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CONGENITAL CATARACT
BY: DR NIKITA JAISWAL
PG 1ST YEAR
IMS AND SUM HOSPITAL
THESE CATARACTS ARE PRESENT AT BIRTH OR THAT
DEVELOP WITHIN THE FIRST YEAR OF LIFE ARE
CALLED CONGENITAL /INFANTILE CATARACT.
FAIRLY OCCURRING IN 1 OF EVERY 2000 LIVE BIRTHS
-SOME LENS OPACITIES DO NOT PROGRESS AND ARE USUALLY
INSIGNIFICANT
-OTHERS CAN PRODUCE PROFOUND VISUAL IMPAIRMENT
CONGENITAL CATARACT -- UNILATERAL
-- BILATERAL
IN GENERAL THESE CONGENITAL CATARACT
1/3RD EXTENSIVE SYNDROMES
1/3RD INHERITED TRAIT
1/3RD UNDETERMINED CAUSE
BASED ON ETIOLOGY
• BILATERAL
• IDIOPATHIC
• HEREDITARY-AUTOSOMAL DOMINANT
-AUTOSOMAL RECESSIVE/X-LINKED
• GENETIC/METABOLIC DISEASE
-DOWN SYNDROME,MARFAN SYNDROME
-HYPOGLYCAEMIA,HYPOPARATHYROIDISM
-MYOTONIC DYSTROPHY
• MATERNAL INFECTION
-
RUBELLA,CMV,VARICELLA,SYPHILIS,TOXOPLASM
OSIS
• OCULAR ANOAMLIES-ANIRIDIA
• TOXIC –CORTICOSTEROIDS,RADIATION
• UNILATERAL
• IDIOPATHIC
• OCULAR ANOMALIES
-POST.LENTICONUS
-POST POLE TUMORS
-PERSISTENT FETAL VASCULATURE
• TRAUMATIC
• RUBELLA
• MASKED B/L CATARACT
CONGENITAL CATARACT IN A VARIETY OF MORPHOLOGIC
CONFIGURATION
LAMELLAR
POLAR
SUTURAL
CORONARY
CERULEAN
CAPSULAR
COMPLETE & MEMBRANOUS
LAMELLAR: IT IS ALSO KNOWN AS ZONULAR CATARACT
-THESE ARE AUTOSOMAL DOMINANT TRAIT
-EFFECTONVISUALACUITYWITHTHE SIZE & DENSITY OFTHE OPACITY
-THESE ARE OPACIFICATIONS OF SPECIFIC LAYERS/ZONES OF THE LENS
-VISIBLE AS AN OPACIFIED LAYER THAT SURROUNDS A CLEARER CENTER & IS ITSELF SURROUNDED BY A LAYER OF CLEAR CORTEX
-DISC SHAPED CONFIGURATION
-RIDERS-THESE ARE HORSESHOE SHAPED OPACITIES.
POLAR CATARACT:LENS OPACITY INVOLVES SUBCAPSULAR
CORTEX&CAPSULE OF ANTERIOR OR POSTERIOR POLE OF THE LENS.
ANT POLAR CAT.-IT IS A.D
SMALL,B/L SYMMETRIC,NON PROGRESSIVE OPACITIES THAT DO NOT IMPAIR VISION.
POST POLAR CAT.-IT PRODUCES MORE VISUAL IMPAIRMENT BECAUSE IT TENDS TO BE LARGER IN
SIZE
THEY MAY BE-FAMILIAL-USUALLY B/L
SPORADIC-OFTEN UNILATERAL
SUTURAL:THE SUTURAL OR STELLATE CATARACT IS AN OPACIFICATION OF THE “Y” SUTURES OF THE
FETAL NUCLEUS
-IT DOESNOT IMPAIR VISION
-THESE OPACITIES OFTEN HAVE BRANCHES OR KNOBS PROJECTING FROM THEM.
