[en] The aim of this study was to compare the image quality of a saturation-recovery gradient-recalled echo (GRE; TurboFLASH) and a saturation-recovery SSFP (SR-TrueFISP) sequence for myocardial first-pass perfusion MRI. Eight patients with chronic myocardial infarction and 8 volunteers were examined with a TurboFLASH (TR 2.1 ms, TE 1 ms, FA 8 ) and a SR-TrueFISP sequence (TR 2.1 ms, TE 0.9 ms, FA, 50 ) on a 1.5 T scanner. During injection of 0.05 mmol/kg BW Gd-DTPA at 4 ml/s, three short axis slices (8 mm) of the left ventricle (LV) were simultaneously scanned during breath-hold. Maximum signal-to-noise ratio (SNR), contrast-to-noise ratio (CNR) between infarcted and normal myocardium, and percentage signal intensity change (PSIC) were measured within the LV lumen and in four regions of the LV myocardium for the three slices separately. For the LV lumen, SR-TrueFISP was superior in SNR and PSIC (factor 3.2 and 1.6, respectively). Mean maximum SNR, PSIC, and CNR during peak enhancement in the LV myocardium were higher for SR-TrueFISP compared with TurboFLASH (factor 2.4, 1.25, and 1.24, respectively). The SNR was higher in the septal portion of the ventricle than in anterior/posterior and lateral regions. The SR-TrueFISP provides higher SNR and improves image quality compared with TurboFLASH in first-pass myocardial perfusion MRI. (orig.)

[en] We sought to compare a three-dimensional, contrast-enhanced, magnetic resonance angiogram (3D CE MRA) sequence combining parallel-imaging (generalised autocalibrating partially parallel acquisitions (GRAPPA)) with a time-resolved echo-shared angiographic technique (TREAT) in an intraindividual comparison to a standard 3D MRA sequence. Four healthy volunteers (27-32 years), and 11 patients (11-82 years) with vascular pathologies of the hand were examined on a 1.5-Tesla (T) MR system (Magnetom Avanto, Siemens, Erlangen, Germany) using two multichannel receiver coils. Following automatic injection (flow rate 2.5 cc/s) of 0.1 mmol/kg gadoterate (Dotarem, Guerbet, Roissy, France), 32 consecutive 3D data sets were collected with the TREAT sequence (TR/TE: 4.02/1.31 ms, FA: 10 , GRAPPA acceleration factor: R=2, TREAT factor: 5, voxel size: 1.0 x 0.7 x 1.3 mm³) and a T1-wighted 3D gradient-echo sequence (TR/TE: 5.3/1.57 ms, FA: 30 , GRAPPA acceleration factor: 2, voxel size: 0.71 x 0.71 x 0.71 mm^3,). MR data sets were evaluated and compared for image quality and visualisation of vascular details. In the volunteer group, all MR imaging was successful while technical problems prevented acquisition of the standard protocol in two patients. For the corresponding segments, the number of visible segments was equal on both sequences. Overall image quality was significantly better on the standard protocol than on the TREAT protocol. TREAT MRA provided functional information in lesions with rapid blood flow, e.g. detection of feeding and draining vessels in an haemangioma. TREAT-MRA is a robust technique that combines morphological and functional information of the hand vasculature and deals with the very special physiological demands of vascular lesions, such as quick arteriovenous transit time. (orig.)

[en] Array coils can potentially offer increased signal-to-noise ratio (SNR) over standard coils adjacent to the array elements, while preserving the SNR at the center of the volume. The SNR advantage should theoretically increase with the number of array elements. Parallel acquisition techniques (PAT), on the other hand, can benefit acquisition times or spatial resolution at a cost to SNR as well as image quality. This study examines the question of whether SNR and image quality are still acceptable with two different array coils (four and eight channels) in conjunction with PAT when compared to standard imaging with a volume coil. All imaging was on a 1.5 T MR scanner. T2-weighted, FLAIR, diffusion-weighted, and time of flight (TOF) angiography images were performed with and without PAT in a phantom and in ten healthy volunteers. The phantom measurements demonstrated superior SNR for the eight-channel coil versus the four-channel and standard head coils. Using the eight-channel head coil for in vivo imaging, image quality with PAT (acceleration factor=2) was scored similar to images without PAT using the volume coil. The four-channel head coil suffered from inhomogeneity, lower SNR and poorer image quality when using PAT compared to standard imaging with the volume head coil. Both the in vivo and the phantom results indicate that the eight-channel head coil should be used for the highest quality brain images; this coil can be combined with PAT sequences for shorter acquisition time without a significant decrease in image quality relative to a volume coil without PAT. (orig.)

