Cardiovascular Radiology, F-59000 Lille, France
3
MR Product Innovation and Definition, Magnetic Resonance, Siemens Healthcare GmbH, 91052 Erlangen, Germany
4
Scientific Partnerships, Siemens Healthcare France, 93200 Saint-Denis, France
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2021, 10(11), 2417; https://doi.org/10.3390/jcm10112417
Submission received: 16 March 2021 / Revised: 24 May 2021 / Accepted: 26 May 2021 / Published: 29 May 2021

Abstract

:
Background and objective: Real-time compressed sensing cine (CSrt) provides reliable quantification for both ventricles but may alter image quality. The aim of this study was to assess image quality and the accuracy of left (LV) and right ventricular (RV) volumes, ejection fraction and mass quantifications based on a retrogated segmented compressed sensing 2D cine sequence (CSrg). Methods: Thirty patients were enrolled. Each patient underwent the reference retrogated segmented steady-state free precession cine sequence (SSFPref), the real-time CSrt cine and the segmented retrogated prototype CSrg sequence providing the same slices. Functional parameters quantification and image quality rating were performed on SSFPref and CSrg images sets. The edge sharpness, which is an estimate of the edge spread function, was assessed for the three sequences. Results: The mean scan time was: SSFPref = 485.4 ± 83.3 (SD) s (95% CI: 454.3–516.5) and CSrg = 58.3 ± 15.1 (SD) s (95% CI: 53.7–64.2) (p < 0.0001). CSrg subjective image quality score (median: 4; range: 2–4) was higher than the one provided by CSrt (median: 3; range: 2–4; p = 0.0008) and not different from SSFPref overall quality score (median: 4; range: 2–4; p = 0.31). CSrg provided similar LV and RV functional parameters to those assessed with SSFPref (p > 0.05). Edge sharpness was significantly better with CSrg (0.083 ± 0.013 (SD) pixel−1; 95% CI: 0.078–0.087) than with CSrt (0.070 ± 0.011 (SD) pixel−1; 95% CI: 0.066–0.074; p = 0.0004) and not different from the reference technique (0.075 ± 0.016 (SD) pixel−1; 95% CI: 0.069–0.081; p = 0.0516). Conclusions: CSrg cine provides in one minute an accurate quantification of LV and RV functional parameters without compromising subjective and objective image quality.

1. Introduction

Cardiac magnetic resonance (CMR) is the reference standard method for quantification of volumes, ejection fraction (EF) and mass of left (LV) and right ventricles (RV) [1,2,3]. Reliable volumes assessment is required since EF has a strong prognostic value regarding clinical outcomes and survival [4,5,6]. However, besides steady-state free precession cine images essential for quantification, phase contrast angiography, gadolinium enhanced imaging, and additional sequences may be recommended depending on heart conditions, leading to an extended scan time, which may be difficult to handle for patients suffering from cardiac-related shortness of breath, since multiple breath-holdings are required for the acquisition [7].
To reduce acquisition time, compressed sensing (CS) has recently been applied to magnetic resonance imaging, especially CMR [8]. Based on Candès et al.’s work on signal recovery from incomplete sampling, Donoho proposed the CS acquisition [9,10]. Since the signal compression required for archiving and transfer implies the deletion of most acquired data, the principle of CS is to acquire only the pieces of information that would be preserved after this compression, sparing the time necessary for the acquisition of the data that would finally be purged during this process. Three prerequisites are mandatory for CS [11]. First, contrary to most medical images, the signal must be compressible. This means a sparsifying transform is required for most transformed coefficients to be insignificant, making the transformed image compressible. Second, the undersampling must be incoherent to provide noise-like overfolding and avoid ambiguity. Finally, non-linear iterative reconstructions enforcing image consistency with measured signal and transformed image sparsity are needed. In the case of cine imaging, the redundancy in the cardiac cycle provides a strong spatiotemporal correlation, which can be exploited for additional acceleration [12,13,14]. Undersampling is not only performed in plane but also in the temporal domain by using variable sampling density maps for successive frames.
The first-generation real-time CS sequence (CSrt) has already been widely evaluated regarding volumes, EF and mass for both ventricles, at 1.5 and 3-Tesla [15,16,17,18,19,20,21,22,23,24,25]. These studies used 80 iterations to reconstruct CSrt data, this setting being supposed to provide the best compromise between image quality and reconstruction time [17]. Nevertheless, computing times over one minute per slice were reported, making such a setting not compatible with clinical use [26,27]. Vermersch et al. evaluated the same sequence halving the number of iterations and demonstrated a similar agreement for the quantification of volumes, EF and mass quantification than previously reported in the literature, extending the use of CSrt in clinical practice [22]. To provide an acceleration factor compatible with single-breath-hold real-time imaging, additional sensitivity encoding imaging (SENSE) and partial Fourier are implemented, the latter being a potential cause of edge sharpness impairment [28]. Another limitation is the limited temporal resolution of 49 ms which may provide variable numbers of frames per slice in the case of heart rate variability. To allow post-processing, a 25-frame per slice interpolation is performed. Besides the border blurring induced by this normalization, end-systolic volumes may be overestimated in the case of a fast heart rate [29,30].
A new generation of retrogated CS sequence (CSrg) has been released. It features segmented acquisition to improve temporal resolution and partial Fourier switch-off to improve edge sharpness. The purpose of this study was to assess the image quality and the ventricular functional parameters in comparison with CSrt and the reference retrogated segmented steady-state free precession cine sequence (SSFPref).

