Dr Arindam Pande,
Consultant Cardiologist,
Academic Coordinator: DNB Cardiology and PGDCC Training
Apollo Gleneagles Hospital, Kolkata
“OCT- few basic facts you must
know”
OCT Imaging
Pre-Intervention
Assessment
Stent Deployment
Complication
and Post Procedural
Assessments
Intravascular OCT Imaging
1. How to acquire the image
2. Assess plaque composition
3. Identify reference segments
4. Choose stent size
5. Determine expansion/MSA
6. Determine apposition
7. Rule out geographical miss
8. Identify edge dissections
9. Identify tissue protrusion
10.Confirm procedural success
OCT Technology
 Console Ilumien, Ilumien Optis, OptisI integrated
 Rapid exchange (Rx) imaging catheter (Dragonfly)
 Flush Media Clearance
 Fast acquisition: 7.5 – 5.4cm pullback in 3.0 – 2.1sec
1. Image acquisition: Outside the Body
Imaging core
Imaging sheath
Optical Lens
1) Purge the catheter with
flush media (3 drips)
2)Connect the catheter
to
the dock
3)Set flush media
injection
• Left coronary: 4cc/s, total 14
• Right coronary: 3cc/s, total 12
• Large vessel: 4cc/s, total 20
• Manual injection: 16cc in 20cc
syringe
*The key to adequate clearance is
time not volume on automatic
pullback.
4.Select pullback length and
image acquisition method.
*Manual pullback is useful in small
vessels, tight stenoses or very
large vessels.
High-resolution pullback: 54 mm, 10 frames/mm 3.0 sec
D1
LRP
LRP
Landing Zone
Long pullback : 75 mm, 5
frames/mm
2.1 sec
Pullback lengths
1. Image acquisition: Inside the body
1) Advance OCT catheter to
region of interest on “Standby”
2) Engage guide catheter
• Avoid sideholes
• Administer IC NTG
3) Enable “Live Image” and Inject
flush media to deliver NTG and
ensure adequate blood
clearance
*Do not waste contrast
*Plan your angiographic view (avoid
overlap)
4) Purge the OCT catheter
*This minimizes signal dampening
Distal Marker
Lens Marker
Proximal Marker
1. Image acquisition: Inside the body
5) Press enable on the OCT dock
or console to calibrate
6) Cine - Enable - Inject
Proximal
Marker
Lens
Marker
Distal
Marker
Region of Interest – Vessel
Segment Imaged During
Pullback
Markers
20 mm apart
Pullback
length: 5
cm
Lens
1. Co-registering
1) Select co-register
2) Select a minimum of 3
points along the guidewire
towards the guide.
*The co-registration is dependent on
the lens
*Selecting more that 3 points is
acceptable but not necessarily
beneficial.
*If co-registration fails, select points
starting just below the lens
towards the guide.
Calcific
• Rotablator
•High
Pressure
Necrotic Core
• Cutting
Balloon
• High
Pressure
2. Assess Plaque
CompositionFibrous Fibro-Fatty
•BAS • BAS
LCX
Dx
LM
MLA 1.95 mm2
Ø = 1.56 mm, AS = 76.5%
LLeseisoionnlelnenggthth2
826mmmm
Area 8.29 mm2
Ø = 3.12 mm
Area 8.32 mm2
Ø = 3.04 mm
Area 8.79 mm2
Ø = 3.25 mm
3. Identify Reference Segments
1) Scroll reference vessel
markers to proximal and
distal lesion edges.
2) Attempt to identify segment
of vessel within 5mm with
at least >180 degrees of
visible EEL
3) Reposition reference
scroll marker accordingly
Area 8.79 mm2 Ø = 3.55 mm
Lesion length 28 mm
LCX
LM
Dx
MLA 1.95 mm2
Ø = 1.56 mm, AS = 76.5%
Area 8.32 mm2
Ø = 3.24 mm
Increasingly aggressive
•Largest reference lumen (prox or dist)
•Mid-wall
•Media-to-media (typically discounted)
3. Choose Stent Length
How Big?
