Free breathing real-time cardiac cine imaging with improved spatial resolution at 3 T.

OBJECTIVES: The aim of this study was to evaluate free-breathing single-shot real-time cine imaging for functional cardiac imaging at 3 T with increased spatial resolution. Special emphasis of this study was placed on the influence of parallel imaging techniques. MATERIALS AND METHODS: Gradient echo phantom images were acquired with GRAPPA and modified SENSE reconstruction using both integrated and separate reference scans as well as TGRAPPA and TSENSE. In vivo measurements were performed for GRAPPA reconstruction with an integrated and a separate reference scan, as well as TGRAPPA using balanced steady-state free precession protocols. Three clinical protocols, rtLRInt (Tres = 51.3 milliseconds; voxel, 2.5 × 5.0 × 10 mm³), rtMRSep (Tres = 48.8 milliseconds; voxel, 1.9 × 3.1 × 10 mm³), and rtHRSep (Tres = 48.3 milliseconds; voxel, 1.6 × 2.6 × 10 mm), were investigated on 20 volunteers using GRAPPA reconstruction with internal as well as separate reference scans. End-diastolic volume, end-systolic volume, ejection fraction, peak ejection rate, peak filling rate, and myocardial mass were evaluated for the left ventricle and compared with an electrocardiogram-triggered segmented readout cine protocol used as standard of reference. All studies were performed at 3 T. RESULTS: Phantom and in vivo data demonstrate that the combination of GRAPPA reconstruction with a separate reference scan provides an optimal compromise of image quality as well as spatial and temporal resolution. Functional values (P values) for the standard of reference, rtLRInt, rtMRSep, and rtHRSep end-diastolic volume were 141 ± 24 mL, 138 ± 21 mL, 138 ± 19 mL, and 128 ± 33 mL, respectively (P = 0.7, 0.7, 0.4); end-systolic volume, 55 ± 15 mL, 61 ± 14 mL, 58 ± 12 mL, and 55 ± 20 mL, respectively (P = 0.23, 0.43, 0.62); ejection fraction, 61% ± 5%, 57% ± 5%, 58% ± 4%, and 56% ± 8%, respectively (P = 0.01, 0.11, 0.06); peak ejection rate, 481 ± 73 mL/s, 425 ± 62 mL/s, 434 ± 67 mL/s, and 381 ± 86 mL/s, respectively (P = 0.03, 0.04, 0.01); peak filling rate, 555 ± 80 mL/s, 480 ± 70 mL/s, 500 ± 70 mL/s, and 438 ± 108 mL/s, respectively (P= 0.007, 0.05, 0.004); and myocardial mass, 137 ± 26 g, 141 ± 25 g, 141 ± 23 g, and 130 ± 31 g, respectively (P = 0.62, 0.54, 0.99). CONCLUSIONS: Using a separate reference scan and high acceleration factors up to R = 6, single-shot real-time cardiac imaging offers adequate temporal and spatial resolution for accurate assessment of global left ventricular function in free breathing with short examination times.

Dynamic MR imaging of a minipig's knee using a high-density multi-channel receive array and a movement device.

OBJECT: To construct an optimised, high-density receive array and a movement device to achieve dynamic imaging of the knee in orthopedic large animal models (e.g., minipigs) at 1.5 T. MATERIALS AND METHODS: A 13-channel RF receive array was constructed, and the crucial choice of the array element size (based on considerations like region of interest, geometry of the minipig's knee, achievable signal-to-noise ratio, applicability of parallel imaging, etc.) was determined using the Q factors of loops with different sizes. A special movement device was constructed to guide and produce a reproducible motion of the minipig's knee during acquisition. RESULTS: The constructed array was electrically characterised and the reproducibility of the cyclic motion was validated. Snapshots of dynamic in vivo images taken at a temporal resolution (308 ms) are presented. Some of the fine internal structures within the minipig's knee, like cruciate ligaments, are traced in the snapshots. CONCLUSION: This study is a step towards making dynamic imaging which can give additional information about joint injuries when static MRI is not able to give sufficient information, a routine clinical application. There, the combination of a high-density receive array and a movement device will be highly helpful in the diagnosis and therapy monitoring of knee injuries in the future.

Cryogenic receive coil and low noise preamplifier for MRI at 0.01T.

We have investigated the design and construction of liquid nitrogen cooled surface coils made from stranded (litz) copper wire for low field MRI applications. If designed correctly, cooled litz coils can provide a competitive alternative to high temperature superconducting (HTS) coils without the complications associated with flux trapping. Litz coils can also be produced with a wider range of shapes and sizes, and at lower cost. Existing models were verified experimentally for flat spiral coils wound from solid and litz wires, operated at room temperature and 77K, and then used to design and optimise a cooled receive coil for MRI at 0.01T (425 kHz). The Q-factor reached 1022 when the coil was cooled to 77K, giving a bandwidth of just 0.42 kHz, so a low noise JFET preamplifier was developed to provide active damping of the coil resonance and thus minimise image intensity artefacts. The noise contribution of the preamplifier was determined using a method based on resistive sources and image noise analysis. The voltage and current noise were measured to be 1.25 nV/Hz(1/2) and 51 fA/Hz(1/2), respectively, and these values were used to estimate a noise figure of 0.32 dB at the resonant frequency of the cooled coil. The coil was used to acquire 0.01T spin echo images, first at room temperature and then cooled to 77K in a low noise liquid nitrogen cryostat. The measured SNR improvement on cooling, by a factor of 3.0, was found to correspond well with theoretical predictions.