2. Materials and Methods

2.1. Study Population

From March to April 2019, 30 consecutive adult patients referred for rest CMR were included. Exclusion criteria were grown-up congenital heart disease work-up or follow-up, underaged patients, patients suffering from arrhythmia for whom the use of prospective ECG gating was necessary, MRI contraindications and patient refusal. Patients gave informed consent, and the protocol was approved by our Institutional Ethics Committee.

2.2. Imaging Protocol

CMR studies were performed on a 1.5-T scanner (MAGNETOM Aera, Siemens Healthcare, Erlangen, Germany). Every patient underwent three series of cine images: first the reference retrogated segmented multi-breath-hold SSFP sequence (SSFPref); then the CS-accelerated SSFP real-time sequence (CSrt) acquired in two breath-holds, and finally the retrogated segmented SSFP prototype with CS-fashioned acceleration requiring three breath-holds (CSrg). One LV 2-chamber, one RV 2-chamber, one 4-chamber slice and a LV short-axis stack covering the entire ventricles were acquired with the three above-cited sequences, providing identical slice position, thickness, and number. Imaging parameters for the three sequences are summarized in Table 1.

2.3. Cine Images Quality Assessment

A 3-step evaluation was performed for the three sequences.
First, a subjective overall image quality was assessed using a 4-point Likert scale (1: non diagnostic, 2: fair, 3: good, 4: excellent).
Then acquisition quality was evaluated using a standardized score based on the “LV-function cine SSFP” section of the criteria established from the European CMR registry, evaluating the artifact detection [15] (p. 3). This score was modified, removing its four last items since their score was systematically null, accordingly to our center practice (Table 2). This score increased with acquisition impairment.
Finally, the edge sharpness (ε) between myocardium and LV blood pool was measured on end-diastole 4-chamber view (Figure 1). This assessment was performed using a MATLAB (version R2015a, The MathWorks, Natick, MA, USA) homemade script. An intensity profile line was drawn perpendicularly to the mid-cavity interventricular septum border with the LV blood pool at end-diastole [31,32,33]. The ε value was a spatial frequency (pixel−1) calculated as the inverse of the distance separating the two points corresponding to 20% and 80% of the difference between the minimum and maximum intensities along this line.

2.4. Functional Evaluation

Assessment of end-diastolic volumes (EDV), end-systolic volumes (ESV), stroke volumes (SV) and EF were performed for both ventricles as well as LV mass (LVM). These parameters were measured on short-axis stacks with semi-automated segmentation with manual correction of the LV endocardium and epicardium while manual segmentation of the RV endocardium was necessary, using dedicated 4D analysis software (Cardiac MR analysis workflow, Syngo.via VB30A, Siemens Healthcare, Erlangen, Germany). Four-chamber, LV and RV 2-chamber slices were used to define mitral and tricuspid valve planes to ensure optimal assessment of ventricular bases.

2.5. Conditions of Image Analysis

The three datasets were independently analyzed by a 4-year experience CMR radiologist (LG). After anonymization and randomization performed for each sequence, each dataset was analyzed separately. Each analysis session, which evaluated all the images of the same sequence, was separated from the previous one by one month. A second radiologist with 11 years of experience in CMR (BL) segmented both ventricles on CSrg images for interrater variability assessment.

2.6. Statistics Analysis

Categorical data were presented as numbers (percentage) and continuous variables as mean ± standard deviation (SD) (95% confidence interval (CI)) in the case of normal distribution or median (range: minimum–maximum) in other cases. Variable normality was assessed using the D’Agostino–Pearson test.
Paired Wilcoxon signed-rank test was used to compare subjective image qualities and acquisition qualities between CSrg and SSFPref or CSrt. An analysis of variance was performed to compare edge sharpness and acquisition times of the three sequences. CSrg and SSFPref mean functional parameters were compared using a Student’s t test, with linear regression and Bland–Altman analysis to assess the agreements between both methods. Inter and intra-observer variabilities were assessed using intra-class coefficient correlation. Significance of the test was defined by values of p < 0.05.
As for valvular regurgitations and WMD visualization, a receiver operating characteristic (ROC) curve was used. Statistical analysis was performed using dedicated commercially available software (MedCalc 14.8.1.0, MedCalc Software, Ostend, Belgium).

