Optic Coherence
Tomography
DR BHAVIN J PATEL
SR NEUROLOGY
MBS HOSPITAL AND GMC, KOTA
Introduction
Imaging technique use to screen various superficial structures…
Noncontact & Non invasive
Nonradiation
Fast, Efficient and Safe
Micron resolution
Reproducible diagnostic imaging
Bhende M,Optical coherence tomography: A guide to interpretation of common macular diseases.
Indian J Ophthalmol 2018;66:20-35
History
Bhende M,Optical coherence tomography: A guide to interpretation of common macular diseases.
Indian J Ophthalmol 2018;66:20-35
Principle of OCT
Bhende M,Optical coherence tomography: A guide to interpretation of common macular diseases.
Indian J Ophthalmol 2018;66:20-35
Types of oct
Time domain Spectral domain
Reference mirror moves Reference mirror stationary
1 pixel at a time 2048 pixel at a time
Slow Rapid
Motion artifacts present No motion artifacts
Less sharp images Sharper and clear images
Generations of OCT
Curr Opin Ophthalmol. 2013 May ; 24(3): 213–221.
Analysis of OCT
Qualitative analysis
Morphology and anomalous structures
Reflectivity: hyper, hypo and shadowing
Quantitative analysis
 Thickness
 Volume
 Area
Curr Opin Ophthalmol. 2013 May ; 24(3): 213–221.
Qualitative analysis
High reflectivity:-
 Nerve Fiber Layer, RPE
ERM, hemorrhage, cotton‐wool spots, hemorrhage, hard exudates, drusen, RPE
hyperplasia
Medium reflectivity:- Plexiform layers Nuclear layers
Low reflectivity:- Photoreceptors, fluid, cysts
Curr Opin Ophthalmol. 2013 May ; 24(3): 213–221.
Anatomy of Retina on OCT
Curr Opin Ophthalmol. 2013 May ; 24(3): 213–221.
Quantitative Analysis
Quantitative Analysis
Type of Scan
POSTERIOR SEGMENT SCAN
 MACULAR SCAN
 OPTIC DISC SCAN
 RNFL THICKNESS ANALYSIS SCAN
ANTERIOR SEGMENT SCAN
Curr Opin Ophthalmol. 2013 May ; 24(3): 213–221.
Uses
Neurological
Ophthalmological
Other uses
Multiple Sclerosis
Multiple sclerosis (MS) causes both demyelination and axonal loss
pRNFL thickness can be used to assess axonal loss
MS patients who have not experienced a clinical episode of optic neuritis, the
average pRNFL thickness has been shown to be thinner than in healthy controls
Neurol Clin Pract 2015;5:460–469
Multiple Sclerosis
Microcystic retinal edema without a clinically identifiable cause can
be seen in the inner nuclear layer (INL) in patients with MS
GCL and inner plexiform layer (IPL) are preferentially affected.
Combined GCL and IPL thickness has been shown to be superior to
RNFL thickness in correlation to severity of disease.
Neurol Clin Pract 2015;5:460–469
Multiple Sclerosis
The progressive thinning of retinal layers as measured by OCT varies
depending on the subtype Of MS.
RNFL thickness correlates with T1 or T2 lesion volume, grey matter atrophy,
MTR, and diffusion tensor imaging measures (DTI).
Neurol Clin Pract 2015;5:460–469
Multiple Sclerosis
Neurol Clin Pract 2015;5:460–469
NMO
Neuromyelitis optica (NMO) typically follows a more aggressive and
debilitating course.
After at least 3 months, the peripapillary RNFL is typically thinner
following NMO optic neuritis compared to MS optic Neuritis……
Neurol Clin Pract 2015;5:460–469
NMO
In NMO optic neuritis, RNFL loss is more severe, diffuse, and
involves the superior and inferior quadrants.
In MS optic neuritis, RNFL loss is less severe and predominantly
affects the temporal quadrant that contains the papillomacular bundle
Neurol Clin Pract 2015;5:460–469
Demyelinating optic neuritis
Combined GCL - IPL thickness decreases before RNFL thinning in eyes
with optic neuritis
Optic neuritis have diffuse thinning of the pRNFL with preferential
involvement of the temporal quadrant.
