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OCT IN RETINAL DISEASES
DR.SHAH-NOOR HASSAN FCPS,FRCS
Assistant Professor
BSMMU
History
 FIRST OCT IMAGES – 1991 (SHUANG)
OCT technology was conceived in the Department of
Electrical Engineering and Computer Science at
Massachusetts Institute of Technology
 James Fujimoto, Carmen Puliafito, and Eric Swanson
In 1992 the first commercial optical coherence
tomography (OCT) company was started. It was called
Advanced Ophthalmic Devices (AOD)
Advantages
• Noncontact and noninvasive technique
• The cross sectional nature of the image provides depth information
• To detect and objectively measure
- Morphological changes
- Retinal thickness
- NFL thickness
- Retinal volume
- Other parameters of optic disc
• Stored in memory, making comparison over time simple and
accurate.
Limitations
• Being new technology the instruments are relatively expensive
• Scan quality is dependent on the skill of OCT operator
• May not be possible with unco-operative patients
• Exploration is limited to the posterior pole.
• Images are degraded in the presence of media opacity.
OCT of Macula
• Normal Macula
• Role of OCT
• Interpretation of OCT
• Vitreo-retinal interface disorders
• Retinal disorders
• Subretinal disorders
Colour codes
Reflectivity
Optically
empty
Hypo Intermediate Hyper
black Blue-green yellow red
Vitreous Nuclear layers Plexiform
layers
NFL and
RPE
ROLE OF OCT
• Ancillary aid in diagnosis
• Evaluate course of disease
• Monitor treatment efficacy
Image Interpretation
18
Two ways of analyzing OCT scan
1.Qualitative
1. Morphology
2. Reflectivity
2.Quantitative
1. Thickness
2. Volume
3. Area
19
morphological changes:
•Overall retinal structural changes
•Changes in retinal outline
•Intraretinal structural changes
•Changes in posterior layers
Anomalous structures:
1.pre-retinal/epiretinal
2.intraretinal
3.subretinal
Qualitative analysis
20
Quantitative analysis is possible because the OCT 3 software is able
to identify and "trace" two key layers of the retina, the NFL and
RPE.
Thickness
Volumetry
Surface mappings
Caliper can be used to measure any other dimension or distance
Quantitive analysis
21
OCT IMAGING OF MACULA
FOVEOLA
RPE
NERVE FIBER
LAYER
MACULAR
THICKNESS
MAP
INTERPRETATION OF ABNORMAL OCT
FINDINGS
•HEMORRHAGES
• SCARS OR FIBROSIS
• HARD EXUDATES
• INFLAMMATORY INFILTRATE
INTO ANY LAYER OF RETINA
HYPERREFLECTIVITY
INTERPRETATION OF
ABNORMAL OCT FINDINGS
•Retinal Edema
•Serous Fluid
•Hypopigmentation of RPE
HYPOREFLECTIVITY
SEROUS FLUID - OPTICALLY TRANSPARENT
BLOOD – ENHANCED REFLECTIVITY
EXUDATE – MODERATE REFLECTIVITY
INTERPRETATION OF
ABNORMAL OCT FINDINGS
NATURE OF FLUID
Interpretation of OCT ?Interpretation of OCT ?
1.How is the vitreo – retinal interface?
2.What does the foveal contour look like?
3.Features of neurosensory retina ?
4. Is the red line of RPE-CCC intact or disrupted?
VITREO – RETINAL INTERFACE
FOVEAL CONTOUR
PUSHING
MACULAR HOLES
NEUROSENSORY RETINA
RPE - CCC
Vitreo - retinal
interface disorders
ERMERM
•TYPE OF ATTACHMENT TO THE RETINAL SURFACE
•POST OPERATIVE RESOLUTION
Epiretinal membrane
VMT
MACULAR HOLEMACULAR HOLE
•STAGE THE MACULAR HOLE
•POST TREATMENT FOLLOW UP
•DIFFERENTIATE-FULL THICKNESS MACULAR HOLE FROM
LAMMELAR HOLE AND PSEUDO HOLE
LAMELLAR HOLE
PSEUDO HOLEPSEUDO HOLE
PSEUDOHOLE…
PSEUDOHOLE…
Retinal disorders
DIABETIC MACULOPATYDIABETIC MACULOPATY
• SUBTLE THICKNESS
• VMT
• SEROUS DETACHMENT
• CME
• LOCATION OF HARD EXUDATES
Pattern 1. Sponge-like retinal thickening
Hard exudates
Sponge-like
Pattern 2.Cystoid spaces (partial thickness)
Cystic spaces
Pattern 3.Cystoid spaces (full thickness)
Pattern 2.Cystoid spaces (partial thickness)
Pattern 4. Subfoveal serous RD
Pattern 5. Taut Posterior Hyloid memb
(Focal)
Focal foveal
traction
Vitreoschisisis
Retinal Vascular Disorders
p302519
Sub retinal disorders
CNVMCNVM
CLASSIC CNVM
OCCULT CNVM
Juxtapapillary CNVM
PED
PIGMENT EPITHELIAL
DETACHMENT
Elevation of the neurosensory retina
optically clear space (black on OCT)
underneath them
The angle of the edge of detachment is typically
acute
HAEMORRHAGIC PED
SEROUS PED
CSCRCSCR
•OBSERVE THE RESOLUTION
•DIFFERENTIATE FROM
CNVM
•IDENTIFY CYSTOID
MACULAR DEGENERATION
CENTRAL SEROUS
RETINOPATHY
OCT in other ocular diseases
FOVEAL HAEMORRHAGE --
SUBILM HAEMORRHAGE
Retinoschisis
Parsplanitis with CME
IPCV
OPTIC NERVE HEAD PIT
VKH
JUXTAFOVEAL TELANGIECTASIA
Conclusion
• OCT is a revolutionary diagnostic tool in the Era
of modern retinal treatment.
