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Application of single shot free-breathing FIESTA sequence in cardiac MRI Objective To investigate the imaging quality of single shot (SS) fast imaging employing steady state (FIESTA) sequence in contrast-enhanced cardiac magnetic resonance (MR) examination, in comparison with the IR FGRE sequence. Materials and Methods Fifty-two cases with suspected or known heart disease were enrolled in this study, including 24 patients who had enhanced myocardium in myocardial delayed enhancement (MDE). We analyzed the imaging quality of the sequences by measuring the myocardium and blood pool signal-to-noise ratios (SNR) and the contrast-to-noise ratios (CNR) of blood pool relative to normal myocardium and of enhanced myocardium relative to normal myocardium and compared the new sequences with traditional sequence. Results The scanning time of SS FIESTA was significantly shortened as compared to IR FGRE. The differences in the image quality scores, enhanced myocardium (EM) mass and percentages, SNR(bp), SNR(myo), CNR(myo/bp) and CNR(l/bg) were not statistically significant between SS FIESTA and IR FGRE (P> 0.05). However the difference in CNR(em/myo) was statistically significant between SS FIESTA and IR FGRE (P<0.0001), with CNR(em/myo) of IR FGRE higher than SS FIESTA. Conclusion SS FIESTA speeded up the acquisition time, halving it to (27.6±1.8 sec) instead of 146+13.8 sec (IR FGRE), it had higher SNR and CNR, and its image quality did not differ significantly from IR FGRE. The SS FIESTA is more suitable for patients with severely heart diseases or those unable to hold breath. 3D IR FGRE sequence had higher SNR(myo) than the others and it is suitable for displaying the subendocardial scar. However it has more artifacts and poor imaging quality than IR FGRE. Key Words contrast-enhanced cardiac magnetic resonance (CMR); single-shot inversion recovery FIESTA (SS-FIESTA); segmented inversion recovery 2D fast gradient echo (IR FGRE); segmented inversion recovery 3D fast gradient echo (3D IR FGRE) Introduction Cardiac magnetic resonance imaging (MRI) can reveal cardiac anatomical structure, function and many types pathological scars and can diagnose a variety of heart diseases [1-2]. Myocardial delayed enhancement (MDE) MRI for myocardial infarction lesions was first reported in 1993 [3]. With the development of MRI technologies, more research reports have confirmed that as a visual observation method for myocardial infarction, delayed enhancement has important clinical value [4] . In recent years, because of the improvement in high performance gradient echo sequence, MDE has become the diagnostic criterion for myocardial infarction, and can be used for the rapid detection of myocardial lesions. MDE can not only be used to diagnose myocardial infarction, but also be used to observe many other heart diseases, such as myocarditis, infection, cardiomyopathy, cardiac tumors, and congenital or secondary heart disease [5]. However, the biggest bottleneck of cardiac MRI is the lengthy scanning time. Patients who have severe heart diseases or patients who can not hold breath well (such as patients with acute myocardial infarction, dilated cardiomyopathy, and other cardiopulmonary dysfunction) can not tolerate long time of scanning, resulting motion artifacts in MRI images and thereby reducing diagnostic confidence. Therefore, investigating sequences with shorter scanning time and better image quality has become a hot research topic in the field of cardiac MRI both in China and abroad. Single shot (SS) fast imaging employing steady state (FIESTA) (single-shot inversion recovery 2D FIESTA) sequence is a type of fast scan sequence. Due to its high contrast-to-noise ratio (CNR), especially cardiac blood pool CNR [6], it can clearly show the myocardial edge, and in clinical practice, it is often used in delayed enhancement sequence to directly display myocardial lesions. In 2006 it was reported that the average scan time