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Cardiovascular Research FoundationCardiovascular Research Foundation
New York, NYNew York, NY
Pre-Intervention IVUSPre-Intervention IVUS
Gary S. Mintz, MDGary S. Mintz, MD
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Weigh otential ro!le"s #i$e$ %& disease, signi'icantWeigh otential ro!le"s #i$e$ %& disease, signi'icantro(i"al or distal disease)ro(i"al or distal disease)
*ssess lesion severit+*ssess lesion severit+ *ssess unusual lesion "orholog+ #i$e$, aneur+s"s,*ssess unusual lesion "orholog+ #i$e$, aneur+s"s,calciu", thro"!i, high-risk "orholog+, in-stentcalciu", thro"!i, high-risk "orholog+, in-stentrestenosis, etc$)restenosis, etc$)
&easure vessel sie&easure vessel sie
&easure lesion length&easure lesion length eter"ine and 'ine-tune the resultseter"ine and 'ine-tune the results *ssess co"lications*ssess co"lications
&ost o' the concets used in IVUS-guided intervention are&ost o' the concets used in IVUS-guided intervention areno di''erent 'ro" those used in angiograh+-guidedno di''erent 'ro" those used in angiograh+-guided
intervention$ .owever, unlike angiograh+, IVUS is actuall+intervention$ .owever, unlike angiograh+, IVUS is actuall+a!le to "ake recise "easure"ents and assess lesiona!le to "ake recise "easure"ents and assess lesion
"orholog+$"orholog+$
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// 0""0"" 12""12""
Pro(i"alPro(i"alRe'erenceRe'erence
%esion%esionSiteSite
istalistalRe'erenceRe'erence
33& CS* 4 21$533& CS* 4 21$5%u"en CS* 4 6$7%u"en CS* 4 6$7
&a(i"u" lu"en dia"eter 4 02$8&a(i"u" lu"en dia"eter 4 02$8&% 4 2$0&% 4 2$0
P9& CS* 4 33&-%u"en 4 1:$1P9& CS* 4 33&-%u"en 4 1:$13ccentricit+ 4 &a(i"u";"ini"u" P9& 4 0$/;/$13ccentricit+ 4 &a(i"u";"ini"u" P9& 4 0$/;/$1
PlaPla*rea stenosis 4 re'erence-lesion;re'erence lu"en area 4 72>*rea stenosis 4 re'erence-lesion;re'erence lu"en area 4 72>
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0 10 50mm
b
a
c
6% 74%
69%
67%
a
b
c
Mintz et al. J Am Coll Cardiol 1995;25:1479-85Mintz et al. J Am Coll Cardiol 1995;25:1479-85
In 886 native coronar+ arteries, the la
and :2A12> o' la
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Coronar+ Re"odeling .+othesisCoronar+ Re"odeling .+othesis
Co"enator+ 3(ansion&aintains Consistant %u"en
3(ansion
Bverco"e%u"en Narrows
Nor"al
Vessel
&ini"al
C*
&oderate
C*
Severe
C*
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* D
3'
'E
C
F
distal
%u"en
e
!
