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DR.Prashant .P.Patel 
Senior resident, 
Aravind Eye Hospital, Tirunelveli.
Slit lamp Biomicroscopy 
• It is a dynamic examination in which eye and 
ocular adnexa are scanned anteroposteriorly and 
horizontally. 
• Slit Lamp: It is a misnomer since slit is only one 
of the various other diaphragmatic opening 
present in the instrument. 
• Slit lamp biomicroscopy: 
1) Term introduced by Mawas in 1925. 
2) Examination of living eye by means of 
microscope and slit lamp.
• The slit-lamp is one of the important examination tools of 
ophthalmologists. 
• One of the most important advantages of slit-lamp examination is that 
one can examine the eye structure in three dimensions (3D). 
• There are three basic requirements for appreciation of depth with a slit-lamp. 
• The first depends upon the clinician possessing a third grade of binocular 
vision called stereopsis. 
• The second involves the direction of the incoming light source, and is 
dependent upon the fact that the light beam can be moved so it comes in 
from one side or the other. 
• The third involves the shape of the slit.
History 
• Purkinje: One of the first individuals to apply 
microscopy to the living eye , who studied the iris 
with an adjustable microscope by illuminating the 
field of view. 
• Louis de Wecker : He made the uniocular slit-lamp 
combined an eyepiece, objective and adjustable 
condensing lens within a tube. 
• It was improved by Siegfried Czapski who added 
binocularity to the microscope. 
• However, none of the units had sufficient and 
adjustable illumination.
• Allvar Gullstrand: An ophthalmologist and 
1911 Nobel laureate introduced the illumination 
system which had for the first time a slit 
diaphragm, therefore Gullstrand is credited 
with the invention of the slit lamp.
• Henker and Vogt improved upon Gullstrand’s 
device in 1911 by creating an adjustable slit-lamp 
by combining Czapski’s microscope with 
Gullstrand’s slit-lamp illumination.
Basic design of slit lamp 
• The three main components of the modern 
slit-lamp are: 
1) Illumination system 
2)Observation system 
3) Mechanical system
Mechanical system 
• It is mainly concerned with: 
• Positioning of patient. 
• Adjustment for observer and patient. 
• Adjustment of illumination and observations 
system. 
• It generally contains following hard ware.
Fixation light 
Head rest 
Canthal alignment mark 
Chin rest 
Lock for slit lamp base 
Joy stick 
Power unit
Chinrest adjust 
-ment knob 
Height adjustment 
switch
• Mechanical coupling: Mechanical system 
provides coupling of microscope and 
illumination system along a common axis of 
rotation that coincides their focal planes. 
• This arrangement ensures that light falls on 
the point where microscope is focused.
Illumination System 
It is based on Kohler illumination 
•The light source L is imaged in the objective O by the collector 
system K. The objective in turn produces an image at S in the 
mechanical slit located next to the collector system. The image of 
the light source at O is the exit pupil of the system. 
•The filament is imaged on to the objective lens but the 
mechanical slit is imaged on to the patient’s eye.
• Köhler illumination provides a very 
homogeneous slit image.
Illumination System 
• The illumination system of most slit-lamps 
consists of two different designs. 
• The first design: the Haag-Streit type 
illumination, allows de-coupling in the vertical 
meridian. 
• Such vertical de-coupling is particularly useful 
when performing gonioscopy to minimize 
reflections and for indirect fundus examination to 
gain increased peripheral views.
In the Zeiss type the illumination comes from below. 
The second design: the Zeiss type illumination system, does not allow decoupling in 
the vertical meridian.
Illumination system control 
• Angle 
• Width 
• Type 
1.Neutral density2.Red free 
3.Cobalt blue 
• Height 
• Intensity
Observation system 
• Should have following Characteristics : 
• Optimum stereoscopic observation. 
• Selectable magnification. 
• Large field of view. 
• Large depth of field. 
• Enough space in front of the 
microscope for manipulations on the 
eye.
Observation system is composed of 
• An objective lens: Two planoconvex lenses with 
their convexities put together. 
• Magnifying lenses 
• Telescope 
• Pair of prisms: To reinvert the image. 
• Eyepiece 
• Converging tubes: They are converged at an 
angle of 10-15 degree, to provide good 
stereopsis.
• The object is located at the object side focal 
point of the magnifying lens that magnifies 
the object image projecting it virtually to 
infinity. 
