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BUPHTHALMOS
(EVALUATION & TREATMENT)
PRESENTER:
DR.ANKIT AHIR
DR.PRAKHAR CHAUDHARY
MODERATOR:
DR.SHAHINUR TAIYAB
CASE 1
21-06-2019
A 7 month old MALE child ,brought to Paediatric Ophthalmology OPD at
SSN with –
Complain of – watering from left eye (OS) associated with mucopurulent
discharge since last 7 months.
HISTORY OF UNKNOWN EYE DROP INSTILLATION IN LEFT EYE (OS) FOR 3
MONTHS.
OD OS
VISION CSM CSM
LIDS N N
CONJUNCTIVA N N
CORNEA NORMAL NORMAL
COVER TEST ORTHO ORTHO
ANTERIOR CHAMBER NORMAL NORMAL
IRIS NORMAL NORMAL
PUPIL NORMAL NORMAL
LENS CLEAR CLEAR
IOP(FINGER TENSION) NORMAL NORMAL
DISC CDR 0.2 CDR 0.5
DIAGNOSIS : LEFT EYE (OS)- NASOLACRIMAL DUCT OBSTRUCTION
- LARGE DISC
ACTION PLAN : CONJUCTIVAL SWAB FOR SENSITIVITY AND GLAUCOMA CLINIC OPINION
21-06-2019
Case seen by Glaucoma clinic Doctor.
O/E –
Cornea – Clear
Pupil – Dilated
IOP (TONOPEN) OD- 36 OS- 43
ACTION PLAN : OBSERVE FOR SIX WEEKS AND REVIEW AFTER THAT
DIAGNOSIS : OU- NASOLACRIMAL DUCT OBSTRUCTION
- ASYMMETRIC CUP
28-06-2019
Case seen by Pediatric ophthalmologist and based on culture sensitivity
report , the child was started on –
TOBRAMYCIN E/D - 3 TIMES / DAY X 2 weeks
TOBRAMYCIN E/O - 2 TIMES / DAY X 2 weeks
CRIGGLER MASSAGE
ADVICED TO REVIEW AFTER 1 MONTH
30-07-2019
Case seen by Paediatric Ophthalmologist first, and noticed improvement in
symptoms, so was advised to continue CRIGGLER MASSAGE and to Review in
Glaucoma clinic.
GLAUCOMA CLINIC –
O/E –
Cornea – Clear, Appears larger
Pupil – Dilated
No haab’s striae
IOP (TONOPEN) OD- 21 OS- 41/43
DIAGNOSIS : OU- NASOLACRIMAL DUCT OBSTRUCTION
- ASSYMETRIC CUP
OS - CONGENITAL GLAUCOMA
- MEGALOCORNEA
ADVICE: EUA (SEVOFLURANE) +/-
REFRACTION,CCT,BIOMETRY,FUNDUS PHOTO +/- SYRINGING
16-09-2019 OD OS
HEAD CIRCUMFERENCE --- ---
FACE NAD NAD
ORBIT NORMAL NORMAL
LID NORMAL NORMAL
CONJUCTIVA NORMAL NORMAL
CORNEA CLEAR
12 MM
CLEAR
13MM
ANTERIOR CHAMBER DEEP DEEP
IRIS NORMAL NORMAL
PUPIL NORMAL NORMAL
LENS CLEAR CLEAR
IOP (TONOPEN) 17mm of Hg 33mm of Hg
GONIOSCOPY Anterior insertion of iris
with prominent iris process
Anterior insertion of iris
with prominent iris process
FUNDUS 0.5 VCDR ,PINK, HEALTHY 0.2 VCDR,PINK,HEALTHY
KERATOMETRY K1- 38.25
K2- 40.75 *66°
K1- 36.25
K2- 38.25 *27°
ADVICE: GONIOTOMY ON TABLE
Patient was started on –
Tobramycin E/D - 6 TIMES / DAY x 7 DAYS
- 4 TIMES / DAY x 7 DAYS
- 2 TIMES / DAY x 7 DAYS
17-09-2019 ( FIRST POST –OP)
O/E - Clear cornea with white and quite eye
- No abnormal lid swelling noted
ADVICE: EUA , REFRACTION AND IDO AFTER 1 MONTH
19-09-2019 ( SECOND POST OP)
O/E - Clear cornea with white and quite eye
- Minimal conjunctival congestion
- No abnormal lid swelling noted
IOP (Tonopen ) – left eye (OS) - 10 mm Hg
ADVICE: EUA , REFRACTION AND IDO AFTER 1 MONTH
18-10-2019
OD OS
FACE NAD NAD
ORBIT NORMAL NORMAL
LID LACERATION – UPPER EYE LID NORMAL
CONJUCTIVA NORMAL NORMAL
CORNEA ABRASSION ON RIGHT SIDE CLEAR
ANTERIOR CHAMBER DEEP DEEP
IRIS NORMAL NORMAL
PUPIL NORMAL NORMAL
