Literature DB >> 14647981

Optimisation of brain SPET and portability of normal databases.

Leighton R Barnden1, Rochelle L Hatton, Setayesh Behin-Ain, Brian F Hutton, Elizabeth A Goble.   

Abstract

Use of a normal database in quantitative regional analysis of brain single-photon emission tomography (SPET) facilitates the detection of functional defects in individual or group studies by accounting for inter-subject variability. Different reconstruction methods and suboptimal attenuation and scatter correction methods can introduce additional variance that will adversely affect such analysis. Similarly, processing differences across different instruments and/or institutions may invalidate the use of external normal databases. The object of this study was to minimise additional variance by comparing reconstructions of a physical phantom with its numerical template so as to optimise processing parameters. Age- and gender-matched normal scans acquired on two different systems were compared using SPM99 after processing with both standard and optimised parameters. For three SPET systems we have optimised parameters for attenuation correction, lower window scatter subtraction, reconstructed pixel size and fanbeam focal length for both filtered back-projection (FBP) and iterative (OSEM) reconstruction. Both attenuation and scatter correction improved accuracy for all systems. For single-iteration Chang attenuation correction the optimum attenuation coefficient (mu) was 0.45-0.85 of the narrow beam value (Nmu) before, and 0.75-0.85 Nmu after, scatter subtraction. For accurately modelled OSEM attenuation correction, optimum mu was 0.6-0.9 Nmu before and 0.9-1.1 Nmu after scatter subtraction. FBP appeared to change in-plane voxel dimensions by about 2% and this was confirmed by line phantom measurements. Improvement in accuracy with scatter subtraction was most marked for the highest spatial resolution system. Optimised processing reduced but did not remove highly significant regional differences between normal databases acquired on two different SPET systems.

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Year:  2003        PMID: 14647981     DOI: 10.1007/s00259-003-1362-3

Source DB:  PubMed          Journal:  Eur J Nucl Med Mol Imaging        ISSN: 1619-7070            Impact factor:   9.236


  8 in total

1.  Experimental performance assessment of SPM for SPECT neuroactivation studies using a subresolution sandwich phantom design.

Authors:  Koenraad J Van Laere; Jan Versijpt; Michel Koole; Stefaan Vandenberghe; Philippe Lahorte; Ignace Lemahieu; Rudi A Dierckx
Journal:  Neuroimage       Date:  2002-05       Impact factor: 6.556

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Journal:  IEEE Trans Med Imaging       Date:  1991       Impact factor: 10.048

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Journal:  Ann Nucl Med       Date:  1996-02       Impact factor: 2.668

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Journal:  J Nucl Med       Date:  2003-04       Impact factor: 10.057

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Journal:  Eur J Nucl Med       Date:  1987

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Journal:  Phys Med Biol       Date:  1985-02       Impact factor: 3.609

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Authors:  S R Meikle; B F Hutton; D L Bailey
Journal:  J Nucl Med       Date:  1994-02       Impact factor: 10.057

  8 in total
  1 in total

1.  Individual voxelwise dosimetry of targeted 90Y-labelled substance P radiotherapy for malignant gliomas.

Authors:  Stefan Kneifel; Peter Bernhardt; Helena Uusijärvi; Stephan Good; Ludwig Plasswilm; Carlos Buitrago-Téllez; Jan Müller-Brand; Helmut Mäcke; Adrian Merlo
Journal:  Eur J Nucl Med Mol Imaging       Date:  2007-01-31       Impact factor: 9.236

  1 in total

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