for this sequence was 10 minutes 13 ± 45 sec [7], and in 2010 Lene Rosendah [8] reported a scan time of 4.4 ± 1.6 min. Our studies used partial sample collection along the X- and Y-axes, and collected more than 90 sequences within 190 ms, with 3~4 ms for each sequence. Our scan time was fast, and one collection can be completed every two heartbeats. We also investigated whether we could obtain clear cardiac images on top of significantly shortened scan time, therefore enabling patients unable to hold breath to benefit from this examination technique. This study enrolled 52 cases of clinically diagnosed or suspected heart diseases. The patients were examined by MDE MRI using the SS FIESTA sequence, 3D IR FGRE (segmented inversion recovery 3D fast gradient echo) sequence and IR FGRE (segmented inversion recovery 2D fast gradient echo) sequence that acted as the conventional sequence. By measuring and analyzing the myocardial signal-to-noise ratio (SNR) and CNR of 52 cases (including the comparison of CNR between enhanced myocardium and normal myocardium in 24 myocardial lesion cases), we observed and compared the SS FIESTA and 3D IR GRE sequences with the conventional IR FGRE sequence, and examined whether the images showed significant difference in image quality and contained rich imaging information on the basis of significantly shortened scan time to correctly diagnose heart disease. Materials and Methods Subjects We enrolled a total of 52 cases of suspected or confirmed heart disease, including 39 males and 14 females. The patients aged between 16 and 76 years, with a mean of 54 years. And there were 22 cases of ischemic heart diseases (including 14 cases undergone reexamination 3 months after coronary artery bypass and bone marrow stem cell transplantation), 5 cases of hypertrophic cardiomyopathy, 4 cases of dilated cardiomyopathy, 1 case of cardiac amyloidosis (confirmed by pathological examination) and 2 cases of myocardial fibrosis. This study was approved by the ethics committee of our hospital, and all patients signed the consent form. MR image collection We used a 1.5 T scanner (Signa Excite HD Twinspeed, GE Healthcare, Milwaukee, Wisconsin, USA) with a gradient of 40 mT/m and a slew rate of 150 mT/m-1/ms-1. All patients were in the supine position with foot entering first. The antecubital vein was placed with an indwelling intravenous catheter. An 8-channel phased array coil dedicated for cardiac MRI was used, the electrocardiogram (ECG) leads were placed in the precordium for vectorcardiogram gating (or a peripheral pulse gating device was placed around the fingers), and the respiratory gating device was placed on the abdomen. According to the myocardial segments defined by the American Heart Association (AHA), cardiac MRI mostly uses long axis, three-chamber, four-chamber or short axis views [9]. Delayed scanning often scans the entire left ventricular short axis, generally with 8-10 layers. For delayed enhancement scan, each subject was injected with 30 ml of contrast agent and 20 ml of normal saline at 2 ml/s through the antecubital vein using high-pressure syringes (binoculars pressure syringe, U.S. Gomal Medical Products Co., Ltd.). The contrast agent that we used was gadopentetate dimeglumine with a dose of 0.1 mmolkg-1 and a maximum dose of 30 ml (Schering, Germany). After 8 minutes of delay, we examined whether the left ventricular myocardium was black. If the left ventricular myocardium was confirmed to be black, it indicated that the contrast agent had entered fully into the myocardium, and the delayed enhancement scan could be initiated. The scanning order of the three kinds of delayed enhancement sequences, SS FIESTA, 3D IR FGRE and IR FGRE, was random. The parameters of the three scan sequences were listed in Table 1. The scan was ECG-gated and respiratory-triggered. The IR FGRE sequence had about 12 heartbeats for each breath hold, and the ECG-based triggering was 25% of the R-wave phase on the ECG [10-11]. The SS FIESTA