3. Results

3.1. Population Description

Demographics data are listed in Table 3. The 30 patients (22 men, 8 women; mean age: 48.0 ± 21.0 (SD) years; 95% CI: 40.2–55.9 years) were referred for: heart valve disease (n = 7/30; 23.3%), ischemic cardiopathy (n = 5/30; 16.7%); dilated cardiomyopathy (n = 5/30; 16.7%), myocarditis (n = 5/30; 16.7%), left ventricular hypertrophy (n = 5/30; 16.7%) and infiltrative cardiomyopathy (n = 3/30; 10%). All patients could fully complete CSrt and CSrg breath-holdings.

3.2. Scan Time and Image Quality

SSFPref mean scan time was 485.4 ± 83.3 (SD) s (95% CI: 454.3–516.5 s) while CSrt scan time was 23.9 ± 5.2 (SD) s (95% CI: 21.9–25.8 s) and CSrg scan time was 58.3 ± 15.1 (SD) s (95% CI: 53.7–64.2 s) (p < 0.0001). Compared to SSFPref, the mean acceleration factor provided by CSrg was 8.7 ± 2.6 (SD) (95% CI: 4.5–15.7). A mean number of 15.0 ± 1.2 (SD) slices (95% CI: 14.6–15.4 slices) was acquired with each technique. For CSrg reconstruction of the full dataset, the mean time was 82.9 ± 23.4 (SD) s (95% CI: 77.4–110.1 s).
All images were rated as diagnostic. CSrg subjective quality score (median: 4; range: 2–4) was higher than the one provided by CSrt (median: 3; range: 2–4; p = 0.0008). SSFPref overall quality score (median: 4; range: 2–4) was not different from CSrg score (p = 0.31).
Regarding the acquisition quality based on the EuroCMR registry, the CSrg sequence (median: 0; range: 0–3) was not different from either the SSFPref acquisition (median: 0; range: 0–3; p = 0.38) or the CSrt cine (median: 0; range: 0–3; p = 0.83).
The CSrg demonstrated a significantly better edge sharpness than CSrtCSrg = 0.083 ± 0.013 (SD) pixel−1 (95% CI: 0.078–0.087 pixel−1) versus εCSrt = 0.070 ± 0.011 (SD) pixel−1 (95% CI: 0.066–0.074 pixel−1); p = 0.0004). Moreover, no significant difference was demonstrated between CSrg and SSFPrefSSFPref = 0.075 ± 0.016 (SD) pixel−1 (95% CI: 0.069–0.081 pixel−1); p = 0.0516) (Figure 2; Figure 3; Video S1; Video S2 (Supplementary Materials)).

3.3. Volumes, Functions and Mass Quantification

Good agreements were yielded by Bland–Altman and linear regression analyses for both LV (Figure 4) and RV (Figure 5) assessments. No significant difference was demonstrated regarding LVM, LV and RV volumes (EDV, ESV, SV) and EF (p > 0.05) (Table 4). Intrarater variability was excellent, demonstrating intraclass correlation coefficients (ICC) greater than 0.99 for both ventricles, as were interrater variabilities for LV (ICC ≥ 0.97) and RV (ICC ≥ 0.96).