• Being noninvasive it is safe and accessible to the
patients.
• Both in the anterior and posterior segment it has
proven to be an accurate tool for diagnosis and
treatment.
• Per operative use of OCT has taken it to a new
height.
Thank you
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
Optical Coherence Tomography (OCT)
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Optical Coherence Tomography (OCT)

Hinweis der Redaktion

  1. OCT technology was conceived in the Department of Electrical Engineering and Computer Science at Massachusetts Institute of Technology. James G. Fujimoto, PhD, professor of electrical engineering and computer science, and his students had collaborated with Carmen A. Puliafito, MD, MBA, OSN Retina/Vitreous Section Editor, who was then at the Massachusetts Eye and Ear Infirmary. “The [initial] collaboration was investigating the applications of femtosecond lasers for surgery,” Dr. Fujimoto told OSN. “At that time, we were also interested in using femtosecond light pulses to measure distances in the eye.” In the late 1980s, this technology was being investigated for the measurement of anterior structures. Joel S. Schuman, MD, an OSN Glaucoma Section Member, was a glaucoma fellow at Massachusetts Eye and Ear at the time and was working on another project in Dr. Puliafito’s laser laboratory in 1989. “I became aware of the technology and realized that it could have an application for measuring retinal thickness,” Dr. Schuman said. In 1991, David Huang, MD, PhD, who was a student under Dr. Fujimoto in the Harvard/MIT Health Sciences and Technology program, was working on this project, and he had the idea of generalizing axial scans to transverse images. “I thought this is much more useful as an imaging modality than just a ranging or thickness measurement,” Dr. Huang said. “So we got a bunch of data and plotted it out [on a false color scale] to get the image, and it looked amazing.” The team demonstrated the first OCT images, which were done in the retina ex vivo, and the data were reported in Science in 1991. Dr. Huang was the first author of the paper, which is widely regarded as the first demonstration of OCT
  2. Instead of a knife, light is used.  Instead of viewing a stained section under a microscope, we are presented with a "false-color" view with micron level resolution.
  3. This sources that can emit light over a broad range of frequencies Light from a broadband, near infrared source 820 nm and a visible aiming beam is combined and coupled into one branch of fiber-optic Michelson interferometer. has a short coherence length………………………,either constructively and destructively
  4. that is reflected and backscattered from different microstructures in the retina and light reflected from reference mirror at known distances
  5. As against B-scan and fluorescein, depth information similar to using a thin slit on a cornea with a slitlamp microscope. Resulting images can be- -Compared with images obtained during follow-up examinations
  6. The coherent light is only minimally visible to the patient, so is very comfortable and
  7. to purchase e.g in dense cataract Thus OCT is difficult/impossible to perform in cases of:
  8. Qualitative analysis of the OCT scan includes observation of the reflective qualities of the retinal structures.  The OCT software assigns "cooler" colors (green, blue) to structures with lower reflectivity.  It assigns "warmer" colors (yellow, orange, red) to more highly reflective structures.  White represents the most highly reflective structures, and black represents the least reflective structures The most highly reflective anatomical layers are the NFL and the RPE. 
