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Examination of
Eye
-RESHMA ANN MATHEW
 External Examination of eye
 Fundus Examination
 Visual field examination
External Examination
 Examination of-
• Iris
• Pupil
• Lens
 Intra-ocular pressure (IOP)
Examination of IRIS
 COLOUR –
 Light blue or green in Caucasians and Dark brown in
orientals
 Heterochromia iridium- different colour
of 2 iris
 Heterochromia iridis-different colour of sectors of the
same iris
It occurs due to involved iris being lighter or darker than the
normal
 Iris lighter than normal-
• congenital heterochromia,
• atrophic patches in chronic uveitis,
• metastatic carcinoma
 Iris darker than normal-
• Iris naevi-appear as freckles
• ocular melanocytosis,
• haemosiderosis,
• siderosis bulbi,
• retained iris foreign body,
• malignant melanoma of iris
• lymphoma
 PATTERN OF NORMAL IRIS
o Pattern occurs due to presence of collarette, crypts and radial
striations on its anterior surface
o It is disturbed in
i. Acute iridocyclitis-muddy iris
ii. Healed iridocyclitis-atrophy of iris
 PERSISTENT PUPILLARY MEMBRANE
o It is seen as abnormal congenital tags of iris tissue
adherent to the collarette area
 SYNECHIAE
o It is the adhesion of iris to other intraocular structures
o Types-
i. Anterior- in Adherent leucoma
ii. Posterior- in Iridocyclitis; can be total, annular or segmental
 IRIDODONESIS
o It is the tremulousness(trembling) of the iris
o Seen in aphakia and subluxation of lens (since posterior
support is lost)
 NODULES ON THE IRIS SURFACE
o Seen in granulomatous uveitis, melanoma,
tuberculoma and gumma of iris
 RUBEOSIS IRIDIS
o New vessel formation on the iris
o Seen in diabetic retinopathy, central retinal vein occlusion,
chronic uveitis, chronic retinal detachment, retinoblastoma
 GAP OR HOLE IN THE IRIS
o May be due to congenital coboloma or due to iridectomy(surgical
coboloma)
o Iridodialysis-separation of iris from ciliary body
 ANIRIDIA OR IRIDEREMIA
o Complete absence of iris
o Rare congenital condition
 IRIS CYST
o In patients using strong miotic drops, it may be seen
in the pupillary margin
Examination of PUPIL
 NUMBER
o Normal: 1 pupil
o Rarely: more than 1 pupil (polycoria)
 LOCATION
o Normal: almost centre of the iris, slightly nasal
o Rarely: congenitally eccentric (corectopia)
 SIZE
o Normal: 3-4mm depending upon illumination
o It may be abnormally small (miosis) or large(mydriasis)
o Anisocoria- It is a condition where there is difference
between the size of two pupils
o Causes of Miosis
• Effect of local miotic drugs-Parasympathomimetic drugs
• Iridocyclitis-narrow, irregular, non-reacting pupil
• Head injury-pontine haemorrhage
• Senile rigid miotic pupil
• Due to effect of strong light
• During sleep pupil is pinpoint
o Causes of Mydriasis
• Effect of topical sympathomimetic drugs-Adrenaline,
phenylephrine
• Effect of topical parasympatholytic drugs-Atropine,
homatropine, tropicamide, cyclopentolate
• Acute congestive glaucoma
• Absolute glaucoma
 SHAPE
o Normal: circular
o Irregular narrow- iridocyclitis
o Festooned- effect of mydriatics on posterior
segment synechiae
o Vertically oval/pear shaped/updrawn- postoperatively (due to
incarceration of iris or vitreous in the wound at 12 o’clock postion)
 COLOUR
o Normal: greyish black
o Aphakia-jet black
o Immature senile cortical cataract-greyish white
o Mature cortical cataract-pearly white
o Hypermature cataract-milky white
o Cataracta brunescens-brown
o Cataracta nigra-brownish black
o Leucocoria-white reflex in pupil
o Glaucoma-greenish hue
o Iridocyclitis-dirty white exudates
 PUPILLARY REACTIONS
o Direct light reflex-