4. Discussion

Our clinical study performed a comprehensive evaluation of a retrogated CS sequence in daily practice. Results are in line with preliminary CSrg tests on eight healthy volunteers reported by Forman et al., regarding LVEF, LVEDV and LVESV, which were similar to SSFPref quantification [34]. However, the study population was small and LVM, RV volumes and EF were not assessed. In the present study, no significant difference was demonstrated regarding LVM, LV and RV volumes (EDV, ESV and SV) and EF.
First-generation 49-ms temporal resolution CSrt sequence provided LVEDV underestimation and LVM overestimation, which were clinically insignificant or smaller than intra or interrater variabilities [17,22,25,26,35]. Moreover, LVEDV underestimation was also reported with other acceleration techniques such as radial gradient-echo or k-space parallel imaging [36,37]. These differences were not depicted with CSrg. This might be explained by the improved edge sharpness facilitating segmentation, retrospective ECG gating allowing acquisition of the last phases of the cardiac cycle and the better temporal resolution (37 ms) [38]. This observation is in line with previous studies suggesting an optimal temporal resolution for accurate steady-state free precession quantification below 45 ms [29]. Since quantification is a major CMR point of interest, the absence of significant difference regarding each LV and RV parameter seems promising for clinical implementation [1]. Moreover, the high intra and interrater reproducibility allows the use of CSrg for chronic status follow-up such as heart failure, anthracycline induced cardiotoxicity and other cardiomyopathies [39,40,41].
The overall image quality alteration using CSrt has already been assessed in a previous publication [22]. The higher score provided by CSrg confirmed the image quality improvement. Indeed, CSrt interpolation was responsible for smoothed images, which required physicians to get used to this rendering. The absence of difference between acquisitions qualities (EuroCMR quality score) was expected. Indeed, no difference had been demonstrated regarding the first-generation CS sequence. The evaluated prototype features partial Fourier switch-off and segmented acquisition, which were not supposed to generate more artifacts. Regarding edge sharpness, the absence of interpolation and acquisition of more data improves boarder delineation. Not only was εCSrg better than εCSrg but it was similar to εSSFPref. Edge sharpness was chosen as a metric for intrinsic image quality assessment due to its simple and reproducible implementation. Moreover, edge sharpness is an estimate of the edge spread function whose derivative is a line-spread function [33]. Fast Fourier transform of the latter gives the task-based modulation transfer function (MTFTask); edge sharpness can be considered as a reasonable approximation of MTFTask, which is widely used to evaluate the spatial frequency response of an imaging system, even using iterative reconstructions [42].
Predictably, CSrg scan time was approximatively twice as long as the first-generation CS sequence since acquisitions were segmented on two heart beats in contrast to real-time imaging. However, as compared to SSFPref, the mean CSrg scan time of about 60 s still provides an 8.7-fold acceleration factor. The study protocol divided CSrg acquisition in 3 stacks to shorten breath-holdings. Nevertheless, this setting is adjustable, such as the number of heart beats required for one slice to reduce apneas or increase spatiotemporal resolution. We chose to use CS to improve scan time, with workflow fluency being a major point of concern. However, it is possible to take advantage of this acceleration to improve spatial resolution, or maybe more interestingly, temporal resolution. Indeed, in the field of feature tracking in CMR, a resolution at least over 30 frames per cycle is recommended for accurate strain assessment, which is more time-consuming when using SSFPref [43]. Such settings may facilitate further feature tracking studies, though the impact of CS based reconstructions should be evaluated regarding strain analysis reliability.
The image quality improvement provided by the prototype CSrg as compared to the first-generation real-time CSrt should facilitate the spread of CS use in daily practice. However, the 2-shot acquisition is responsible for the loss of the real-time acquisition. Futures generations of CS cine sequences, maintaining the CSrt real-time feature and the CSrg image quality, should be oriented towards the application of additional motion correction algorithms to provide free-breathing acquisition with preserved image quality.

Limitations

The size of the population was limited and cannot represent the whole variety of cardiac conditions encountered in daily practice. Nevertheless, the main objective of this study was to assess the image quality recovery as compared to SSFPref and CSrt. To facilitate the standardized assessment of edge sharpness, we chose to exclude congenital heart disease anatomy. Among the cardiac conditions assessed by CMR, dilated cardiomyopathy is a frequent pathology, usually responsible for shortness of breath, in which the LV wall may be thinned. The decreased wall thickness may be challenging for endocardium and epicardium delineation, thus impairing LV mass assessment. The impact of LV wall thickness for this assessment, for instance in dilated cardiomyopathy, could not be evaluated because of an insufficient subgroup. Nevertheless, we assume that the edge sharpness provided by CSrg should help to distinguish the endocardium from the epicardium as compared to the first-generation CSrt cine that provided blurrier borders. Although a high acceleration factor was demonstrated using CSrg, the improvement of CMR tolerance can only be assumed since this parameter was not evaluated. However, we suppose that the lower number of breath-holdings required by CSrg should help dyspneic or claustrophobic patients undergo CMR examinations. This acceleration might be overestimated and must be interpreted cautiously since the two 1.6 × 1.6 mm2 in-plane resolution CS sequences were compared with a 1.3 × 1.3 mm2 in-plane resolution reference sequence. However, Miller et al. demonstrated that the maximal accuracy for functional parameters quantification using SSFP sequence was reached between 1 and 2-mm in-plane spatial resolution [29]. Even though further acquisitions could be performed during CSrg reconstruction during this study (SSFPref images were acquired first and available), up to 2 min were necessary for images to be reconstructed and displayed to set the next sequences orientation in case of exclusive use of CSrg. Wall motion abnormalities were not evaluated, but the increased temporal resolution provided by segmented acquisition and the absence of interpolation should not impair their visualization on CSrg since the first generation of compressed sensing cine was demonstrated to be reliable for this evaluation (Video S3 (Supplementary Materials)) [44]. The heart rate of the evaluated patients ranged from 54 to 101 beats per minute (R–R intervals: 594 ms to 1111 ms). Since CSrg is a 2-shot sequence and its temporal resolution is constant (37 ms), the amount of data acquired during the acquisition must vary and may have an impact on the quality of the reconstructed cine images and consequently on functional assessment. The impact of heart rate on image quality was not evaluated in this study due to the limited size of the study population. Finally, only sinus rhythm patients were enrolled in this study. Even though a real-time acquisition is more robust than a segmented acquisition versus arrhythmia, the need of only two heart beats per slice should be more arrhythmia-proof than the conventional 8-heart-beat SSFPref. Further comparison with other acceleration techniques such as generalized autocalibrating partial parallel acquisition would be interesting since the later requires more heart beats for identical temporal and spatial resolutions [45].

