These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Diffusion tensor imaging of the median nerve at 3.0 T using different MR scanners: agreement of FA and ADC measurements.
    Author: Guggenberger R, Nanz D, Bussmann L, Chhabra A, Fischer MA, Hodler J, Pfirrmann CW, Andreisek G.
    Journal: Eur J Radiol; 2013 Oct; 82(10):e590-6. PubMed ID: 23768611.
    Abstract:
    OBJECTIVE: To assess the agreement of fractional anisotropy (FA) and apparent diffusion coefficient (ADC) values of the median nerve on 3.0 T MR scanners from different vendors. MATERIALS AND METHODS: IRB approved study including 16 healthy volunteers (9 women; mean age 30.6 ± 5.3 years). Diffusion tensor imaging (DTI) of the dominant wrist was performed on three 3.0 T MR scanners (GE, Siemens, Philips) using similar imaging protocols and vendor-proprietary hard- and software. Intra-, inter-reader and inter-vendor agreements were assessed. RESULTS: ICCs for intra-/inter-reader agreements ranged from 0.843-0.970/0.846-0.956 for FA, and 0.840-0.940/0.726-0.929 for ADC, respectively. ANOVA analysis identified significant differences for FA/ADC measurements among vendors (p < 0.001/p < 0.01, respectively). Overall mean values for FA were 0.63 (SD ± 0.1) and 0.999 × 10(-3)mm(2)/s (SD ± 0.134 × 10(-3)) for ADC. A significant negative measurement bias was found for FA values from the GE scanner (-0.05 and -0.07) and for ADC values from the Siemens scanner (-0.053 and -0.063 × 10(-3)mm(2)/s) as compared to the remainder vendors CONCLUSION: FA and ADC values of the median nerve obtained on different 3.0 T MR scanners differ significantly, but are in comparison to the standard deviation of absolute values small enough to not have an impact on larger group studies or when substantial diffusion changes can be expected. However, caution is warranted in an individual patient when interpreting diffusion values from different scanner acquisitions.
    [Abstract] [Full Text] [Related] [New Search]