eE
!E
%u"en
Positive Re"odelingPositive Re"odeling
Negative Re"odelingNegative Re"odeling
c
cE
distal
33&33&
33&33&
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Re"odeling is not ust acade"ic$Re"odeling is not ust acade"ic$Positive re"odeling is associated withPositive re"odeling is associated with
Acute coronary syndrome at presentationAcute coronary syndrome at presentation CK-MB elevation after percutaneous coronary interventionCK-MB elevation after percutaneous coronary intervention No reflow in primary infarct angioplastyNo reflow in primary infarct angioplasty Recurrent ischemia within one month after thrombolysisRecurrent ischemia within one month after thrombolysis
for acute myocardial infarctionfor acute myocardial infarction
arget lesion revasculari!ation in patients undergoingarget lesion revasculari!ation in patients undergoingnonstent intervention and intimal hyerplasia in patientsnonstent intervention and intimal hyerplasia in patientsundergoing bare metal stent interventionundergoing bare metal stent intervention
Ma"or adverse coronary events in patients with unstableMa"or adverse coronary events in patients with unstableangina undergoing any form of revasculari!ationangina undergoing any form of revasculari!ation
#n-hospital complications$ ma"or adverse coronary events$#n-hospital complications$ ma"or adverse coronary events$restenosis$ and new lesion formation in patients withrestenosis$ and new lesion formation in patients with
stable angina undergoing single vessel intervention%stable angina undergoing single vessel intervention%
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%esion Calci'ication #n41177)%esion Calci'ication #n41177)
Calci'ication
&o
fangiographiclesions
#'() *uadrants of calcium
Suer'icial calci'ication
&o
fangiographiclesions
#'() *uadrants ofsuperficial calcium
Mintz et al. Circlation1995;91:1959-65.Mintz et al. Circlation1995;91:1959-65.
Ghe onl+ redictor o' IVUS calciu" was angiograhic calci'icationGhe onl+ redictor o' IVUS calciu" was angiograhic calci'icationelsewhere in the coronar+ tree$elsewhere in the coronar+ tree$ +u!cu et al% , AM Coll Cardiol ../0123451-46+u!cu et al% , AM Coll Cardiol ../0123451-46
0
5
1 0
1 5
2 0
2 5
3 0
N o n eO n e T w o T h r e eF o u r
S ev e r e
M od e r a t e
N o n e / M il d
0
5
1 0
1 5
2 0
2 5
3 0
3 5
4 0
N o n eO n e T w o T h r e eF o u
S ev e r e
M od e r a t e
N o n e / M il d
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%esion 3ccentricit+ #n41665)%esion 3ccentricit+ #n41665)
Mintz et al. Circlation 1996;9!:924-9!1Mintz et al. Circlation 1996;9!:924-9!1
0
1 0
2 0
3 0
4 0
5 0
6 0
1 . 0 - 3. 0 3 . 0 - 5. 0 5 . 0 - 7. 0 > 7. 0
Y es
N o
3ccentricit+
&o
fangiographiclesions
#'() Ma78Min
9:M hic;ness
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&a(i"u" la
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Unusual %esion &orholog+Unusual %esion &orholog+
*ngiograhic 'illing de'ects*ngiograhic 'illing de'ects Ghro"!iGhro"!i Calci'ied nodulesCalci'ied nodules
*ngiograhic aneur+s"s*ngiograhic aneur+s"s Grue aneur+s"sGrue aneur+s"s Pseudoaneur+s"sPseudoaneur+s"s Co"le(;rutured la
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B
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0?/31/->0?/31/->
@istance from coronary ostium +mm6@istance from coronary ostium +mm6
of ruptured pla*ues of ruptured pla*ues
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IVUS Classi'ication o'*ngiograhic *neur+s"s
B' :: angiograhic aneur+s"s 21 #2:>) true aneur+s" 0 #6>) seudoaneur+s" 12 #15>) co"le( la) nor"al seg"ent adacent to one or "ore
stenoses
Grue*neur+s"
PS* Co"le(Pla
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0 2.5 10.0mm
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0 3.5 17.5mm
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0 1.5 7.5mm
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Ghree Vessel IVUS I"aging in 26Ghree Vessel IVUS I"aging in 26Pts with *CS and Positive GnPts with *CS and Positive Gn
7/ rutured la
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Rutured la
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%ocation o' 2:0 rutured la
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Co"arison o' Culrit Non-Culrit Ruture Sites inCo"arison o' Culrit Non-Culrit Ruture Sites in*CS Patients and Ruture Sites in Non-*CS Patients*CS Patients and Ruture Sites in Non-*CS Patients
4/$//14/$//1 4/$//14/$//1
ACS Culprit PlaqueACS Culprit Plaque
Ruptures (N=35)Ruptures (N=35)
ACS NonCulprit PlaqueACS NonCulprit Plaque
Ruptures (N=!")Ruptures (N=!")
