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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

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