sequence had 2 heartbeats for each breath hold. Analysis of MR images Quality evaluation According to the contrast of myocardium and cardiac chambers to the background on cardiac MRI images, it was possible to freely adjust the window width and position, in order to achieve the best visual effects of the images. Myocardial hypo- or hyper-signal was determined according to the myocardial segmentation defined by AHA, and the image quality was divided into five grades of scores. MDE image quality was determined according to the following four conditions: (i) whether there were breathing artifacts, (ii) evaluation of cardiac artifacts, (iii) whether the myocardium was sufficiently suppressed, without enhanced myocardial signal intensity (black), (iv) whether the endocardium adjacent to the left ventricular endocardial cavity was sharp. All image quality was divided into grades 1-5 (1 is very poor, 2 is poor, 3 is acceptable, 4 is good, and 5 is excellent) [12]. Image quality was rated by two experienced cardiovascular MRI physicians. Disagreement was solved by discussion, and the consensus was used as the final result. SNR and CNR When measuring myocardial SNR and CNR, the regions of interest (ROIs) were placed in the center of areas such as the left ventricular blood pool (bp), normal left ventricular myocardium (myo), background (bg) (chest air), lung tissue (l), and abnormally enhanced myocardium (em) to measure signal intensity (I) and standard deviation (SD). ROI was placed in the corresponding position of each slice of short axis images, with an area of about 3 ± 0.7 mm2. The measured data included: blood pool SNR (SNR(bp) = Ib/SDbg), myocardial SNR (SN (myo) = Imyo/SDbg), lung tissue minus background CNR (CNR(l/bg) = (Il-Ibg)/SDbg), blood pool minus myocardium CNR (CNR(bp/myo) = (Ibp-Imyo)/SDbg) and abnormal myocardium minus normal myocardium CNR (CNR(em/myo)) = (Iem-Imyo)/SDbg). Statistics We statistically analyzed the average elapsed time for the three kinds of sequences, and evaluated the image quality of the three kinds of sequences. We compared the images obtained using the two fast scanning sequences with the traditional IR FGRE sequence, and measured the image SNR and CNR, including SNR(myo), SNR(bg), SNR(bp) and SNR(l), CNR(bp/myo), MDE CNR(em/myo) and CNR(l/bg). The SSPS17.0 software was used to analyze and compare whether there were statistically significant differences in image SNR and CNR. According to conventional standards, image quality was examined using the homogeneity of variance test. In the presence of homogeneous variance, the chi-square test for two independent samples was used. In the presence of heterogeneous variance, the rank sum test for two independent samples of non-normal data was used. P <0.05 indicated statistically significant difference, and P> 0.05 indicated no significant difference. Results 1 Scanning time and image quality 1.1 Scan time: The SS FIESTA sequence required 2-3 times of breath hold, each lasting 7 ± 1.3 seconds, 3-4 slices (each with an average of 1.7 ± 0.5 sec) were obtained, and the total scan time was 27.6 ± 1.8 s (not including the intervals between breath-hold). IR FGRE required one breath hold per slice of scanning, each breath hold lasted 10 ± 2.3 seconds, and the total scan time was 146 ± 13.8 sec (not including the intervals between breath-hold). 3D IR FGRE required only once breath hold lasting 30.4 ± 4.0 seconds, and the images of segmentations 24-26 of the left ventricle were obtained (table 2). Compared with IR FGRE, the scan time of 3D IR FGRE sequence was reduced by 81%, and that of SS FIESTA sequence was reduced by 79%. The comparisons between the two fast sequences and IR FGRE sequence both had P <0.001. And 50 out of 52 patients had successful examinations, and the success rate was about 96.2%. 