[en] To investigate the feasibility of 7T MR imaging of the kidneys utilising a custom-built 8-channel transmit/receive radiofrequency body coil. In vivo unenhanced MR was performed in 8 healthy volunteers on a 7T whole-body MR system. After B₀ shimming the following sequences were obtained: 1) 2D and 3D spoiled gradient-echo sequences (FLASH, VIBE), 2) T1-weighted 2D in and opposed phase 3) True-FISP imaging and 4) a T2-weighted turbo spin echo (TSE) sequence. Visual evaluation of the overall image quality was performed by two radiologists. Renal MRI at 7T was feasible in all eight subjects. Best image quality was found using T1-weighted gradient echo MRI, providing high anatomical details and excellent conspicuity of the non-enhanced vasculature. With successful shimming, B₁ signal voids could be effectively reduced and/or shifted out of the region of interest in most sequence types. However, T2-weighted TSE imaging remained challenging and strongly impaired because of signal heterogeneities in three volunteers. The results demonstrate the feasibility and diagnostic potential of dedicated 7T renal imaging. Further optimisation of imaging sequences and dedicated RF coil concepts are expected to improve the acquisition quality and ultimately provide high clinical diagnostic value. (orig.)

[en] The purpose of the study was to estimate T₁ values of blood and myocardium after a single injection of Vasovist trademark and to assess Vasovist trademark for magnetic resonance coronary angiography (MRCA). For all exams 0.05 mmol/kg of Vasovist trademark was injected. T₁ values of blood and myocardium were estimated over 30 min after injection. Twelve volunteers were examined on a 1.5-T Siemens system using a SSFP sequence with incrementally increasing inversion times for T₁-estimation and a breath-hold 3D IR-FLASH sequence for MRCA. Eleven examinations were performed on 1.5-T Philips system using the Look-Locker approach for T₁ estimation and a whole-heart inversion-prepared, 3D SSFP sequence for MRCA. SNR, CNR and image quality were assessed. T₁ values of blood (5 min: 230 ms vs. 30 min: 275 ms) and myocardium (5 min: 99 ms vs. 30 min: 130 ms) increased over time. Whereas the blood SNR (1 min: 23.6 vs. 30 min: 21.2) showed no significant differences, the blood-to-myocardium CNR (1 min: 18.1 vs. 30 min: 13.8) and the image quality (1 min: 2.9 vs. 30 min: 3.8) degraded over time. Due to long plasma half-time the T1-shortening effect of Vasovist trademark remains effective over 30 min, which allows for multiple breath-hold or high-resolution MRCA. (orig.)

[en] Endoscopy for evaluation of hoarseness is an invasive procedure and the result depends, to a large extent, on the patient's cooperation. Successful laryngoscopy can also be hampered by unfavourable anatomic conditions, a severely impaired general condition, or severe coagulopathy. We evaluated the feasibility of doing ultra-fast magnetic resonance imaging (MRI), using a recent dedicated coil design and a sequence with inherently high signal-to-noise ratios (SNR), for the detection of motility disorders of the vocal cords. Twelve consecutive patients (eight males and four females) in the age range of 24–80 years (mean age 60 years) with persistent hoarseness and presumed vocal cord palsy were included in this blinded prospective study. Two two-element phased-array carotid coils were used for signal reception. The first coronal real-time steady-state free precession (SSFP) sequence was performed during silence (i.e., with no vocal cord motion) and the second while phonating ‘heee.’ Qualitative MRI findings were compared with the results of the endoscopic examination. The examination time for setup, patient instruction and positioning, localization scans, and real-time SSFP scans was less than 10 min. Seven patients with laryngoscopically-confirmed unilateral palsy of the vocal cord were correctly identified with MRI. The five remaining patients had hoarseness due to causes other than vocal cord palsy; they showed normal motion of the vocal cords on MRI and endoscopy. Compared to preceding studies, the image quality in this study is supported by excellent SNR (carotid phased-array coils and SSFP sequence with higher SNR if compared to a spoiled gradient-echo sequence or an EPI sequence). Further studies, with larger groups of patients, are necessary to show if this protocol can serve as an alternative to endoscopy in selected cases

[en] To evaluate a TGRAPPA (temporal parallel acquisition technique)-accelerated, single breath-hold multi-slice cine imaging approach for the assessment of left ventricular (LV) function. One hundred eleven patients were examined at 1.5 T. Cine imaging was performed with single-slice breath-hold acquisitions in short-axis orientation using a SSFP (TR 2.63 ms, TE 1.12 ms, FA 72 ) sequence and a TGRAPPA SSFP (TR 2.66 ms, TE 1.11 ms, FA 72 , AF 3) sequence, which covered the entire LV in multiple short-axis slices during a single breath-hold. End-diastolic (EDV), end-systolic (ESV), stroke volumes (SV), ejection fraction (EF), muscle mass (MM) and regional wall motion were assessed for both data sets. Single breath-hold imaging was feasible in 108 patients. Excellent correlations were observed for all volumetric parameters derived from both data sets (all r > 0.97). While EDV and ESV showed marginally lower values for single breath-hold imaging (EDV: -1.6 ± 7.9 ml; ESV: -1.8 ± 6.0 ml, p < 0.05), no differences were observed for SV, EF, MM and regional wall motion assessment. Single breath-hold imaging required significant shorter acquisition times (28 ± 6 s vs. 335 ± 87 s). TGRAPPA-accelerated multi-slice SSPF imaging allows for fast and accurate assessment of regional and global LV function within a single breath-hold. (orig.)

