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How Are Left Main and non Left How Are Left Main and non Left Main Bifurcations Unique: Main Bifurcations Unique:
Insights from ImagingInsights from ImagingInsights from ImagingInsights from Imaging
Akiko Maehara, MDAkiko Maehara, MD
Cardiovascular Research Foundation/Cardiovascular Research Foundation/Columbia University Medical CenterColumbia University Medical Center
New York City, NYNew York City, NY
Disclosure Statement of Financial InterestWithin the past 12 months, I or my spouse/partner have had a financial Interest /arrangement or affiliation with the organization(s) listed below
Affiliation/Financial Relationship CompanyGrant/ Research Support: Boston Scientific Corp.
Speaker Fee Volcano Corp.
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Plaque Distribution by IVUS (n=140)Plaque Distribution by IVUS (n=140)1/1,1,1LMCA (1/1)
1/0,1,1LMCA (1/0)
1/0,1,0LMCA (1/0)
LCX (1)LAD (1)
62% 14% 14%LCX (1)LAD (1) LCX (0)LAD (1)
0/1,1,1LMCA (0/1)
0/0,1,0LMCA (0/0)
0/0,1,1LMCA (0/0)
0/1,0,1LMCA (0/1)
4% 3% 2% 1%
In 90% plaque extends from LMCA-LAD
LCX (1)LAD (1) LCX (0)LAD (1) LCX (1)LAD (1) LCX (1)LAD (0)
Oviedo C et al. Circ Cardiovasc Interv 2010;3:105Oviedo C et al. Circ Cardiovasc Interv 2010;3:105--12.12.
Plaque Distribution LMCA Plaque Distribution LMCA vsvs LAD/D1LAD/D1Inclusion: angiographically significant bifurcation disease
90%
96%
Yakushiji @ CRF
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Plaque Composition in Plaque Composition in 256 Bifurcations256 Bifurcations
Han SH et al. Eurointervention 2010;6:313Han SH et al. Eurointervention 2010;6:313--320.320.
Necrotic Core (NC) & Dense Calcium (DC)
%NC and %DC were greater in the LAD (15.7%, 8.8%) than in the LM (11.8%, 4.5%) or LCX (10.9%, 4.5%) - p=0.002 &
p=0 0004 respectively
Plaque Composition in Each Vessel
15.7 56.2 19.4
24.411.8 56
LAD
LMNecrotic Corep=0.0004Dense Calciump=0.002Fibrous
p=0.0004, respectively.
10.9 57.2 27.5
0% 50% 100%
LCX
Fibrous p=0.7FibroFatty p=0.001
Oviedo @ CRF
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The distribution by vessel of the 168 eccentric plaques differed according to plaque type
(p=0.035)
Plaque Phenotype in Each Vessel
LAD
LM
TCFAThCFAPIT
0% 50% 100%
LCX
Oviedo @ CRF
Pre -PCI FinalCarina Carina ShiftShift
LMCA LCX
LCX
LAD
5
12.0
m2 )
5.4mm2 4.0mm225.0
m2 )
11.8mm2 9.6mm2
3.0
rina
1.22 1.47
p<0.001
MLA within LCX ostium EEM area at MLA EEM eccentricity
Carina Shift Carina Shift (n=23, LCX DS<50%)(n=23, LCX DS<50%)
2.0
4.0
6.0
8.0
10.0
MLA
with
in L
CX
ost
ium
(mm
5.0
10.0
15.0
20.0
EE
M a
rea
at th
e M
LA s
ite (m
m
1.0
1.5
2.0
2.5
ecce
ntric
ity in
dex
at L
CX
car
p=0.009 p=0.048
p
0pre post-stenting
0pre post-stenting
E
0.5pre post-stentingE
EM
p 0.009 p 0.048
78% showed a >10% reduction of MLA within LCX ostium after cross-over stenting
Kang et al. Circulation Cardiovasc Interv 2011;4:355Kang et al. Circulation Cardiovasc Interv 2011;4:355--6161
Pre -PCI FinalPlaque Plaque ShiftShift
LMCA LCX
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Carina & Plaque ShiftCarina & Plaque Shift-- 38 Pre & Post 3D Comparison 38 Pre & Post 3D Comparison --
