Open in TheBrain

2012 Contrast Echocardiography Jonathan Lindner

<p>Oct 20, 2014 07:45 PM &nbsp;This is outstanding!!! &nbsp;(LIFE-CHANGING!!)

will give CVI talk On Oct 21 at noon.</p>

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This is a talk from 2012...</p>

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microbubbles contrast aents... cannot deflate on way to microvasc.

shells: &nbsp;albumin; &nbsp;lipids, put in gases... rings in the sono... abt 1/3 diam of rbc

(in his slide mm = micron = micrometer) &nbsp;bubble are abt 2-3 microns.

shell and special gas... move thru capillaries.</p>

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use it for LV opacification...

where do bubble help you...</p>

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imrpoves dx; &nbsp;improves interp segments, &nbsp;post-exercise studies;</p>

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huge improvement with contrast;</p>

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using this on obese pts; &nbsp;weent from tech difficult to easily interp. &nbsp;saves money by

avoiding other tests.</p>

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study kinetics of LV;</p>

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do this with exercise echo; &nbsp;can see hypokinessi;</p>

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results of the stress echo with contrast are... &nbsp;multivessel- high risk...</p>

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angio &nbsp;3 vessel CAD is compared; &nbsp;shows occlus RCA;</p>

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can see contrast as it moves thur microcirc... see microbubbles!!!</p>

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see min 16:21 &nbsp;!!!!! &nbsp;&nbsp;we do this daily; &nbsp;helps pt of care decisions!!!

perfusion imaging; &nbsp;our microbubbles &nbsp;behave just like RBCs...

small arterioles... &nbsp;they don't lodge... shows graph of velocities!

can see it move thru microcirc of muscle!!! &nbsp;unique look at perfusion...</p>

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infuse microbubbles; &nbsp;&nbsp;sono at high power; &nbsp;apical 4 chamber;

destroy a slab of bubbles... destroy bubble and watch how fast they come back!!!

femoral artery... &nbsp;&nbsp;can see vaso vasorum;</p>

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how fast do they come backin and how bright does it get...</p>

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can measure volume of blood... fits to an expon function...</p>

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can get quantit and spatial &nbsp;idea of regional perfusion...

can quantify blood flow &nbsp;spatially...</p>

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Note:&nbsp;at &nbsp;<b>22:32 &nbsp;quality of video greatly improves</b>!!!</p>

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see an actual slide: &nbsp;major determinants of infarct size:</p>

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time of occlusion; &nbsp;O2 demand during occlusion; extent of collat;

size of perfusion terrir of IRA;= infarct related artery

can check reflow...</p>

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get good recovery of func if resid blood flow &nbsp;(collateral or resid antegrade flow etc. &nbsp;minute 26....

wall is destined to improve (if any residual flow)...</p>

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pt got outside &nbsp;thrombolytic rx;.

&nbsp;DX of CAD

daily basis to dx CAD;;; do STRESS;

vast majority of pts with CAD do not have flwo limiting stenosis;

nl flow is 1-2 ml per min per gram of tissue

must havve 85% stenosis &nbsp;before &nbsp;flow is limited at rest;

if moder

nl blood flow is 1 ml per minute per gram of tissue...</p>

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should incr &nbsp;flow by 3 to 5 fold &nbsp;with dipyrid or with dobut/ stress;</p>

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see a little rim of darkness after the flash...

flow limiting stenosis at rest!!! &nbsp;(restin ghypperfusion)

critical stenosis in LAD... dx in 2 mins at bedside...</p>

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remember this relationship; &nbsp;flow and radial wall thickening during dobutamine...

at peak dobut. &nbsp;dog model graded cor stensosis...</p>

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normal wall thickening is abt 30% at rest...

at mild to moder stenosis you do NOT see wall thickening... &nbsp;only has sensit in 70s

its NOT there... will not see moder stenosis.</p>

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minute 29....</p>

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see little rim of darkness after flash in end systolic frames &nbsp;only get this if critical stenosis

like > 85%...</p>

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stress echo only has &nbsp;sensit in the 70s... its not there!

wall thickening is not there...

must use &nbsp;perfusion to see it...</p>

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from Tom Porter;;

compare perfusion to wall thickening...