CORONARY: A.D
GROUP OF CLUB SHAPED CORTICAL OPACITIES THAT
ARE ARRANGED AROUND THE EQUATOR OF LENS LIKE A
CROWN
--THEY CANT BE SEEN UNTILL THE PUPILS ARE DILATED
--USUALLY DO NOT AFFECT THE VISUAL ACUITY
CERULEAN:SMALL BLUISH OPACITIES
LOCATED IN THE LENS CORTEX
--HENCE THEY ARE ALSO K/AS BLUE DOT
CATARACT
--NON-PROGRESSIVE
USUALLY DO NOT CAUSE VISUAL SYMPTOMS
CAPSULAR-THESE CATARACTS ARE SMALL
OPACIFICATIONOF THE LENS EPITHELIUM & ANTERIOR
LENS CAPSULE THAT SPARE THE CORTEX
COMPLETE- ALSO K/AS TOTAL CATARACT
ALL THE LENS FIBRES ARE OPACIFIED.
THE RED REFLEX IS TOTALLY OBSCURED
RETINA CANT BE SEEN BY DIRECT /INDIRECT OPH.
SPOKE LIKE FABRY’S DISEASE
VACUOLES MANNOSIDOSIS
DIABETES
MULTICOLOR FLECKS HYPOPARATHYRODISM
MYOTONIC DYSTROPHY
GREEN “SUNFLOWER” WILSON’S DISEASE
THIN DISCIFORM LOWE’S SYNDROME
LAMELLAR GALACTOSEMIA
HYPOGLYCEMIA
RUBELLA- CAUSED BY RUBELLA
VIRUS
CAN CAUSE FETAL DAMAGE
ESPECIALLY IF THE INFECTION
OCCURRS IN 1st TRIMESTER OF
PREGNANCY.
PEARLY WHITE
OPACIFICATIONS
ENTIRE LENS IS
OPACIFIED & CORTEX
MAY LIQUEFY
LIVE VIRUS PARTICLES
MAY BE RECOVERED AS
LATE AS 3 YRS AFTER
BIRTH
CATARACT REMOVAL MAY BE
COMPLICATED BY EXCESSIVE POST-
OP INFLAMMATION RELEASE BY
THESE LIVE VIRUS
MANAGEMENT
-DETAILED HISTORY
-CAREFUL CLINICAL EVALUATION
-BASIC ASSESSMENT OF CHILD’S VISION
-IOP
-FUNDUS EXAMINATION UNDER DILATATION
-B-SCAN FOR POSTERIOR SEGMENT
A-SCAN TO MEASURE AXIAL LENGTH OF BOTH
THE EYES
TIME OF SURGERY
SURGICAL TECHNIQUE
TYPE OF OPTICAL REHABILITATION
POST-OP MANAGEMENT OF AMBLYOPIA
CONGENITAL CATARACTS:LABORATORY EVALUATION
RESULT POSSIBLE DIAGNOSIS
+ REDUCING SUBSTANCE
AMINOACIDURIA
HEMATURIA ,
PROTEINURIA
‘’MALTESE CROSS”
FIGURES
GALACTOKINASE DEFICIENCY
LOWE’S SYNDROME
FABRY’S DISEASE
ERYTHROCYTE
ENZYMES
GLUCOSE
TORCH titres,VDRL test
CALCIUM,
PHOSPHORUS
GALACTOKINASE DEFICIENCY
HYPER/HYPO GLYCEMIA
RUBELLA.TOXOPLASMOSIS,CMV,H
ERPES,SYPHILIS,HYPOPARATHYRO
IDISM
urine
Blood
CONGENITAL CATARACT:DIAGNOSTIC EVALUATION
CONDITION LABORATORY TEST
GALACTOSEMIA URINE REDUCING SUBSTANCE
RUBELLA ANTIBODY TITERS
SYPHILIS VDRL TEST
HYPOPARATHYROIDISM SERUM
CALCIUM,PHOSPHORUS,ALKALINE
PHOSPHATASE
WILSON’S DISEASE SERUM CERULOPLASMIN
HYPERGLYCEMIA/HYPOGLYCEMIA BLOOD GLUCOSE
FABRY’S DISEASE URINE”MALTESE CROSS”(POLARIZED
IIGHT)
LOWE’S SYNDROME URINE AMINO ACIDS
TREATMENT IS INDICATED ONLY IF
THE VISION IS CONSIDERABLY
IMPAIRED
--MEDICAL
--SURGICAL
MEDICAL
• IF THE PATIENT HAS SMALL
OPACITIES IN WHOM THE RED
REFLEX IS NOT CONSIDERED
SIGNIFICANTLY IMPAIRED
• IN SOME PATIENTS WITH SMALL
CENTRAL OPACITY{3 MM OR LESS}
• PATCHING
• DILATATION WITH TROPICAMIDE
0.5%OR CYCLOPENTOLATE 0.5%
• IF VISION IMPROVES 6/18 THEN NO
SURGERY REQUIRED
• WHO REQUIRES CHRONIC
CYCLOPLEGIC AGENTS TO MAINTAIN
DILATION & IN VISUAL ACUITY HAS
IMPROVED –SURGICAL OPTICAL
IRIDECTOMY SHOULD BE
CONSIDERED.