1.1. Narrow LAD/LCX AngleNarrow LAD/LCX Angle22 Less Plaque Burden atLess Plaque Burden at2.2. Less Plaque Burden at Less Plaque Burden at
LCX LCX OstiumOstium3.3. 60% of 60% of LumenLumen Decrease Decrease
Due to Carina Shift Due to Carina Shift
Xiu & Choi et al @ CRF
20
30
40
20
30
40 BMSDistal
LMCA 55%
Distal LMCA:100%All SES
Crush
Location of Restenosis after LMCA StentingLocation of Restenosis after LMCA Stenting
LCX
0
10
20
40
0
10SES Cross-
Over
Distal LMCA:100%SES: 84%
SES PES
4 10
LCX Ostium
0
10
20
30 Crush/T
Cross-Over
ISR:9% ISR:29%
4 10
Pan. et al, Am Heart J 2007; 88: 153, Kim Am J Cardiol 2006; 97:1957-1601, He Y, AHA 2009
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Criteria for stent Criteria for stent underexpansionunderexpansion at the at the distal LMCA bifurcation (n=403)distal LMCA bifurcation (n=403)
98 1%
LCX ostium
90.2%
98.1%
4 Cardiac death2 Late stent thrombosis
Kang et al. Circulation Kang et al. Circulation CardiovascCardiovasc IntervInterv 2011; 4:5622011; 4:562--569569
SB Stent Underexpansion After CrushSB Stent Underexpansion After CrushFinal angiographic result
SB stent ostium
MV
SB distal stent
MVMV SBSB PP
MSA, mmMSA, mm22 6.56.5±±1.71.7 3.93.9±±1.01.0 <0.0001<0.0001
Stent expansion, % Stent expansion, % 92.192.1±±16.616.6 79.979.9±±12.312.3 0.020.02
MSA <4 mmMSA <4 mm22 10%10%(2/20)(2/20)
55% 55% (11/20)(11/20)
0.0070.007
MSA <5 mmMSA <5 mm22 20%20%(4/20)(4/20)
90%90%(18/20)(18/20)
<0.0001<0.0001
Costa et al. J Am Coll Cardiol. 2005;46:599-605
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The Optimal Cutoff Value of Post-Procedural MSA to Predict a Follow-up MLA ≥4mm2 After
Bifurcatoin T-Stenting
Hahn et al. J Am Coll Cardiol 2009;54:110-7
AUC=0.81 (95%CH=0.64-0.99)
AUC=0.88 (95%CH=0.80-0.95)
Take Home MessageTake Home Message1.1. 90% of plaque distribution is LAD dominant in the 90% of plaque distribution is LAD dominant in the
LMCA, LAD/D1 bifurcation, no matter the angiographic LMCA, LAD/D1 bifurcation, no matter the angiographic appearance.appearance.
22 I LMCA bif ti d d th l iI LMCA bif ti d d th l i2.2. In LMCA bifurcations, advanced atherosclerosis In LMCA bifurcations, advanced atherosclerosis ((fibroatheromafibroatheroma, calcification) is more in the proximal , calcification) is more in the proximal LAD than LMCA or LCX. However, in nonLAD than LMCA or LCX. However, in non--LM bifurcation LM bifurcation lesions, the proximal segment had more plaque than lesions, the proximal segment had more plaque than the distal segment.the distal segment.
3.3. In LMCA lesions, carina shift is related to the narrow In LMCA lesions, carina shift is related to the narrow angle of LAD/LCX and minimum plaque at LCXangle of LAD/LCX and minimum plaque at LCX ostiumostium..angle of LAD/LCX and minimum plaque at LCX angle of LAD/LCX and minimum plaque at LCX ostiumostium..
4.4. The main difference between LMCA and LAD/D1 The main difference between LMCA and LAD/D1 bifurcation are 1) size of vessel and 2) angle which may bifurcation are 1) size of vessel and 2) angle which may relate to different mechanism of lumen compromise at relate to different mechanism of lumen compromise at side branch side branch ostiumostium and acute outcome (=minimum and acute outcome (=minimum lumen area).lumen area).