• The image is than viewed with respective 
magnification through telescope.
Change in magnification 
• Grenough type: 
• Galilean changer type: 
• Czapskiscope with rotating objective: 
• Zoom system:
The Grenough type(Classical Haag 
Streit) 
Flip lever to change 
magnification
• The Galilean Magnification 
changer
The Galilean Magnification changer 
• It utilises the Galilean telescopes to alter the 
magnification. 
• It has two optical components: 
• 1)Positive lens 2)Negative lens 
• Lenses are arranged in turret arrangement. 
• It provides large range of magnifications, 
typically five.
The Galilean Magnification changer
The Galilean Magnification changer 
Knob to change 
magnification (3 
or 5step)
Czapskiscope with rotating objectives 
• The different objectives are usually placed on 
a turret type of arrangement that allows them 
to be fairly rapidly changed during 
examination.
Zoom System 
• Zoom system allows continuously various 
degree of magnification. 
• E.g, Nikon photo slit lamp &Zeiss-75 Sl
Magnification can also be changed 
by changing the eyepiece power
Clinical Procedure 
• Before using the slit-lamp, it is important to 
ensure that the instrument is correctly set up. 
• The eyepieces should be focused for the observer 
for his/her own refractive error. 
• Often a little more minus correction is required 
than the observer’s actual refractive error due to 
accommodation and proximal convergence. 
• The Pupillary distance (pd) is adjusted for the 
observer (perhaps the pd should be slightly less 
than that usually measured to account for 
proximal convergence).
• Check that the observation and illumination 
systems are coupled, and the slit-beam is of 
even illumination and has sharply demarcated 
edge (otherwise irregularity of the beam may 
be falsely interpreted as irregularity of 
tissues). 
• The slit-lamp examination is conducted in a 
semi dark room.
• Patient is seated in front of slit-lamp on an 
adjustable stool and his/her head is steadied by 
placing chin on chin-rest and his forehead rests 
on the bar of head-rest. 
• Adjust the chin-rest so that the patient’s eyes are 
approximately level with the black marker on 
the side of the head rest. 
• Focus the slit-beam on the eye by moving the 
joystick either towards or away from the patient.
• The examination should be commenced using the 
X10 eyepieces and the lower powered objective 
to locate the pathology and higher magnification 
should then be used to examine it. 
• Use the lowest voltage setting on the 
transformer. 
• Select the longest slit-length by means of the 
appropriate lever. 
• The angulation between the observation arm and 
the illumination arm is adjusted.
Examination methods – 
Types of Illumination. 
• Slit lamp Provides three basic types of Illuminations. 
• 1)Focal Illumination: 
Achieved by narrowing the slit horizontally or 
vertically, provides isolation of the specific areas of eye 
/cornea for observation. 
• 2) Oblique illumination: It is essential for detecting and 
examining findings in different layers of the cornea. 
• 3)The Optical Section: The narrow slit beam slices 
through the eye revealing the internal details of the 
tissue at all layers.
Types of Illumination 
• Dffuse Illumination: 
Terminology :It is the type encountered in everyday life. 
For example light from sun or a light bulb that 
diffusely illuminate one’s surroundings. 
Principle :It is a Initial survey examination of the face, 
eyelids and ocular surface. 
If one directly proceeds with the magnified 
examination one is likely to miss skin disorders( such 
as acne rosacea), eyelid lesions ( such as molluscum 
contagiosum, small chalasion, mild ptosis). 
Technique: It can be done with torch light ,
Diffuse illumination with slit lamp 
1)Swing the microscope aside or keep it at 30- 
40’ of angle. 
2)Opening the slit beam to full height and width. 
3)Dialing in the neutral density filter. 
• Beam is only 8-14 mm diameter and 
therefore must be moved over the eyelids and 
ocular surface. 
• It can reveal location and general pattern of 
eyelid, conjunctival, corneal lesions.
Sclerotic Scatter 
• Terminology :In this technique for illuminating cornea, the 
slit beam is directed at the scleral limbus and illumination 
is transmitted into cornea by total internal reflection. 
• Opacities within the cornea scatter the light back to the 
observer. 
• Principle: Opaque sclera scatters the light at the point of 
illumination, some of the light is directed in to corneal 
stroma, where it travels through the entire cornea by 
repeatedly reflecting from its anterior and posterior 
surfaces. 