1.2 Evaluation MDE image quality: we compared the image quality of the SS FIESTA sequence and IR FGRE sequence at free-breathing state. SS FIESTA had an average score of 1.8 ± 0.2, which was better than IR FGRE (0.7 ± 0.1), and statistical analysis showed that there were significant differences between the two (P <0.05). In contrast, the image quality of 3D IR FGRE had a score of only 0.2 ± 0.04, with the worst image quality, and there were significant differences between 3D IR FGRE and IR FGRE (table 2) (Figure A). In the breath-holding state, IR FGRE had a score of 3.9 ± 0.8, SS FIESTA had a score of 3.8 ± 0.7, and 3 D IR FGRE had a score of 2.9 ± 0.9. There was no significant difference between SS FIESTA and IR FGRE, while there was significant difference between 3D IR FGRE and IR FGRE (P <0.0001) (table 2) (Figure B). 2 Diagnostic performances 2.1 Delayed enhancement quality and percentage measurements Among 52 cases successful undergone cardiac MRI examination, 24 cases had myocardial delayed enhancement. The mass and percentage of enhanced left ventricular myocardium were automatically calculated in the ADW4.3 workstation using the MASS software. The results were as follows: SS FIESTA showed an enhanced myocardial mass of 25.4 ± 17.3 g, accounting for 15.1 ± 9.2% of the left ventricular mass; 3D IR FGRE showed an enhanced myocardial mass of 33.2 ± 19.1g, accounting for 21.9 ± 11.1% of the left ventricular mass; and IR FGR showed an enhanced myocardial mass 26.7 ± 17.2g, accounting for 15.4 ± 9.7% of the left ventricular mass. Compared with IR FGRE, SS FIESTA did not show statistically significant differences in terms of lesioned myocardial mass and percentage (P> 0.05), while 3D IR FGRE showed statistically significant difference in lesioned myocardial mass and no statistically significant difference in the percentage of lesioned myocardium (table 3) (Figure C). 2.2 SNR and CNR Compared with IR FGRE sequence, SS FIESTA sequence did not show statistically significant differences in SNRbp, SNRmyo, CNRbp/myo, and CNRl/bg (P> 0.05), but SS FIESTA differed significantly from IR FGRE in CNRem/myo (P <0.05), with IR FGRE higher than SS FIESTA (table 3). Compared with IR FGRE sequence, 3D IR FGRE sequence showed statistically significant differences in SNRbp, SNRmyo, CNRbp/myo, CNRl/bg and CNRem/myo, and all parameters except CNRem/myo were higher than those of IR FGRE (Table 3). CNRem/myo of IR FGRE was significantly higher than the other two sequences, and was statistically different from that of SS FIESTA and 3D IR FGRE (Table 4). 3 SNR of intracardiac blood pool and various segments of myocardium IR FGRE sequence showed that intracardiac blood pool had the highest SNR. However, the SNR of each myocardial segment in 3D IR FGRE sequences was superior to IR FGRE and SS FIESTA. The two fast sequences showed statistically significant differences as compared with IR FGRE (P <0.001) (Table 5). These two sequences also clearly revealed the myocardium, endocardium and epicardium, and had unique advantages for subendocardial infarction (Figure D). Table 1 Scan parameters for the three group of myocardial delayed enhancement MRI Scan Parameters 2D IR FGRE 3D IR FGRE 2D SS FIESTA TR/TE FA TI Segment per heartbeat Matrix FOV Slice thickness/gap Number of excitation Acquisition time(RR) 4.0/1.8 20 250 1/12 heartbeat 3.3/1.4 15 200-250 1/heartbeat 3.4/1.4 45 200-400 3/8 heartbeat 256×256 35 8/3mm 2 10-15 phases /R-R 256×256 35 5/-4mm 256×256 35 8/3mm 1 17-19 phases /R-R 15-20 phases /R-R Table 2 Image quality scores and the mass and percentage of myocardium with delayed enhancement for the three delayed enhancement cardiac MRI sequences MDE image SS FIESTA 3D IR FGRE Free-breathing image score Breath-holding image score Scan time (s) 1.8±0.2 0.2±0.04 3.8±0.7 2.9±0.9 3.9±0.8 27.6±1.8 30.4±4.0 146+13.8 P value IR GRE 0.7±0.1 0.000﹙<0.0001﹚△ 0.000﹙<0.0001=● 0.43﹙>0.05﹚△ 0.000﹙<0.0001=● 0.000﹙<0.0001﹚△ 0.000﹙<0.0001﹚● △ P value for the comparison of SS FIESTA and IR GRE sequences ● P value for the comparison of 3D IR FGRE and IR GRE sequences Table 3 Comparison of the SS FIESTA and IR FGRE sequences and of the 3D IR FGRE and IR FGRE sequences in