Classic eg.-peter anomaly –central cataract + corneal opacity but has a clear peripheral lens &
cornea
optical iridectomy better than corneal transplant & cataract extraction.
SURGICAL
• IF DENSE UNILATERAL OR BILATERAL CRITICAL PERIOD
APPEARS TO BE WITHIN THE FIRST 2 MONTHS.
• FIRST 6 WKS –PRECORTICAL STAGE
6-8 WKS-CORTICAL STAGE
• UNILATERAL CAT.--OPERATED ON BY AGE 6 WKS
• BILATERAL CAT.—SLIGHTLY LARGER WINDOW 8--10 WKS
BILATERAL PARTIAL-MAY
NOT REQUIRE SURGERY
MONITOR LENS OPACITIES
AND VISUAL FUNCTION &
INTERVENE LATER IF
VISION DETERIOTES
UNILATERAL DENSE- URGENT Sx
FOLLOWED BY AGGRESSIVE anti AMBLYOPIA
therapy
IF DETECTED AFTER 16 WKS OF AGE THEN
PROGNOSIS IS VERY POOR
PARTIAL UNILATERAL-CAN
USUALLY BE OBSERVED OR
TREATED NON SURGICALLY
WITH PUPILLARY DILATATION
AND CONTRALATERAL
OCCLUSION
HISTORICAL LANDMARKS
BEFORE 1960 – MOST CONGENITAL CATARACTS WERE
REMOVED BY AN EXTRACAPSULAR TECHNIQUE.
IN 1960- SCHEIE INTRODUCED DISCISSION & ASPIRATION
TECHNIQUE
IN 1972-MACHEMAR ET AL DEVELOPED A NEW INSTRUMENT
{VISC} VITREOS INFUSION SUCTION CUTTER
CURRENT SURGICAL TECHNIQUE: VITRECTOMY CUTTING
INSTRUMENTS, IRRIGATION/ASPIRATION,PHACO OR SOME
COMBINATION OF THIS TECHNIQUE
CURRENT SURGICAL TECHNIQUE
• INCISION_ USUALLY THE INCISIONS WE TAKE ARE SELF HEALING BUT IN
CHILDREN THE CORNEAL TISSUE IS LESS LIKELY TO HEAL THUS SUTURE
CLOSURE OF TUNNEL WOUNDS RE ADVISED.
• ANTERIOR CAPSULORHEXIS:A 1.4% SODIUM HYLURONATE IS RECOMMENDED
FOR PAEDIATRIC SURGERY TO MAINTAIN THE A.C STABILITY ABD INCREASED
VITREOUS UPTHRUST.THE ANT. CAPSULOTOMY SHAPE,SIZE AND INTEGRITY
ARE IMPORTANT TO LONG TERM CENTRATION OF IOL.{THE FUGO PLASMA
BLADE IS A NEW TOOL FOR PERFORMING ANT CAPSULOTOMY IN CHILDREN.
• HYDRODISSECTION:TO ENSURE MAXIMUM REMOVAL OF LENS CORTEX AND
LENS EPITHELIAL CELLS, MAY BE A SINGLE OR MULTIPLE SITE ---------
PRERFORMED BY INJECTING RL OR BALANCED SALT SOLUTION INN 2 ML
DISPOSABLE SYRINGE AVOIDED IN CATARACT WITH POST. LENTICONUS OR
POST POLAR CATARACT
CATARACT REMOVAL-LENS MATERIAL MAY BE REMOVED WITH
PHACOASPIRATIONOR IRRIGATION AND ASPIRATION.
