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CONCEPT, MAGNITUDE & MANAGEMENT OF COMMUNICAL &
NON COMMUNICAL COMMON OCULAR CONDITIONs
/DISORDERs SUCH AS TRACHOMA, CATARACT, DIABETIC
RETINOPATHY, VARIOUS CORNEAL INFECTIONs & CONJUNCTIVAL
INFECTIONs
Dr. Vinit Kumar
Cataract
Dr. Vinit
Classification
• A. Etiological classification
• I. Congenital and developmental cataract
• II. Acquired cataract
• 1. Senile cataract
• 2. Traumatic cataract
• 3. Complicated cataract
• 4. Metabolic cataract
• 5. Electric cataract
• 6. Radiational cataract
• 7. Toxic cataract e.g.,
• i Corticosteroid-induced cataract
• ii. Miotics-induced cataract
• iii. Copper (in chalcosis) and iron (in siderosis)
• induced cataract.
• 8. Cataract associated with skin diseases
• (Dermatogenic cataract).
• 9. Cataract associated with osseous diseases.
• 10. Cataract with miscellaneous syndromes e.g.,
• i. Dystrophica myotonica
• ii. Down's syndrome.
• iii. Lowe's syndrome
• iv. Treacher - Collin's syndrome
• B. Morphological classification
• 1. Capsular cataract. It involves the capsule and
• may be:
• i. Anterior capsular cataract
• ii. Posterior capsular cataract
• 2. Subcapsular cataract. It involves the
• superficial part of the cortex (just below the
• capsule) and includes:
• i. Anterior subcapsular cataract
• ii. Posterior subcapsular cataract
• 3. Cortical cataract. It involves the major part
• of the cortex.
• 4. Supranuclear cataract. It involves only the
• deeper parts of cortex (just outside the nucleus).
• 5. Nuclear cataract. It involves the nucleus of the
• crystalline lens.
• 6. Polar cataract. It involves the capsule and
• superficial part of the cortex in the polar region
• only and may be:
• i. Anterior polar cataract
• ii. Posterior polar cataract
• Etiology
• A. Factors affecting age of onset, type and
maturation of senile cataract.
1. Heredity. incidence, age of onset and maturation
of senile cataract
2. Ultraviolet irradiations- exposure to UV
irradiation from sunlight
3. Dietary factors- proteins, amino acids, vitamins
4. Dehydrational crisis.
5. Smoking
• B. Causes of presenile cataract. The term
presenile
• before 50 years of age
1. Heredity
2. Diabetes mellitus. Nuclear cataract progress
rapidly.
3. Myotonic dystrophy
4. Atopic dermatitis
• C. Mechanism of loss of transparency - different in
nuclear and cortical senile cataracts.
• 1. Cortical senile cataract.
• Nuclear senile cataract.
• the total protein content and distribution of
cations remain normal.
• Stages of maturation
• [A] Maturation of the cortical type of senile
• cataract
• 1. Stage of lamellar separation.
• demarcation of cortical fibres owing to their
separation by fluid.
• demonstrated by slit-lamp
• reversible.
• 2. Stage of incipient cataract. In this stage early
• detectable opacities with clear areas between
them are seen.
• (a) Cuneiform senile cortical cataract
• (b) Cupuliform senile cortical cataract
• 3. Immature senile cataract (ISC).
• Greyish white
• iris shadow is visible.
• 4. Mature senile cataract (MSC)
• 5. Hypermature senile cataract (HMSC).
• (a) Morgagnian hypermature cataract
• (b) Sclerotic type hypermature cataract
• [B] Maturation of nuclear senile cataract
• diffusely cloudy (greyish) or tinted (yellow to
black) due to deposition of pigments.
• amber, brown (cataracta brunescens) or black
(cataracta nigra)
• reddish (cataracta rubra) in colour
• Clinical features
• Symptoms.
• 1. Glare- intolerance of bright light; such as direct
sunlight or the headlights ofan oncoming motor
vehicle.