• The light emerges around circumference of the cornea, 
where it encounters the opaque sclera and create a 
glowing halo.
• Should be used early in the examination 
because, 
1) The patient acclimates to bright light of the 
slit lamp before it is directed in to the pupil. 
2) It accurately reveals the presence and 
pattern of corneal opacities. 
3) It helps to identify faint opacities that are 
difficult to see in direct illumination.
• Technique: 
• SLIT BEAM : Moderate width, Directed at the 
3- or 9-o’clock scleral limbus 
• MICROSCOPE: Independently focused onto 
the cornea.
Direct focal slit illumination 
• Terminology : Projection , of a narrow slit beam at an 
angle, to the corneal surface, producing an optical section 
that slices through the cornea and eye. 
• Principle: A direct narrow slit beam optically cuts through 
the cornea , providing a cross sectional view that reveals 
its contour and its internal structure. 
• It forms two parallel curved surface, one that follows 
anterior corneal surface and one that posterior corneal 
surface. 
• Two surfaces are joined by a block of light scattered in the 
stroma to create a geometric figure that resembles an 
elongated ice cube. 
• This is known as parallelepiped/ optical block/optical 
section.
• Technique: 
• Best used after the lesion is located by 
sclerotic scatter, diffuse illumination. 
• Examiner than focuses narrow slit of light 
over this lesion. 
• SLIT BEAM: Narrow 
• Approximately 30’ angle between slit beam 
and microscope, can be increased up to 90’.
Broad tangential illumination 
• Terminology: A wide beam is oriented at an 
extremely oblique illumination angle, causing it 
to project tangentially across the corneal surface. 
• Principle : Extreme angle of incidence of the slit 
beam results in decrease of light reflected and 
scattered by the cornea, this in turn reduces 
background glare causes surface abnormalities to 
stand out. 
• It is most useful for examining corneal surface.
• Technique: 
• SLIT BEAM: wide 
• ANGLE between slit beam and microscope: 
70-80’. 
• This highlights irregularities of corneal 
surface such as epithelial defect, PEES etc.
Proximal( indirect) illumination 
• Terminology: It requires that the slit beam is directed 
adjacent (proximal) to the area of interest to illuminate it 
indirectly. 
• Principle: It combines the Principle of Sclerotic Scatter and 
Retro illumination. 
• When directed adjacent to opaque area of the cornea, the 
illumination of the slit beam is internally reflected within 
the cornea causing light to spread throughout the stroma, 
light striking the opacity is scattered and some of the 
scattered light is reflected back to the observer. 
• It is used to define the an opaque area of the cornea and 
to identify details within the opacity.
• Technique: 
• SLIT Beam: 
• Short: 2-3 mm 
• Slightly broad: 0.2 mm 
• Directed adjacent to area of interest. 
• Angle between microscope and slit lamp is 15 
degree.
Retroillumination from Iris 
• Terminology: It is a technique of illuminating 
an area of cornea using light reflected from 
structure posterior to cornea such as iris. 
• Direct type: Cornea illuminated by light is 
viewed directly. 
• Indirect type: Cornea viewed adjacent to area 
of illuminated by the reflected light.
Direct type of Retro illumination
Indirect type of Retro illumination 
from Iris
• Principle: When light of direct illumination strikes 
a corneal opacity, it scatters and some of the light 
is reflected back towards the examiner. This form 
of illumination often washes out and obscures 
details of the lesion and provide little 
information about optical qualities and internal 
structure of small lesion. 
• When retroillumination is used these details 
stands out more prominently because the lesion 
is less likely to scatter and more likely to obstruct 
and refract the reflected light.
• Observer looks for three optical phenomena in 
retroillumination. 
• 1) Obstruction of light by densely opaque 
abnormalities appear black against the light 
beam. e.g, pigment deposit. 
• 2)Substructure of the droplets or refractile 
material in retroillumination. 
• 3)Distortion of light especially near the edge of 
the abnormality by refractile lesions that have 
different refractive index than the media in which 
they are contained.
Technique: 
Slit beam: narrow to medium, slit height is 
reduced, area of corneal pathology is 
positioned directly over the slit beam light 
reflected from the iris, either by moving the 
instrument or by altering the patient’s gaze.
Direct retroillumination
Indirect retroillumination.