 RNFL thickness below 75 mm are more likely to have persistent visual
field defects
Neurol Clin Pract 2015;5:460–469
Leber Hereditary Optic Neuropathy
As papillomacular bundle thickens at the presymptomatic stage, pRNFL
thickness (pRNFLT) increases.
mGCC thickness decreases at presentation as atrophy of the macular retinal
ganglion cells (RGC) sets in
mGCC damage begins as early as 6 weeks before the onset of visual loss in
LHON
Curr Opin Ophthalmol 2017, 28:000–000
Papilledema
OCT can also aid in differentiation of optic nerve head drusen (i.e.,
pseudo papilledema) from papilledema
Degree of pRNFL thickening of more than 127 microns gave a 73%
sensitivity and specificity
OCT volumetric measurements correlate well with clinical grading
of optic nerve head photographs,
Curr Opin Ophthalmol 2017, 28:000–000
Optic pathway glioma
Patients with neurofibromatosis-1 (NF1) with OPGs were found to have
thinner peripapillary RNFL and maculae than healthy controls
Similarly, combined macular GCL-IPL thickness was thinner in children
with OPGs and vision loss
Curr Opin Ophthalmol 2017, 28:000–000
Compressive optic neuropathy
Enlargement of the optic cup and thinning of the RNFL
More thinning nasally and temporally in compressive optic neuropathy
OCT can be used to predict the likelihood of postoperative visual recovery
Patients with thinning (less than 97.5%of normal) of the RNFL were less
likely to show any improvement in visual acuity or visual fields
Curr Opin Ophthalmol 2017, 28:000–000
NAION
Ganglion cell complex measurements have shown to correlate well with the
severity and location of visual field loss.
NAION eyes showed significant thinning of macular ganglion cell inner
plexiform layer (GCIPL) as early as 2.2 days after symptoms onset.
Degree of initial pRNFL swelling correlated with the severity of atrophy, as
well as the level of functional impairment,…
Alzheimer disease
Decreased macular thickness and RNFL thinning are associated with
abnormalities on electroretinogram.
There is decreased choroidal thickness in patients with AD compared
to healthy controls
Rev Neurol Dis. 2009;6(4):E105-E120 doi: 10.3909/rind0243
Parkinson disease
Ophthalmologic manifestations of Parkinson disease (PD) include:-
Decreased visual acuity,
Decreased contrast sensitivity,
Hallucinations,
Altered color perception,
Prolonged visual evoked potential latency
The meta-analysis found a higher prevalence of RNFL thinning at the
temporal quadrant compared to other quadrants.
Rev Neurol Dis. 2009;6(4):E105-E120 doi: 10.3909/rind0243
Parkinson disease
GCL thickness was inversely correlated with disease duration and severity.
The differential thicknesses of the outer nuclear layer and outer plexiform
layer could help distinguish PSP from MSA.
Rev Neurol Dis. 2009;6(4):E105-E120 doi: 10.3909/rind0243
Amyotrophic lateral sclerosis
In a study of 24 patients with ALS, there were significantly lower
measures of average RNFL, INL, and macular thickness compared to
controls.
Rev Neurol Dis. 2009;6(4):E105-E120 doi: 10.3909/rind0243
Drug Toxicity
Vigabatrin-attributed visual field loss is asymptomatic at early stage
with normal fundoscopy or subtle retinal changes only.
Fingolimod asso macular edema(FAME) can be diagnosed by
macular OCT.
Rev Neurol Dis. 2009;6(4):E105-E120 doi: 10.3909/rind0243
Opthalmological uses
For purposes of analysis, the OCT image of the retina can be
subdivided vertically into four regions
Pre-retina
Epi-retina
Intra-retina
Sub-retina
Pre retinal pathology
Anomalous structures
 pre-retinal membrane
 epi-retinal membrane
 vitreo-retinal strands
 vitreo-retinal traction
 pre-retinal neovascular membrane
 pre-papillary neovascular membrane
Intra retinal pathology
 Choroidal neovascular membrane
 Diffuse intra-retinal edema
 Cystoid macular edema
 Drusen
 Hard exudates
 Scar tissue
 RPE tear
OCT IN GLAUCOMA
Diagnosing and monitoring the glaucomatous change.
 Evaluating the RNFL for early (pre- perimetric) glaucoma detection.
 Evaluation of cystoid macular edema after combined cataract and
glaucoma surgery.
ANTERIOR SEGMENT OCT
Corneal thickness and keratoconus evaluation
Anterior chamber angle
 Assessing the fit of intraocular lens implants
Results of corneal implants
Other Uses
Imaging of non transparent tissue.