the means, standard deviations and statistical significances of SNR (bp), SNR (myo), CNR (bp /myo), CNR (l/bg), and CNR (em/myo) Parameter SNR(bp) SNR(myo) CNR (bp/myo) CN R(l/bg) CNR (em/myo) SS FIESTA (SD) 30.2(14.1) 7.2(2.7) 23.1(12.9) 3D IR FGRE (SD) 83.8(51) 48.5(48.7) 37 (14.8) IR FGRE (SD) P value 25.4(11.7) 0.108 △ 0.000 ● 7.6(2.5) 0.412 △ 0.000 ● 17.9(10.4) 0.108 △ 0.000 ● 1.5(1.7) 8.1(4.6) 1.7(2.8) 0.8 △ 0.000 ● 21(13.7) 15.7(13.8) 36.7(24.6) 0.000 △ 0.000 ● 0.306 △ 0.02 ● EM mass (g) 25.4±17.3 33.2±19.1 26.7±17.2 EM (%) 15.1±9.2 21.9±11.1 15.4±9.7 0.59 △ 0.07 ● △ P value for the comparison of SS FIESTA and IR GRE sequences ● P value for the comparison of 3D IR FGRE and IR GRE sequences Table 4 Comparison of the three sequences, SS FIESTA, 3D IR GFRE and IR FGRE, in CNRem/myo between myocardium with delayed enhancement and normal myocardium, with the former two showing significantly differences compared with the latter Table 5 Compared with IR EGRE, the SS FIESTA and 3D IR FGRE sequences showed statistically significant difference in SNR of all LV myocardial segments (P<0.0001) SS FIESTA (SD) 3D IR FGRE (SD) IR GRE (SD) LV blood pool 123 (67.7) 54.7(21.1) 178.2(55.7) ISEP 45(38.1) 88.1(46.2) 24.3(12.2) ASEP 56.2(48.8) 85.9(48.9) 26.7(12.9) ANT 48.3(38.5) 72.7(56.1) 23.6(12.9) ALAT 39(30.1) 77.3(33.6) 21(11.8) ILAT 42.5(34.2) 81.1(37.9) 21.4(11.7) INF 43 (35.1) 23.6(12.1) 94.3(43.8) Mean 45.2(35.8) 84.1(36.9) 22.8(10.4) P value 0.000﹙<0.0001﹚△ 0.000﹙<0.0001﹚● 0.000﹙<0.0001﹚△ 0.000﹙<0.0001﹚● 0.000﹙<0.0001﹚△ 0.000﹙<0.0001﹚● 0.000﹙<0.0001﹚△ 0.000﹙<0.0001﹚● 0.000﹙<0.0001﹚△ 0.000﹙<0.0001﹚● 0.000﹙<0.0001﹚△ 0.000﹙<0.0001﹚● 0.000﹙<0.0001﹚△ 0.000﹙<0.0001=● 0.000﹙<0.0001﹚△ 0.000﹙<0.0001﹚● △ P value for the comparison of SS FIESTA and IR GRE sequences ● P value for the comparison of 3D IR FGRE and IR GRE sequences Figure A. Comparison of the image qualities of the three free breathing sequences, SS FIESTA, 3D IR FGRE and IR GRE. The cardiac fine structures were unclear in 3D IR FGRE images with more artifacts, and the diaphragm (narrow short arrow) and intrapulmonary large vessel (long arrow) had significant motion artifacts. The pulmonary vessel was not revealed clearly in IR FGRE. Figure B. Under the breath hold condition, IR FGRE and SS FIESTA clearly displayed the myocardium (white arrow) and the border of papillary muscle (black arrow), while 3D IR FGRE had artifacts. Figure C. Comparison of the three sequences, IR FGRE, SS FIESTA and 3D IR FGRE, in the volume and area of revealed myocardial infarction (long white arrow indicated the anterior interventricular septum, and short black arrow indicated the left ventricular inferior wall and inner wall). Statistical analysis showed that there were no statistically significant differences between IR FGRE sequence and other sequences. Figure D. Compared with other sequences, 3D IR-FGRE displayed the subendocardial myocardial infarction (black arrowhead) more clearly. Discussion Contrast-enhanced cardiac MR images can reveal acute or chronic myocardial lesions well due to its high resolution [13]. Therefore, contrast-enhanced cardiac MRI is often used in clinical practice as the gold standard for the diagnosis of myocardial infarction. In particular, it can reveal micro-subendocardial myocardial infarction, and can measure the infarct size and volume [14], predict the functional recovery of lesioned myocardium [15], guide revascularization therapy and accurately determine the disease progression of patients [16]. In this study, we compared the myocardium with delayed enhancement in the re-examinations for 14 myocardial ischemia cases 3 months after the initial surgery of coronary artery bypass graft and bone marrow stem cell transplantation and determined that the lesions showed varying degrees of improvement as compared with those three months ago. However, the bottleneck of cardiac MRI is the lengthy scan time, preventing it being used widely in clinical applications, especially for those suffering