DSE = dobut &nbsp;stress ech.... &nbsp;he can see an RCA stensosis;

sensitivity is incr at even intermed DB &nbsp;(sometimes we don't get pts up to max dose DB = dobut)</p>

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no &nbsp;indications for this in US yet &nbsp;(in 2012)...we use it a lot for off label uses...</p>

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future stuff: &nbsp;research apps &nbsp;in 2012: the future stuff...

easy cheap way for looking at perfusion; &nbsp;using contrast ultrasound...

sonothrombolysis;</p>

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quantit &nbsp;assessment of perfusion;</p>

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studying ESC rx!

can make bubbles smart....

use them for dissolving thrombus!</p>

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hyperlipidemia decr flow reserve; blood becomes more viscous;

induces hyperlipidemia and shows RBCs slowing down during hyperlipidemia;</p>

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<b>hyperlipidemia causes endothel dysfunction</b>

<b>rbc's don't deform as much &nbsp;&nbsp;minute 35...</b>

<b>RBC &nbsp;move much more slowly during hyperlipidemia...</b>

<b>effect of hyperlipid on Rheology !!!! &nbsp;holy fk!!</b></p>

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nasty stiff RBCs would not move thru caps...

(<b>Throw away the butter!</b>!)</p>

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shows PNH pt; &nbsp;parox &nbsp;nocturnal hemo.

put siliris... &nbsp;&nbsp;rate of mvmt of RBCs improved...</p>

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rate of mvmt thru microcirculation!!!</p>

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* &nbsp;now fun future stuff</p>

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nuclear, MRI, CT... molec imaging &nbsp;and same for contrast echo... portable, rapid...

smart contrast agents.... &nbsp;info immed to clinician.</p>

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shows leukocytes rolling in a venule... &nbsp;upreg of selectins...

grabs leukocytes...

molec imaging... close to 1st clinical trials... &nbsp;see &nbsp;leukocytes...

look venules... selectins... &nbsp;&nbsp;adhesion molecules...

WBCs are sniffing... do we need a full blown inflam response or not...

selectins will stay upreg for 16 to 24 hours....

WBCs bind to PSGL1... &nbsp;smart bubbles stick to same thing

smart microbubbles... IV inject wait 5 mins....

fluor bubbles targeted to selectins...

they only get stuck if ischemic...(in post ischemia bubbles get stuck)</p>

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"I had chest pain 2 or 5 hours ago... was it ischemia or was it &nbsp;bad dumplings..."

at bedside &nbsp;was CP due to ischemia or not... &nbsp;works all the way out to 16 to 18 hours.</p>

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did mouse model... did tempor &nbsp;cor occlusion and then can detect it later...</p>

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detect CAD at v early stage! &nbsp;I think&nbsp;its a <b>curable disease if you can find it early enuf</b>...

mice study: &nbsp;10, 20 40 weeks: at 40 weeks of age: &nbsp;big &nbsp;plaques...

almost none at 10 weeks - early just see monocytes entering vessel wall; earliest start;

give smart bubbles... stick to same areas where monocytes are sticking...</p>

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the voice of crystal bubble, charms us at once away from all our troubles;</p>

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if not using &nbsp;contrast sono... you are doing a <b>disservice</b> to your pts...

eg Bill Zogby lab... &nbsp;&nbsp;Jon is vice chair &nbsp;of Natl board of echo...

he runs a meeting... Echo Hawaii &nbsp;every January... &nbsp;&nbsp;we do discuss contrast.

fair amt of contrast in the echo boards! &nbsp;(so learn it)</p>

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lecture ends around min 50 or so then demo by his tech &nbsp;(can skip);</p>

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