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Myopia
By: Dr. Saif Aldeen AlRyalat
Department of Ophthalmology, The University of Jordan
saifryalat@yahoo.com
Definition
• Myopia: Focusing the image in
front of the retina.
• Due to:
- High axial length
- High refractive power
High myopia
• Refractive error with spherical
equivalent exceeding −6 diopters (D)
AND/OR
• Axial length longer than 26.5 mm.
Pathological myopia
• High axial myopia.
AND
• Characteristic pathological
changes at the posterior pole.
Also called degenerative or
malignant myopia
Epidemiology
• The prevalence varies from 1% to 4% in the general population.
• More prevalent in the Asian population.
• Higher prevalence of PM in women than in men.
Pathophysiology
• Excessive axial elongation resulting in
chorioretinal stretching and subsequent
thinning.
• Myopia-related complications increase
proportionally with increase in axial length.
• Choroidal neovascularization (CNV)
Outcome
• CNV observed in 5.2% of eyes with pathological myopia.
• Myopic CNV may account for as much as 62% of CNV occurring in
patients younger than 50 years of age.
• Several studies observed poor long-term visual acuity outcome after
CNV.
Features
Posterior staphyloma
Posterior staphyloma
• Local bulging of the sclera at the posterior
pole of the eye.
• Has a radius of less than the surrounding
curvature of the wall of the eye.
• Pathognomonic for pathological myopia.
• The best way to diagnose by an indirect
ophthalmoscope.
Posterior staphyloma
• It is seen as a secondary
depression with bending of
vessels at the margin and a dark
crescentic nasal reflex
Features
Myopic maculopathy
Classification for maculopathy
• Available classification systems:
- Curtin and Karlin on 1970 (didn’t cover all lesions).
- Avila et al. on 1984 (do not progress sequentially).
- Hayashi et al. on 2010 (do not progress sequentially).
• On 2015, a new study published in AJO by META-analysis for
pathologic myopia study group proposed a new classification system
to overcome previous limitations.
The new classification
• 5 categories from 0 to 4.
• 3 plus lesions: Do not fit into
any particular category, and
can develop from, or co-exist,
in eyes with any of the myopic
maculopathy categories.
• % are rates of progression over
13 years.
The new classification
• The classification is
based on risk of
developing myopic
choroidal
neovascularization
(myopic CNV) from
different categories
(incidence % over 13
years)
Tessellated fundus
• Generalized depigmentation due
to retinal pigment epithelium
atrophy following the myopic
axial elongation.
Diffuse chorioretinal atrophy
• Appears as yellowish-
white of posterior pole
of an eye.
Patchy chorioretinal atrophy
• Appears as well defined, grayish-
white lesions.
• characterized by a complete loss
of choriocapillaris and can
progress to an absence of outer
retina and RPE.
Macular atrophy
• Macular atrophy is a well-defined,
round chorioretinal atrophic lesion
which is grayish-white or whitish
and enlarges with time.
• Macular atrophy is centered on the
central fovea and has a round
shape. Whereas patchy
chorioretinal atrophy is not
centered on the fovea and has
irregular margins.
Lacquer cracks (Lc)
• Lacquer cracks are
mechanical breaks of
Bruch’s membrane and are
observed as yellowish thick
linear pattern.
• Lacquer cracks can lead to
bleeding (arrows).
Myopic CNV
• An active CNV is determined by
the presence of a CNV and
exudative changes.
• They are located in the
subretinal space, as opposed to
the sub-RPE space in age-
related macular degeneration
(AMD)
• Serous retinal detachments
associated with the CNV can be
present.
Fuchs’ spot (Fs)
• Fuchs’ spot is a pigmented
spot representing the
scaring phase of myopic
choroidal
neovascularization.
• Fuchs’ spot is a
consequence of myopic CNV.
Features
Others
Myopic conus/crescent
• A sharply defined
concentric area of
depigmentation
adjacent to the optic
disc where the inner
surface of sclera is
visible
Myopic Macular Retinoschisis
• A schisis-like (i.e. cleft)
thickening of neurosensory
retina into a thicker inner
layer and a thinner outer
layer at the macula.
• Alternatively described as
myopic traction maculopathy
(MTM).
Prevention
Prevention
• Increased time spent outdoors is the only known protective factor.
• Atropine eye drops are under investigation.
• No intervention can reverse pathological myopia. However,
treatments available for CNV.
Management
Management: Before 1990s
• Photothermal laser ablation of the new vessels.
• High rate of recurrence
• High tendency of the photocoagulation scars to expand over time and
significantly risked central vision
Management: Late 1990s
• Photodynamic therapy (PDT).
• Photosensitive intravenous drug,
verteporfin in combination with a
low power, long duration infrared
laser.
Management: Late 1990s
• Selectively target neovascular vessels with lesser collateral damage.
• Photodynamic Therapy has been limited by these observations:
- Up to 13% still have moderate vision losses despite treatment
- Up to 57% with persistent leakage at one year.
- Almost no effect at two years.
Management: Nowadays
• Anti-VEGF therapy is now considered first line intervention in patients
with myopic CNV.
• Used off-label for the treatment of myopic CNV.
• A growing number of prospective and randomized trials have been
published or are currently underway.
Management: Nowadays
• RADIANCE (A Randomized Controlled Study of Ranibizumab in
Patients with Choroidal Neovascularization Secondary to Pathologic
Myopia).
• Comparing intravitreal ranibizumab to PDT.
• Concluded: “Ranibizumab treatment, irrespective of retreatment
criteria, provided superior BCVA gains versus PDT"
Management: Role of vitrectomy
• Patients with decreased vision in the setting of maculoschisis or
foveoschisis.