LENS CLEAR CLEAR
IOP (TONOPEN) 9mm of Hg 13/14mm of Hg
GONIOSCOPY Anterior insertion of iris with
prominent iris process
Anterior insertion of iris with
prominent iris process
FUNDUS 0.4:1 0.9:1
REFRACTION -1.50 D sph -1.50 D sph
OS- SUTURE REMOVED
ADVICE: REPEAT EUA AFTER 6 MONTHS, VISUAL REHABILITATION IN PEDIATRIC OPHTHALMOLOGY CLINIC
ADV: TOBRAMYCINE E/D-
TDS x 7 DAYS
DEFINITION
Buphthalmos is a term used to describe the abnormal enlargement of
an infant’s eye secondary to elevated IOP.
In extreme cases,these eyes are vulnerable to lens-subluxationand
rupture even with even minor trauma.
Isolated congenital glaucoma
1. Isolated maldevelopment of the trabecular meshwork
2. No other developmental ocular anomalies or ocular diseases that can raise IOP.
3. Recognized with in first month
Infantile glaucoma
1. Synonymous with congenital glaucoma.
2. 1 month to 3 years
Juvenile glaucoma
1. Primary glaucoma occurring later in child hood or early adulthood
2. 3 years to 35 years
Three years of age is generally taken as the division between infantile and
juvenile glaucoma.
After this age the eye no longer expands in response to raised intraocular
pressure.
 Juvenile glaucoma doesn’t havecorneal enlargement or Haabstriae
EPIDEMIOLOGY
1. 1 in 10000births
2. 50%isolated congenital
3. 60%diagnosed by 6 months and 80%by 1 year
4. 65%affected are males
5. 70%bilateral involvement
CLINICALFEATURES
Classic Triad ……symptoms
1. Epiphora
2. Photophobia
3. Blepharospasm
Other symptoms are
cloudy cornea , red eye, enlarged cornea or eye , irritability , poor vision and pain
In older children, astigmatism, progressive axial myopia cause symptomatic decreased VA and
refractive amblyopia.
SIGNS
IOP
Cornealoedema Haabsstriae
1. Breaks in Descmet’s membrane –as
cornea stretches- acute localized edema
& deposition of new basement
membrane into hyalineridges.
2. Horizontal, curvilinear and parallel to
the limbus in the peripheralcornea.
Haab’s striae
SIGNS
IOP
buphthalmos Sclerathin
andblue
SIGNS
IOP
Flatand
subluxatedlens iridodonesis
1. Anterior chamber becomesdeep
2. Optic nerve cupping
◦ Develop early and rapidly
◦ Reversalof cupping with IOPreduction
EVALUATION
Examination in clinic
Observe
1. Cornea Size and Clarity
2. degree of tearing/photophobia
3. Any discharge /swelling –sac area
4. Iris/pupil Hypoplasia/corectopia andAniridia
EVALUATION UNDERGA
OTHER USEFUL DIAGNOSTIC TESTS:
 CCT
 Ultrasound (Axial Length Measurement / B
Scan)
 Optic Nerve Photography
 Refraction
1. Vision Testing (Acuity and Visual field)
2. Tonometry ( After Induction And Before Intubation )
3. External Examination
4. Anterior Segment Examination
5. Corneal Diameter Measurement
6. Gonioscopy
7. Optic Nerve &Fundus Examination
VISION TESTING :
 Varies with patient’s age and Cognitive function
 Central , maintained fixation behaviour and absent Nystagmus – Infants
 Optotype Testing with Proper Refraction – Older Children
VISUAL FIELD TESTING:-
 Difficult in children with Nystgmus and in Young Children.