NonACS PlaqueNonACS Plaque
Ruptures (N=!)Ruptures (N=!)
(mm!)
(nde)endent )redictor* o+ AC, ere MA and t$rom/* #/ot$ )0.01%(nde)endent )redictor* o+ AC, ere MA and t$rom/* #/ot$ )0.01%
Fuji et al. Circulation 2003;108:2473-8Fuji et al. Circulation 2003;108:2473-8
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2""2"" 5""5""//
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00 1.01.0 6.0mm6.0mm
' ' '
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What is the 'ate o' non-'low-li"itingWhat is the 'ate o' non-'low-li"itingrutured la) vs
no statin-treated atient #4/$11)$no statin-treated atient #4/$11)$
%esions re
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Su!clinical la
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0 3.0 12.0mm
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0 8 40mm
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The HCI SCAD Registry
)CA@ N15
Med R7 without stent or CAB
N?
#nitial 9C# attempted
N5
Coronary stenting without CAB
N5
#nitial med R7 attempted
N4
#nitial CAB
N5
9C# after initial med R7
N1
CAB after 9C# attempt
N
CAB after initial med R7N
Med R7 after failed
thrombectomy
N
CAB
N/
9C# attempted otal
N>
hrombolysis N1
Coronary AngiogramsN15
#(to et al. JACC Cardio3a*clar (nter3ention* in )re**%#(to et al. JACC Cardio3a*clar (nter3ention* in )re**%
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WrinklingWrinkling
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0 1.5 9.0mm
Attenuated 9la*ueAttenuated 9la*ue
Dee et al% ,ACC Cardiovasc #nterv% 1==.013/>-21
Eu et al$ Am , Cardiol 1==0=>3?4->5
Attenuated pla*ues were observed in 5.%/& of )FM#$ 2%/& of N)FM#$ and =&
of stable angina%
Attenuate pla*ues were associated with more fibroatheromas and a larger necroticcore +on '
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Validation o' IVUS assess"ent o' ische"ia-Validation o' IVUS assess"ent o' ische"ia-
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Validation o' IVUS assess"ent o' ische"ia-Validation o' IVUS assess"ent o' ische"ia-roducing stenoses #oler FloWire,roducing stenoses #oler FloWire,
SP3CG, and Pressure Wire)SP3CG, and Pressure Wire)
??5.5.CHRCHR 1%=1%=
121211CHR G 1%=CHR G 1%=
#'() MDAG?%=mm1
#'() MDAI?%=mm1
@iagnostic accuracy .1&%@iagnostic accuracy .1&%Abi!aid et al% Am , Cardiol ..40413?1-4Abi!aid et al% Am , Cardiol ..40413?1-4
1=1=- )pect- )pect
?1?1??J )pectJ )pect
#'() MDAG?%=mm1
#'() MDAI?%=mm1
@iagnostic accuracy .5&%@iagnostic accuracy .5&%Nishio;a et al% , Am Coll Cardiol ...055342=-4Nishio;a et al% , Am Coll Cardiol ...055342=-4
a;agi$ et al% Circulationa;agi$ et al% Circulation...0==31>=->...0==31>=->
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85 ts
Nishioka G,
M*CC 1===
Gakagi et al
Cir$ 1===
*!iaid et al
*MC 1==8
:/ lesions
62 ts
&%* #""2) 0$092$0 0$=A2$/ 6$6A2$/
&V* #""2) 10$2A6$6
*rea stenosis> 77A26 60A26
Cut-o'' o' &%*
#""2)
6$/
#Ghalliu" 9)
0$/
#FFR /$:7)
J 6$/
#CFR J2$/)
OC* V #"")S #>)
IVUS vs FFR in 2/1 ts #205
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Sensitivit+4=/>Seci'icit+45/>
PPV40:>
NPV4=5>
*ccurac+458>
IVUS vs FFR in 2/1 ts #205inter"ediate lesions)
= 1= ?= /= 4= ==
==-)pecificity
==
4=
/=
?=
1=
=
)ens
itivity
Cut-o'' 42$62""2
A(C=%4==
.>& C#=%2?1-=%4?4
"an' et al. Circlation Cardio3a*clar (nter3ention* in )re**
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&%* ""2
/>?51=
=%4
FFR J/$8
2$6 ""2
FFR /$8
V3RICG Pil tV3RICG Pil t
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V3RICG PilotV3RICG Pilot
9rospective$ multicenter$ non-randomi!ed$ non-blinded study in
5== intermediate coronary lesions
+@) ?=& - G4=&$ R'@ 1%2> L ?%= mm6
HHR and '
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C$ ctober ? th $ 1==4C$ ctober ? th $ 1==4