from severe heart disease and unable to cope with breath holding. Traditional IR FGRE is two-dimensional inversion recovery fast gradient echo sequence. Its advantages include high image spatial resolution and high CNRem/myo, facilitating the clear visualization of lesion. Its disadvantage is that repeated scans are required to collect multiple sets of data when scanning the entire left ventricle, the total scan time is too long, and satisfactory image quality can not be obtained for patients having trouble to hold breath [16]. Single-shot FIESTA (GE company) is an ultra-fast pulse train and its signal mainly consists of spin-echo signal weights. The imaging principle of this sequence is similar to spin-echo without spin refocusing in the excitation process. This principle is in contrast to that of the spoiled gradient echo sequence. In order to correct proton dephasing caused by spatial encoding gradient field and phase drift caused by flow, after the acquisition of each echo, FIESTA applies a corresponding gradient field with the same gradient strength and time integration and the opposite direction at the slice selection phase, the phase encoding phase and the frequency encoding phase. When selecting a very short repetition time (TR) and large flip angle (FA), the lateral and longitudinal magnetization vectors achieve true steady state [17]. The SS FIESTA pulse sequence in this study used a very short TR (3.3 ms) and a single shot FA (350-750), transformed the the original T2-weighted image into the T1-weighted, and then inverted to null the myocardium. At this point, the normal myocardium signal is black, while the myocardial lesions present high signal. After FIESTA sequences were routinely used in movie sequences of cardiac MRI examination [18], Kim [15] and Simonetti [19] improved the application of FIESTA in T1-weighted enhanced sequences of infarcted myocardium, and obtained strong T1-weighted images. Simonetti compared 10 pulse sequences and found that contrast enhanced images of myocardial infarction from the FIESTA sequence had the strongest signal strength, which differs from our results. Our results showed that 3D IR FGRE sequence had the strongest signal strength of myocardial infarction. But in the current literature, the FIESTA sequence is considered to be the fastest sequence with the best image quality [41520-22]. It has been reported [7] that this sequence not only can shorten the scan time (an average of 16 ± 3.2 seconds per slice, and the total scan time of 10 minutes 13 ± 45 seconds), but also can accurately reflect the subacute and acute myocardial infarct size. In this study, FIESTA sequence required 3-4 times of breath hold per scan, each breath hold lasted for 7 ± 1.3 seconds, 3-4 slices of images (an average of 1.7 ± 0.5 seconds per slice) were obtained, the total scan time was 27.6 ± 1.8 seconds, and the delayed scan speed was significantly improved. After comparing the SS FIESTA, 3D IR FGRE and IR FGRE sequences, this study proved that the three sequences were all feasible to act as MDE methods to reveal various myocardial segments. SS FIESTA, which is a fast sequence, has the scan time only ¼ of the conventional sequence (IR FGRE sequence), without showing statistically significant differences in the size and the percentage of infarcted myocardium as compared with IR FGRE. This is consistent with the related reports [23] . Compared with IR FGRE sequence, SS FIESTA sequence could lead to images of high quality in many aspects. However, the size and percentage of myocardium with delayed enhancement were high, which may be due to the fact that SS FIESTA sequence has higher SNR and CNR, thus displaying more clearly the border between myocardium and lesion. High SNR can increase spatial resolution and shorten the scan time. High CNR can better reveal the myocardial edge and fine structure of the heart, and help to identify small lesions. Therefore, high SNR and CNR are very important for cardiac MRI [7]. Our results showed