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Cataracts: Classification
Cataracts: Classification
Cataracts: Classification
Classification
1. Based on age of onset
• Congenital,
• Infantile,
• Juvenile,
• Adult,
• Presenile,
• Senile.
2. Based on site of opacity
• Capsular,
• Subcapsular,
• Cortical,
• Supranuclear,
• Nuclear,
• Polar,
• Total.
3. Based on degree of opacity/morphology
• Incipient,
• Immature, (partial/scattered opacification)
• Mature, (completely opaque lens)
• Intumescent, (lens is swollen due to imbibition of water)
• Hypermature, (anterior capsule becomes wrinkled and cortex a soft pultaceous
mass, may produce phacolytic glaucoma)
• Morgagnian. (complete liquefaction of cortex and nucleus sinks inferiorly).
4. Based on acquisition
• Congenital,
• Acquired.
5. Based on Aetiology
• Ageing/senility (MCC),
• Traumatic (2nd MCC),
• Secondary (due to an independent disease process e.g. DM, myotonic
dystrophy, atopic dermatitis, etc),
• Radiation,
• Ocular/Complicated (e.g. uveitis, corneal ulcer, retinitis pigmentosa, etc.),
• Toxic (from drugs - including Amiodarone, Busulphan, Chlorpromazine,
Dexamethasone)
• Associated with various syndromes (Down’s, Lowe’s, Miller’s, Rothman’s,
Werner’s).
Investigations
• CBC
• ESR
• Hep B & C
• Blood urea + creatinine
• Blood sugar
• Lipid profile
• BP
• ECG
• Biometry (keratometry + A-scan)
• B-scan
• Pachymetry
CONGENITAL CATARACT
The opacification of the crystalline lens, present at birth, or that may occur in early
childhood.
Inheritance
• Most commonly (2/3) autosomal dominant inheritance. Those inherited this way are usually
bilateral.
• Unilateral cataracts are more sporadic, without family history or systemic disease.
Types
• Capsular (anterior/posterior) cataract
• Polar (anterior and posterior, involving the central part of the capsule) cataract
• Sutural (following the anterior and posterior Y sutures),
• Nuclear (confined to the embryonic/fetal nucleus),
• Lamellar/Zonular (opacities affecting a particular lamella of the lens)
• Most common type (40-50%),
• Involves circular lamella of the lens both anteriorly and posteriorly which appears as a
sharply demarcated opacity with clear lens fibres within and around it,
• Results from an insult to the developing fibres during embryonic development,
• Usually bilateral & AD.
• Central Oil Droplet cataract
• Characteristic of galactosemia,
• The nucleus and deep cortex are opacified.
• Coronary/Supranuclear cataract
• Commonly occurs at puberty, and is a common form,
• Cataract is in the deep cortex and surrounds the nucleus,
• Central (axial) portion of the lens is clear so vision is unaffected,
• Autosomal dominant.
• Punctate/Blue-dot (multiple, small, opaque, scattered stationery dots seen, that don’t affect
vision) cataract
• Membranous (when the lens material is absorbed, leaving behind a thin membrane) cataract,
• Complete cataract
• Very common,
• Dense white nuclear cataract.
Aetiology
Maternal Causes
• Infections e.g. Rubella (20% of congenital cataracts),
• Intrauterine hypoxia/Placental insufficiency e.g. eclampsia,
• Radiation exposure,
• Drugs e.g. corticosteroids,
• Endocrine disorders e.g. DM.
Fetal Causes
• Heredity accounts for approx 25% of cases, mostly AD but can also be AR or X-linked,
• Chromosomal disorders e.g. Down’s,
• Ocular anomalies e.g. aniridia, persistent hyperplastic primary vitreous,
• Metabolic disorders e.g. galactosemia,
• Trauma, e.g. forceps delivery.
Unknown causes account for approx 30-50% of cases.
Signs
• Whitish reflex in pupillary area (Leukocoria)
• Abnormal eye movements
• Reduced vision
• Squint, usually convergent
• Nystagmus
• Slit lamp exam reveals the type of cataract
D/Ds of Leukocoria
• Congenital cataract
• Retinoblastoma
• Retrolental fibroplasia
• Anterior persistent hyperplastic primary vitreous (APHPV)
• Coat's Disease
• Endophthalmitis
• Toxocarial granuloma
Ocular Assessment
• Density and morphology of cataract are noted based on vision.