POSTERIOR CONT.. CURVILINEAR CAPSULOREXHIS{PCCC}: WE PERFORM THIS
AT THE AGE LESS THAN 6-8 YEARS & ANY CHILDREN WITH NYSTAGMUS WHERE
FUTURE YAG MAY BE DIFFICULT
IT IS DONE TO PREVENT THE PCO AS IT IS AMBLYOGENIC AND THE SURGEON IS
DEFEATED IN ACHIEVING THE TARGET
USE OF HIGH VISCOSITY VISCOELASTIC HELPS TO ACHIEVE PCCC.THE
DESIRABLE SIZE OF POST RHEXIS IS 3-3.5 MM.
ANT.VITRECTOMY.
IOL LENS IMPLANTATION: CAPSULAR BAG IMPLANTATION IS THE BEST CHOICE AS
IOL & UVEAL TISSUE CONTACT IS LESSER& CENTRATION IS ACHIEVED{AIOS
ADVICE IT TO BE DONE BY PAEDIATRIC OPHTHALMOLOGISTS}
IOL SELECTION: PMMA IOLS WERE THE ONLY CHOICE
THE SINGLE PIECE HYDROPHOBIC ACRYLIC IOLS ARE IDEAL FOR IMPLANTATION
NOW MULTIFOCAL IOL ARE GAINING GROUNDS AS IT GIVES THE GOOD
COMPATIBILITY WITH NEAR AND FAR VISION OF CHILD
LIMITATIONS :IOL POWER PREDICTABILITY
VISUAL DEVELOPMENT
INCISION CLOSURE
Birth 34.4
0-1yr 28.7
1-2yr 26.4
2-3yr 23.0
3-4yr 22.1
4-5yr 20.9
5-6yr 19.5
INTRAOCULAR LENSES POWER TO ACHIEVE
EMMETROPIA
UNDERCORRECTING BIOMETRY BY 10% IN 2-8
YRS
FOR CHILDREN YOUNGER THAN 2 YRS UNDER
CORRECT BY 20%
1 year +6D
2 year +5 D
3 year +4 D
4 year +3 D
5 year +2 D
6 year +1 D
7year PLANO
8 year -1 TO -2 D
21MM 22.00D
20MM 24.00D
19MM 26.00D
18MM 27.00D
17MM 28.00D
AXIAL
LENGTH
POWER
VISUAL REHABILITATION
1. GLASSES {APHAKIC SPECTACLES}
2. CONTACT LENS
3. EPIKERATOPHAKIA
4. INTRAOCULAR LENS
APHAKIC SPECTACLES
ADVANTAGES: THEY CAN EASILY BE
UPDATED TO MATCH THE RAPIDLY
CHANGING REFRACTIONS IN YOUNG
CHILDREN
DISADVANTAGES:LENS THIKNESS & WEIGHT
AS WELL AS OPTICAL DISTORTIONS
IN NEW BORNS LENS POWER OF +24 TO
+26D
Which can be accomplished with very thick
bubble shaped lens in older children the thinner
high ensity aphakic specs can be used .
Patching of normal eye is necessary when the child
is using aphakic specs
CONTACT
LENS
MOST COMMON METHOD
FOR BOTH BILATERAL AND
UNILATERAL APHAKIA.
ADVANTAGES:OPTICAL QUALITY IS
GOOD *SOME CL CAN BE WORN
THROUGHOUT 24 HOURS A DAY
DISADVANTAGES-
-RELATIVELY THICK
-CAN BE WASHED OR RUBBED
OUT EASILY
-TIDIOUS FOR PARENTS
-ASSOCIATED WITH CORNEAL
COMPLICATIONS AS INFECTIONS
& ULCERS
LENS : SILICONE – HIGH O2 PERMEABILITY
CHILDREN YOUNGER THAN 6 MONTHS-36 D
Gas permeable lens can also be used
EPIKERATOPHAKI
A
IN 1980’S FIRST PERFORMED
BECAUSE OF PROBLEM IN
SPECS & C.L’S
PROCEDURE:- REMOVING A CENTRAL
HALF THICKNESS OF THE CORNEA &
THEN SUTURING PREDETERMINED
CORNEAL DONOR TISSUE.
• DISADVANTAGES:PERSISTENT
HAZINESSESPECIALLY AT THE
INTERFACE BETWEEN HOST & THE
GRAFT THAT COULD TAKE UP AN
YEAR TO CLEAR.