  9. The software can then measure the distance between these two layers, which represents retinal thickness.  Multiple thickness measurements can be interpolated into a volume measurement of the
  10. THE NORMAL FOVEA IS IDENTIFIED BY ITS CHARACTERISTIC DEPRESSION OF THE INNER RETINAL BORDER SECONDARY TO THE LATERAL DISPLACEMENT OF TISSUE ANTERIOR TO NERVE FIBER LAYER . THE UPPERMOST FIGURE IS COLOR CODED , CROSS SECTIONAL MAP ALONG THE VERTICAL LINE . THE CENTRAL THINNING CORRESPONDS TO FOVEOLA AND WHITE LINES MARK THE VITREORETINAL AND RPE BOUNDARIES OF RETINA . THE LOWER LEFT MAP IS THE COLOR CODED MACULAR THICKNESS MAP WHEREIN BLUE COLOR REPRESENTS THINNER RETINA AND YELLOW GREEN ,THICKER RETINA. THE CENTER MAP GIVES THE QUANTATIVE MEASUREMENTS OF NINE SECTORS.
  11. REFLECTIVITY PATTERN OF THE SCANNED IMAGES IS USED TO INTERPRET ABNORMAL FINDING AS FOLLOWS ; HYPERREFLECTIVITY CAN BE CAUSED BY HEMORRHAGES , SCARS OR FIBROSIS , HARD EXUDATES AND INFLAMMATORY INFILTRATE INTO ANY LAYERS OF RETINA.
  12. HYPOREFLECTIVITY MEANS REDUCED BACK SCATTERING MAY BE CAUSED BY RETINAL EDEMA , SEROUS FLUID HYPOPIGMENTATION OF RPE .
  13. DISTINCTION BETWEEN BLOOD SEROUS FLUID AND EXUDATE IS MADE ON THE BASIS OF REFLECTIVITY SEROUS FLUID IS OPTICALLY TRANSPARENT , BLOOD HAS BOTH ENHANCED REFLECTIVITY AND INCREASED ATTENUATION OF ENHANCED LIGHT .EXUDATE TYPICALLY HAS INTERMEDIATE APPEARANCE BETWEEN BLOOD AND SEROUS FLUID ON OCT IMAGES.
  14. ERM 1. CLEAR SPACE BETWEEN ERM AND INNER RETINAL LAYERS 2 NO SPACE GLOBALLY ADHERENTERM SEE WHAETER IS UNDERLYING TRACTION…1. CELLOPHANE MACULOPATHY, 2. CRINKLED CELLOPAHNE MACULOPATHY, 3. MACULAR PUCKER IT HELPS SURGEON IN IDENTIFTING THE RIGHT PLANE OF CLEV AGE….
  15. CONFINED TO OUTER RETINAL LAYERES GIVES A SHADOWING EFFECT AND HARD EXUDATES ARE SEEN AS HYPERREFLECTIVE SHADOWS…
  16. OCT SHOWS MACULAR THICKENING WITH FULL THICKNES CYSTIOD SPACES UNDER THE FOVEA WITH INTERVENING SEPTAE..WITH ADJOINING SMALL SEPTAE…
  17. OCT SHOWS LARGE CYSTOID SPACES WITH INTERVENING SEPTAE…
  18. OCT SHOWS MACULAR THICKENING..IN THE FOVEA WITH HYPOREFLECTIVE SPACESIN ADDITION THERE IS HYPOREFLECTIVE AREA IN THE SUFOVEAL REGION CONSISTENT WITH SUBFOVEAL SEROUS RETINAL DETACHMENT
  19. INCREASED RETINAL THICKENING WITH VITREOSCHISIS..I.E SEPERATION OF POSTERIOR VITREOUS PHASE IN TO TWO LAMELLAE AND THE POSTERIOR LAMELLA CAUSES FOCAL TRACTION ON THE FOVEA SUBSEQUENTLY TRD
  20. A TYPICAL CSR OF SMOKE STACK PATTERN THEY CAN BE 1 SEROUS RETINAL DETACHMENT WITH FLUID ACCUMULATION BETWEEN NEUROSENSORY RETINA AND RPE 2. SEROUS RD WITH PED ARTYPICAL CSR MAY 1 SMALL PEDS, 2. SICK RPE WITH PED 3.
  21. FOCAL AREA OF ENHANCED BACKSCATTER OR HIGH REFLECTIVITY UNDERLYING ILM THAT BLOCKS ALL CLINICAL REFLECTIONS FROM CHORIOD AND SCLERA
  22. THERE IS SEROUS RETINAL DETACHMENT OPTIC PIT IS CONDUIT CHANNEL FOR CSF FLUID ENTERING I TO THE SUBRETINAL SPACE…ALSO SHOWS SOME CYSTIC CAVITIES
  23. Fa shows telangiectasia in the early phase and late staning IT SHOWS HYPERPLASIA OF RPE EXTENDING IN TO THE INNER RETINAL LAYERS