Retroillumination from the fundus: 
• Terminology : Light entering the pupil is 
reflected from RPE and choroid and emerges 
from the pupil with orange red glow, 
commonly called as red reflex. 
• When examiner views the cornea against this 
reflex he/she is able to detect lesions that 
are to subtle for visualization by other 
techniques.
• Principle: Same that of the Retroillumination 
from iris. 
• Dense scars : Obstructs the reflected and they 
appear as dark silhouettes. 
• Translucent/transparent objects: Corneal 
guttae, DM Folds, Lattice corneal dystrophy, 
epithelial oedema stands out as brightly 
refractile contours.
• Technique: Slit lamp is aligned coaxial with 
microscope. Then decentered to the edge of 
the pupil. 
• Slit width: Medium and curved at one edge to 
fit in pupil. 
• Slit height: Reduced to 1/3 .
Specular reflection 
• Terminology: The smooth surfaces of cornea 
reflect incident light like a plain mirror 
following SNELL’S LAW. 
• When angle of incidence is equal to angle of 
reflection as measured from line drawn 
perpendicular to the surface. THIS IS KNOWN 
AS SPECULAR REFLECTION.
• Principle: Surface light reflex from the tear air 
interface is brightest specular reflection emanating 
from the cornea, but this does not permit examination 
of individual epithelial cells, because the light is 
reflected from tear film. 
• Intensity of anterior reflection is great because the 
difference in refractive index between air and tears is 
large. 
• Intensity of posterior reflection from endothelial 
surface is much less because the difference in index of 
refraction between aqueous humor and endothelium 
is much less.
• Light Reflected from the endothelium is 0.22% of 
total incident light. 
• Because cornea is curved , only a small part of 
the incident light beam is reflected in a specular 
manner which forces the observer to narrow the 
slit beam in to eliminate the surrounding glare. 
• Mirror smooth posterior surface of endothelium 
is broken by the intercellular spaces, which do 
not reflect the light, thus appears dark 
boundaries outlining a regular mosaic.
• The regular endothelial mosaic pattern can be 
disrupted by various pathologic entities. 
• 1) large and small cells may form a heterogeneous 
population. 
• 2)Irregularities in Descemet’s membrane e.g., cornea 
guttata , ridges, folds may displace the endothelial 
cells from the plane of reflected light so that they can 
not be clearly visualised and localised black area is 
viewed. 
• 3)Pigment deposits/ keratic precipitates on the 
posterior surface of the endothelium may reflect light 
and may be seen as focal bright spots.
• Technique: It requires a more systematic, stepwise, 
careful approach. 
• Patient is asked to look straight ahead. 
• Slit beam is projected on the central cornea from the 
temporal side. 
• The height of beam : 3 to 4 mm 
• Width of beam: Moderately wide (0.5mm) 
• Angle of slit beam and microscope should be same 
from the perpendicular to the corneal surface. 
• With this settings observer sees three lights:
• 1. Slit beam parallelepiped in the cornea. 
• 2) Beam reflected from the iris nasal to the 
parallelepiped. 
• 3) The corneal light reflex( First Catoptric 
image) temporal to parallelepiped. 
• Examiner focuses the slit beam at the level of 
the endothelium and slowly moves it 
temporally towards the first catoptric image.
• As this being done entire corneal parallelepiped 
changes in appearance from grey black to lighter 
and brighter structure. 
• When the corneal parallelepiped passes in front 
of the catoptric reflection, the bright surface 
reflex from the tear air interface dazzles the 
examiner and faint mosaic pattern of the 
endothelium becomes apparent, at this point 
magnification is changed to high power.
Aqueous flare and cells 
• Conical beam: is a small circular beam used to 
examine the presence of cells and flare. 
• Beam: Small circular pattern. 
• Light Source:45-60’ Temporally and directed in to 
the pupil. 
• Biomicroscope: Directly in front of the eye. 
• Magnification: High 
• Focusing: Beam is focused between cornea and 
anterior lens surface.
Filters 
• Sodium fluorescein is applied gently to the bulbar conjunctiva. 
• The patient should blink once or twice for the dye to be dispersed 
over the eye. 
• If the epithelium of the conjunctiva or the cornea is damaged, the 
fluorescein stains the underlying tissue. 
• The remaining dye fluoresces a yellow green colour when excited 
by the blue light. 
