This document discusses various classification and staging systems used in ophthalmology. It covers classifications for corneal and external eye diseases, glaucoma, uveitis, vitreo-retinal diseases, and others. For each condition, it provides details on the classifications used to describe risk factors, pathogenesis, clinical features, severity, investigations, and management approaches. The classifications discussed include international standardized systems as well as other commonly used staging methods.
3. General Classifications
• Risk factors
• E.g. modifiable/not, ocular/systemic
• Pathogenesis
• E.g. Ischemic/occlusive/haemorrhagic, necrotic/fibrotic
• Aetiology/causes
• Clinical features/Severity/Progression/Complications
• Investigation/tests
• E.g. ocular/systemic, invasive/not
• Management
• E.g. conservative/medical/laser/surgical
• E.g. factors to be considered
• Primary vs Secondary
• Systemic vs Ocular
• Congenital vs Acquired
• Anatomical approach
• Etiological approach (VITAMINS, VEINS, VINDICATE)
• Most common, important. life/sight threatening
6. Global Consensus on Keratoconus and
Ectatic Diseases 2015
• Currently there is no clinically adequate
classification system for keratoconus
• Currently, there is no consistent or clear definition
of ectasia progression
8. Belin ABCD KC Staging
• Ant & Back radius of
curvature (3mm),
• Corneal thickness
(minimal)
• Distance VA (DCVA)
9. Pentacam for KC
• K Max & ABCD & Thinnest pachy progression
• Indices colour code, KISA (60-100), IS (1.4-1.9)
• BAD D (enhanced ectasia) screening & colour code
(change/different: ant 5-7 & post 12-16 )
• Covis biomechanical: CBI & TBI
• Asphericity/Q value: normal -0.01 to -0.8
• Q-val <0/-ve/oblate = normal or KC or post hyperop LVC
• Q-val >0/+ve/prolate = post myopic LVC
• Q-val=0/sphere
10. IC3D 2015 (International Classification of Corneal
Dystrophies)
- Genetic (chromosomal/gene)
- Clinical (pattern/anatomical layer)
- Pathology (histo/biochem/confocal)
11. DEWS 2017 (International Dry Eye Workshop)
Classification: Aqueous deficiency VS evaporative
• Aq deficiency
– Sjogren VS Non Sjogren
• Evaporative
– Intrinsic VS Extrinsic
Dry Eye Severity Grading Scheme
• Symptoms + Signs (conj/cornea/tear/lid & gland) + Tests (TBUT/Schimer)
12. VKC- classification
• Limbal/bulbar vs palbebral vs mixed
• Chronic vs intermittent
• VKC Grade 0-4 (various)
• Mild/mod/severe (just noticeable/most of the
day/interrupt daily routine) & vision threatening
• Papillae Grading 0-4 (size: 0.3-1-3mm, location:
tarsal-limbus)
• Shield ulcer Grading 1-3 (content: clear-debris-
plaque, treatment response/re-epithelised)
15. Trachoma: WHO classification & SAFE strategy
SAFE strategy: Surgery for in-turned eyelashes, Antibiotics for active disease, Face washing (or
promotion of facial cleanliness), and Environmental improvement to reduce transmission.
21. International Workshop on Ocular Sarcoidosis (IWOS)
• 7signs:
– (1) mutton-fat keratic precipitates (KPs)/small granulomatous KPs and/or iris nodules
(Koeppe/Busacca),
– (2) trabecular meshwork (TM) nodules and/or tent-shaped peripheral anterior synechiae (PAS),
– (3) vitreous opacities displaying snowballs/strings of pearls,
– (4) multiple chorioretinal peripheral lesions (active and/or atrophic),
– (5) nodular and/or segmental peri-phlebitis (± candlewax drippings) and/or retinal macroaneurism in
an inflamed eye,
– 6) optic disc nodule(s)/granuloma(s) and/or solitary choroidal nodule, and
– (7) bilaterality
• 5labs/imaging Ix:
– (1) negative tuberculin skin test in a BCG-vaccinated patient or in a patient having had a positive
tuberculin skin test previously,
– (2) elevated serum angiotensin converting enzyme (ACE) levels and/or elevated serum lysozyme,
– (3) chest x-ray revealing bilateral hilar lymphadenopathy (BHL),
– (4) abnormal liver enzyme tests, and
– (5) chest CT scan in patients with a negative chest x-ray result.
• Four levels of certainty for the diagnosis of ocular sarcoidosis (diagnostic criteria) were
recommended in patients in whom other possible causes of uveitis had been excluded:
– (1) biopsy-supported diagnosis with a compatible uveitis was labeled as definite ocular sarcoidosis;
– (2) if biopsy was not done but chest x-ray was positive showing BHL associated with a compatible
uveitis, the condition was labeled as presumed ocular sarcoidosis;
– (3) if biopsy was not done and the chest x-ray did not show BHL but there were 3 of the above
intraocular signs and 2 positive laboratory tests, the condition was labeled as probable ocular
sarcoidosis; and
– (4) if lung biopsy was done and the result was negative but at least 4 of the above signs and 2
positive laboratory investigations were present, the condition was labeled as possible ocular
sarcoidosis
29. • Narrow slit beam
• Perpendicular to the most peripheral part of the cornea
• Slit beam angle of about 60°
• Compare the thickness of the cornea & visible aqueous
30. Becker Goniogram
Means of drawing gonioscopic findings
Allow description of the variable anatomy of an angle within a quadrant
Record synechiae, tumors, foreign bodies, and so on
37. DR & DME- classification
• International classification of DR (ICDR) disease severity scale
• mild-mod-severe NDPR, PDR
• DRS & ETDRS
• NPDR severe/very severe, PDR early/high risk
• NVD >/= 1/3 DD
• NVD <1/3 DD with VH/PRH
• NVE >/= ½ DD with VH/PRH
• DME
– center involvement: CMT (center 1mm) >250um
– vision impairment: VA =/< 6/9
– focal: micro-aneurysm with circinate ring
– diffuse: cystoid ME
– +- VMT
• International classification of DME (ICDME) disease severity scale
• DME absent vs present (mild-mod-severe)
• CSME (ETDRS)
– retinal edema within 500um center of fovea
– HE with retinal thickening within 500um center of fovea
– retinal thickening >1DD located within 1DD center of fovea
38.