Normal: pupil reacts briskly and constricts
o Consensual light reflex
Normal: contralateral pupil should also constrict
o Swinging flash light test-(when RAPD is suspected)
• Normal: both pupils constrict equally and the pupil to which
light is transferred remains tightly constricted
• RAPD present: affected pupil will dilate when flash light is
moved from normal eye to abnormal eye. This is called
Marcus Gunn Pupil
o Near reflex- Pupil constricts while looking at a near object
Abnormal pupillary reactions are seen in
i. Amaurotic pupil
ii. Efferent pathway defect
iii. Wernicke’s hemianopic pupil
iv. Marcus Gunn pupil
v. Argyll Robertson pupil
vi. Tonic pupil
Examination of LENS
 Can be examined using oblique illumination, slit lamp
biomicroscopy and distant direct ophthalmoscopy with FULLY
DILATED PUPILS
 POSITION
o Normal: patellar fossa by the zonules
o Dislocation of lens: lens not present in its normal position
i. Anterior dislocation-present in anterior chamber
ii. Posterior dislocation-present in vitreous cavity either
floating(LENSA NUTANS) or fixed to the retina(LENSA
FIXATE)
o Subluxation of lens-lens is partially displaced from its position
• Causes-trauma, marfan’s syndrome, homocystinuria
o Aphakia-absence of lens
• It is diagnosed by
i. jet black pupil, deep anterior chamber, empty patellar fossa by slit
lamp biomicroscopy
ii. hypermetropic eye on ophthalmoscopy, retinoscopy
iii. ABSENCE of 3rd and 4th purkinje images
o Pseudophakia-
• When posterior chamber IOL is present, it is diagnosed by black
pupil, deep anterior chamber, shining reflexes (from anterior surface of
IOL) and PRESENCE of all the four Purkinje images
 SHAPE
o Normal: biconvex structure, on slit lamp-optical section shows
embryonic, foetal, infantile and adult nuclei, cortex and capsule
o Spherophakia-spherical
o Lenticonus anterior-anterior cone shaped bulge (Alport
syndrome)
o Lenticonus posterior-posterior cone shaped bulge
o Coloboma of lens-Notch in the lens
 Colour
o Normal: In young age, it is almost clear or gives a faint blue hue
o Old age-greyish white (mistaken to be cataract)
o CORTICAL cataract- greyish white (immature), pearly white
(mature), milky white (hypermature)
o NUCLEAR cataract-amber, brown or black
o Cataractous lens with siderosis bulbi-rusty (orange)
 TRANSPARENCY
o Normal: transparent
o Any opacity in the lens is called CATARACT
o Complicated cataract-breadcrumb appearance (polychromatic
lustre)
o True diabetic cataract-snow flake opacities
o Wilson’s disease-sunflower cataract
o Concussion injury of lens-rosette shaped cataract
 DEPOSITS ON ANTERIOR SURFACE OF LENS-
o Vossius ring-in blunt trauma
o Pigmented clumps-iridocyclitis
o Dirty white exudates-uveitis, endophthalmitis
o Rusty deposits-siderosis bulbi (deposition of ferrous ions)
o Greenish deposits-chalcosis(deposition of copper ions)
 PURKINJE IMAGES TEST
o It WAS used to diagnose mature cataract and aphakia
o Normal-
• When a strong beam of light is shown to the eye,
4 images (purkinje images) are formed from the
four different reflecting surfaces [ant & post
surfaces of cornea and lens]
o Mature cataract-4th image is absent (post surface of lens)
o Aphakia-3rd and 4th are absent (ant & post surface of lens)
Intraocular pressure
 Digital tonometry-
o IOP raised-fluctuation produced is feeble or absent, eyeball-firm to hard
o IOP low-eyeball-soft
 Indentation and Applanation tonometers are frequently used
 Normal IOP=10-21mm Hg
 Hypotony- IOP < 10mm Hg
• Causes-ruptured globe, retinal/choroidal detachment, postoperative wound
leak
 Glaucoma suspected when IOP>21mm Hg