 Children with associated Neurological condition ( sturgeweber
syndrome) may have underlying homonymous hemifield vision loss
independent of Glaucoma.
EXTERNAL EXAMINATION:
 Important to identify evidence of other associated abnormalities –
o Neurofibromatosis
o Facial haemangioma
o Photophobia
o Nasolacrimal duct obstruction
o Facial features s/o Metabolic disorder , Connective tissue disorder, Chromosomal
abnormalities.
 -Exclude other causes of epiphora, photophobia and blepharospasm.
 -Most common cause of epiphora in new-born and infant – congenital NLDO
 -Others :- Conjunctivitis (infectious, chemical)
Corneal epithelial defect/ abrasion
Keratitis
Inflamed ant segment (uveitis, trauma)
CORNEAL EXAMINATION :
REF: SHIELD’S TEXTBOOK OF GLAUCOMA – 6TH
EDITION
Horizontal diameter from white to white……..
The vertical diameter is fallaciously lowered by
encroachment of sclera at the superior limbus
Also Document
Corneal edema/ clouding, breaks in Descemet’s membrane (Haab’s striae)
Other causes of corneal clouding
Sclerocornea
Tears in D membrane
Ulcers
Metabolic disease
Peters anomaly
Endothelial dystrophies
Dystrophy e.g congenital hereditary stromal dystrophy
TONOMETRY:
1. IOPshould be measured using Perkin’shand-held applanation tonometer or
tonopen
2. Most anesthetic agents reduceIOP
3. Should be measured early during earliest possible moments afteranesthesia
induction, before intubation.
4. AsymmetricIOPmore suggestiveof abnormality than B/Lborderline IOP
Chloralhydrate isthe agent doesn’t haveanyeffect onIOP,so best…..
ANTERIOR SEGMENT EXAMINATION
(BIO-MICROSCOPY) :
 Assess corneal size, symmetry, clarity.
 Bio microscopy ( handheld slit lamp) adds improved examination and detail of
corneal architecture specially Haab’s striae.
 IOP normalised  Descemet's tear repair  corneal edema clears , but
linear corneal opacities persists  associated with reduced endothelial count
 Permanent scaring  Refractive errors.
 Limbus may be dramatically stretched and thinned by ocular stretching in
infant eye with Glaucoma and Anterior chamber deepens.
GONIOSCOPY:
Koeppe (14-16mm) lens provides surgeon with appropriate view of the
angle.- Infants
Indirect Goniocopy – Zeiss or Sussman lens – Older Children.
In normal newborn
1. Iris inserts posterior to scleral spur.
2. TM appears more translucent than that of adult.
In primary congenital glaucoma
1. Anterior insertion of iris (flat or concave) directly into TM.
2. Surface of TM has stippled appearance and meshwork may appear thicker
3. Occasionally loops of blood vessels from major arterial circle may be seen
(LOCH NESS monster phenomenon)
OPTICNERVE & FUNDUS:
1. C:D ratio >0.3 and asymmetry are suggestive evidence of glaucoma.
2. The infant glaucomatous cup is more often round , steep walled central &
surrounded by uniform pink NRR. Tends to enlarge circumferentially with
progression of glaucoma.
3. Cupping is reversible
REFRACTION :-
 Enlargement of globe due to elevated IOP , creates myopic shift in refractive
error  Amblyopia , if significant anisometropia is present.