• 2. Uniocular polyopia (i.e., doubling or trebling of
• objects)
• 3. Coloured haloes
• 4. Black spots in front of eyes
5. Image blur, distortion of images and misty vision
6. Loss of vision
• second sight- improved near vision
• Nuclear sclerosis
• Signs.
1. Visual acuity testing.
2. Oblique illumination examination.
3. Test for iris shadow.
4.Distant direct ophthalmoscopic examination
5.Slit-lamp examination
• Grading of nucleus hardness on slit-lamp
biomicroscopy.
• Grade of Description of Colour of hardness of
nucleus
• Grade I Soft White or greenish yellow
• Grade II Soft-medium Yellowish
• Grade III Medium-hard Amber
• Grade IV Hard Brownish
• Grade V Ultrahard Blackish (rock-hard)
Immature senile cataract versus
nuclear sclerosis
• 1. Painless progressive loss of
vision
• 2. Greyish colour of lens
• 3. Iris shadow is present
• 4. Black spots against red
fundal glow observed on
distant direct
ophthalmoscopy
• 5. Slit-lamp examination
reveals area of cataractous
cortex
• 6. Visual acuity does not
improves on pin-hole testing
testing
• 1. Painless progressive loss of
vision
• 2. Greyish colour of lens
• 3. Iris shadow is absent
• 4. No black spots / glow are
observed on seen against red
glow in DDO
• 5. Slit-lamp examination
reveals clear lens
• 6.Visual acuity usually
improve on pin-hole
• Complications
• 1. Phacoanaphylactic uveitis.
• A hypermature cataract may leak lens proteins into anterior
chamber. These proteins may act as antigens and induce
antigenantibody reaction leading to uveitis.
• 2. Lens-induced glaucoma.
• It may occur by different mechanisms e.g., due to intumescent
lens (phacomorphic glaucoma) and leakage of proteins into the
anterior chamber from a hypermature cataract (phacolytic
glaucoma).
• 3. Subluxation or dislocation of lens
Cataract

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Cataract

  • 1. CONCEPT, MAGNITUDE & MANAGEMENT OF COMMUNICAL & NON COMMUNICAL COMMON OCULAR CONDITIONs /DISORDERs SUCH AS TRACHOMA, CATARACT, DIABETIC RETINOPATHY, VARIOUS CORNEAL INFECTIONs & CONJUNCTIVAL INFECTIONs Dr. Vinit Kumar
  • 3. Classification • A. Etiological classification • I. Congenital and developmental cataract • II. Acquired cataract • 1. Senile cataract • 2. Traumatic cataract • 3. Complicated cataract • 4. Metabolic cataract • 5. Electric cataract • 6. Radiational cataract
  • 4. • 7. Toxic cataract e.g., • i Corticosteroid-induced cataract • ii. Miotics-induced cataract • iii. Copper (in chalcosis) and iron (in siderosis) • induced cataract. • 8. Cataract associated with skin diseases • (Dermatogenic cataract). • 9. Cataract associated with osseous diseases. • 10. Cataract with miscellaneous syndromes e.g., • i. Dystrophica myotonica • ii. Down's syndrome. • iii. Lowe's syndrome • iv. Treacher - Collin's syndrome
  • 5. • B. Morphological classification • 1. Capsular cataract. It involves the capsule and • may be: • i. Anterior capsular cataract • ii. Posterior capsular cataract • 2. Subcapsular cataract. It involves the • superficial part of the cortex (just below the • capsule) and includes: • i. Anterior subcapsular cataract • ii. Posterior subcapsular cataract • 3. Cortical cataract. It involves the major part • of the cortex. • 4. Supranuclear cataract. It involves only the • deeper parts of cortex (just outside the nucleus). • 5. Nuclear cataract. It involves the nucleus of the • crystalline lens.