Nico
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*NIB-grou
N46=5
FFR-grou
N47/=
9-value9-value
# indicated lesions per patient# indicated lesions per patient 2$: A /$= 2$8 A 1$/ =%5?=%5?
FFR resultsFFR results
Desions succesfully measured$Desions succesfully measured$ No +&6No +&6 - 102= #=8>) --
Desions with HHR I =%4=$Desions with HHR I =%4=$ No +&6No +&6 - 8:6 #50>) --
Desions with HHR P =%4=$Desions with HHR P =%4=$ No +&6No +&6 - 710 #0:>) --
Stents per patientStents per patient 2$: A 1$2 1$= A 1$0 G=%==G=%==
Desions succesfully stentedDesions succesfully stented +&6+&6 =2> =6> --
@F)$ total$@F)$ total$ NoNo 107= =8/ --
HAMF study3HAMF study3 9rocedural Results9rocedural Results
HAMF t dHAMF t d F t f ) i lF t f ) i l
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HHR-guided
5= days1%.& .= days
5%4& 4= days
?%.& 5/= days
>%5&
Angio-guided
absolute difference in MACF-free survival
HAMF study3HAMF study3 Fvent-free )urvivalFvent-free )urvival
B' all the coronar+ seg"ents, the %&C* hasB' all the coronar+ seg"ents, the %&C* has
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Hisher et al% Cathet Cardiovasc @iagn .41043>/>-2>
Comparison between percent stenosisComparison between percent stenosisassessment from the *uality control +QC6 lab vsassessment from the *uality control +QC6 lab vs
the clinical site in the CA)) )tudythe clinical site in the CA)) )tudy
area of the s*uare is proportional to the number of casesarea of the s*uare is proportional to the number of cases
QC labQC lab
Clinical siteClinical site
====
== ======
B' all the coronar+ seg"ents, the %&C* hasB' all the coronar+ seg"ents, the %&C* hasthe greatest angiograhic assess"entthe greatest angiograhic assess"ent
varia!ilit+ - Ivaria!ilit+ - I
B' all the coronar+ seg"ents, the %& hasB' all the coronar+ seg"ents, the %& has
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B' all the coronar+ seg"ents, the %& hasB' all the coronar+ seg"ents, the %& hasthe greatest angiograhic assess"entthe greatest angiograhic assess"ent
varia!ilit+ - IIvaria!ilit+ - II
Cameron et al% Circulation .450/43?4?-?4.