Fundus Examination
 To diagnose diseases of vitreous, optic nerve head, retina and choroid
 For thorough examination, pupils to be dilated with 5%phenylephrine and/or
1%tropicamide eye drops
Techniques of Fundus Examination
1) Ophthalmoscopy
a) Distant direct ophthalmoscopy
b) Direct ophthalmoscopy
c) Indirect ophthalmoscopy
2) Slit lamp bio-microscopic examination by
a) Indirect slit lamp bio-microscopy
b) Hruby lens bio-microscopy
c) Contact lens bio-microscopy
 OCULAR MEDIA
o Normal- transparent
o Opacities-black against red glow (distant direct
ophthalmoscopy)
• Causes-corneal opacity, lenticular opacity, vitreous opacity
 OPTIC DISC
o SIZE: normal-1.5mm; hypermetropes-smaller;
myopes-larger
o SHAPE: normal-circular; high astigmatism-oblong
o MARGINS: normal-well defined; blurring of margins-
papilloedema, papillitis
o COLOUR: normal-pinkish with central pallor;
Hyperaemia-papilloedema
Pale-partial optic atrophy
Chalky white-primary optic atrophy
Yellow waxy-consecutive optic atrophy
o CUP DISC RATIO: Normal-0.3;
Large cup-physiological or glaucomatous;
Cup full-papilloedema, papillitis
o SPLINTER HAEMORRHAGES: seen in primary open
angle glaucoma, papilloedema
o NEOVASCULARISATION: diabetic retinopathy
o PERIPAPILLARY CRESENT: myopia
 MACULA
o Situated at posterior pole with its centre (foveolar) about 2 disc diameters
lateral to temporal margin of disc
o Normal-slightly darker than surrounding retina, its centre imparts a bright
reflex-foveal reflex
o Abnormalities-
• MACULAR HOLE
• MACULAR HAEMORRHAGE
• CHERRY RED SPOTS- Neimann Pick’s disease, Gaucher’s disease,
central retinal artery occlusion
• MACULAR OEDEMA- trauma, intraocular operations
• PIGMENTARY DISTURBANCES- after trauma, solar burn, chloroquine
toxicity
• BULL’S EYE MACULAR LESIONS- age related macular degeneration,
chloroquine retinopathy
• HARD EXUDATES-hypertensive retinopathy, exudative diabetic
maculopathy
• MACULAR SCARRING- trauma, disciform macular degeneration
 RETINAL BLOOD VESSELS
o Normal: arterioles-bright red, veins-purplish
o Abnormalities-
• NARROWING OF ARTERIOLES-hypertensive retinopathy,
arteriosclerosis, central retinal artery occlusion
• TORTUOSITY OF VEINS-diabetes mellitus, central retinal vein
occlusion
• SHEATHING OF VESSELS-hypertensive retinopathy
• VASCULAR PULSATIONS- venous pulsations (seen normally in some),
arterial pulsations ( seen in patients with aortic regurgitation, aneurysm,
exophthalmic goitre)
 GENERAL BACKGROUND
o Normal-pinkish red
o Abnormal-
• SUPERFICIAL RETINAL HAEMORRHAGES-hypertension, diabetes,
trauma
• DEEP RETINAL HAEMORRHAGES-diabetic retinopathy
• COTTON WOOL SPOTS(SOFT EXUDATES)-
hypertensive retinopathy, diabetic retinopathy,
anaemias, collagen disorders
• HARD EXUDATES-Hypertensive retinopathy,
diabetic retinopathy
• COLLOID BODIES-senile macular degeneration
• PIGMENTARY DISTURBANCES-retinitis pigmentosa
• MICROANEURYSMS-diabetic retinopathy
• NEOVASCULARISATION of retina- diabetic retinopathy, sickle cell
retinopathy
• TUMOURS of fundus-retinoblastoma
• PERIPHERAL RETINAL DEGENERATION
• RETINAL HOLES
• PROLIFERATIVE RETINOPATHY
• RETINAL DETACHMENT
THANK YOU

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Ophthal examination of eye

  • 2.  External Examination of eye  Fundus Examination  Visual field examination
  • 3. External Examination  Examination of- • Iris • Pupil • Lens  Intra-ocular pressure (IOP)
  • 4. Examination of IRIS  COLOUR –  Light blue or green in Caucasians and Dark brown in orientals  Heterochromia iridium- different colour of 2 iris  Heterochromia iridis-different colour of sectors of the same iris It occurs due to involved iris being lighter or darker than the normal