Lumen
MLD 3.0mm
MSA (πr2) = 7.07mm2
Mid-wall
MWD 3.1mm
MSA (πr2) = 7.55mm2
External Elastic Lamina
EELD 3.2mm
MSA (πr2) = 8.04mm2
3. Choose Stent Diameter
OCT vs IVUS vs Histology
Kubo et al. iJACC 2013;6(10):1095-
Size Matters
de Feyter et al. Circulation 1999;100:1777-83
Final Minimum Stent Area (mm2)
*
*
*
*
*
*
*
* *
*
*
*
*
*
*
*
*
*
*
**
**
*
*
*
*
5. Determine Expansion/MSA
1) Scroll reference vessel markers
to distal stent edge and
midpoint of stent.
2) Identify “automated measures”
yellow box to determine MSA.
3) Identify respective “automated
measures” reference blue box
to determine residual area
stenosis.
Distal Half
5. Determine Expansion/MSA
1) Scroll reference vessel markers
to distal stent edge and
midpoint of stent.
2) Identify “automated measures”
yellow box to determine MSA.
3) Identify respective “automated
measures” reference blue box
to determine residual area
stenosis.
Proximal Half
Lumen Area, Stent Area, Strut-Lumen
Distance
Strut-Vessel
Wall
Distance
Protruding
Covered
MalapposedEmbedded
6. Determine
Apposition
Malapposition
Alloy Strut Polymer Total Thickness Embedded Contact Malapposed
Cypher 140 7 154 <80 80-160 >160
Taxus 97 15 127 <65 65-130 >130
Zotarolimus 91 8 107 <55 55-110 >110
Everolimus 81 7 88* <54 50-100 >108
6. Determine
Apposition
Major
Strut
Minor
Strut
Lumen Area; 12.36mm2
Stent Area; 10.95mm2
Lumen Area; 5.47mm2
Stent Area; 4.32mm21mm
1mm
• Associated with
stent
underexpansion
• Not Associated
with stent
underexpansion
OCT
7. Rule out geographic miss
1) Peruse OCT longitudinal
image for geographic miss
Stented Segment
8. Identify Edge Dissections
Major Category
1) >60° / >3mm
2)Flow limiting (TIMI)
3)Inadequate MLA
8. Identify Edge Dissections
LCX-post BVS implantation
LCX-post BVS implantation
LCX – OCT run
9. Identify Tissue Protrusion
Major
Minor
• Effective MLA
<5.5mm2
Effective Lumen Area; 2.70 mm2
Protrusion Area/Stent Area ≥ 10%
Effective Lumen Area; 6.30 mm2
Protrusion Area/Stent Area < 10%
Tissue protrusion
Tissue protrusion
1mm
1mm
Effective MLA
>5.5mm2
LAD – during BVS implantation
LAD – during BVS implantation
LAD – post aspiration
10. Confirm Procedural Success
Adequate stent expansion: The MSA within the stented segment must
be
≥90% the mean proximal and distal reference lumen areas.
Proximal Reference = 7.9mm2, Distal Reference = 7.1mm2 , mean = 7.45mm2
• Target =≥90% of 7.45mm2 = 6.70mm2
•Final MSA = 7.15mm2 (Adequate Stent Expansion Achieved)
OCT – ISR - BVS
Modality Advantages Disadvantages
IVUS - High tissue penetration
- Good imaging of fiber, calcium
- Plaque burden
- LMCA
- No flush required
- Large installed base
- Outcomes data
- Operator Experience
- Cost
- Slow
- Inferior resolution
- Difficult to resolve lipid, thrombus, stents,
dissections
- Apposition
- Dissection
- Calcium shadowing
- Virtual histology reliability
OCT - High resolution
- < 3 second pullback
- Non-occlusive
- Follow-up for apposition, dissection
- High sens/spec for lesion identification (lipid, calcium,
fiber, thrombus)
- Low crossing profile
- Bioabsorbable stents
- Lack of outcome data
- LMCA
- Poor tissue penetration
- Ostial
- Very tight lesions
- Very large vessels
- Adds contrast load
IVUS versus OCT
Very Tight Lesions  Pre-dilation with 1.5-2.0mm balloon
Very Large Vessels Injection via Guideliner
Contrast Load
Obstacles to OCT
Visipaque Dextran-40
Thank You

OCT - few basic facts

  • 1.