Hive grades of DMHive grades of DM
severityseverity
33 =-1?& @) =-1?& @)1313 1>-?.& @)1>-?.& @)
5353 >=-2?& @)>=-2?& @)
?3?3 2>-4.& @)2>-4.& @)
>3>3 .=-==&@).=-==&@)
of grades of difference in assessment of grades of difference in assessment
of DM severityof DM severity
=3=3 no differenceno differenceJ or -3J or -3 grade difference grade difference
J1 or -13J1 or -13 1 grades of difference1 grades of difference
J5 or -53J5 or -53 5 grades of difference5 grades of difference
J? or -?3J? or -?3 ? grades of difference? grades of difference
Clinical site vsClinical site vs
Quality controlQuality control
Clinical site vsClinical site vs
)tudy roup)tudy roup
)tudy roup vs)tudy roup vs
Quality controlQuality control
Dut surel+ we are !etter toda+ IQDut surel+ we are !etter toda+ IQ
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Lindstaedt et al. Int J Cardiol 200!"202$%&'"
Dut surel+ we are !etter toda+ - IQDut surel+ we are !etter toda+ - IQ
> intermediate or e*uivocal DM lesions were evaluated by> intermediate or e*uivocal DM lesions were evaluated byHHR and angiography% Hour e7perienced interventionalHHR and angiography% Hour e7perienced interventional
cardiologists visually classified lesions as SsignificantT$ Snotcardiologists visually classified lesions as SsignificantT$ Snot
significantT$ or Sunsure%TsignificantT$ or Sunsure%T he ? e7perienced interventional cardiologists achievedhe ? e7perienced interventional cardiologists achieved
correct lesion classification in no more thancorrect lesion classification in no more than UU>=& of each>=& of each
case regardless of the HHR threshold +I=%2> or I=%4=6%case regardless of the HHR threshold +I=%2> or I=%4=6% #nterobserver variability was large$ resulting in unanimous#nterobserver variability was large$ resulting in unanimous
correct lesion classification in only 1.&Vcorrect lesion classification in only 1.&V
Which o' these %&C* lesions isWhich o' these %&C* lesions is
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Which o' these %&C* lesions isWhich o' these %&C* lesions issigni'icant and, there'ore, should !esigni'icant and, there'ore, should !e
treated *nd which is nottreated *nd which is not
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0 1.5 6.0mm
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0 3.0 9.0mm
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0 2.0 5.0mm
&%*46$5""2
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0 2.0 8.0mm
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0 1.0 4.0mm
IVUS deter"inants o' %&C* FFRIVUS deter"inants o' %&C* FFR
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IVUS deter"inants o' %&C* FFRIVUS deter"inants o' %&C* FFR/$:7/$:7
,asti,astiet al% Circulationet al% Circulation1==?0=3145-/1==?0=3145-/
IVUS Criteria 'or aIVUS Criteria 'or a Signi'icantT %&C*Signi'icantT %&C*
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IVUS Criteria 'or aIVUS Criteria 'or a Signi'icantT %&C*Signi'icant %&C*StenosisStenosis
&ost IVUS %&C* studies show either insigni'icant disease&ost IVUS %&C* studies show either insigni'icant diseaseor critical diseaseor critical disease
*!solute lu"en CS* 5$/""*!solute lu"en CS* 5$/""22#or &% 0$/"") is the#or &% 0$/"") is the
suggested criterion 'or a signi'icant %&C* stenosissuggested criterion 'or a signi'icant %&C* stenosis
Correlates with a %&C* FFR/$:7Correlates with a %&C* FFR/$:7
oes not deend on 'inding a disease-'ree re'erenceoes not deend on 'inding a disease-'ree re'erence
seg"entseg"ent
%ong ter" data #%IGRB registr+)%ong ter" data #%IGRB registr+)
It is not clear whether the sa"e criteria should !e used 'orIt is not clear whether the sa"e criteria should !e used 'or
ostial %& lesions as 'or "id-sha't;distal !i'urcation lesionsostial %& lesions as 'or "id-sha't;distal !i'urcation lesionsand 'or ositivel+ vs negativel+ re"odeled lesionsand 'or ositivel+ vs negativel+ re"odeled lesions
#'() assessment of DM disease#'() assessment of DM disease
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9la*ue burden +9:M8FFM6 /4&9la*ue burden +9:M8FFM6 /4&