that compared with the IR FGRE sequence, SS FIESTA sequence did not show statistically significant differences in SNRmyo, SNRbp, and CNRl/bg. The most prominent feature of 3D IR FGRE sequence is its short total inspection time, and one breath hold (with multiple cardiac cycles) is sufficient for data collection on the entire left ventricle. Images are of thin slices (5 mm), with high myocardial noise SNR, can more clearly show small lesions and also can be used for a comprehensive understanding of myocardial scar. The study found that 3D IR FGRE sequence had the highest SNR and CNR among the three sequences, and could clearly reveal subendocardial myocardial infarction[24]. However, excessively long breath-hold time and acquisition time often lead to failed scan and more artifacts in the images, therefore limiting its clinical application. Our results also showed that this sequence required a breath-hold time of 30 seconds, which is difficult even for people with normal respiratory function, not to mention in patients with abnormal cardiac function. It has been reported [25-26] that 3D IR FGRE sequences can shorten the acquisition time without affecting the image quality and diagnostic accuracy by using a variety of improved technologies and image reconstruction method. For studies using delayed enhancement scan sequence, the selection of the best inversion time (TI) is crucial for delayed scan [5]: the TI value for the scanning of this group of cases was in general set to start from 200 ms, and increased by 50 ms after scanning one sequence. References [1] [2] [3] [4] [5] [6] [7] [8] [9] [10] [11] Berman DS, Hachamovitch R, Shaw LJ, Friedman JD, Hayes SW, Thomson LE, Fieno DS, Germano G, Slomka P, Wong ND, Kang X, Rozanski A. Roles of nuclear cardiology, cardiac computed tomography, and cardiac magnetic resonance: assessment of patients with suspected coronary artery disease. J Nucl Med, 2006, 47(1): 74-82 Yang Q, Li K, Liu X, Bi X, Liu Z, An J, Zhang A, Jerecic R, Li D. Contrast-Enhanced Whole-Heart Coronary Magnetic Resonance Angiography at 3.0-T. Journal of the American College of Cardiology. 2009, 54, (1): 69-76 Dulce MC, Duerinckx AJ, Hartiala J, Caputo GR, O'Sullivan M, Cheitlin MD, Higgins CB. MR imaging of the myocardium using nonionic contrast medium: signal-intensity changes in patients with subacute myocardial infarction. AJR Am J Roentgenol. 1993, 160 (5): 963–970 Kim RJ, Fieno DS, Parrish TB, Harris K, Chen EL, Simonetti O, Bundy J, Finn JP, Klocke FJ, Judd RM. Relationship of MRI delayed contrast enhancement to irreversible injury, infarct age, and contractile function. Circulation. 1999, 100 (19): 1992–2002 Vogel-Claussen J, Rochitte CE, Wu KC, Kamel IR, Foo TK, Lima JA, Bluemke DA. Delayed Enhancement MR Imaging: Utility in Myocardial Assessment1. RadioGraphics. 2006, 26 (3): 795-810 Thiele H, Nagel E, Paetsch I, Schnackenburg B, Bornstedt A, Kouwenhoven M, Wahl A, Schuler G, Fleck E. Functional cardiac MR imaging with steady-state free precession (SSFP) significantly improves endocardial border delineation without contrast agents. J Magn Reson Imaging (2001); 14: 362–367. Huber A, Schoenberg SO, Spannagl B, Rieber J, Erhard I, Klauss V, Reiser MF. Single-Shot Inversion Recovery TrueFISP for Assessment of Myocardial Infarction. AJR. 2006, 186(3): 627-633 Lene Rosendahl, Britt-Marie Ahlander, Per-Gunnar Björklund, Peter Blomstrand, Lars Brudin, Jan E. Engvall. Image quality and myocardial scar size determined with magnetic resonance imaging in patients with permanent atrial fibrillation: a comparison of two imaging protocols. Clinical Physiology and Functional Imaging, 2010, 30(2): 122–129 Cheng LQ, Gao YG, Sheng FG, Cai YQ. Imaging Planes Plotting and Anatomy of the Heart on MRI. Chinese Journal of Medical Imaging, 2004, 12 (5) :321-324. Gupta A, Lee VS, Chung YC, Babb JS, Simonetti OP. Myocardial infarction: optimization of inversion times at delayed contrast-enhanced MR imaging. Radiology. 