 Haab’s striae  significant Astigmatism  Amblyopia ,especially in unilateral /
asymmetric cases.
ULTRASONOGRAPHY:-
 Important ,because stabilisation and even reduction in axial length can occur
in enlarged eye with stable IOP.
 In aphakic eyes of infants after filtration surgery OR implantation of Glaucoma
drainage device – axial length changes within days after a significant IOP
reduction.
 Glaucoma filtration surgery – size of implant
 B- scan helps in confirming Retinal status in eyes with opaque media -- aids in
assessing patency of glaucoma drainage devices when bleb is not seen.
CENTRAL CORNEAL THICKNESS:-
 CHILDREN ( 6- 23 MONTHS ) – 540 µm
 OLDER CHILDREN – 550- 560 µm
 White people thinner CCT than Black people.
 CCT is thinner in children with congenital glaucoma than other children.
 Eyes with Aniridia, Aphakia -- thicker CCT
 Importance of CCT in evaluation & management in children with Glaucoma
is still uncertain…...
IMAGING TECHNIQUES:-
FUNDUS PHOTOGRAPHY -
OPTICAL COHERENCE TOPOGRAPHY (OCT) –
 Documentation
 OCT – measure thickness of peripapillary nerve fibre layer ,
Macular area ,
Volume
 Newly developed Handheld Spectral- domain OCT may be used, in uncoop
or children who can not assessed by standard technology.
DIFFERENTIAL DIAGNOSIS:
EXCESSIVE
WATERING
LARGE CORNEA TEAR IN DESCEMET’S
MEMBRANE
CORNEAL
OPACIFICATION
• NLD OBSTRUCTION
• RED EYE
• UVEITIS
• KERATITIS
• MEGALOCORNEA
• HIGH MYOPIA
• FORCEPS DELIVERY
- VERTICAL & OBLIQUE
• HAAB’S STRIAE
- HORIZONTAL & CONCENTRIC
• DEVELOPMENTAL-
SCLEROCORNEA
• DYSTROPHIES
• CHORISTOMAS
• EDEMA DUR TO BIRTH
TRAUMA
• IUI
• METABOLIC D/S
THANK YOU..!!!

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Congenital glaucoma -Evaluation

  • 1. BUPHTHALMOS (EVALUATION & TREATMENT) PRESENTER: DR.ANKIT AHIR DR.PRAKHAR CHAUDHARY MODERATOR: DR.SHAHINUR TAIYAB
  • 2. CASE 1 21-06-2019 A 7 month old MALE child ,brought to Paediatric Ophthalmology OPD at SSN with – Complain of – watering from left eye (OS) associated with mucopurulent discharge since last 7 months. HISTORY OF UNKNOWN EYE DROP INSTILLATION IN LEFT EYE (OS) FOR 3 MONTHS.
  • 3. OD OS VISION CSM CSM LIDS N N CONJUNCTIVA N N CORNEA NORMAL NORMAL COVER TEST ORTHO ORTHO ANTERIOR CHAMBER NORMAL NORMAL IRIS NORMAL NORMAL PUPIL NORMAL NORMAL LENS CLEAR CLEAR IOP(FINGER TENSION) NORMAL NORMAL DISC CDR 0.2 CDR 0.5 DIAGNOSIS : LEFT EYE (OS)- NASOLACRIMAL DUCT OBSTRUCTION - LARGE DISC ACTION PLAN : CONJUCTIVAL SWAB FOR SENSITIVITY AND GLAUCOMA CLINIC OPINION
  • 4. 21-06-2019 Case seen by Glaucoma clinic Doctor. O/E – Cornea – Clear Pupil – Dilated IOP (TONOPEN) OD- 36 OS- 43 ACTION PLAN : OBSERVE FOR SIX WEEKS AND REVIEW AFTER THAT DIAGNOSIS : OU- NASOLACRIMAL DUCT OBSTRUCTION - ASYMMETRIC CUP