  • 5.  Iris lighter than normal- • congenital heterochromia, • atrophic patches in chronic uveitis, • metastatic carcinoma
  • 6.  Iris darker than normal- • Iris naevi-appear as freckles • ocular melanocytosis, • haemosiderosis, • siderosis bulbi, • retained iris foreign body, • malignant melanoma of iris • lymphoma
  • 7.  PATTERN OF NORMAL IRIS o Pattern occurs due to presence of collarette, crypts and radial striations on its anterior surface o It is disturbed in i. Acute iridocyclitis-muddy iris ii. Healed iridocyclitis-atrophy of iris  PERSISTENT PUPILLARY MEMBRANE o It is seen as abnormal congenital tags of iris tissue adherent to the collarette area
  • 8.  SYNECHIAE o It is the adhesion of iris to other intraocular structures o Types- i. Anterior- in Adherent leucoma ii. Posterior- in Iridocyclitis; can be total, annular or segmental  IRIDODONESIS o It is the tremulousness(trembling) of the iris o Seen in aphakia and subluxation of lens (since posterior support is lost)
  • 9.  NODULES ON THE IRIS SURFACE o Seen in granulomatous uveitis, melanoma, tuberculoma and gumma of iris  RUBEOSIS IRIDIS o New vessel formation on the iris o Seen in diabetic retinopathy, central retinal vein occlusion, chronic uveitis, chronic retinal detachment, retinoblastoma
  • 10.  GAP OR HOLE IN THE IRIS o May be due to congenital coboloma or due to iridectomy(surgical coboloma) o Iridodialysis-separation of iris from ciliary body  ANIRIDIA OR IRIDEREMIA o Complete absence of iris o Rare congenital condition  IRIS CYST o In patients using strong miotic drops, it may be seen in the pupillary margin
  • 11. Examination of PUPIL  NUMBER o Normal: 1 pupil o Rarely: more than 1 pupil (polycoria)  LOCATION o Normal: almost centre of the iris, slightly nasal o Rarely: congenitally eccentric (corectopia)  SIZE o Normal: 3-4mm depending upon illumination o It may be abnormally small (miosis) or large(mydriasis) o Anisocoria- It is a condition where there is difference between the size of two pupils
  • 12. o Causes of Miosis • Effect of local miotic drugs-Parasympathomimetic drugs • Iridocyclitis-narrow, irregular, non-reacting pupil • Head injury-pontine haemorrhage • Senile rigid miotic pupil • Due to effect of strong light • During sleep pupil is pinpoint
  • 13. o Causes of Mydriasis • Effect of topical sympathomimetic drugs-Adrenaline, phenylephrine • Effect of topical parasympatholytic drugs-Atropine, homatropine, tropicamide, cyclopentolate • Acute congestive glaucoma • Absolute glaucoma
  • 14.  SHAPE o Normal: circular o Irregular narrow- iridocyclitis o Festooned- effect of mydriatics on posterior segment synechiae o Vertically oval/pear shaped/updrawn- postoperatively (due to incarceration of iris or vitreous in the wound at 12 o’clock postion)
  • 15.  COLOUR o Normal: greyish black o Aphakia-jet black o Immature senile cortical cataract-greyish white o Mature cortical cataract-pearly white o Hypermature cataract-milky white o Cataracta brunescens-brown o Cataracta nigra-brownish black o Leucocoria-white reflex in pupil o Glaucoma-greenish hue o Iridocyclitis-dirty white exudates
  • 16.  PUPILLARY REACTIONS o Direct light reflex- Normal: pupil reacts briskly and constricts o Consensual light reflex Normal: contralateral pupil should also constrict
  • 17. o Swinging flash light test-(when RAPD is suspected) • Normal: both pupils constrict equally and the pupil to which light is transferred remains tightly constricted • RAPD present: affected pupil will dilate when flash light is moved from normal eye to abnormal eye. This is called Marcus Gunn Pupil o Near reflex- Pupil constricts while looking at a near object