• In partial cataract, fundus examination and retinoscopy is done.
• In total cataract, B-scan ultrasonography is useful to assess the posterior segment of the eye to
rule out associated retinoblastoma or retinal detachment.
• A-scan ultrasonography is done to record and compare the axial lengths of the two eyes.
• IOP is noted.
Lab Investigations
• Urinalysis - to check for galactosemia or Lowe’s syndrome.
• Serum biochemistry - to check FBS, calcium, phosphorus, galactokinase and RBC transferase.
• Serological test - to check antibody titres for TORCH infections.
Treatment
The surgical technique used depends on the type and density of the cataract, and age of the patient.
• Lens aspiration
• Lensectomy
Post-Operative Complications
• Posterior capsule opacification due to proliferation of lens epithelium
• Secondary membrane
• Secondary glaucoma
• Amblyopia, which is treated with spectacles or contact lenses or intraocular implantation.
SENILE CATARACT
Symptoms
• Painless gradual deterioration of vision
• Glare
• Monocular diplopia/polyopia
• Coloured halos
• Change in refractive power (myopic/hypermetropic shift)
• Worsening of vision during daytime
• Secondary lens induced glaucoma is also possible presentation.
Signs
• Decreased visual acuity
• Opacification of the lens
Diagnosis
• Simple torch
• DDO
• Slit lamp examination
Complications
• Phacomorphic glaucoma
• Phacolytic glaucoma
• Phacoantigenic Uveitis
• Dislocation of lens
• Incarceration into the pupil causing pupillary block glaucoma.
Cataract Extraction
Extra Capsular Cataract Extraction (ECCE)
Removal of lens nucleus and cortex through an opening in the anterior capsule. Posterior capsule
stays intact.
Types
1. Phacoemulsification: most common method of the cataract extraction. Lens is fragmented
(emulsified) by ultrasound vibrations and aspirated with probe of phacoemulsifier. *small
incision so rapid healing, less astigmatism, early visual rehabilitation
2. Femtosecond Laser (FSL): glass laser generates focused ultrashort pulse creating
cavitation and bubbles within the tissue. *it is better than the hand-held surgical tool
3. Manual small extraction surgery: cataract is removed through a suture less, self-sealing
sclero corneal tunnel incision
4. Conventional extracapsular cataract extraction: it is the removal of cataract through
limbal or corneal section. Anterior capsulotomy, nucleus is removed intact and the residual
cortical matter is aspirated
Anesthesia
Local Anesthesia
Topical (surface)
o Xylocaine, proparacaine, tetracaine, lidocaine gel. Adequate but less effective
o Can cause endothelial and epithelial toxicity allergy and surface keratopathy
Retrobulbar block
o Anesthetic is injected behind the eyeball in the muscle cone near the ciliary body
o Ciliary nerves, ciliary ganglion, oculomotor nerve and abducens nerve is anesthetized
Subtenon block
o 5mm from the limbus, injected through an incision in the conjunctiva and sub-tenon capsule
o Chemosis and subconjunctival complications are common
Peribulbar block
o Injected to the peripheral spaces of the orbit
o Orbital compression is placed for 15 mins which allows the anesthetic to infiltrate into the
retro bulbar capsule
Phacoemulsification
Self-sealing clear corneal or sclerocornal incision using a keratome
Anterior chamber is maintained by injecting viscoelastic substance
A second incision is made at right angle to the first incision
Anterior capsulotomy (capsulorhexis) circular
Hydrodissection is performed with water to separate the capsule from the cortex
Hydrodelineation is performed to separate the epinucleus from nucleus
Nucleus is rotated within the capsular bag
Nucleus is cracked using a chopper
Aspiration
Capsular bag is inflated with viscoelastic substance and foldable IOL is inserted through the same
incision or rigid IOL is inserted by enlarging the incision
No suturing required, pad and bandage
Aphakia