  • 5. 28-06-2019 Case seen by Pediatric ophthalmologist and based on culture sensitivity report , the child was started on – TOBRAMYCIN E/D - 3 TIMES / DAY X 2 weeks TOBRAMYCIN E/O - 2 TIMES / DAY X 2 weeks CRIGGLER MASSAGE ADVICED TO REVIEW AFTER 1 MONTH
  • 6. 30-07-2019 Case seen by Paediatric Ophthalmologist first, and noticed improvement in symptoms, so was advised to continue CRIGGLER MASSAGE and to Review in Glaucoma clinic. GLAUCOMA CLINIC – O/E – Cornea – Clear, Appears larger Pupil – Dilated No haab’s striae IOP (TONOPEN) OD- 21 OS- 41/43 DIAGNOSIS : OU- NASOLACRIMAL DUCT OBSTRUCTION - ASSYMETRIC CUP OS - CONGENITAL GLAUCOMA - MEGALOCORNEA ADVICE: EUA (SEVOFLURANE) +/- REFRACTION,CCT,BIOMETRY,FUNDUS PHOTO +/- SYRINGING
  • 7. 16-09-2019 OD OS HEAD CIRCUMFERENCE --- --- FACE NAD NAD ORBIT NORMAL NORMAL LID NORMAL NORMAL CONJUCTIVA NORMAL NORMAL CORNEA CLEAR 12 MM CLEAR 13MM ANTERIOR CHAMBER DEEP DEEP IRIS NORMAL NORMAL PUPIL NORMAL NORMAL LENS CLEAR CLEAR IOP (TONOPEN) 17mm of Hg 33mm of Hg GONIOSCOPY Anterior insertion of iris with prominent iris process Anterior insertion of iris with prominent iris process FUNDUS 0.5 VCDR ,PINK, HEALTHY 0.2 VCDR,PINK,HEALTHY KERATOMETRY K1- 38.25 K2- 40.75 *66° K1- 36.25 K2- 38.25 *27°
  • 8. ADVICE: GONIOTOMY ON TABLE Patient was started on – Tobramycin E/D - 6 TIMES / DAY x 7 DAYS - 4 TIMES / DAY x 7 DAYS - 2 TIMES / DAY x 7 DAYS
  • 9. 17-09-2019 ( FIRST POST –OP) O/E - Clear cornea with white and quite eye - No abnormal lid swelling noted ADVICE: EUA , REFRACTION AND IDO AFTER 1 MONTH 19-09-2019 ( SECOND POST OP) O/E - Clear cornea with white and quite eye - Minimal conjunctival congestion - No abnormal lid swelling noted IOP (Tonopen ) – left eye (OS) - 10 mm Hg ADVICE: EUA , REFRACTION AND IDO AFTER 1 MONTH
  • 10. 18-10-2019 OD OS FACE NAD NAD ORBIT NORMAL NORMAL LID LACERATION – UPPER EYE LID NORMAL CONJUCTIVA NORMAL NORMAL CORNEA ABRASSION ON RIGHT SIDE CLEAR ANTERIOR CHAMBER DEEP DEEP IRIS NORMAL NORMAL PUPIL NORMAL NORMAL LENS CLEAR CLEAR IOP (TONOPEN) 9mm of Hg 13/14mm of Hg GONIOSCOPY Anterior insertion of iris with prominent iris process Anterior insertion of iris with prominent iris process FUNDUS 0.4:1 0.9:1 REFRACTION -1.50 D sph -1.50 D sph OS- SUTURE REMOVED ADVICE: REPEAT EUA AFTER 6 MONTHS, VISUAL REHABILITATION IN PEDIATRIC OPHTHALMOLOGY CLINIC ADV: TOBRAMYCINE E/D- TDS x 7 DAYS
  • 11. DEFINITION Buphthalmos is a term used to describe the abnormal enlargement of an infant’s eye secondary to elevated IOP. In extreme cases,these eyes are vulnerable to lens-subluxationand rupture even with even minor trauma.