• LATE MYOPIA & ASTIGMATISM IN MANY
EYES
THANK YOU

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Congenital cataract & ITS MANAGEMENT

  • 1. CONGENITAL CATARACT BY: DR NIKITA JAISWAL PG 1ST YEAR IMS AND SUM HOSPITAL
  • 2. THESE CATARACTS ARE PRESENT AT BIRTH OR THAT DEVELOP WITHIN THE FIRST YEAR OF LIFE ARE CALLED CONGENITAL /INFANTILE CATARACT. FAIRLY OCCURRING IN 1 OF EVERY 2000 LIVE BIRTHS -SOME LENS OPACITIES DO NOT PROGRESS AND ARE USUALLY INSIGNIFICANT -OTHERS CAN PRODUCE PROFOUND VISUAL IMPAIRMENT
  • 3. CONGENITAL CATARACT -- UNILATERAL -- BILATERAL IN GENERAL THESE CONGENITAL CATARACT 1/3RD EXTENSIVE SYNDROMES 1/3RD INHERITED TRAIT 1/3RD UNDETERMINED CAUSE
  • 4. BASED ON ETIOLOGY • BILATERAL • IDIOPATHIC • HEREDITARY-AUTOSOMAL DOMINANT -AUTOSOMAL RECESSIVE/X-LINKED • GENETIC/METABOLIC DISEASE -DOWN SYNDROME,MARFAN SYNDROME -HYPOGLYCAEMIA,HYPOPARATHYROIDISM -MYOTONIC DYSTROPHY • MATERNAL INFECTION - RUBELLA,CMV,VARICELLA,SYPHILIS,TOXOPLASM OSIS • OCULAR ANOAMLIES-ANIRIDIA • TOXIC –CORTICOSTEROIDS,RADIATION • UNILATERAL • IDIOPATHIC • OCULAR ANOMALIES -POST.LENTICONUS -POST POLE TUMORS -PERSISTENT FETAL VASCULATURE • TRAUMATIC • RUBELLA • MASKED B/L CATARACT
  • 5. CONGENITAL CATARACT IN A VARIETY OF MORPHOLOGIC CONFIGURATION LAMELLAR POLAR SUTURAL CORONARY CERULEAN CAPSULAR COMPLETE & MEMBRANOUS
  • 6. LAMELLAR: IT IS ALSO KNOWN AS ZONULAR CATARACT -THESE ARE AUTOSOMAL DOMINANT TRAIT -EFFECTONVISUALACUITYWITHTHE SIZE & DENSITY OFTHE OPACITY -THESE ARE OPACIFICATIONS OF SPECIFIC LAYERS/ZONES OF THE LENS -VISIBLE AS AN OPACIFIED LAYER THAT SURROUNDS A CLEARER CENTER & IS ITSELF SURROUNDED BY A LAYER OF CLEAR CORTEX -DISC SHAPED CONFIGURATION -RIDERS-THESE ARE HORSESHOE SHAPED OPACITIES.
  • 7. POLAR CATARACT:LENS OPACITY INVOLVES SUBCAPSULAR CORTEX&CAPSULE OF ANTERIOR OR POSTERIOR POLE OF THE LENS. ANT POLAR CAT.-IT IS A.D SMALL,B/L SYMMETRIC,NON PROGRESSIVE OPACITIES THAT DO NOT IMPAIR VISION. POST POLAR CAT.-IT PRODUCES MORE VISUAL IMPAIRMENT BECAUSE IT TENDS TO BE LARGER IN SIZE THEY MAY BE-FAMILIAL-USUALLY B/L SPORADIC-OFTEN UNILATERAL
  • 8. SUTURAL:THE SUTURAL OR STELLATE CATARACT IS AN OPACIFICATION OF THE “Y” SUTURES OF THE FETAL NUCLEUS -IT DOESNOT IMPAIR VISION -THESE OPACITIES OFTEN HAVE BRANCHES OR KNOBS PROJECTING FROM THEM.
