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SLIT LAMP – BIO MICROSCOPY OF EYE
 By- Dr. Paresh Vijay Nichlani
Moderators- Dr. K Srikanth
Dr N Swathi
NEED OF SLIT LAMP ???
 Magnified View
 Stereoscopic view
 Quantitative measurement
EVOLUTION OF SLIT LAMP
 Purkinje (1823)- One hand held lamp and one hand held lens
 De Wecker (1863)- mono-ocular microscope
 Albert & Greenough (1891)- Binocular microscope
 Czapski (1897)- binocular corneal microscope
 Gullstrand (1911)- Illumination system with a slit
 Henker (1916) – Combined the two
 Hans Goldmann (1933) – Both the lamp and slit beam with
horizontal and vertical adjustment were placed on single stage,
Haag-Streit model
 Littmann (1950) - incorporated rotatory magnification changer-
galilean teliscopee – zeiss slit lamp
PARTS OF MODERN SLIT LAMP
 Observation system (Microscope)
 Illumination system
 Mechanical system
BRUSHUP
• Ray of light
passing from
optical center will
not be refracted.
• Rays coming
from infinity ( zero
vergence ) will
converge to focal
point
• Rays originating
from focus will
come parallel after
refracting
OBSERVATION SYSTEM – MICROSCOPE
 Based on principle of Keplerian telescope
OBSERVATION SYSTEM
1. Objective lens – two Plano convex
lens, convexities put together -
+22.00 D
2. Eye piece - +10.00 D, Tubes
converged at an angle of 10-15
degrees- stereopsis
3. Prisms- rectify problem of inverted
image
GALILEAN MAGNIFICATION CHANGER
Based on principle of Galilean Telescope
MAGNIFICATION SYSTEM
Haag Streit magnification system- Grenough typeGalilean Magnification changer
PRINCIPLE OF ILLUMINATION SYSTEM
 Kohler illumination principle
 Converts light source to a beam of homogenous
brightness with minimal glare
 Advantage is that a very sharp and bright light is
obtained
ILLUMINATION SYSTEM
1. Light source – nerst lamp > arc lamp > Mercury
vapour lamp > halogen Lamp> LED lamps
Illumination – 2*105 to 4*105 lux
2. Condenser lens – coupled Plano convex lens
3. Slit and other diaphragm – horizontal and
vertical diaphragm
4. Filters – cobalt blue filter, red free filter
5. Projection lens - diameter of lens is smaller
- Better quality image
- Increases depth of focus of slit
– better optical section.
6. Reflecting mirror/ prism – illumination axis do
not obstruct field of
vision
TYPES – LOCATION OF ILLUMINATION SYSTEM
MECHANICAL SUPPORT SYSTEM
Joystick
Patient support arrangement
Fixation target
Mechanical coupling
TYPES OF ILLUMINATION
 Depending upon the structures and there
different optical property we use different
types of illumination.
1. DIFFUSE ILLUMINATION
Settings
- Slit fully opened (annular diaphragm)
- Inserted diffuser
- Microscope positioned at 0°
-Angle of slit illumination system approx. 30° - 50°
-Magnification – 5-12x
Uses
- general surveys of anterior eye segments
- general observation of the surfaces
of crystalline lens and cornea
- assessment of the lachrymal reflex
-assessment of soft contact lenses
-It can be used with filters
Pterygium
2. DIRECT FOCAL ILLUMINATION
• Slit beam is regulated until it
coincides with exact focus of the
microscope
• Settings – Narrow slit at oblique
angle (30), slit 2-3mm , 5-45x
• 3d layered view
- cornea lens and ant.
Phase of vitreous disperse light and
gets visible against dark back
ground.