  • 12. Isolated congenital glaucoma 1. Isolated maldevelopment of the trabecular meshwork 2. No other developmental ocular anomalies or ocular diseases that can raise IOP. 3. Recognized with in first month Infantile glaucoma 1. Synonymous with congenital glaucoma. 2. 1 month to 3 years Juvenile glaucoma 1. Primary glaucoma occurring later in child hood or early adulthood 2. 3 years to 35 years
  • 13. Three years of age is generally taken as the division between infantile and juvenile glaucoma. After this age the eye no longer expands in response to raised intraocular pressure.  Juvenile glaucoma doesn’t havecorneal enlargement or Haabstriae
  • 14. EPIDEMIOLOGY 1. 1 in 10000births 2. 50%isolated congenital 3. 60%diagnosed by 6 months and 80%by 1 year 4. 65%affected are males 5. 70%bilateral involvement
  • 15. CLINICALFEATURES Classic Triad ……symptoms 1. Epiphora 2. Photophobia 3. Blepharospasm Other symptoms are cloudy cornea , red eye, enlarged cornea or eye , irritability , poor vision and pain In older children, astigmatism, progressive axial myopia cause symptomatic decreased VA and refractive amblyopia.
  • 17. 1. Breaks in Descmet’s membrane –as cornea stretches- acute localized edema & deposition of new basement membrane into hyalineridges. 2. Horizontal, curvilinear and parallel to the limbus in the peripheralcornea. Haab’s striae
  • 20. 1. Anterior chamber becomesdeep 2. Optic nerve cupping ◦ Develop early and rapidly ◦ Reversalof cupping with IOPreduction
  • 21. EVALUATION Examination in clinic Observe 1. Cornea Size and Clarity 2. degree of tearing/photophobia 3. Any discharge /swelling –sac area 4. Iris/pupil Hypoplasia/corectopia andAniridia
  • 22. EVALUATION UNDERGA OTHER USEFUL DIAGNOSTIC TESTS:  CCT  Ultrasound (Axial Length Measurement / B Scan)  Optic Nerve Photography  Refraction 1. Vision Testing (Acuity and Visual field) 2. Tonometry ( After Induction And Before Intubation ) 3. External Examination 4. Anterior Segment Examination 5. Corneal Diameter Measurement 6. Gonioscopy 7. Optic Nerve &Fundus Examination
  • 23. VISION TESTING :  Varies with patient’s age and Cognitive function  Central , maintained fixation behaviour and absent Nystagmus – Infants  Optotype Testing with Proper Refraction – Older Children VISUAL FIELD TESTING:-  Difficult in children with Nystgmus and in Young Children.  Children with associated Neurological condition ( sturgeweber syndrome) may have underlying homonymous hemifield vision loss independent of Glaucoma.
  • 24. EXTERNAL EXAMINATION:  Important to identify evidence of other associated abnormalities – o Neurofibromatosis o Facial haemangioma o Photophobia o Nasolacrimal duct obstruction o Facial features s/o Metabolic disorder , Connective tissue disorder, Chromosomal abnormalities.  -Exclude other causes of epiphora, photophobia and blepharospasm.  -Most common cause of epiphora in new-born and infant – congenital NLDO  -Others :- Conjunctivitis (infectious, chemical) Corneal epithelial defect/ abrasion Keratitis Inflamed ant segment (uveitis, trauma)
  • 25. CORNEAL EXAMINATION : REF: SHIELD’S TEXTBOOK OF GLAUCOMA – 6TH EDITION
  • 26. Horizontal diameter from white to white…….. The vertical diameter is fallaciously lowered by encroachment of sclera at the superior limbus
  • 27. Also Document Corneal edema/ clouding, breaks in Descemet’s membrane (Haab’s striae) Other causes of corneal clouding Sclerocornea Tears in D membrane Ulcers Metabolic disease Peters anomaly Endothelial dystrophies Dystrophy e.g congenital hereditary stromal dystrophy
  • 28. TONOMETRY: 1. IOPshould be measured using Perkin’shand-held applanation tonometer or tonopen 2. Most anesthetic agents reduceIOP 3. Should be measured early during earliest possible moments afteranesthesia induction, before intubation. 4. AsymmetricIOPmore suggestiveof abnormality than B/Lborderline IOP
  • 29.
