Accuracy of T1 measurement in dynamic contrast-enhanced breast MRI using two- and three-dimensional variable flip angle fast low-angle shot

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Abstract

In vivo T1 measurements, used to monitor the uptake of contrast agent by tissues, are typically performed as a first step in implementing compartmental analysis of contrast-enhanced breast magnetic resonance imaging (MRI) data. We have extended previously described methodology for in vivo T1 measurement (using a variable nip-angle gradient-recalled echo technique) to two-dimensional (2D), fast low-angle shot (FLASH), This approach requires computational modeling of slice-selective radiofrequency (RF) excitation to correct for nonrectangular slice profiles. The accuracy with which breast tissue T1 values can be measured by this approach is examined: T1 measurements from phantom and in vivo image data acquired with 2D and 3D FLASH imaging sequences are presented. Significant sources of error due to imaging pulse sequence quality and RF transmit field nonuniformity in the breast coil device that will have detrimental consequences for compartmental analysis are identified. Rigorous quality assurance programs with calibrated phantoms are thus recommended, to verify the accuracy with which T1 measurements are obtained. J, Magn, Reson. Imaging 1999;9:163-171, (C) 1999 Wiley-Liss, Inc.

Original languageEnglish
Pages (from-to)163-171
Number of pages9
JournalJournal of Magnetic Resonance Imaging
Volume9
Issue number2
DOIs
Publication statusPublished - Feb 1999

Keywords

  • accuracy
  • T1 measurement
  • contrast-enhanced breast MRI
  • compartmental analysis
  • relaxation time measurements
  • quantitative analysis
  • agent uptake
  • flash
  • DTPA
  • selection
  • sequence

Cite this

@article{1f14c0a06a0e4c9f8c02a212f2b22d4b,
title = "Accuracy of T1 measurement in dynamic contrast-enhanced breast MRI using two- and three-dimensional variable flip angle fast low-angle shot",
abstract = "In vivo T1 measurements, used to monitor the uptake of contrast agent by tissues, are typically performed as a first step in implementing compartmental analysis of contrast-enhanced breast magnetic resonance imaging (MRI) data. We have extended previously described methodology for in vivo T1 measurement (using a variable nip-angle gradient-recalled echo technique) to two-dimensional (2D), fast low-angle shot (FLASH), This approach requires computational modeling of slice-selective radiofrequency (RF) excitation to correct for nonrectangular slice profiles. The accuracy with which breast tissue T1 values can be measured by this approach is examined: T1 measurements from phantom and in vivo image data acquired with 2D and 3D FLASH imaging sequences are presented. Significant sources of error due to imaging pulse sequence quality and RF transmit field nonuniformity in the breast coil device that will have detrimental consequences for compartmental analysis are identified. Rigorous quality assurance programs with calibrated phantoms are thus recommended, to verify the accuracy with which T1 measurements are obtained. J, Magn, Reson. Imaging 1999;9:163-171, (C) 1999 Wiley-Liss, Inc.",
keywords = "accuracy, T1 measurement, contrast-enhanced breast MRI, compartmental analysis, relaxation time measurements, quantitative analysis, agent uptake, flash, DTPA, selection, sequence",
author = "Brookes, {J A} and Redpath, {Thomas William} and Gilbert, {Fiona Jane} and Murray, {Alison Dorothy} and Staff, {Roger T}",
year = "1999",
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T1 - Accuracy of T1 measurement in dynamic contrast-enhanced breast MRI using two- and three-dimensional variable flip angle fast low-angle shot

AU - Brookes, J A

AU - Redpath, Thomas William

AU - Gilbert, Fiona Jane

AU - Murray, Alison Dorothy

AU - Staff, Roger T

PY - 1999/2

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N2 - In vivo T1 measurements, used to monitor the uptake of contrast agent by tissues, are typically performed as a first step in implementing compartmental analysis of contrast-enhanced breast magnetic resonance imaging (MRI) data. We have extended previously described methodology for in vivo T1 measurement (using a variable nip-angle gradient-recalled echo technique) to two-dimensional (2D), fast low-angle shot (FLASH), This approach requires computational modeling of slice-selective radiofrequency (RF) excitation to correct for nonrectangular slice profiles. The accuracy with which breast tissue T1 values can be measured by this approach is examined: T1 measurements from phantom and in vivo image data acquired with 2D and 3D FLASH imaging sequences are presented. Significant sources of error due to imaging pulse sequence quality and RF transmit field nonuniformity in the breast coil device that will have detrimental consequences for compartmental analysis are identified. Rigorous quality assurance programs with calibrated phantoms are thus recommended, to verify the accuracy with which T1 measurements are obtained. J, Magn, Reson. Imaging 1999;9:163-171, (C) 1999 Wiley-Liss, Inc.

AB - In vivo T1 measurements, used to monitor the uptake of contrast agent by tissues, are typically performed as a first step in implementing compartmental analysis of contrast-enhanced breast magnetic resonance imaging (MRI) data. We have extended previously described methodology for in vivo T1 measurement (using a variable nip-angle gradient-recalled echo technique) to two-dimensional (2D), fast low-angle shot (FLASH), This approach requires computational modeling of slice-selective radiofrequency (RF) excitation to correct for nonrectangular slice profiles. The accuracy with which breast tissue T1 values can be measured by this approach is examined: T1 measurements from phantom and in vivo image data acquired with 2D and 3D FLASH imaging sequences are presented. Significant sources of error due to imaging pulse sequence quality and RF transmit field nonuniformity in the breast coil device that will have detrimental consequences for compartmental analysis are identified. Rigorous quality assurance programs with calibrated phantoms are thus recommended, to verify the accuracy with which T1 measurements are obtained. J, Magn, Reson. Imaging 1999;9:163-171, (C) 1999 Wiley-Liss, Inc.

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KW - compartmental analysis

KW - relaxation time measurements

KW - quantitative analysis

KW - agent uptake

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KW - selection

KW - sequence

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