• This type of illumination can be
used with 3 types of different
beam
1. Optical Section
2. parallelepiped
3. conical beam effect
OPTICAL SECTION
 A narrow slit is focused obliquely 2-
3mm, 30-45, – knife like histological
sections of cornea, lens & ant. phase
of vitreous
 Optical section of cornea –
1.Tear layer- ant. Most bright zone
2. Epithelium- dark line
3. Bowman’s membrane – bright line
4. Stroma- Wider granular grey zone
5. Descemet’s membrane – bright
zone
 Uses – 1. corneal curvature
2. Corneal thickness
3. Location of corneal pathology
4. Van Her-rick method of ac depth
OPTICAL SECTION OF LENS
 Optical section of lens
1. Ant capsule 2. sub capsular clear zone – c1 3. Bright narrow zone of discontinuity 4.second clear
cortical zone – c2
5.Light scratting zone of deep cortex – c3 6.Clear zone of deep cortex. 7. Nucleus
 Parallelopiped – 2-
3mm wide focal slit –
used for pathologies
on epithelial and
stroma
 Conical beam- small
circular beam –
examining aqueous
for cells and flares –
at 45-60 degrees, at
high mag.
3 INDIRECT ILLUMINATION
 Slit beam is focused beside the
area to be observed- The axes of
illuminating and viewing path do
not intersect at the point of image
focus.
 Angle-60, variable, slit max height
Uses –
1. Corneal infiltrates
2. Corneal microcytes
3. Corneal vacuoles
4. Epithelial cells
4RETRO ILLUMINATION
• Light is reflected off from iris
or fundus
• system and observation axis are
set to 0°.
• it is essential that the pupil is
• dilated as otherwise the resulting
relatively small field of view
through a normal size pupil
makes observation
• almost impossible.
• Direct- Observer is in direct pathway of light reflected from structure. Pathology-
against illuminating background.
• Indirect – observer right angled to observing structure. Not in line with light ,
Pathology – against dark non illuminated background.
GRAVES – PATHOLOGY- OPTICAL PROPERTIES
 Obstructive- opaque to
light- dark against bright
background eg- pigments
 Respersive- scatter light
but do not obstruct –
brightly against dark
background epithelial
edema, precipitates.
 Refrectile- distort view as
refrective index is different
from surrounding. Eg –
vacuole.
5. SPECULAR REFLECTION
 Reflection accurse – beam
of light incident on optical
surface- zone of
discontinuity
 Observer in path of
reflected light – dazzling
reflex - specular reflex –
dark areas in reflex
 Technique – Pt to look 30
degree temporally , light
beam focused from opp.
side, focused under high
magnification, 3-4 mm from
limbus- slit is rotated more
temporally to about 60
degree (i=r)
 Uses – endothelial cell
count
6. SCLEROTIC SCATTER
Uses- outline finest corneal
pathology
COBALT BLUE FILTER
 This throws a blue
light,
 Principle –
fluorescence – these
substance absorbs
light of a colour and
then emit a light of
other colour in this
case it absorbs blue
and emits yellowish
green.
 Uses – corneal ulcer,
scidel test etc, tear
BUT etc.
RED FREE FILTER
 This filter emits green
light – This causes
obscure red colour
 Blood vessels and
haemorrhages appear
black
 Areas of episclera with
lymphocyte appears
yellow
 Fleischer ring
ACCESSORY DEVICES
 Gonioscopy
 Fundus examination using lens
 Pachymetry
 Applenation tonometry
 Slit lamp photography
 Slit lamp video graphy
 Slit lamp – argon, diode and yag laser
 Others
WHAT DO WE KNOW??
WHAT WE HAVE LEARNT??