[en] Objectives: Preoperative magnetic resonance (MR) guided wire localization is a frequently used tool to target MR-only visible breast lesions. Different techniques are available. Targeting can be performed using automated software or a manual approach. Aim of this study therefore was to compare manually and automated software assisted wire localization of suspicious breast lesions regarding to image time and accurate positioning. Methods: 60 females with suspicious breast lesions underwent MR-guided wire localization. In 30 patients a manual target calculation and in another 30 patients a software calculated approach was used. Time measurements for MR imaging as well as calculation of the target coordinates were performed. Furthermore size measurements of (i) lesions, (ii) distance to wire anchor as well as, (iii) distance to skin were performed. A Mann-Whitney-test was used for statistical evaluation. Results: Total imaging time was shorter for the automated software calculated approach but failed to show a statistical significant difference (p = 0.13). Time for localization of the lesions was significantly shorter for the software based method (p < 0.001). Lesion sizes, distances to wire anchor and skin showed no statistically significant differences. Conclusions: Preoperative MR-guided wire localization of suspicious lesions that are accessible horizontally, a manually or automated software generated target calculation can be used. As MR guided wire localization of breast lesions needs its time in total, a minimal time consuming approach and therefore an automated software calculated targeting (if available) should be preferred

[en] To assess the diagnostic accuracy of phonocardiogram (PCG) gated velocity-encoded phase contrast magnetic resonance imaging (MRI). Flow quantification above the aortic valve was performed in 68 patients by acquiring a retrospectively PCG- and a retrospectively ECG-gated velocity-encoded GE-sequence at 1.5 T. Peak velocity (PV), average velocity (AV), forward volume (FV), reverse volume (RV), net forward volume (NFV), as well as the regurgitant fraction (RF) were assessed for both datasets, as well as for the PCG-gated datasets after compensation for the PCG trigger delay. PCG-gated image acquisition was feasible in 64 patients, ECG-gated in all patients. PCG-gated flow quantification overestimated PV (Δ 3.8 ± 14.1 cm/s; P = 0.037) and underestimated FV (Δ -4.9 ± 15.7 ml; P = 0.015) and NFV (Δ -4.5 ± 16.5 ml; P = 0.033) compared with ECG-gated imaging. After compensation for the PCG trigger delay, differences were only observed for PV (Δ 3.8 ± 14.1 cm/s; P = 0.037). Wide limits of agreement between PCG- and ECG-gated flow quantification were observed for all variables (PV: -23.9 to 31.4 cm/s; AV: -4.5 to 3.9 cm/s; FV: -35.6 to 25.9 ml; RV: -8.0 to 7.2 ml; NFV: -36.8 to 27.8 ml; RF: -10.4 to 10.2 %). The present study demonstrates that PCG gating in its current form is not reliable enough for flow quantification based on velocity-encoded phase contrast gradient echo (GE) sequences. (orig.)

[en] The purpose of this study was to evaluate the diagnostic efficacy of magnetic resonance (MR)-guided biopsy of focal liver lesions within a short, wide-bore 1.5-T MR system and to determine the duration and accuracy of needle placement using MR fluoroscopy guidance in 25 patients. Accuracy of needle placement was evaluated in two orthogonal planes, and the out-of-plane angle of needle deflection was measured. Needle positioning was characterised subjectively as centred, peripheral, or exterior relative to the lesion. Exterior positioning was corrected by a step-by-step procedure. Surgical resection (n = 6), previous histologies (n = 8), or clinical/radiological follow-up (n = 11) served as the 'gold standard'. The guidance needle could be placed successfully using MR fluoroscopy in 20 of 25 patients (80%). Needle placement was rated as 'centred' in 11 and as 'peripheral' in nine patients. Median needle deflection was 2.6 degrees, with a median deviation of 3.4 mm. In five patients, the direct approach failed or was rated as 'exterior'; therefore, repositioning after needle stabilisation with a stainless-steel stylet was necessary. The diagnostic yield of all biopsies was: sensitivity 95.5%, specificity 100.0% and accuracy 96.0%. In conclusion, MR-guided biopsies in a short, wide-bore MR system yielded highly reliable biopsy results, and in most cases the direct approach with MR fluoroscopy guidance proved to be fast and accurate. (orig.)