  • 6. • 6. Polar cataract. It involves the capsule and • superficial part of the cortex in the polar region • only and may be: • i. Anterior polar cataract • ii. Posterior polar cataract
  • 7. • Etiology • A. Factors affecting age of onset, type and maturation of senile cataract. 1. Heredity. incidence, age of onset and maturation of senile cataract 2. Ultraviolet irradiations- exposure to UV irradiation from sunlight 3. Dietary factors- proteins, amino acids, vitamins 4. Dehydrational crisis. 5. Smoking
  • 8. • B. Causes of presenile cataract. The term presenile • before 50 years of age 1. Heredity 2. Diabetes mellitus. Nuclear cataract progress rapidly. 3. Myotonic dystrophy 4. Atopic dermatitis
  • 9. • C. Mechanism of loss of transparency - different in nuclear and cortical senile cataracts. • 1. Cortical senile cataract.
  • 10. • Nuclear senile cataract. • the total protein content and distribution of cations remain normal.
  • 11. • Stages of maturation • [A] Maturation of the cortical type of senile • cataract • 1. Stage of lamellar separation. • demarcation of cortical fibres owing to their separation by fluid. • demonstrated by slit-lamp • reversible.
  • 12. • 2. Stage of incipient cataract. In this stage early • detectable opacities with clear areas between them are seen. • (a) Cuneiform senile cortical cataract • (b) Cupuliform senile cortical cataract • 3. Immature senile cataract (ISC). • Greyish white • iris shadow is visible.
  • 13. • 4. Mature senile cataract (MSC) • 5. Hypermature senile cataract (HMSC). • (a) Morgagnian hypermature cataract • (b) Sclerotic type hypermature cataract
  • 14. • [B] Maturation of nuclear senile cataract • diffusely cloudy (greyish) or tinted (yellow to black) due to deposition of pigments. • amber, brown (cataracta brunescens) or black (cataracta nigra) • reddish (cataracta rubra) in colour
  • 15. • Clinical features • Symptoms. • 1. Glare- intolerance of bright light; such as direct sunlight or the headlights ofan oncoming motor vehicle. • 2. Uniocular polyopia (i.e., doubling or trebling of • objects) • 3. Coloured haloes • 4. Black spots in front of eyes 5. Image blur, distortion of images and misty vision 6. Loss of vision • second sight- improved near vision • Nuclear sclerosis
  • 16. • Signs. 1. Visual acuity testing. 2. Oblique illumination examination. 3. Test for iris shadow. 4.Distant direct ophthalmoscopic examination 5.Slit-lamp examination
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  • 45. • Grading of nucleus hardness on slit-lamp biomicroscopy. • Grade of Description of Colour of hardness of nucleus • Grade I Soft White or greenish yellow • Grade II Soft-medium Yellowish • Grade III Medium-hard Amber • Grade IV Hard Brownish • Grade V Ultrahard Blackish (rock-hard)
  • 46. Immature senile cataract versus nuclear sclerosis • 1. Painless progressive loss of vision • 2. Greyish colour of lens • 3. Iris shadow is present • 4. Black spots against red fundal glow observed on distant direct ophthalmoscopy • 5. Slit-lamp examination reveals area of cataractous cortex • 6. Visual acuity does not improves on pin-hole testing testing • 1. Painless progressive loss of vision • 2. Greyish colour of lens • 3. Iris shadow is absent • 4. No black spots / glow are observed on seen against red glow in DDO • 5. Slit-lamp examination reveals clear lens • 6.Visual acuity usually improve on pin-hole
  • 47. • Complications • 1. Phacoanaphylactic uveitis. • A hypermature cataract may leak lens proteins into anterior chamber. These proteins may act as antigens and induce antigenantibody reaction leading to uveitis. • 2. Lens-induced glaucoma. • It may occur by different mechanisms e.g., due to intumescent lens (phacomorphic glaucoma) and leakage of proteins into the anterior chamber from a hypermature cataract (phacolytic glaucoma). • 3. Subluxation or dislocation of lens