MDA2%1mmMDA2%1mm11
#'() assessment of DM disease#'() assessment of DM diseasesignificance is based on lumensignificance is based on lumendimensions$ not pla*ue burdendimensions$ not pla*ue burden
??S"all@ %& 4 i''use %&C* diseaseS"all@ %& 4 i''use %&C* disease
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S"all %& 4 i''use %&C* diseaseS"all %& 4 i''use %&C* disease
&urra+&urra+Ts %awTs %aw
%&C*%&C*rr00
44 %*%*rr00
99 %C%Crr00
Fractal eo"etr+Fractal eo"etr+
%&C*%&C* 4 /$5:8 # 4 /$5:8 #%*%* 9 9 %C%C))
(C) DS *+
Fractal (C) DS *+/
2/
:/
/
2/
:/
Matreff et al% Furointervention 1==0>32=.->
-rospectie application o/ prede/ined I1S criteria /or-rospectie application o/ prede/ined I1S criteria /or
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-rospectie application o/ prede/ined I1S criteria /orospect e app cat o o p ede ed 1S c te a oreascularization o/ interediate le/t ain coronary arteryreascularization o/ interediate le/t ain coronary artery
lesions Results at 2 years /ro t3e LI4R5 studylesions Results at 2 years /ro t3e LI4R5 study
5>? patients5>? patients
MDAMDA /%=mm/%=mm11
+n4/6+n4/6MDA G/%=mmMDA G/%=mm11
+n/46+n/46
2 revasculari!ed2 revasculari!ed
No DMCA revasculari!ationNo DMCA revasculari!ation
+n2.$ ./&6+n2.$ ./&6DMCA revasculari!ationDMCA revasculari!ation
+n>1$ .=&6+n>1$ .=&6
/ not revasculari!ed/ not revasculari!ed
>/& 9C# of other vessels>/& 9C# of other vessels>>& CAB>>& CAB
?>& 9C# +J other vessels in /1&?>& 9C# +J other vessels in /1&
@e Da orre
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reascularization *ML) 7'reascularization *ML) 7'22
Surial /ree o/ cardiac
deat3, MI and anyreascularization
-80.22
De/er *n8"9
Reascularization *n8"$2
Surial /ree o/ cardiac
deat3-80.20
De/er
Reascularization
Surial /ree o/ cardiac
deat3, MI and LMC)reascularization at 2
years 9%.2+
Surial /ree o/ LMC)
reascularization at 2years 9'.$+
Surial /ree o/ cardiacdeat3 at 2 years 9.++
@e Da orre
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@e Da orre =
?=
5=
1=
-=
=
ime
De/er *edical t3erapy 6it3 ML) :'2*n8"9
De/er *edical t3erapy 6it3 ML) ;'2
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IVUS vs FFR in %&C* iseaseIVUS vs FFR in %&C* isease
here is probably more agreement between #'() and HHR inhere is probably more agreement between #'() and HHR in
assessing DMCA lesion significance than in assessing non-assessing DMCA lesion significance than in assessing non-
DMCA lesion significanceDMCA lesion significance Dimited variability in DMCA lengthDimited variability in DMCA length Dimited variability in amount of supplied myocardiumDimited variability in amount of supplied myocardium
Darge DMCA si!eDarge DMCA si!e Both have theoretical and practical limitationsBoth have theoretical and practical limitations
DA@ and8or DCW disease L HHRDA@ and8or DCW disease L HHR #t is necessary to image the DM from both the DA@ and#t is necessary to image the DM from both the DA@ and
DCW - #'()DCW - #'()
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#n 1>& of patients$ the left main MDA differed#n 1>& of patients$ the left main MDA differedby mmby mm11when imaged from a pullbac;when imaged from a pullbac;
beginning in the DA@ vs a pullbac; beginningbeginning in the DA@ vs a pullbac; beginning
in the DCW%in the DCW%
)ince #'() can artificially increase$ but not)ince #'() can artificially increase$ but notdecrease lumen dimensions$ the smallest MDAdecrease lumen dimensions$ the smallest MDA
is always the most accurateis always the most accurate
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00 1.01.0 4.0mm4.0mm
00 1.01.0 5.0mm5.0mm
LC=LC=
L)DL)D
#'() assessment of DCW ostium from the DA@-#'() assessment of DCW ostium from the DA@-
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3valuation o' the %* 'ro"
the %&-%C ull!ack
3valuation o' the %C 'ro"
the %&-%* ull!ack
-
i''erence!etweenesti"atedand
directl+"easuredlu"en
dia"eters#"")
-
i''erence!etweenesti"atedand
directl+"eas
uredlu"en
dia"eters#"")
DM +or vice versa6 - MD@DM +or vice versa6 - MD@
viedo et al% Am , Cardiol 1==0=>3.?4->?