    Dr Arindam Pande, ConsultantCardiologist, Academic Coordinator: DNB Cardiology and PGDCC Training Apollo Gleneagles Hospital, Kolkata “OCT- few basic facts you must know”
  • 2.
    OCT Imaging Pre-Intervention Assessment Stent Deployment Complication andPost Procedural Assessments Intravascular OCT Imaging 1. How to acquire the image 2. Assess plaque composition 3. Identify reference segments 4. Choose stent size 5. Determine expansion/MSA 6. Determine apposition 7. Rule out geographical miss 8. Identify edge dissections 9. Identify tissue protrusion 10.Confirm procedural success
  • 3.
    OCT Technology  ConsoleIlumien, Ilumien Optis, OptisI integrated  Rapid exchange (Rx) imaging catheter (Dragonfly)  Flush Media Clearance  Fast acquisition: 7.5 – 5.4cm pullback in 3.0 – 2.1sec
  • 4.
    1. Image acquisition:Outside the Body Imaging core Imaging sheath Optical Lens 1) Purge the catheter with flush media (3 drips) 2)Connect the catheter to the dock 3)Set flush media injection • Left coronary: 4cc/s, total 14 • Right coronary: 3cc/s, total 12 • Large vessel: 4cc/s, total 20 • Manual injection: 16cc in 20cc syringe *The key to adequate clearance is time not volume on automatic pullback. 4.Select pullback length and image acquisition method. *Manual pullback is useful in small vessels, tight stenoses or very large vessels.
  • 5.
    High-resolution pullback: 54mm, 10 frames/mm 3.0 sec D1 LRP LRP Landing Zone Long pullback : 75 mm, 5 frames/mm 2.1 sec Pullback lengths
  • 6.
    1. Image acquisition:Inside the body 1) Advance OCT catheter to region of interest on “Standby” 2) Engage guide catheter • Avoid sideholes • Administer IC NTG 3) Enable “Live Image” and Inject flush media to deliver NTG and ensure adequate blood clearance *Do not waste contrast *Plan your angiographic view (avoid overlap) 4) Purge the OCT catheter *This minimizes signal dampening Distal Marker Lens Marker Proximal Marker
  • 7.
    1. Image acquisition:Inside the body 5) Press enable on the OCT dock or console to calibrate 6) Cine - Enable - Inject Proximal Marker Lens Marker Distal Marker Region of Interest – Vessel Segment Imaged During Pullback Markers 20 mm apart Pullback length: 5 cm Lens
  • 8.
    1. Co-registering 1) Selectco-register 2) Select a minimum of 3 points along the guidewire towards the guide. *The co-registration is dependent on the lens *Selecting more that 3 points is acceptable but not necessarily beneficial. *If co-registration fails, select points starting just below the lens towards the guide.
  • 9.
    Calcific • Rotablator •High Pressure Necrotic Core •Cutting Balloon • High Pressure 2. Assess Plaque CompositionFibrous Fibro-Fatty •BAS • BAS
  • 10.
    LCX Dx LM MLA 1.95 mm2 Ø= 1.56 mm, AS = 76.5% LLeseisoionnlelnenggthth2 826mmmm Area 8.29 mm2 Ø = 3.12 mm Area 8.32 mm2 Ø = 3.04 mm Area 8.79 mm2 Ø = 3.25 mm 3. Identify Reference Segments 1) Scroll reference vessel markers to proximal and distal lesion edges. 2) Attempt to identify segment of vessel within 5mm with at least >180 degrees of visible EEL 3) Reposition reference scroll marker accordingly
  • 11.
    Area 8.79 mm2Ø = 3.55 mm Lesion length 28 mm LCX LM Dx MLA 1.95 mm2 Ø = 1.56 mm, AS = 76.5% Area 8.32 mm2 Ø = 3.24 mm Increasingly aggressive •Largest reference lumen (prox or dist) •Mid-wall •Media-to-media (typically discounted) 3. Choose Stent Length
  • 12.