  • 18. Abnormal pupillary reactions are seen in i. Amaurotic pupil ii. Efferent pathway defect iii. Wernicke’s hemianopic pupil iv. Marcus Gunn pupil v. Argyll Robertson pupil vi. Tonic pupil
  • 19. Examination of LENS  Can be examined using oblique illumination, slit lamp biomicroscopy and distant direct ophthalmoscopy with FULLY DILATED PUPILS  POSITION o Normal: patellar fossa by the zonules o Dislocation of lens: lens not present in its normal position i. Anterior dislocation-present in anterior chamber ii. Posterior dislocation-present in vitreous cavity either floating(LENSA NUTANS) or fixed to the retina(LENSA FIXATE)
  • 20. o Subluxation of lens-lens is partially displaced from its position • Causes-trauma, marfan’s syndrome, homocystinuria o Aphakia-absence of lens • It is diagnosed by i. jet black pupil, deep anterior chamber, empty patellar fossa by slit lamp biomicroscopy ii. hypermetropic eye on ophthalmoscopy, retinoscopy iii. ABSENCE of 3rd and 4th purkinje images o Pseudophakia- • When posterior chamber IOL is present, it is diagnosed by black pupil, deep anterior chamber, shining reflexes (from anterior surface of IOL) and PRESENCE of all the four Purkinje images
  • 21.  SHAPE o Normal: biconvex structure, on slit lamp-optical section shows embryonic, foetal, infantile and adult nuclei, cortex and capsule o Spherophakia-spherical o Lenticonus anterior-anterior cone shaped bulge (Alport syndrome) o Lenticonus posterior-posterior cone shaped bulge o Coloboma of lens-Notch in the lens
  • 22.  Colour o Normal: In young age, it is almost clear or gives a faint blue hue o Old age-greyish white (mistaken to be cataract) o CORTICAL cataract- greyish white (immature), pearly white (mature), milky white (hypermature) o NUCLEAR cataract-amber, brown or black o Cataractous lens with siderosis bulbi-rusty (orange)
  • 23.  TRANSPARENCY o Normal: transparent o Any opacity in the lens is called CATARACT o Complicated cataract-breadcrumb appearance (polychromatic lustre) o True diabetic cataract-snow flake opacities o Wilson’s disease-sunflower cataract o Concussion injury of lens-rosette shaped cataract
  • 24.  DEPOSITS ON ANTERIOR SURFACE OF LENS- o Vossius ring-in blunt trauma o Pigmented clumps-iridocyclitis o Dirty white exudates-uveitis, endophthalmitis o Rusty deposits-siderosis bulbi (deposition of ferrous ions) o Greenish deposits-chalcosis(deposition of copper ions)
  • 25.  PURKINJE IMAGES TEST o It WAS used to diagnose mature cataract and aphakia o Normal- • When a strong beam of light is shown to the eye, 4 images (purkinje images) are formed from the four different reflecting surfaces [ant & post surfaces of cornea and lens] o Mature cataract-4th image is absent (post surface of lens) o Aphakia-3rd and 4th are absent (ant & post surface of lens)
  • 26. Intraocular pressure  Digital tonometry- o IOP raised-fluctuation produced is feeble or absent, eyeball-firm to hard o IOP low-eyeball-soft  Indentation and Applanation tonometers are frequently used  Normal IOP=10-21mm Hg  Hypotony- IOP < 10mm Hg • Causes-ruptured globe, retinal/choroidal detachment, postoperative wound leak  Glaucoma suspected when IOP>21mm Hg
  • 27. Fundus Examination  To diagnose diseases of vitreous, optic nerve head, retina and choroid  For thorough examination, pupils to be dilated with 5%phenylephrine and/or 1%tropicamide eye drops