• Vitrectomy relieve traction on the fovea and prevent formation of
macular holes or macular retinal detachment.
Thank you

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Myopia

  • 1. Myopia By: Dr. Saif Aldeen AlRyalat Department of Ophthalmology, The University of Jordan saifryalat@yahoo.com
  • 2. Definition • Myopia: Focusing the image in front of the retina. • Due to: - High axial length - High refractive power
  • 3. High myopia • Refractive error with spherical equivalent exceeding −6 diopters (D) AND/OR • Axial length longer than 26.5 mm.
  • 4. Pathological myopia • High axial myopia. AND • Characteristic pathological changes at the posterior pole. Also called degenerative or malignant myopia
  • 5. Epidemiology • The prevalence varies from 1% to 4% in the general population. • More prevalent in the Asian population. • Higher prevalence of PM in women than in men.
  • 6. Pathophysiology • Excessive axial elongation resulting in chorioretinal stretching and subsequent thinning. • Myopia-related complications increase proportionally with increase in axial length. • Choroidal neovascularization (CNV)
  • 7. Outcome • CNV observed in 5.2% of eyes with pathological myopia. • Myopic CNV may account for as much as 62% of CNV occurring in patients younger than 50 years of age. • Several studies observed poor long-term visual acuity outcome after CNV.
  • 9. Posterior staphyloma • Local bulging of the sclera at the posterior pole of the eye. • Has a radius of less than the surrounding curvature of the wall of the eye. • Pathognomonic for pathological myopia. • The best way to diagnose by an indirect ophthalmoscope.
  • 10. Posterior staphyloma • It is seen as a secondary depression with bending of vessels at the margin and a dark crescentic nasal reflex
  • 12. Classification for maculopathy • Available classification systems: - Curtin and Karlin on 1970 (didn’t cover all lesions). - Avila et al. on 1984 (do not progress sequentially). - Hayashi et al. on 2010 (do not progress sequentially). • On 2015, a new study published in AJO by META-analysis for pathologic myopia study group proposed a new classification system to overcome previous limitations.
  • 13. The new classification • 5 categories from 0 to 4. • 3 plus lesions: Do not fit into any particular category, and can develop from, or co-exist, in eyes with any of the myopic maculopathy categories. • % are rates of progression over 13 years.
  • 14. The new classification • The classification is based on risk of developing myopic choroidal neovascularization (myopic CNV) from different categories (incidence % over 13 years)
  • 15. Tessellated fundus • Generalized depigmentation due to retinal pigment epithelium atrophy following the myopic axial elongation.
  • 16. Diffuse chorioretinal atrophy • Appears as yellowish- white of posterior pole of an eye.
  • 17. Patchy chorioretinal atrophy • Appears as well defined, grayish- white lesions. • characterized by a complete loss of choriocapillaris and can progress to an absence of outer retina and RPE.
  • 18. Macular atrophy • Macular atrophy is a well-defined, round chorioretinal atrophic lesion which is grayish-white or whitish and enlarges with time. • Macular atrophy is centered on the central fovea and has a round shape. Whereas patchy chorioretinal atrophy is not centered on the fovea and has irregular margins.
  • 19. Lacquer cracks (Lc) • Lacquer cracks are mechanical breaks of Bruch’s membrane and are observed as yellowish thick linear pattern. • Lacquer cracks can lead to bleeding (arrows).
  • 20. Myopic CNV • An active CNV is determined by the presence of a CNV and exudative changes. • They are located in the subretinal space, as opposed to the sub-RPE space in age- related macular degeneration (AMD) • Serous retinal detachments associated with the CNV can be present.
  • 21. Fuchs’ spot (Fs) • Fuchs’ spot is a pigmented spot representing the scaring phase of myopic choroidal neovascularization. • Fuchs’ spot is a consequence of myopic CNV.
  • 23. Myopic conus/crescent • A sharply defined concentric area of depigmentation adjacent to the optic disc where the inner surface of sclera is visible
  • 24. Myopic Macular Retinoschisis • A schisis-like (i.e. cleft) thickening of neurosensory retina into a thicker inner layer and a thinner outer layer at the macula. • Alternatively described as myopic traction maculopathy (MTM).
  • 26. Prevention • Increased time spent outdoors is the only known protective factor. • Atropine eye drops are under investigation. • No intervention can reverse pathological myopia. However, treatments available for CNV.
  • 28. Management: Before 1990s • Photothermal laser ablation of the new vessels. • High rate of recurrence • High tendency of the photocoagulation scars to expand over time and significantly risked central vision
  • 29. Management: Late 1990s • Photodynamic therapy (PDT). • Photosensitive intravenous drug, verteporfin in combination with a low power, long duration infrared laser.
  • 30. Management: Late 1990s • Selectively target neovascular vessels with lesser collateral damage. • Photodynamic Therapy has been limited by these observations: - Up to 13% still have moderate vision losses despite treatment - Up to 57% with persistent leakage at one year. - Almost no effect at two years.
  • 31. Management: Nowadays • Anti-VEGF therapy is now considered first line intervention in patients with myopic CNV. • Used off-label for the treatment of myopic CNV. • A growing number of prospective and randomized trials have been published or are currently underway.
  • 32. Management: Nowadays • RADIANCE (A Randomized Controlled Study of Ranibizumab in Patients with Choroidal Neovascularization Secondary to Pathologic Myopia). • Comparing intravitreal ranibizumab to PDT. • Concluded: “Ranibizumab treatment, irrespective of retreatment criteria, provided superior BCVA gains versus PDT"
  • 33. Management: Role of vitrectomy • Patients with decreased vision in the setting of maculoschisis or foveoschisis. • Vitrectomy relieve traction on the fovea and prevent formation of macular holes or macular retinal detachment.