首页> 外文期刊>Journal of computer assisted tomography >Liver MRI at 3.0 tesla: Comparison of image quality and lesion detectability between single-source conventional and dual-source parallel radiofrequency transmissions
【24h】

Liver MRI at 3.0 tesla: Comparison of image quality and lesion detectability between single-source conventional and dual-source parallel radiofrequency transmissions

机译:3.0特斯拉肝脏MRI:单源常规和双源并行射频传输之间图像质量和病变可检测性的比较

获取原文
获取原文并翻译 | 示例
           

摘要

OBJECTIVE: To prospectively and intraindividually compare liver magnetic resonance imaging (MRI) using single-source and dual-source parallel radiofrequency (RF) transmissions at 3.0-T for image quality, lesion detectability, and lesion contrast. METHODS: Ninety-nine patients with 139 liver lesions underwent liver MRI at 3.0-T. Two radiologists performed a consensus review of T2-weighted images (T2WI), heavily T2WI (HT2WI), gadoxetic acid-enhanced hepatobiliary images, and diffusion-weighted imaging using single-source and dual-source RF transmissions with regard to image quality and lesion detectability. Contrast ratios between liver lesions and liver parenchyma were also calculated. RESULTS: Image quality was better with dual-source than with single-source at T2WI and HT2WI (P < 0.05), but lesion detectabilities were similar for all sequences. There was no significant difference in mean contrast ratios for all sequences (P > 0.05). CONCLUSION: Dual-source RF transmission provides a better image quality with T2WI and HT2WI than with single-source. However, 2 techniques showed similar lesion detectability.
机译:目的:前瞻性和个体化地比较采用3.0-T单源和双源并行射频(RF)传输的肝脏磁共振成像(MRI)的图像质量,病变检测能力和病变对比度。方法:99例有139例肝脏病变的患者在3.0-T接受了MRI检查。两名放射科医生就图像质量和病变情况对T2加权图像(T2WI),重度T2WI(HT2WI),加多西酸增强的肝胆图像和扩散加权成像进行了共识性审查可检测性。还计算了肝脏病变与肝实质之间的对比度。结果:在T2WI和HT2WI上,双源图像质量优于单源图像(P <0.05),但所有序列的病变检测能力均相似。所有序列的平均对比度没有显着差异(P> 0.05)。结论:T2WI和HT2WI的双源RF传输比单源具有更好的图像质量。但是,有2种技术显示了相似的病变检测能力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号