#f you want to *uantify the degree of lumen compromise$ you
must image the daughter branches directly%
#'() assessment of DCW ostium from the#'() assessment of DCW ostium from the
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Sensitivit+ Seci'icit+
9la*ueburdenP?=&
>.& ?>&
9la*ueburdenP2=&
24& ?1&
3valuation o' the %* 'ro"
the %&-%C ull!ack
Sensitivit+ Seci'icit+
9la*ueburdenP?=&
/2& >>&
9la*ueburdenP2=&
44& ?1&
3valuation o' the %C 'ro"
the %&-%* ull!ack
#'() assessment of DCW ostium from the#'() assessment of DCW ostium from theDA@-DM +or vice versa6 L pla*ue burdenDA@-DM +or vice versa6 L pla*ue burden
#f you want to *uantify the pla*ue burden$ you must image the
daughter branches directly%
viedo et al% Am , Cardiol 1==0=>3.?4->?
IVUS la
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%C #1)%* #1)
%&C* #1;1)
52> 16> 16>
6> 0> 2> 1>
%C #1)%* #1) %C #/)%* #1)
%C #1)%* #1) %C #/)%* #1) %C #1)%* #1) %C #1)%* #/)
%&C* #1;/) %&C* #1;/)
%&C* #/;1) %&C* #/;/) %&C* #/;/) %&C* #/;1)
1;1,1,1 1;/,1,1 1;/,1,/
/;1,1,1 /;/,1,/ /;/,1,1 /;1,/,1
-1
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=& ==&
&edina 1,1,1#n421)
&edina 1,1,/#n4=)
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&edina /,1,/#n416)
&edina /,/,1#n412)
&edina /,/,/#n45/)
*ll lesions#n48/)
Bthers
viedo et al% Circ Cardiovasc #nterv% 1==053=>-1
Inter"ediate in-stent restenosis lesions IIInter"ediate in-stent restenosis lesions II
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Inter"ediate in stent restenosis lesions IIInter"ediate in stent restenosis lesions II=-"onth "ini"u" lu"en area that redicts 0-+ear &*C3-=-"onth "ini"u" lu"en area that redicts 0-+ear &*C3-
'ree survival in atients 'ro" G*US IV, V, and VI'ree survival in atients 'ro" G*US IV, V, and VI
n4068n4068 D&SD&S
C-statisticC-statistic Cuto''Cuto''
&ini"u" lu"en area&ini"u" lu"en area /$:0/$:0 6$/""6$/""22
n4071n4071 Ga(usGa(us
C-statisticC-statistic Cuto''Cuto''
&ini"u" lu"en area&ini"u" lu"en area /$:7/$:7 6$2""6$2""22
+@oi et al Circulation #nterventions 1==403-4%%
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D*
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3
diastole systole diastole
C
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00 2.52.5 12.5mm12.5mm
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0 5.0 15.0mm
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00 2.52.5 10.0mm10.0mm
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/ 2$7"" 1/$/""
Pro(i"alPro(i"al
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0 1.5 6.0mm
0 1.5 6.0mm