ISNVD Abstract Book
ISNVD Abstract Book
ISNVD Abstract Book
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GeneralMagneticResonanceImaging(MRI)ProtocolfortheStudyofChronicCerebrospinalVenous<br />
Insufficiency(CCSVI)inMultipleSclerosisPatients<br />
<br />
TheMRICCSVIProtocolusesaconventionalneuroimagingprotocolforMSwithadditionalspecialized<br />
sequencestostudythevasculatureinthebrain,neckandspineaswellastheironcontentinthebrain.<br />
Onthevascularside,bothanatomicandflowinformationiscollected.AmajorbenefitofusingMRIis<br />
thatitprovidestheneurologistwithwhatheneedsforassessingMS,itprovidestheinterventionalist3D<br />
planninganditprovidesallpartieswithcriticalflowinformationwhichmaywellbecomeakeymarker<br />
fordecidingwhenorwhennottotreatapatient.MRIisalsooperatorindependentforthemostpart<br />
andthesameprotocolscanberunonmostmanufacturers’systems.Thedataarealsoeasilyreproduced<br />
when run on the same equipment from site to site.Potential biomarkers for CCSVI and MS can be<br />
identifiedfromthedata.MRIcanalsolongitudinallytracktheprogressofthe diseaseovertimevia<br />
lesioncountsandtype,physiologicchangeslikebloodflowandcerebrospinalfluid(CSF)dynamics,and<br />
provideabaselineforfuturescans.<br />
<br />
Thefollowingimagingprotocolispresentedfora3TeslaSiemensScannerbutcanbeextendedtoother<br />
field strengths and manufacturers.The scans proposed are: 2D time of flight MR venography (TOF<br />
MRV), timeresolved contrast enhanced 3D MR angiography and venography (MRAV), 3D volumetric<br />
interpolatedbreathholdexamination(VIBE),phasecontrastflowdataatdifferentlevelsintheneckand<br />
thoracic cavity, as well as the conventional T2 weighted imaging (WI), T2 fluid attenuated inversion<br />
recovery(FLAIR),susceptibilityweightedimaging(SWI),andpreandpostcontrastT1weightedimaging<br />
(WI)ormagnetizationpreparedrapidgradientecho(MPRAGE)imaging.Perfusionscanningcanalsobe<br />
addedintothisprotocolforasmallincrementintime(roughly3minutesextra).<br />
<br />
2DTOFMRVscansareusedtodetectbloodflowinarteriesandveins.Usingasaturationband,anyflow<br />
towardthehead(arterialflow)willbesaturated,andtheflowtowardstheheart(venousflow)willbe<br />
highlightedinavelocitydependentmanner.Fromthissequence,veinsarewellvisualizedanditcanbe<br />
determinediftheyarepatent,occluded,orstenosed.Sincethedataarecollectedwithhighresolution,<br />
vesselcrosssectioncanalsobecalculatedtoevaluatethedegreeofstenosis.<br />
<br />
3DCEMRAVcanalsobeusedtoevaluatevascularabnormalities.ThescanusesaT1reducingcontrast<br />
agentwhichpassesthroughallvesselsandleadstoincreasedsignalforvesselsinT1weightedscans.<br />
Fromthedata,3Danatomicalassessmentscanbedonetoevaluatevesselpatency.Atresias,aplasias,<br />
truncularmalformations,valveissues,andstenosescanbedetected.<br />
<br />
3D VIBE pre and postcontrast can be used to evaluate structural patency of vessels as well as<br />
inhomogeneousenhancementofthetissue.Itisanalternateapproachtothe3DdynamicCEapproach<br />
justdiscussedandtakesmuchlonger(althoughstillrelativelyfast).<br />
<br />
2DPCMRIimagesareusedtoassessflowdynamicsintheheadandneckveinsandarteries,theazygous<br />
vein,andCSFattheC2cervicallevel.Thisinformationisvaluablebecauseitcanbothcorroborateand<br />
complimenttheinformationseeninthe2DTOFMRVand3DCEMRAV.Itisnotuncommontovisualize<br />
themajorveinsonlylatertofindthatmanyoftheveinshavecompromisedbloodflow.<br />
<br />
Susceptibility Weighted Imaging (SWI) is useful because the image contrast is based on the intrinsic<br />
susceptibilitiesoftissues.Forexample,veinsarerichindeoxyhemoglobinwhichisparamagneticand<br />
providesclearvisibilityofvenousstructures.Quantificationofironinthegraymatteraswellaslesions<br />
canbeaccomplishedusingT2*,phaseorsusceptibilitymappingfromthephaseimages.SWIisalso