  • 28. Techniques of Fundus Examination 1) Ophthalmoscopy a) Distant direct ophthalmoscopy b) Direct ophthalmoscopy c) Indirect ophthalmoscopy 2) Slit lamp bio-microscopic examination by a) Indirect slit lamp bio-microscopy b) Hruby lens bio-microscopy c) Contact lens bio-microscopy
  • 29.  OCULAR MEDIA o Normal- transparent o Opacities-black against red glow (distant direct ophthalmoscopy) • Causes-corneal opacity, lenticular opacity, vitreous opacity
  • 30.  OPTIC DISC o SIZE: normal-1.5mm; hypermetropes-smaller; myopes-larger o SHAPE: normal-circular; high astigmatism-oblong o MARGINS: normal-well defined; blurring of margins- papilloedema, papillitis o COLOUR: normal-pinkish with central pallor; Hyperaemia-papilloedema Pale-partial optic atrophy Chalky white-primary optic atrophy Yellow waxy-consecutive optic atrophy
  • 31. o CUP DISC RATIO: Normal-0.3; Large cup-physiological or glaucomatous; Cup full-papilloedema, papillitis o SPLINTER HAEMORRHAGES: seen in primary open angle glaucoma, papilloedema o NEOVASCULARISATION: diabetic retinopathy o PERIPAPILLARY CRESENT: myopia
  • 32.  MACULA o Situated at posterior pole with its centre (foveolar) about 2 disc diameters lateral to temporal margin of disc o Normal-slightly darker than surrounding retina, its centre imparts a bright reflex-foveal reflex o Abnormalities- • MACULAR HOLE • MACULAR HAEMORRHAGE • CHERRY RED SPOTS- Neimann Pick’s disease, Gaucher’s disease, central retinal artery occlusion • MACULAR OEDEMA- trauma, intraocular operations
  • 33. • PIGMENTARY DISTURBANCES- after trauma, solar burn, chloroquine toxicity • BULL’S EYE MACULAR LESIONS- age related macular degeneration, chloroquine retinopathy • HARD EXUDATES-hypertensive retinopathy, exudative diabetic maculopathy • MACULAR SCARRING- trauma, disciform macular degeneration
  • 34.  RETINAL BLOOD VESSELS o Normal: arterioles-bright red, veins-purplish o Abnormalities- • NARROWING OF ARTERIOLES-hypertensive retinopathy, arteriosclerosis, central retinal artery occlusion • TORTUOSITY OF VEINS-diabetes mellitus, central retinal vein occlusion • SHEATHING OF VESSELS-hypertensive retinopathy • VASCULAR PULSATIONS- venous pulsations (seen normally in some), arterial pulsations ( seen in patients with aortic regurgitation, aneurysm, exophthalmic goitre)
  • 35.  GENERAL BACKGROUND o Normal-pinkish red o Abnormal- • SUPERFICIAL RETINAL HAEMORRHAGES-hypertension, diabetes, trauma • DEEP RETINAL HAEMORRHAGES-diabetic retinopathy • COTTON WOOL SPOTS(SOFT EXUDATES)- hypertensive retinopathy, diabetic retinopathy, anaemias, collagen disorders • HARD EXUDATES-Hypertensive retinopathy, diabetic retinopathy • COLLOID BODIES-senile macular degeneration • PIGMENTARY DISTURBANCES-retinitis pigmentosa
  • 36. • MICROANEURYSMS-diabetic retinopathy • NEOVASCULARISATION of retina- diabetic retinopathy, sickle cell retinopathy • TUMOURS of fundus-retinoblastoma • PERIPHERAL RETINAL DEGENERATION • RETINAL HOLES • PROLIFERATIVE RETINOPATHY • RETINAL DETACHMENT

Notas del editor

  1. Pic-posterior synechiae-adherent to ant. Crystalline lens Subluxation of lens-2nd pic
  2. 1st pic-coboloma
  3. Festooned- irregular pupil after patchy dilatation
  4. Relative afferent pathway defect-RAPD=> earliest indication of optic nerve disease in the presence of normal visual acquity
  5. Patellar foassa-space between vitreous and back of iris
  6. Subluxation of lens Jet black lens Shining reflex
  7. Alport syndrome-pic
  8. From text pic
  9. Ophthalmoscopy is clinical examination of the interior of the eye by means of an ophthalmoscope
  10. Vitreous opacity
  11. Chalky white
  12. Splinter, neovascularisation, peripapillary cresecnt
  13. Macular scar