 Evolution of slit lamp
 Parts of slit lamp
 Optics of slit lamp
 Uses
 Types of illumination
 Accessory devices
 The future- dime
illumination coupled
with electronic light
amplification system
Slit lamp – biomicroscopy of eye

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Slit lamp – biomicroscopy of eye

  • 1. SLIT LAMP – BIO MICROSCOPY OF EYE  By- Dr. Paresh Vijay Nichlani Moderators- Dr. K Srikanth Dr N Swathi
  • 2. NEED OF SLIT LAMP ???  Magnified View  Stereoscopic view  Quantitative measurement
  • 3. EVOLUTION OF SLIT LAMP  Purkinje (1823)- One hand held lamp and one hand held lens  De Wecker (1863)- mono-ocular microscope  Albert & Greenough (1891)- Binocular microscope  Czapski (1897)- binocular corneal microscope  Gullstrand (1911)- Illumination system with a slit  Henker (1916) – Combined the two  Hans Goldmann (1933) – Both the lamp and slit beam with horizontal and vertical adjustment were placed on single stage, Haag-Streit model  Littmann (1950) - incorporated rotatory magnification changer- galilean teliscopee – zeiss slit lamp
  • 4. PARTS OF MODERN SLIT LAMP  Observation system (Microscope)  Illumination system  Mechanical system
  • 5. BRUSHUP • Ray of light passing from optical center will not be refracted. • Rays coming from infinity ( zero vergence ) will converge to focal point • Rays originating from focus will come parallel after refracting
  • 6. OBSERVATION SYSTEM – MICROSCOPE  Based on principle of Keplerian telescope
  • 7. OBSERVATION SYSTEM 1. Objective lens – two Plano convex lens, convexities put together - +22.00 D 2. Eye piece - +10.00 D, Tubes converged at an angle of 10-15 degrees- stereopsis 3. Prisms- rectify problem of inverted image
  • 8. GALILEAN MAGNIFICATION CHANGER Based on principle of Galilean Telescope
  • 9. MAGNIFICATION SYSTEM Haag Streit magnification system- Grenough typeGalilean Magnification changer
  • 10. PRINCIPLE OF ILLUMINATION SYSTEM  Kohler illumination principle  Converts light source to a beam of homogenous brightness with minimal glare  Advantage is that a very sharp and bright light is obtained
  • 11. ILLUMINATION SYSTEM 1. Light source – nerst lamp > arc lamp > Mercury vapour lamp > halogen Lamp> LED lamps Illumination – 2*105 to 4*105 lux 2. Condenser lens – coupled Plano convex lens 3. Slit and other diaphragm – horizontal and vertical diaphragm 4. Filters – cobalt blue filter, red free filter 5. Projection lens - diameter of lens is smaller - Better quality image - Increases depth of focus of slit – better optical section. 6. Reflecting mirror/ prism – illumination axis do not obstruct field of vision
  • 12. TYPES – LOCATION OF ILLUMINATION SYSTEM
  • 13. MECHANICAL SUPPORT SYSTEM Joystick Patient support arrangement Fixation target Mechanical coupling
  • 14. TYPES OF ILLUMINATION  Depending upon the structures and there different optical property we use different types of illumination.
  • 15. 1. DIFFUSE ILLUMINATION Settings - Slit fully opened (annular diaphragm) - Inserted diffuser - Microscope positioned at 0° -Angle of slit illumination system approx. 30° - 50° -Magnification – 5-12x Uses - general surveys of anterior eye segments - general observation of the surfaces of crystalline lens and cornea - assessment of the lachrymal reflex -assessment of soft contact lenses -It can be used with filters
  • 17.
  • 18. 2. DIRECT FOCAL ILLUMINATION • Slit beam is regulated until it coincides with exact focus of the microscope • Settings – Narrow slit at oblique angle (30), slit 2-3mm , 5-45x • 3d layered view - cornea lens and ant. Phase of vitreous disperse light and gets visible against dark back ground. • This type of illumination can be used with 3 types of different beam 1. Optical Section 2. parallelepiped 3. conical beam effect
  • 19. OPTICAL SECTION  A narrow slit is focused obliquely 2- 3mm, 30-45, – knife like histological sections of cornea, lens & ant. phase of vitreous  Optical section of cornea – 1.Tear layer- ant. Most bright zone 2. Epithelium- dark line 3. Bowman’s membrane – bright line 4. Stroma- Wider granular grey zone 5. Descemet’s membrane – bright zone  Uses – 1. corneal curvature 2. Corneal thickness 3. Location of corneal pathology 4. Van Her-rick method of ac depth
  • 20.