  • 9. CORONARY: A.D GROUP OF CLUB SHAPED CORTICAL OPACITIES THAT ARE ARRANGED AROUND THE EQUATOR OF LENS LIKE A CROWN --THEY CANT BE SEEN UNTILL THE PUPILS ARE DILATED --USUALLY DO NOT AFFECT THE VISUAL ACUITY
  • 10. CERULEAN:SMALL BLUISH OPACITIES LOCATED IN THE LENS CORTEX --HENCE THEY ARE ALSO K/AS BLUE DOT CATARACT --NON-PROGRESSIVE USUALLY DO NOT CAUSE VISUAL SYMPTOMS
  • 11. CAPSULAR-THESE CATARACTS ARE SMALL OPACIFICATIONOF THE LENS EPITHELIUM & ANTERIOR LENS CAPSULE THAT SPARE THE CORTEX COMPLETE- ALSO K/AS TOTAL CATARACT ALL THE LENS FIBRES ARE OPACIFIED. THE RED REFLEX IS TOTALLY OBSCURED RETINA CANT BE SEEN BY DIRECT /INDIRECT OPH.
  • 12. SPOKE LIKE FABRY’S DISEASE VACUOLES MANNOSIDOSIS DIABETES MULTICOLOR FLECKS HYPOPARATHYRODISM MYOTONIC DYSTROPHY GREEN “SUNFLOWER” WILSON’S DISEASE THIN DISCIFORM LOWE’S SYNDROME LAMELLAR GALACTOSEMIA HYPOGLYCEMIA
  • 13. RUBELLA- CAUSED BY RUBELLA VIRUS CAN CAUSE FETAL DAMAGE ESPECIALLY IF THE INFECTION OCCURRS IN 1st TRIMESTER OF PREGNANCY. PEARLY WHITE OPACIFICATIONS ENTIRE LENS IS OPACIFIED & CORTEX MAY LIQUEFY LIVE VIRUS PARTICLES MAY BE RECOVERED AS LATE AS 3 YRS AFTER BIRTH CATARACT REMOVAL MAY BE COMPLICATED BY EXCESSIVE POST- OP INFLAMMATION RELEASE BY THESE LIVE VIRUS
  • 15. -DETAILED HISTORY -CAREFUL CLINICAL EVALUATION -BASIC ASSESSMENT OF CHILD’S VISION -IOP -FUNDUS EXAMINATION UNDER DILATATION -B-SCAN FOR POSTERIOR SEGMENT A-SCAN TO MEASURE AXIAL LENGTH OF BOTH THE EYES
  • 16. TIME OF SURGERY SURGICAL TECHNIQUE TYPE OF OPTICAL REHABILITATION POST-OP MANAGEMENT OF AMBLYOPIA
  • 17. CONGENITAL CATARACTS:LABORATORY EVALUATION RESULT POSSIBLE DIAGNOSIS + REDUCING SUBSTANCE AMINOACIDURIA HEMATURIA , PROTEINURIA ‘’MALTESE CROSS” FIGURES GALACTOKINASE DEFICIENCY LOWE’S SYNDROME FABRY’S DISEASE ERYTHROCYTE ENZYMES GLUCOSE TORCH titres,VDRL test CALCIUM, PHOSPHORUS GALACTOKINASE DEFICIENCY HYPER/HYPO GLYCEMIA RUBELLA.TOXOPLASMOSIS,CMV,H ERPES,SYPHILIS,HYPOPARATHYRO IDISM urine Blood
  • 18. CONGENITAL CATARACT:DIAGNOSTIC EVALUATION CONDITION LABORATORY TEST GALACTOSEMIA URINE REDUCING SUBSTANCE RUBELLA ANTIBODY TITERS SYPHILIS VDRL TEST HYPOPARATHYROIDISM SERUM CALCIUM,PHOSPHORUS,ALKALINE PHOSPHATASE WILSON’S DISEASE SERUM CERULOPLASMIN HYPERGLYCEMIA/HYPOGLYCEMIA BLOOD GLUCOSE FABRY’S DISEASE URINE”MALTESE CROSS”(POLARIZED IIGHT) LOWE’S SYNDROME URINE AMINO ACIDS
  • 19. TREATMENT IS INDICATED ONLY IF THE VISION IS CONSIDERABLY IMPAIRED --MEDICAL --SURGICAL
  • 20. MEDICAL • IF THE PATIENT HAS SMALL OPACITIES IN WHOM THE RED REFLEX IS NOT CONSIDERED SIGNIFICANTLY IMPAIRED • IN SOME PATIENTS WITH SMALL CENTRAL OPACITY{3 MM OR LESS} • PATCHING • DILATATION WITH TROPICAMIDE 0.5%OR CYCLOPENTOLATE 0.5% • IF VISION IMPROVES 6/18 THEN NO SURGERY REQUIRED • WHO REQUIRES CHRONIC CYCLOPLEGIC AGENTS TO MAINTAIN DILATION & IN VISUAL ACUITY HAS IMPROVED –SURGICAL OPTICAL IRIDECTOMY SHOULD BE CONSIDERED. Classic eg.-peter anomaly –central cataract + corneal opacity but has a clear peripheral lens & cornea optical iridectomy better than corneal transplant & cataract extraction.