5. Conclusions

CSrg allows reliable quantification of LV and RV volumes, EF and mass providing similar objective and subjective image quality to SSFPref. Performed in clinical conditions, CSrg is promising in terms of workflow improvement and image quality recovering in comparison with the first-generation real-time CSrt.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/jcm10112417/s1, Video S1: Short-axis cine stacks in a 45-year-old woman referred for myocarditis follow-up; Video S2: Four-chamber cine slice in the same patient as Video S1; Video S3, short-axis mid-cavity cine slice in a 68-year-old patient referred for viability assessment after myocardial infarction, demonstrating inferolateral akinesia.

Author Contributions

B.L.: study conception and design, data collection, interpretation and analysis, drafting of the manuscript, critical revision for important intellectual content; C.V.G.: data collection and interpretation, critical revision for important intellectual content; A.C.: study conception, critical revision for important intellectual content; L.G.: data collection, interpretation and analysis, drafting of the manuscript; V.S.: data collection and interpretation, critical revision for important intellectual content; J.P.: data collection and interpretation, critical revision for important intellectual content; A.S.: data collection and interpretation, critical revision for important intellectual content; J.H.: data collection and interpretation, critical revision for important intellectual content; M.S.: study conception and design, critical revision for important intellectual content; C.F.: study conception and design, critical revision for important intellectual content; S.T.: study conception and design, critical revision for important intellectual content; D.M.: study conception, critical revision for important intellectual content; F.P.: study conception and design, data collection, interpretation and analysis, drafting of the manuscript, critical revision for important intellectual content. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was approved by the research ethics committee of Lille University Hospital.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data presented in this study are available on reasonable request from the corresponding author, subject to approval by the research ethics committee of Lille University Hospital.

Conflicts of Interest

B.L.; C.V.G; A.C.; L.G.; V.S.; J.P.; A.S.; J.H.; D.M.; F.P. have no competing interest. They are employed by an institution engaged in a contractual collaboration with Siemens Healthcare. M.S.; C.F.; S.T. are employees of Siemens Healthcare GmbH.