Neoplasia, vol 2, jan-apr, 2000 pp 9-25
Other Uses
Optical biopsy and detecting early neoplastic changes
Neoplasia, vol 2, jan-apr, 2000 pp 9-25
Other Uses
Cathater and endoscopic oct imaging  Cellular level oct imaging
Neoplasia, vol 2, jan-apr, 2000 pp 9-25
NEWER OCT’s
 OCT- SLO
 3D OCT
OCT-angiography
Enhanced depth imaging
Retinal single-layer imaging
Neoplasia, vol 2, jan-apr, 2000 pp 9-25
Artifacts
Misidentification of inner or outer retinal layer
Off center artifact
Off register artifact
Motion artifact
Blink artifact
Limitations
Quality of OCT depends on the transparency of the ocular media
OCT is operator dependent
The statistical analysis is based on a control population, which may not be
accurate depending on the population studied
Conclusion
Helps in diagnosis, treatment monitoring and deciding prognosis of
neurological illness.
Can replace need of tissue biopsy in future.
Required further research to make it more clinically applicable.
Novel and developing imaging modality.
References
Neoplasia, vol 2, jan-apr, 2000 pp 9-25
Review Neurological Dis. 2009;6(4):E105-E120 doi: 10.3909/rind0243
Curr Opin Ophthalmol 2017, 28:000–000
Neurology Clinical Pract 2015;5:460–469
Curr Opin Ophthalmol. 2013 May ; 24(3): 213–221.
Bhende M,Optical coherence tomography: A guide to interpretation of
common macular diseases. Indian J Ophthalmol 2018;66:20-35
Uptodate.com
Thank you
Anatomy of Retina on OCT
Curr Opin Ophthalmol. 2013 May ; 24(3): 213–221.
Summary
Rev Neurol Dis. 2009;6(4):E105-E120 doi: 10.3909/rind0243

Optic coherence tomography

  • 1.
    Optic Coherence Tomography DR BHAVINJ PATEL SR NEUROLOGY MBS HOSPITAL AND GMC, KOTA
  • 2.
    Introduction Imaging technique useto screen various superficial structures… Noncontact & Non invasive Nonradiation Fast, Efficient and Safe Micron resolution Reproducible diagnostic imaging Bhende M,Optical coherence tomography: A guide to interpretation of common macular diseases. Indian J Ophthalmol 2018;66:20-35
  • 3.
    History Bhende M,Optical coherencetomography: A guide to interpretation of common macular diseases. Indian J Ophthalmol 2018;66:20-35
  • 4.
    Principle of OCT BhendeM,Optical coherence tomography: A guide to interpretation of common macular diseases. Indian J Ophthalmol 2018;66:20-35
  • 5.
    Types of oct Timedomain Spectral domain Reference mirror moves Reference mirror stationary 1 pixel at a time 2048 pixel at a time Slow Rapid Motion artifacts present No motion artifacts Less sharp images Sharper and clear images
  • 6.
    Generations of OCT CurrOpin Ophthalmol. 2013 May ; 24(3): 213–221.
  • 8.
    Analysis of OCT Qualitativeanalysis Morphology and anomalous structures Reflectivity: hyper, hypo and shadowing Quantitative analysis  Thickness  Volume  Area Curr Opin Ophthalmol. 2013 May ; 24(3): 213–221.
  • 9.
    Qualitative analysis High reflectivity:- Nerve Fiber Layer, RPE ERM, hemorrhage, cotton‐wool spots, hemorrhage, hard exudates, drusen, RPE hyperplasia Medium reflectivity:- Plexiform layers Nuclear layers Low reflectivity:- Photoreceptors, fluid, cysts Curr Opin Ophthalmol. 2013 May ; 24(3): 213–221.
  • 10.
    Anatomy of Retinaon OCT Curr Opin Ophthalmol. 2013 May ; 24(3): 213–221.
  • 11.
  • 12.
  • 13.
    Type of Scan POSTERIORSEGMENT SCAN  MACULAR SCAN  OPTIC DISC SCAN  RNFL THICKNESS ANALYSIS SCAN ANTERIOR SEGMENT SCAN Curr Opin Ophthalmol. 2013 May ; 24(3): 213–221.
  • 14.
  • 15.
    Multiple Sclerosis Multiple sclerosis(MS) causes both demyelination and axonal loss pRNFL thickness can be used to assess axonal loss MS patients who have not experienced a clinical episode of optic neuritis, the average pRNFL thickness has been shown to be thinner than in healthy controls Neurol Clin Pract 2015;5:460–469
  • 16.
    Multiple Sclerosis Microcystic retinaledema without a clinically identifiable cause can be seen in the inner nuclear layer (INL) in patients with MS GCL and inner plexiform layer (IPL) are preferentially affected. Combined GCL and IPL thickness has been shown to be superior to RNFL thickness in correlation to severity of disease. Neurol Clin Pract 2015;5:460–469
  • 17.