    How Big? Lumen MLD 3.0mm MSA(πr2) = 7.07mm2 Mid-wall MWD 3.1mm MSA (πr2) = 7.55mm2 External Elastic Lamina EELD 3.2mm MSA (πr2) = 8.04mm2 3. Choose Stent Diameter
  • 13.
    OCT vs IVUSvs Histology Kubo et al. iJACC 2013;6(10):1095-
  • 14.
    Size Matters de Feyteret al. Circulation 1999;100:1777-83 Final Minimum Stent Area (mm2) * * * * * * * * * * * * * * * * * * * ** ** * * * *
  • 15.
    5. Determine Expansion/MSA 1)Scroll reference vessel markers to distal stent edge and midpoint of stent. 2) Identify “automated measures” yellow box to determine MSA. 3) Identify respective “automated measures” reference blue box to determine residual area stenosis. Distal Half
  • 16.
    5. Determine Expansion/MSA 1)Scroll reference vessel markers to distal stent edge and midpoint of stent. 2) Identify “automated measures” yellow box to determine MSA. 3) Identify respective “automated measures” reference blue box to determine residual area stenosis. Proximal Half
  • 17.
    Lumen Area, StentArea, Strut-Lumen Distance Strut-Vessel Wall Distance Protruding Covered MalapposedEmbedded 6. Determine Apposition Malapposition Alloy Strut Polymer Total Thickness Embedded Contact Malapposed Cypher 140 7 154 <80 80-160 >160 Taxus 97 15 127 <65 65-130 >130 Zotarolimus 91 8 107 <55 55-110 >110 Everolimus 81 7 88* <54 50-100 >108
  • 18.
    6. Determine Apposition Major Strut Minor Strut Lumen Area;12.36mm2 Stent Area; 10.95mm2 Lumen Area; 5.47mm2 Stent Area; 4.32mm21mm 1mm • Associated with stent underexpansion • Not Associated with stent underexpansion
  • 19.
  • 20.
    7. Rule outgeographic miss 1) Peruse OCT longitudinal image for geographic miss Stented Segment
  • 21.
    8. Identify EdgeDissections
  • 22.
    Major Category 1) >60°/ >3mm 2)Flow limiting (TIMI) 3)Inadequate MLA 8. Identify Edge Dissections
  • 23.
  • 24.
  • 25.
  • 26.
    9. Identify TissueProtrusion Major Minor • Effective MLA <5.5mm2 Effective Lumen Area; 2.70 mm2 Protrusion Area/Stent Area ≥ 10% Effective Lumen Area; 6.30 mm2 Protrusion Area/Stent Area < 10% Tissue protrusion Tissue protrusion 1mm 1mm Effective MLA >5.5mm2
  • 27.
    LAD – duringBVS implantation
  • 28.
    LAD – duringBVS implantation
  • 29.
    LAD – postaspiration
  • 30.
    10. Confirm ProceduralSuccess Adequate stent expansion: The MSA within the stented segment must be ≥90% the mean proximal and distal reference lumen areas. Proximal Reference = 7.9mm2, Distal Reference = 7.1mm2 , mean = 7.45mm2 • Target =≥90% of 7.45mm2 = 6.70mm2 •Final MSA = 7.15mm2 (Adequate Stent Expansion Achieved)
  • 31.
  • 32.
    Modality Advantages Disadvantages IVUS- High tissue penetration - Good imaging of fiber, calcium - Plaque burden - LMCA - No flush required - Large installed base - Outcomes data - Operator Experience - Cost - Slow - Inferior resolution - Difficult to resolve lipid, thrombus, stents, dissections - Apposition - Dissection - Calcium shadowing - Virtual histology reliability OCT - High resolution - < 3 second pullback - Non-occlusive - Follow-up for apposition, dissection - High sens/spec for lesion identification (lipid, calcium, fiber, thrombus) - Low crossing profile - Bioabsorbable stents - Lack of outcome data - LMCA - Poor tissue penetration - Ostial - Very tight lesions - Very large vessels - Adds contrast load IVUS versus OCT
  • 33.
    Very Tight Lesions Pre-dilation with 1.5-2.0mm balloon Very Large Vessels Injection via Guideliner Contrast Load Obstacles to OCT Visipaque Dextran-40
  • 34.