  • 21. SURGICAL • IF DENSE UNILATERAL OR BILATERAL CRITICAL PERIOD APPEARS TO BE WITHIN THE FIRST 2 MONTHS. • FIRST 6 WKS –PRECORTICAL STAGE 6-8 WKS-CORTICAL STAGE • UNILATERAL CAT.--OPERATED ON BY AGE 6 WKS • BILATERAL CAT.—SLIGHTLY LARGER WINDOW 8--10 WKS
  • 22. BILATERAL PARTIAL-MAY NOT REQUIRE SURGERY MONITOR LENS OPACITIES AND VISUAL FUNCTION & INTERVENE LATER IF VISION DETERIOTES UNILATERAL DENSE- URGENT Sx FOLLOWED BY AGGRESSIVE anti AMBLYOPIA therapy IF DETECTED AFTER 16 WKS OF AGE THEN PROGNOSIS IS VERY POOR PARTIAL UNILATERAL-CAN USUALLY BE OBSERVED OR TREATED NON SURGICALLY WITH PUPILLARY DILATATION AND CONTRALATERAL OCCLUSION
  • 24. BEFORE 1960 – MOST CONGENITAL CATARACTS WERE REMOVED BY AN EXTRACAPSULAR TECHNIQUE. IN 1960- SCHEIE INTRODUCED DISCISSION & ASPIRATION TECHNIQUE IN 1972-MACHEMAR ET AL DEVELOPED A NEW INSTRUMENT {VISC} VITREOS INFUSION SUCTION CUTTER CURRENT SURGICAL TECHNIQUE: VITRECTOMY CUTTING INSTRUMENTS, IRRIGATION/ASPIRATION,PHACO OR SOME COMBINATION OF THIS TECHNIQUE
  • 25. CURRENT SURGICAL TECHNIQUE • INCISION_ USUALLY THE INCISIONS WE TAKE ARE SELF HEALING BUT IN CHILDREN THE CORNEAL TISSUE IS LESS LIKELY TO HEAL THUS SUTURE CLOSURE OF TUNNEL WOUNDS RE ADVISED. • ANTERIOR CAPSULORHEXIS:A 1.4% SODIUM HYLURONATE IS RECOMMENDED FOR PAEDIATRIC SURGERY TO MAINTAIN THE A.C STABILITY ABD INCREASED VITREOUS UPTHRUST.THE ANT. CAPSULOTOMY SHAPE,SIZE AND INTEGRITY ARE IMPORTANT TO LONG TERM CENTRATION OF IOL.{THE FUGO PLASMA BLADE IS A NEW TOOL FOR PERFORMING ANT CAPSULOTOMY IN CHILDREN. • HYDRODISSECTION:TO ENSURE MAXIMUM REMOVAL OF LENS CORTEX AND LENS EPITHELIAL CELLS, MAY BE A SINGLE OR MULTIPLE SITE --------- PRERFORMED BY INJECTING RL OR BALANCED SALT SOLUTION INN 2 ML DISPOSABLE SYRINGE AVOIDED IN CATARACT WITH POST. LENTICONUS OR POST POLAR CATARACT
  • 26. CATARACT REMOVAL-LENS MATERIAL MAY BE REMOVED WITH PHACOASPIRATIONOR IRRIGATION AND ASPIRATION. POSTERIOR CONT.. CURVILINEAR CAPSULOREXHIS{PCCC}: WE PERFORM THIS AT THE AGE LESS THAN 6-8 YEARS & ANY CHILDREN WITH NYSTAGMUS WHERE FUTURE YAG MAY BE DIFFICULT IT IS DONE TO PREVENT THE PCO AS IT IS AMBLYOGENIC AND THE SURGEON IS DEFEATED IN ACHIEVING THE TARGET USE OF HIGH VISCOSITY VISCOELASTIC HELPS TO ACHIEVE PCCC.THE DESIRABLE SIZE OF POST RHEXIS IS 3-3.5 MM. ANT.VITRECTOMY. IOL LENS IMPLANTATION: CAPSULAR BAG IMPLANTATION IS THE BEST CHOICE AS IOL & UVEAL TISSUE CONTACT IS LESSER& CENTRATION IS ACHIEVED{AIOS ADVICE IT TO BE DONE BY PAEDIATRIC OPHTHALMOLOGISTS}