    Multiple Sclerosis The progressivethinning of retinal layers as measured by OCT varies depending on the subtype Of MS. RNFL thickness correlates with T1 or T2 lesion volume, grey matter atrophy, MTR, and diffusion tensor imaging measures (DTI). Neurol Clin Pract 2015;5:460–469
  • 18.
    Multiple Sclerosis Neurol ClinPract 2015;5:460–469
  • 19.
    NMO Neuromyelitis optica (NMO)typically follows a more aggressive and debilitating course. After at least 3 months, the peripapillary RNFL is typically thinner following NMO optic neuritis compared to MS optic Neuritis…… Neurol Clin Pract 2015;5:460–469
  • 20.
    NMO In NMO opticneuritis, RNFL loss is more severe, diffuse, and involves the superior and inferior quadrants. In MS optic neuritis, RNFL loss is less severe and predominantly affects the temporal quadrant that contains the papillomacular bundle Neurol Clin Pract 2015;5:460–469
  • 21.
    Demyelinating optic neuritis CombinedGCL - IPL thickness decreases before RNFL thinning in eyes with optic neuritis Optic neuritis have diffuse thinning of the pRNFL with preferential involvement of the temporal quadrant.  RNFL thickness below 75 mm are more likely to have persistent visual field defects Neurol Clin Pract 2015;5:460–469
  • 22.
    Leber Hereditary OpticNeuropathy As papillomacular bundle thickens at the presymptomatic stage, pRNFL thickness (pRNFLT) increases. mGCC thickness decreases at presentation as atrophy of the macular retinal ganglion cells (RGC) sets in mGCC damage begins as early as 6 weeks before the onset of visual loss in LHON Curr Opin Ophthalmol 2017, 28:000–000
  • 23.
    Papilledema OCT can alsoaid in differentiation of optic nerve head drusen (i.e., pseudo papilledema) from papilledema Degree of pRNFL thickening of more than 127 microns gave a 73% sensitivity and specificity OCT volumetric measurements correlate well with clinical grading of optic nerve head photographs, Curr Opin Ophthalmol 2017, 28:000–000
  • 24.
    Optic pathway glioma Patientswith neurofibromatosis-1 (NF1) with OPGs were found to have thinner peripapillary RNFL and maculae than healthy controls Similarly, combined macular GCL-IPL thickness was thinner in children with OPGs and vision loss Curr Opin Ophthalmol 2017, 28:000–000
  • 25.
    Compressive optic neuropathy Enlargementof the optic cup and thinning of the RNFL More thinning nasally and temporally in compressive optic neuropathy OCT can be used to predict the likelihood of postoperative visual recovery Patients with thinning (less than 97.5%of normal) of the RNFL were less likely to show any improvement in visual acuity or visual fields Curr Opin Ophthalmol 2017, 28:000–000
  • 26.
    NAION Ganglion cell complexmeasurements have shown to correlate well with the severity and location of visual field loss. NAION eyes showed significant thinning of macular ganglion cell inner plexiform layer (GCIPL) as early as 2.2 days after symptoms onset. Degree of initial pRNFL swelling correlated with the severity of atrophy, as well as the level of functional impairment,…
  • 27.
    Alzheimer disease Decreased macularthickness and RNFL thinning are associated with abnormalities on electroretinogram. There is decreased choroidal thickness in patients with AD compared to healthy controls Rev Neurol Dis. 2009;6(4):E105-E120 doi: 10.3909/rind0243
  • 28.
    Parkinson disease Ophthalmologic manifestationsof Parkinson disease (PD) include:- Decreased visual acuity, Decreased contrast sensitivity, Hallucinations, Altered color perception, Prolonged visual evoked potential latency The meta-analysis found a higher prevalence of RNFL thinning at the temporal quadrant compared to other quadrants. Rev Neurol Dis. 2009;6(4):E105-E120 doi: 10.3909/rind0243
  • 29.
    Parkinson disease GCL thicknesswas inversely correlated with disease duration and severity. The differential thicknesses of the outer nuclear layer and outer plexiform layer could help distinguish PSP from MSA. Rev Neurol Dis. 2009;6(4):E105-E120 doi: 10.3909/rind0243
  • 30.
    Amyotrophic lateral sclerosis Ina study of 24 patients with ALS, there were significantly lower measures of average RNFL, INL, and macular thickness compared to controls. Rev Neurol Dis. 2009;6(4):E105-E120 doi: 10.3909/rind0243
  • 31.
    Drug Toxicity Vigabatrin-attributed visualfield loss is asymptomatic at early stage with normal fundoscopy or subtle retinal changes only. Fingolimod asso macular edema(FAME) can be diagnosed by macular OCT. Rev Neurol Dis. 2009;6(4):E105-E120 doi: 10.3909/rind0243
  • 32.