2004, 233 (3): 921–926 Simonetti OP, Kim RJ, Fieno DS, Hillenbrand HB, Wu E, Bundy JM, Finn JP, Judd RM. An improved MR imaging technique for the visualization of myocardial infarction. Radiology. 2001, 218(1): 215–223 [12] [13] [14] [15] [16] Bongartz G, Golding SJ, Jurik AG, Leonardi M, Van Meerten E, Geleijns J, Jessen KA, Panzer W, Shrimpton PC, Tose G, Menzel H-G, Schibilla H, Teunen D The 1999 CEC European Guidelines on Quality Criteria for Computed Tomography, EUR 16262 EN (2000). The Luxembourg Office for publication of the European Communities, Brussels, CEC, 1999 Cerqueira MD, Weissman NJ, Dilsizian V, Jacobs AK, Kaul S, Laskey WK, Pennell DJ, Rumberger JA, Ryan T, Verani MSCerqueira MD.Standardized Myocardial Segmentation and Nomenclature for Tomographic Imaging of the Heart. Circulation. 2002, 105(4): 539-542 Wagner A, Mahrholdt H, Holly TA, Elliott MD, Regenfus M, Parker M, Klocke FJ, Bonow RO, Kim RJ, Judd RM. Contrast-enhanced MRI and routine single photon emission computed tomography (SPECT) perfusion imaging for detection of subendocardial myocardial infarcts: an imaging study. Lancet.2003, 361(9355):374–9 Kim RJ, Wu E, Rafael A, Chen EL, Parker MA, Simonetti O, Klocke FJ, Bonow RO, Judd RM. The use of contrast-enhanced magnetic resonance imaging to identify reversible myocardial dysfunction. N Engl J Med. 2000, 343(20): 1445–53 Bear FM, Erdmann E, Methods of assessment and clinical relevance of myocardial hibernation and stunning. Assessment of myocardial viability. Thorac Cardiovasc Surg. 1998, 46(suppl 2): 264-269 [17] Jahnke C,Gebker R,Manka R, Schnackenburg B, Fleck E, Paetsch I. [17] [18] [19] [20] [21] [22] Navigator-gated 3D blood oxygen level-dependent CMR at 3.0-T for detection of stress-induced myocardial ischemic reactions. JACC Cardiovasc Imaging. 2010, 3(4):375-384 Nitz W. Imaging sequences in magnetic resonance tomography and their clinical application (Part 2). Electromedica.1996,64:48-51 Gorrie A, Warren FM 3rd, de la Garza AN, Shelton C, Wiggins RH 3rd. Is there a correlation between vascular loops in the cerebellopontine angle and unexplained unilateral hearing loss. Otol Neurotol. 2010, 31(1):48–52 Simonetti OP, Kim RJ, Fieno DS, Hillenbrand HB, Wu E, Bundy JM, Finn JP, Judd RM. An improved MR imaging technique for the visualization of myocardial infarction. Radiology. 2001; 218(1): 215–223 Breuckmann F, Möhlenkamp S, Nassenstein K, Lehmann N, Ladd S, Schmermund A, Sievers B, Schlosser T, Jöckel KH, Heusch G, Erbel R, Barkhausen J. Myocardial late gadolinium enhancement: prevalence, pattern, and prognostic relevance in marathon runners. Radiology. 2009; 251(1): 50 –7 Bello D, Shah DJ, Farah GM, Di Luzio S, Parker M, Johnson MR, Cotts WG, Klocke FJ, Bonow RO, Judd RM, Gheorghiade M, Kim RJ. Gadolinium cardiovascular magnetic resonance predicts reversible myocardial dysfunction and remodeling in patients with heart failure undergoing beta-blocker therapy. Circulation. 2003; 108(16):1945–1953 Jiménez, Borreguero LJ, Ruiz-Salmerón R. Assessment of myocardial viability in patients before revascularization. Rev Esp Cardiol. 2003, 56(7): 721–733 Huber A, Schonberg SO, Spannagl B, Rieber J, Klauss V, Reiser MF. Determining myocardial vitality in myocardial infarction: comparison of single and multislice MRI techniques with TurboFLASH and TrueFISP sequences [in German]. Radiologe. 2004, 44(2): 146–151 [24] Li W, Li BS, Polzin JA, Mai VM, Prasad PV, Edelman RR. Myocardial delayed enhancement imaging using inversion recovery single-shot steady-state free precession: initial experience. J Magn Reson Imagin. 2004, 20(2): 327–330 [25] Wen H, Denison TJ, Singerman RW, Balaban RS. The intrinsic signal-to-noise ratio in human cardiac imaging at 1.5, 3, and 4 T. J Magn Reson.1997, 125(1): 65–71 [26] Jogiya R, Kozerke S, Morion G, et a1. Validation of dynamic 3.0 dimensional whole heart magnetic resonance myocardial perfusion imaging against fractional flow reserve for the detection of significant coronary artery disease[J]. J Am Coil Cardiol, 2012, 60: 756-765. [23]