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Figure 1. Edge sharpness measurement. An orthogonal profile line is drawn across the border between the interventricular myocardium and the left ventricular blood pool (blue line) on a 4-chamber view at end-diastole provided by (a) the reference segmented SSFP sequence, (b) the real-time compressed sensing sequence and (c) the retrogated compressed sensing prototype, providing intensity profiles (blue curves) along the line for (d) reference, (e) real-time and (f) prototype sequences. The edge sharpness was calculated as the inverse of the distance d (in pixels) from the positions corresponding to 20% and 80% (red stars) of the difference between the maximum and minimum signal intensities (black crosses) along the profile line and was expressed in pixel−1. Abbreviations: SSFPref, reference steady-state free precession; CSrt, real-time compressed sensing; CSrg, retrogated compressed sensing; ε, edge sharpness; Ymax, maximum signal intensity; Ymin, minimum signal intensity; d, distance along the intensity (pixels).
Figure 1. Edge sharpness measurement. An orthogonal profile line is drawn across the border between the interventricular myocardium and the left ventricular blood pool (blue line) on a 4-chamber view at end-diastole provided by (a) the reference segmented SSFP sequence, (b) the real-time compressed sensing sequence and (c) the retrogated compressed sensing prototype, providing intensity profiles (blue curves) along the line for (d) reference, (e) real-time and (f) prototype sequences. The edge sharpness was calculated as the inverse of the distance d (in pixels) from the positions corresponding to 20% and 80% (red stars) of the difference between the maximum and minimum signal intensities (black crosses) along the profile line and was expressed in pixel−1. Abbreviations: SSFPref, reference steady-state free precession; CSrt, real-time compressed sensing; CSrg, retrogated compressed sensing; ε, edge sharpness; Ymax, maximum signal intensity; Ymin, minimum signal intensity; d, distance along the intensity (pixels).
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Figure 2. Midventricular short-axis cine slice acquired with the three cine sequences in a 37-year-old patient referred for myocarditis suspicion. (a) Reference steady-state free precession cine: Likert scale = 4/4; EuroCMR score = 0/10; ε = 0.082 pixel−1; LVEF = 59%, LVEDV = 135 mL, LVM = 83 g, RVEF = 63%, RVEDV = 159 mL; (b) Real-time compressed sensing cine: Likert scale = 4/3; EuroCMR score = 0/10; ε = 0.056 pixel−1; LVEF = 60%, LVEDV = 133 mL, LVM = 81 g, RVEF = 61%, RVEDV = 153 mL; (c) Retrogated compressed sensing cine: Likert scale = 4/4; EuroCMR score = 0/10; ε = 0.081 pixel−1; LVEF = 58%, LVEDV = 133 mL, LVM = 86 g, RVEF = 62%, RVEDV = 164 mL. Abbreviations: ε, edge sharpness; LVEF, left ventricular ejection fraction; LVEDV, left ventricular end-diastolic volume; LVM, left ventricular myocardial mass; RVEF, right ventricular ejection fraction; RVEDV, right ventricular end-diastolic volume.
Figure 2. Midventricular short-axis cine slice acquired with the three cine sequences in a 37-year-old patient referred for myocarditis suspicion. (a) Reference steady-state free precession cine: Likert scale = 4/4; EuroCMR score = 0/10; ε = 0.082 pixel−1; LVEF = 59%, LVEDV = 135 mL, LVM = 83 g, RVEF = 63%, RVEDV = 159 mL; (b) Real-time compressed sensing cine: Likert scale = 4/3; EuroCMR score = 0/10; ε = 0.056 pixel−1; LVEF = 60%, LVEDV = 133 mL, LVM = 81 g, RVEF = 61%, RVEDV = 153 mL; (c) Retrogated compressed sensing cine: Likert scale = 4/4; EuroCMR score = 0/10; ε = 0.081 pixel−1; LVEF = 58%, LVEDV = 133 mL, LVM = 86 g, RVEF = 62%, RVEDV = 164 mL. Abbreviations: ε, edge sharpness; LVEF, left ventricular ejection fraction; LVEDV, left ventricular end-diastolic volume; LVM, left ventricular myocardial mass; RVEF, right ventricular ejection fraction; RVEDV, right ventricular end-diastolic volume.
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Figure 3. Edge sharpness comparison assessed at end-diastole. (a) There was no significant difference regarding ε between CSrg and SSFPref (p = 0.0516) (b) but CSrg significantly improved ε while compared with CSrt (p = 0.0004). Abbreviations: CSrg, retrogated compressed sensing; CSrt, real-time compressed sensing; SSFPref, reference steady-state free precession; ε, edge sharpness.
Figure 3. Edge sharpness comparison assessed at end-diastole. (a) There was no significant difference regarding ε between CSrg and SSFPref (p = 0.0516) (b) but CSrg significantly improved ε while compared with CSrt (p = 0.0004). Abbreviations: CSrg, retrogated compressed sensing; CSrt, real-time compressed sensing; SSFPref, reference steady-state free precession; ε, edge sharpness.