  • 27. IOL SELECTION: PMMA IOLS WERE THE ONLY CHOICE THE SINGLE PIECE HYDROPHOBIC ACRYLIC IOLS ARE IDEAL FOR IMPLANTATION NOW MULTIFOCAL IOL ARE GAINING GROUNDS AS IT GIVES THE GOOD COMPATIBILITY WITH NEAR AND FAR VISION OF CHILD LIMITATIONS :IOL POWER PREDICTABILITY VISUAL DEVELOPMENT INCISION CLOSURE
  • 28. Birth 34.4 0-1yr 28.7 1-2yr 26.4 2-3yr 23.0 3-4yr 22.1 4-5yr 20.9 5-6yr 19.5 INTRAOCULAR LENSES POWER TO ACHIEVE EMMETROPIA
  • 29. UNDERCORRECTING BIOMETRY BY 10% IN 2-8 YRS FOR CHILDREN YOUNGER THAN 2 YRS UNDER CORRECT BY 20% 1 year +6D 2 year +5 D 3 year +4 D 4 year +3 D 5 year +2 D 6 year +1 D 7year PLANO 8 year -1 TO -2 D 21MM 22.00D 20MM 24.00D 19MM 26.00D 18MM 27.00D 17MM 28.00D AXIAL LENGTH POWER
  • 30. VISUAL REHABILITATION 1. GLASSES {APHAKIC SPECTACLES} 2. CONTACT LENS 3. EPIKERATOPHAKIA 4. INTRAOCULAR LENS
  • 31. APHAKIC SPECTACLES ADVANTAGES: THEY CAN EASILY BE UPDATED TO MATCH THE RAPIDLY CHANGING REFRACTIONS IN YOUNG CHILDREN DISADVANTAGES:LENS THIKNESS & WEIGHT AS WELL AS OPTICAL DISTORTIONS IN NEW BORNS LENS POWER OF +24 TO +26D Which can be accomplished with very thick bubble shaped lens in older children the thinner high ensity aphakic specs can be used . Patching of normal eye is necessary when the child is using aphakic specs
  • 32. CONTACT LENS MOST COMMON METHOD FOR BOTH BILATERAL AND UNILATERAL APHAKIA. ADVANTAGES:OPTICAL QUALITY IS GOOD *SOME CL CAN BE WORN THROUGHOUT 24 HOURS A DAY DISADVANTAGES- -RELATIVELY THICK -CAN BE WASHED OR RUBBED OUT EASILY -TIDIOUS FOR PARENTS -ASSOCIATED WITH CORNEAL COMPLICATIONS AS INFECTIONS & ULCERS LENS : SILICONE – HIGH O2 PERMEABILITY CHILDREN YOUNGER THAN 6 MONTHS-36 D Gas permeable lens can also be used
  • 33. EPIKERATOPHAKI A IN 1980’S FIRST PERFORMED BECAUSE OF PROBLEM IN SPECS & C.L’S PROCEDURE:- REMOVING A CENTRAL HALF THICKNESS OF THE CORNEA & THEN SUTURING PREDETERMINED CORNEAL DONOR TISSUE. • DISADVANTAGES:PERSISTENT HAZINESSESPECIALLY AT THE INTERFACE BETWEEN HOST & THE GRAFT THAT COULD TAKE UP AN YEAR TO CLEAR. • LATE MYOPIA & ASTIGMATISM IN MANY EYES