    Opthalmological uses For purposesof analysis, the OCT image of the retina can be subdivided vertically into four regions Pre-retina Epi-retina Intra-retina Sub-retina
  • 33.
    Pre retinal pathology Anomalousstructures  pre-retinal membrane  epi-retinal membrane  vitreo-retinal strands  vitreo-retinal traction  pre-retinal neovascular membrane  pre-papillary neovascular membrane
  • 34.
    Intra retinal pathology Choroidal neovascular membrane  Diffuse intra-retinal edema  Cystoid macular edema  Drusen  Hard exudates  Scar tissue  RPE tear
  • 35.
    OCT IN GLAUCOMA Diagnosingand monitoring the glaucomatous change.  Evaluating the RNFL for early (pre- perimetric) glaucoma detection.  Evaluation of cystoid macular edema after combined cataract and glaucoma surgery.
  • 36.
    ANTERIOR SEGMENT OCT Cornealthickness and keratoconus evaluation Anterior chamber angle  Assessing the fit of intraocular lens implants Results of corneal implants
  • 37.
    Other Uses Imaging ofnon transparent tissue. Neoplasia, vol 2, jan-apr, 2000 pp 9-25
  • 38.
    Other Uses Optical biopsyand detecting early neoplastic changes Neoplasia, vol 2, jan-apr, 2000 pp 9-25
  • 39.
    Other Uses Cathater andendoscopic oct imaging  Cellular level oct imaging Neoplasia, vol 2, jan-apr, 2000 pp 9-25
  • 40.
    NEWER OCT’s  OCT-SLO  3D OCT OCT-angiography Enhanced depth imaging Retinal single-layer imaging Neoplasia, vol 2, jan-apr, 2000 pp 9-25
  • 41.
    Artifacts Misidentification of inneror outer retinal layer Off center artifact Off register artifact Motion artifact Blink artifact
  • 42.
    Limitations Quality of OCTdepends on the transparency of the ocular media OCT is operator dependent The statistical analysis is based on a control population, which may not be accurate depending on the population studied
  • 43.
    Conclusion Helps in diagnosis,treatment monitoring and deciding prognosis of neurological illness. Can replace need of tissue biopsy in future. Required further research to make it more clinically applicable. Novel and developing imaging modality.
  • 44.
    References Neoplasia, vol 2,jan-apr, 2000 pp 9-25 Review Neurological Dis. 2009;6(4):E105-E120 doi: 10.3909/rind0243 Curr Opin Ophthalmol 2017, 28:000–000 Neurology Clinical Pract 2015;5:460–469 Curr Opin Ophthalmol. 2013 May ; 24(3): 213–221. Bhende M,Optical coherence tomography: A guide to interpretation of common macular diseases. Indian J Ophthalmol 2018;66:20-35 Uptodate.com
  • 45.
  • 46.
    Anatomy of Retinaon OCT Curr Opin Ophthalmol. 2013 May ; 24(3): 213–221.
  • 47.
    Summary Rev Neurol Dis.2009;6(4):E105-E120 doi: 10.3909/rind0243

Editor's Notes

  • #16 through a complex and incompletely understood inflammatory and neurodegenerative process
  • #17 this may independently affect visual function…………… in correlations with scores from the Expanded Disability Status Scale, visionrelated quality of life metrics, as well as high- and low-contrast visual acuity testing
  • #18 Compared to clinically isolated syndrome, both secondary progressive MS and relapsing-remitting MS had significantly thinner measurements
  • #22 Thinning of the GCL can be detected by 1 month
  • #23 LHON may be misdiagnosed, or the diagnosis delayed, especially in LHON patients with normal disc appearance and pupillary reaction
  • #24 differentiating between pseudo-papilledema and true papilledema where for Frisen scale 0 to scale 4 the total retinal volumes were 11.36, 12.53, 14.42, 17.48, and 21.81, respectively
  • #25 , whereas patients with NF1 without OPGs had measurements that were similar to healthy controls……………..
  • #26  following resection of parachiasmal tumor
  • #27 (defined as measurement between ILM to outer boundary of the IPL) A prospective longitudinal study of 16 compared to unaffected eyes,
  • #28 AD with normal visual acuity, normal visual fields, and normal color vision…
  • #32 Although it can be diagnosed and monitored by electrophysiology and perimetry, respectively, these tests may not be feasible or reliable in children or adults with coexisting cognitive limitations thus helping physicians to distinguish visual loss caused by FAME from recurrent optic neuritis