  • 30. Chloralhydrate isthe agent doesn’t haveanyeffect onIOP,so best…..
  • 31. ANTERIOR SEGMENT EXAMINATION (BIO-MICROSCOPY) :  Assess corneal size, symmetry, clarity.  Bio microscopy ( handheld slit lamp) adds improved examination and detail of corneal architecture specially Haab’s striae.  IOP normalised  Descemet's tear repair  corneal edema clears , but linear corneal opacities persists  associated with reduced endothelial count  Permanent scaring  Refractive errors.  Limbus may be dramatically stretched and thinned by ocular stretching in infant eye with Glaucoma and Anterior chamber deepens.
  • 32. GONIOSCOPY: Koeppe (14-16mm) lens provides surgeon with appropriate view of the angle.- Infants Indirect Goniocopy – Zeiss or Sussman lens – Older Children. In normal newborn 1. Iris inserts posterior to scleral spur. 2. TM appears more translucent than that of adult. In primary congenital glaucoma 1. Anterior insertion of iris (flat or concave) directly into TM. 2. Surface of TM has stippled appearance and meshwork may appear thicker 3. Occasionally loops of blood vessels from major arterial circle may be seen (LOCH NESS monster phenomenon)
  • 33. OPTICNERVE & FUNDUS: 1. C:D ratio >0.3 and asymmetry are suggestive evidence of glaucoma. 2. The infant glaucomatous cup is more often round , steep walled central & surrounded by uniform pink NRR. Tends to enlarge circumferentially with progression of glaucoma. 3. Cupping is reversible
  • 34. REFRACTION :-  Enlargement of globe due to elevated IOP , creates myopic shift in refractive error  Amblyopia , if significant anisometropia is present.  Haab’s striae  significant Astigmatism  Amblyopia ,especially in unilateral / asymmetric cases.
  • 35. ULTRASONOGRAPHY:-  Important ,because stabilisation and even reduction in axial length can occur in enlarged eye with stable IOP.  In aphakic eyes of infants after filtration surgery OR implantation of Glaucoma drainage device – axial length changes within days after a significant IOP reduction.  Glaucoma filtration surgery – size of implant  B- scan helps in confirming Retinal status in eyes with opaque media -- aids in assessing patency of glaucoma drainage devices when bleb is not seen.
  • 36. CENTRAL CORNEAL THICKNESS:-  CHILDREN ( 6- 23 MONTHS ) – 540 µm  OLDER CHILDREN – 550- 560 µm  White people thinner CCT than Black people.  CCT is thinner in children with congenital glaucoma than other children.  Eyes with Aniridia, Aphakia -- thicker CCT  Importance of CCT in evaluation & management in children with Glaucoma is still uncertain…...
  • 37. IMAGING TECHNIQUES:- FUNDUS PHOTOGRAPHY - OPTICAL COHERENCE TOPOGRAPHY (OCT) –  Documentation  OCT – measure thickness of peripapillary nerve fibre layer , Macular area , Volume  Newly developed Handheld Spectral- domain OCT may be used, in uncoop or children who can not assessed by standard technology.
  • 38. DIFFERENTIAL DIAGNOSIS: EXCESSIVE WATERING LARGE CORNEA TEAR IN DESCEMET’S MEMBRANE CORNEAL OPACIFICATION • NLD OBSTRUCTION • RED EYE • UVEITIS • KERATITIS • MEGALOCORNEA • HIGH MYOPIA • FORCEPS DELIVERY - VERTICAL & OBLIQUE • HAAB’S STRIAE - HORIZONTAL & CONCENTRIC • DEVELOPMENTAL- SCLEROCORNEA • DYSTROPHIES • CHORISTOMAS • EDEMA DUR TO BIRTH TRAUMA • IUI • METABOLIC D/S