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Figure 4. Bland–Altman plots and linear regression trendlines applied to left ventricular functional parameters quantifications. Left column: Bland–Altman plots for (a) LVEF, (c) LVEDV, (e) LVESV, (g) LVSV and (i) LVM. Solid blue lines are the mean differences between parameters measured with SSFPref and CSrg sequences and dashed red lines are the 95% limits of agreement. Right column: linear regression trend lines for (b) LVEF, (d) LVEDV, (f) LVESV, (h) LVSV and (j) LVM. Abbreviations: SSFPref, reference steady-state free precession; CSrg, retrogated compressed sensing; SD, standard deviation; LVEF, left ventricular ejection fraction; LVEDV, left ventricular end-diastolic volume; LVESV, left ventricular end-systolic volume; LVSV, left ventricular stroke volume; LVM, left ventricular mass.
Figure 4. Bland–Altman plots and linear regression trendlines applied to left ventricular functional parameters quantifications. Left column: Bland–Altman plots for (a) LVEF, (c) LVEDV, (e) LVESV, (g) LVSV and (i) LVM. Solid blue lines are the mean differences between parameters measured with SSFPref and CSrg sequences and dashed red lines are the 95% limits of agreement. Right column: linear regression trend lines for (b) LVEF, (d) LVEDV, (f) LVESV, (h) LVSV and (j) LVM. Abbreviations: SSFPref, reference steady-state free precession; CSrg, retrogated compressed sensing; SD, standard deviation; LVEF, left ventricular ejection fraction; LVEDV, left ventricular end-diastolic volume; LVESV, left ventricular end-systolic volume; LVSV, left ventricular stroke volume; LVM, left ventricular mass.
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Figure 5. Bland–Altman plots and linear regression trendlines applied to right ventricular functional parameters quantifications. Left column: Bland-Altman plots for (a) RVEF, (c) RVEDV, (e) RVESV, and (g) RVSV. Solid blue lines are the mean differences between parameters measured with SSFPref and CSrg sequences and dashed red lines are the 95% limits of agreement. Right column: linear regression trend lines for (b) RVEF, (d) RVEDV, (f) RVESV, and (h) RVSV. Abbreviations: SSFPref, reference steady-state free precession; CSrg, retrogated compressed sensing; SD, standard deviation; RVEF, right ventricular ejection fraction; RVEDV, right ventricular end-diastolic volume; RVESV, right ventricular end-systolic volume; RVSV, right ventricular stroke volume.
Figure 5. Bland–Altman plots and linear regression trendlines applied to right ventricular functional parameters quantifications. Left column: Bland-Altman plots for (a) RVEF, (c) RVEDV, (e) RVESV, and (g) RVSV. Solid blue lines are the mean differences between parameters measured with SSFPref and CSrg sequences and dashed red lines are the 95% limits of agreement. Right column: linear regression trend lines for (b) RVEF, (d) RVEDV, (f) RVESV, and (h) RVSV. Abbreviations: SSFPref, reference steady-state free precession; CSrg, retrogated compressed sensing; SD, standard deviation; RVEF, right ventricular ejection fraction; RVEDV, right ventricular end-diastolic volume; RVESV, right ventricular end-systolic volume; RVSV, right ventricular stroke volume.
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Table 1. Imaging parameters of the reference steady-state free precession cine, real-time compressed sensing cine and segmented retrogated compressed sensing cine.
Table 1. Imaging parameters of the reference steady-state free precession cine, real-time compressed sensing cine and segmented retrogated compressed sensing cine.
ParametersSSFPrefCSrtCSrg
Repetition time—ms3.162.702.70
Echo time—ms1.231.141.14
Flip angle—degrees576060
Field of view—mm2375 × 280360 × 270360 × 270
Matrix—pixels2288 × 216224 × 168224 × 168
Spatial resolution—mm21.3 × 1.31.6 × 1.61.6 × 1.6
Temporal resolution—ms374937
Slice thickness/gap—mm8/28/28/2
Bandwidth—Hz/pixel915900900
Reconstructed cardiac phases—n
Number of acquired cardiac phases
-
25 a
25 a
16.8 ± 3.9
-
25 a
Number of breath-holds15.0 ± 1.22 a3 a
Cycles per slice—n8 a1 a2 a
Cycles of iterative reconstruction—n-4040
Data are expressed as mean ± standard deviation in the absence of any indication. a Constant value. Abbreviations: SSFPref, reference steady-state free precession cine; CSrt, real-time compressed sensing cine; CSrg, segmented retrogated compressed sensing cine.
Table 2.LV-Function cine SSFP” section of the standardized objective quality criteria score based on the European CMR registry. Adapted from [15] (p. 3).
Table 2.LV-Function cine SSFP” section of the standardized objective quality criteria score based on the European CMR registry. Adapted from [15] (p. 3).