  • 21. OPTICAL SECTION OF LENS  Optical section of lens 1. Ant capsule 2. sub capsular clear zone – c1 3. Bright narrow zone of discontinuity 4.second clear cortical zone – c2 5.Light scratting zone of deep cortex – c3 6.Clear zone of deep cortex. 7. Nucleus
  • 22.  Parallelopiped – 2- 3mm wide focal slit – used for pathologies on epithelial and stroma  Conical beam- small circular beam – examining aqueous for cells and flares – at 45-60 degrees, at high mag.
  • 23. 3 INDIRECT ILLUMINATION  Slit beam is focused beside the area to be observed- The axes of illuminating and viewing path do not intersect at the point of image focus.  Angle-60, variable, slit max height Uses – 1. Corneal infiltrates 2. Corneal microcytes 3. Corneal vacuoles 4. Epithelial cells
  • 24. 4RETRO ILLUMINATION • Light is reflected off from iris or fundus • system and observation axis are set to 0°. • it is essential that the pupil is • dilated as otherwise the resulting relatively small field of view through a normal size pupil makes observation • almost impossible.
  • 25. • Direct- Observer is in direct pathway of light reflected from structure. Pathology- against illuminating background. • Indirect – observer right angled to observing structure. Not in line with light , Pathology – against dark non illuminated background.
  • 26. GRAVES – PATHOLOGY- OPTICAL PROPERTIES  Obstructive- opaque to light- dark against bright background eg- pigments  Respersive- scatter light but do not obstruct – brightly against dark background epithelial edema, precipitates.  Refrectile- distort view as refrective index is different from surrounding. Eg – vacuole.
  • 27. 5. SPECULAR REFLECTION  Reflection accurse – beam of light incident on optical surface- zone of discontinuity  Observer in path of reflected light – dazzling reflex - specular reflex – dark areas in reflex  Technique – Pt to look 30 degree temporally , light beam focused from opp. side, focused under high magnification, 3-4 mm from limbus- slit is rotated more temporally to about 60 degree (i=r)  Uses – endothelial cell count
  • 28. 6. SCLEROTIC SCATTER Uses- outline finest corneal pathology
  • 29. COBALT BLUE FILTER  This throws a blue light,  Principle – fluorescence – these substance absorbs light of a colour and then emit a light of other colour in this case it absorbs blue and emits yellowish green.  Uses – corneal ulcer, scidel test etc, tear BUT etc.
  • 30. RED FREE FILTER  This filter emits green light – This causes obscure red colour  Blood vessels and haemorrhages appear black  Areas of episclera with lymphocyte appears yellow  Fleischer ring
  • 31. ACCESSORY DEVICES  Gonioscopy  Fundus examination using lens  Pachymetry  Applenation tonometry  Slit lamp photography  Slit lamp video graphy  Slit lamp – argon, diode and yag laser  Others
  • 32. WHAT DO WE KNOW?? WHAT WE HAVE LEARNT??  Evolution of slit lamp  Parts of slit lamp  Optics of slit lamp  Uses  Types of illumination  Accessory devices  The future- dime illumination coupled with electronic light amplification system

Hinweis der Redaktion

  1. Iop endothelial cell count, pupil size , corneal thickness, ac depth ect
  2. De wecker- heand helf-restedon face- condencer lens,
  3. Zero vergence Eye piece stronger, objective less power Afocal system
  4. Objective plus (low power) eye piece minus (hig power)
  5. Ray diagram
  6. Filament imaged on lens , slit imaged on patient eye
  7. Narrow beam- scattered background light is removed
  8. Tindal phenominon narrow beam and dark pupilary background
  9. 2 % fluorescein dye FDDt- prolonged stay in fornex – defective drainage . Jones 1- dye put – collected in inf meatus. Jones 2 – press saline if dye – occlusion of nld if not canallicular occlusion non fn pump
  10. Fleischer ring – pigment ring in pereferal cornea - ieon deposition in basel epithelial cells - keratoconous .... Kayser f ring copper – willson’s