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MAGNETIC RESONANCE
PERFUSION
Rahman Ud Din
Lecturer Medical Imaging
NWIHS
Introduction
 Blood flow and metabolism of human tissues
 Studied in nuclear medicine with tracer
 Now it is still studied with PET
 But PET lack spatial and temporal resolution
 Also lack in specificity
 Recent methods introduced like CT & MRI
perfusion
 MR perfusion performed with
 Exogenous contrast agent (Gd)
 Endogenous contrast agent (no contrast
administration)
Principles of MRP Imaging
 Perfusion refers to passage of blood from
arterial supply to venous drainage through
microcirculation
 Perfusion is vital for nutritive supply to tissues
 For clearance of products as well
 Perfusion can be affect by various disease
processes
 Hence to detect such changes in perfusion
can help in diagnosis of certain diseases,
monitoring and assessing the treatment
response
 Gd (paramagnetic agents) cause shortening of
both T1 and T2 of the tissue or region in which
they go
 Decrease T1 relaxation time on T1-w images
results into increased signals or brightening
 Decrease in the T2 relaxation time on T2 or
T2*-w images results into signal drop or
blackening
 As Gd passes through the microvasculature in
high concentration there is decrease in signal
in surrounding tissues
 Signal drop (shows disease)
Before and after Gd adminitration
in T1-w Sequence
Technique of MRP with Exogenous
Contrast
 A dose of 0.1mmol/kg of Gd injected IV
 Using power injector at rate of 5ml/s
 Fast T2*-w EPI seq is run to catch first pass of the
contrast through microcirculation
 This seq: takes 15-20 slices from entire brain 1-2 s
 About 60 such run acquired before, during and after
dynamic injection of the contrast media
 Raw data images converted into various color coded
maps using software
 rCBV=relative Cerebral Blood Volume
 CBF= Cerebral blood flow
 TTP=Time to Peak
 MTT =Mean Transit Time
Magnetic Resonance Perfusion
Permeability or Leakiness
 Areas of severe blood-brain barrier
break-down are seen in necrotic
tumor and irradiated tumor beds
 Increase in leakiness bcoz break in
BBB results in accumulation of Gd-
based contrast in extravascular
space
 T1-enhancing effects of
extravascular Gd may predominate
to counteract the T2 signal
Clinical Applications of MRP
 MRP performed in various clinical conditions
 Stroke
 Brain tumors
 Dementia
 Psychiatric illnesses
 Migraine
 Headaches
 Trauma
 Epilepsy
 Multiple sclerosis
MRP in Stroke
 Stroke is brain attack
 To detect brain ischemia & salvageable tissue
in early window period of 3-6 hours
 DWI and PWI or MRP effective for early
ischemia
 PWI more sensitive than DWI detecting
ischemia in early period of after onset of
arterial occlusion
Magnetic Resonance Perfusion
MRP in Brain Tumours
Glioma
Glioblastoma
Other Clinical Conditions
 MRP used to assess ischemic or under
perfused areas
 Like moyamoya disease and CNS vasculities
CNS
vasculities

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Magnetic Resonance Perfusion

  • 1. MAGNETIC RESONANCE PERFUSION Rahman Ud Din Lecturer Medical Imaging NWIHS
  • 2. Introduction  Blood flow and metabolism of human tissues  Studied in nuclear medicine with tracer  Now it is still studied with PET  But PET lack spatial and temporal resolution  Also lack in specificity  Recent methods introduced like CT & MRI perfusion  MR perfusion performed with  Exogenous contrast agent (Gd)  Endogenous contrast agent (no contrast administration)
  • 3. Principles of MRP Imaging  Perfusion refers to passage of blood from arterial supply to venous drainage through microcirculation  Perfusion is vital for nutritive supply to tissues  For clearance of products as well  Perfusion can be affect by various disease processes  Hence to detect such changes in perfusion can help in diagnosis of certain diseases, monitoring and assessing the treatment response
  • 4.  Gd (paramagnetic agents) cause shortening of both T1 and T2 of the tissue or region in which they go  Decrease T1 relaxation time on T1-w images results into increased signals or brightening  Decrease in the T2 relaxation time on T2 or T2*-w images results into signal drop or blackening  As Gd passes through the microvasculature in high concentration there is decrease in signal in surrounding tissues  Signal drop (shows disease)
  • 5. Before and after Gd adminitration in T1-w Sequence
  • 6. Technique of MRP with Exogenous Contrast  A dose of 0.1mmol/kg of Gd injected IV  Using power injector at rate of 5ml/s  Fast T2*-w EPI seq is run to catch first pass of the contrast through microcirculation  This seq: takes 15-20 slices from entire brain 1-2 s  About 60 such run acquired before, during and after dynamic injection of the contrast media  Raw data images converted into various color coded maps using software  rCBV=relative Cerebral Blood Volume  CBF= Cerebral blood flow  TTP=Time to Peak  MTT =Mean Transit Time
  • 8. Permeability or Leakiness  Areas of severe blood-brain barrier break-down are seen in necrotic tumor and irradiated tumor beds  Increase in leakiness bcoz break in BBB results in accumulation of Gd- based contrast in extravascular space  T1-enhancing effects of extravascular Gd may predominate to counteract the T2 signal
  • 9. Clinical Applications of MRP  MRP performed in various clinical conditions  Stroke  Brain tumors  Dementia  Psychiatric illnesses  Migraine  Headaches  Trauma  Epilepsy  Multiple sclerosis
  • 10. MRP in Stroke  Stroke is brain attack  To detect brain ischemia & salvageable tissue in early window period of 3-6 hours  DWI and PWI or MRP effective for early ischemia  PWI more sensitive than DWI detecting ischemia in early period of after onset of arterial occlusion
  • 12. MRP in Brain Tumours Glioma Glioblastoma
  • 13. Other Clinical Conditions  MRP used to assess ischemic or under perfused areas  Like moyamoya disease and CNS vasculities CNS vasculities