39.
40.
41. ARMD- Type & Classification
• Dry vs wet- 90 vs 10% (blindness opposite)
• Normal/normal aging/early/intermediate/late AMD
– drusen size + pigmentary changes → CNV/GA
• Dry- drusen/GA
• Drusen- size (drupelets/63/125=vein diameter at OD margin), morphology
(hard/soft/confluent), +- dystrophic calcification +- pigmentary changes
• PED- x 4 (drusenoid/serous/hrge/FVC)
• Wet- CNV/PED/RAP/PCV
• CNV (FFA/MPS study)
– classic (20%, well defined and early, predominant/minimal), (location:
extra/juxta/subfovea, 200um vs foveola)
– occult (80%, FV PED/LLUS)
• CNV (ICG)
– Hot spot <1DD (less common, for laser)
– Plaque >1DD (more common, poor natural history)
– Combination (rare)
• Wet (CNV)- type 1/2 (subRPE/subretina) or type 3 (RCA with RAP)
• CNV (active/not)- +fluid/hrge/leak on FFA/enlarging CNV membrane/deteriorating
vision
• Variant- RAP x 3 stages (1-3: IRN/SRN/RCA), IPCV
43. GA New OCT Classification
• New classification (OCT)
• Outer retinal atrophy (ORA) only or with RPE (RORA)
• Complete vs incomplete
• cRORA = GA
• iRORA = early GA
• cORA
• iORA
57. High myopia
META-PM (meta-analysis for pathologic myopia) international classification
• for myopic maculopathy
• OCT and colour fundus photography
• retinal changes + choroid, Bruch’s membrane and the RPE
• “no myopic retinal degenerative lesion” (Category 0), “tessellated fundus”
(Category 1), “diffuse chorioretinal atrophy” (Category 2), “patchy chorioretinal
atrophy” (Category 3), and “macular atrophy” (Category 4).
• “plus” lesions: lacquer cracks, myopic choroidal neovascularisation, and Fuchs
spot.
• Posterior staphyloma was considered as a further important sign
ATN classification
• three factors: atrophy, traction and neovascularisation.
62. RAPD
Grading (Bell et al 1993)
• Grade I: Weak constriction then greater dilatation
• Grade II: No initial constriction, stall, then dilatation
• Grade III: Immediate dilatation
• Grade IV: Immediate dilatation following prolonged illumination
of the good eye for six seconds
• Grade V: Immediate dilatation with no secondary constriction
63. Staging for papilloedema (Frisen Scale )
Grade 0-5:
Principle:
- nasal temporal
- border blur grayish opaque
elevation BV obscured
protrusion/expansion/paton’s
line
• Early: hyperemic, blurred + elevated margin, subtle peripapillary NFL edema, dilated disc
capillaries, distended retinal veins, absent spontaneous venous pulsation (SVP).
• Acute: as listed above + peripapillary hemorrhages, CWS, increased NFL edema (may
obscure retinal vessels).
• Chronic: hyperemia, CWS or hemorrhages, variable swelling, usually still elevated; ± drusen-
like deposits and optociliary shunt vessels at the disc (=vintage papilledema).
• Atrophic/late: pale atrophic disc, dswelling, attenuated arterioles.
64. MG
Osserman Grading
• I: Ocular
• II: Generalized
• III: Fulminant and crisis
• IV: Late progressive
• V : Muscle atrophy
MGFA Clinical Classification
• Class I: ocular muscle
weakness only
• Class II to IV= I +
mild/mod/severe
weakness of other
muscles
• Further a or b:
• a: > limb, axial muscles
• b: > oropharyngeal,
respiratory muscles
• Class V: Intubation
78. OTS
• scores range from 1 (most severe injury and worst prognosis at 6 months follow-up) to 5 (least
severe injury and least poor prognosis at 6 months). Each score is associated with a range of
predicted post-injury visual acuities. It has a predictive accuracy of approximately 80%, which
means that the OTS will be accurate 4 out of 5 times
79. BETTS
Closed-globe injuries
• contusion (blunt trauma without break in eyewall)
• lamellar laceration (partial-thickness wound of the eyewall)
• superficial foreign bodies
Open-globe injuries
• rupture (blunt trauma with break in eyewall)
• laceration (full-thickness wound of the eyewall, caused by a sharp
object)
• intraocular foreign bodies, penetrating or perforating
• penetrating injury (entrance break; no exit break in eyewall)
• perforating injury (both entrance and exit breaks in eyewall)
80. Midface fracture
• Midface/Le Fort # (extended maxillary #)
I: low transverse maxillary (above teeth)
II: pyramidal maxillary-nasal/lacrimal/medial orbital
floor/rim
III: facial skeleton-base of skull detachM (orbital
floor/med/lat walls)