Items0123Maximum Score
1. LV coverageFull-No apexBase or ≥1 slice missing5
2. Wrap aroundNo1 slice2 slices≥3 slices3
3. Respiratory ghostNo1 slice2 slices≥3 slices
4. Cardiac ghostNo1 slice2 slices≥3 slices
5. Blurring/MistriggeringNo1 slice2 slices≥3 slices
6. Metallic artifactsNo1 slice2 slices≥3 slices
7. Shimming artifactsNo1 slice2 slices≥3 slices
8. Signal loss (coil inactive)Activated-Not activated 2
9. Orientation of stackCorrect-Incorrect-2
10. Slice thickness≤10 mm11–15 mm->15 mm3
11. Gap≤3 mm3–4 mm->4 mm3
12. Correct LV long axes≥2 mm1-None3
Score 21
Modified score (items 1 to 8) 10
The four last items were nulled since acquisitions were repeated when orientation was not appropriated (item 9 = 0); all acquisitions were performed using a 8-mm thickness (item 10 score = 0) and a 2-mm gap (item 11 score = 0), horizontal and vertical long axis views were systematically acquired (item 12 score = 0). Consequently, italic criteria were not applied, and only bold criteria were used for objective quality assessment in our study, providing a maximum score of 10 points. The more artifacts there were, the higher the score was. Abbreviations: LV, left ventricle; SSFP, steady-state free precession.
Table 3. Study population characteristics.
Table 3. Study population characteristics.
Mean ± SD (95% CI)Minimum ValueMaximum Value
Age—years48.0 ± 21.0 (40.2–55.9)1887
Weight—kg73.9 ± 12.1 (69.4–78.5)53105
Height—cm172.5 ± 8.3 (169.4–175.6)157189
Body surface area—m21.87 ± 0.17 (1.80–1.93)1.552.22
Body mass index—kg/m224.8 ± 3.6 (23.5–26.2)19.833.7
Heart rate—beats per minute73.8 ± 13.5 (68.7–78.9)54101
Abbreviations: SD, standard deviation; 95% CI, 95% confidence interval.
Table 4. Functional parameters segmented on both the reference steady-state free-precession and retrogated compressed-sensing cine.
Table 4. Functional parameters segmented on both the reference steady-state free-precession and retrogated compressed-sensing cine.
SSFPref Sequence
(Mean ± SD (95% CI))
CSrg Sequence
(Mean ± SD (95% CI))
Difference
(Mean ± SD (95% CI))
Paired t Test pICC
InterIntra
LVEF—%52.7 ± 14.1
(47.5–58.0)
52.1 ± 13.8
(47.0–57.3)
−0.6 ± 2.6
(−1.6 to −0.4)
0.210.990.9996
LVEDV—mL174.1 ± 50.3
(155.3–192.9)
173.0 ± 48.0
(155.1–190.9)
−1.2 ± 8.0
(−4.2 to −1.8)
0.430.990.9994
LVESV—mL86.8 ± 49.4
(68.4–105.2)
86.4 ± 48.0
(68.5–104.3)
−0.4 ± 6.5
(−2.8 to −2.0)
0.740.980.9906
LVSV—mL87.5 ± 24.0
(78.6–96.5)
86.7 ± 23.2
(78.0–95.4)
−0.8 ± 5.3
(−2.8 to −1.1)
0.390.980.9932
LVM—g139.5 ± 47.7
(121.6–157.3)
135.9 ± 50.4
(117.0–154.7)
−3.6 ± 13.9
(−8.8 to 1.6)
0.170.970.9994
RVEF—%55.8 ± 9.7
(52.2–59.4)
56.0 ± 9.3
(52.6–59.5)
0.3 ± 2.4
(−0.7 to 1.2)
0.560.960.9965
RVEDV—mL167.0 ± 53.6
(147.0–187.0)
163.2 ± 47.4
(145.5–180.9)
−3.8 ± 18.2
(−10.5 to 3.05)
0.270.980.9968
RVESV—mL74.1 ± 34.3
(61.3–86.9)
73.1 ± 32.0
(61.1–85.0)
−1.0 ± 6.9
(−3.6 to 1.6)
0.450.960.9934
RVSV—mL89.8 ± 24.3
(80.8–98.9)
90.1 ± 24.5
(81.0–99.3)
−0.3 ± 5.7
(−1.8 to 2.4)
0.770.970.9961
ICC assessed the inter and intrarater agreements for ventricular segmentations. The significance of Student’s t test is defined by values of p < 0.05. Abbreviations: SSFPref, reference steady-state free-precession cine; CSrg, retrogated compressed-sensing cine; SD, standard deviation; 95%CI, 95% confidence interval; LV, left ventricular; RV, right ventricular; EF, ejection fraction; EDV, end-diastolic volume; ESV, end-systolic volume; SV, stroke volume; LVM, left ventricular mass; ICC, intraclass correlation coefficient; Inter, interrater; Intra, intrarater.
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Longère, B.; Gkizas, C.V.; Coisne, A.; Grenier, L.; Silvestri, V.; Pagniez, J.; Simeone, A.; Hennicaux, J.; Schmidt, M.; Forman, C.; et al. 60-S Retrogated Compressed Sensing 2D Cine of the Heart: Sharper Borders and Accurate Quantification. J. Clin. Med. 2021, 10, 2417. https://doi.org/10.3390/jcm10112417

AMA Style

Longère B, Gkizas CV, Coisne A, Grenier L, Silvestri V, Pagniez J, Simeone A, Hennicaux J, Schmidt M, Forman C, et al. 60-S Retrogated Compressed Sensing 2D Cine of the Heart: Sharper Borders and Accurate Quantification. Journal of Clinical Medicine. 2021; 10(11):2417. https://doi.org/10.3390/jcm10112417

Chicago/Turabian Style

Longère, Benjamin, Christos V. Gkizas, Augustin Coisne, Lucas Grenier, Valentina Silvestri, Julien Pagniez, Arianna Simeone, Justin Hennicaux, Michaela Schmidt, Christoph Forman, and et al. 2021. "60-S Retrogated Compressed Sensing 2D Cine of the Heart: Sharper Borders and Accurate Quantification" Journal of Clinical Medicine 10, no. 11: 2417. https://doi.org/10.3390/jcm10112417

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