• Healthy epithelium does not stain. 
• Uses: 
• Contact lens fitting, 
• Marginal tear film height measurement, 
• Tear film break up time, 
• Jone’s dye disappearance test
Red free filter 
• The Red-free (green) filter to differentiate 
vascular from pigmented lesions. 
• Blood vessels and small haemorrhages will 
take on a dark appearance with the use of the 
red-free filter, whereas pigmented lesions will 
remain dark. 
• It makes the detail better by improving 
contrast.
Clinical Slit Lamp Microscopy 
• Examiner must integrate various types of illuminations in to flowing 
examination of cornea that permits rapid and accurate observations of 
corneal disease. 
• An example for sequence of illuminations in which the corneal lesion is to 
be seen: 
• 1)Flash light/ diffuse illumination: To locate the pathology. 
• 2)Sclerotic scatter: To see the pattern of abnormality. 
• 3)Focal slit: To know the depth at which the lesion is located. 
• 4)Proximal illumination : For internal details of the lesion. 
• 5)Tangential illumination: For surface characteristics of the lesion. 
• 6)Retroillumination from iris & fundus: For optical qualities of the lesion.
Clinical Drawings of Corneal 
Pathology 
Colour coding: 
• Black: 
• Corneal limbus, 
• Scars , 
• Degenerations, 
• Foreign Bodies, 
• Suture, 
• Contact lens.
• Blue: Designates oedema 
1)Shading: Diffuse stromal oedema. 
2)Small circles: Epithelial Oedema. 
3)Wavy Lines: DM Folds.
• Brown: Indicates Melanin or Iron 
Pigmentations 
1)Pupil 
2)Iris 
3)Deposits of Melanocytes on Posterior 
cornea. 
4)Sundry Iron lines on the epithelium.
• Red 
1) Blood vessels: 
i) Wavy lines: Begin outside the limbus indicates 
subepithelial vessels. 
ii) Straight lines : Begin inside the limbus 
indicates stromal vessels. 
2) Rose bengal stain: RED DOTS indicates area 
stained by rose bengal. 
3)Solid red shades: Indicates haemorrhage.
• Yellow: indicates presence of white blood 
cells. 
• Hypopyon 
• Stromal infiltrate 
• Keratic precipitates
• Green: fluorescein staining of the cornea 
• Green coloured dots: PEES 
• Small Lines: Filaments 
• Shaded Outlines: Epithelial Defect.
Accessory Devices: 
• Gonioscopy. 
• Pachymetry. 
• Applanation tonometry. 
• Slit lamp photography. 
• Slit lamp as a delivery system for argon, 
diode,and YAG laser.
Slit lamp examination lecture

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Slit lamp examination lecture

  • 1. DR.Prashant .P.Patel Senior resident, Aravind Eye Hospital, Tirunelveli.
  • 2. Slit lamp Biomicroscopy • It is a dynamic examination in which eye and ocular adnexa are scanned anteroposteriorly and horizontally. • Slit Lamp: It is a misnomer since slit is only one of the various other diaphragmatic opening present in the instrument. • Slit lamp biomicroscopy: 1) Term introduced by Mawas in 1925. 2) Examination of living eye by means of microscope and slit lamp.
  • 3. • The slit-lamp is one of the important examination tools of ophthalmologists. • One of the most important advantages of slit-lamp examination is that one can examine the eye structure in three dimensions (3D). • There are three basic requirements for appreciation of depth with a slit-lamp. • The first depends upon the clinician possessing a third grade of binocular vision called stereopsis. • The second involves the direction of the incoming light source, and is dependent upon the fact that the light beam can be moved so it comes in from one side or the other. • The third involves the shape of the slit.
  • 4. History • Purkinje: One of the first individuals to apply microscopy to the living eye , who studied the iris with an adjustable microscope by illuminating the field of view. • Louis de Wecker : He made the uniocular slit-lamp combined an eyepiece, objective and adjustable condensing lens within a tube. • It was improved by Siegfried Czapski who added binocularity to the microscope. • However, none of the units had sufficient and adjustable illumination.
  • 5. • Allvar Gullstrand: An ophthalmologist and 1911 Nobel laureate introduced the illumination system which had for the first time a slit diaphragm, therefore Gullstrand is credited with the invention of the slit lamp.
  • 6. • Henker and Vogt improved upon Gullstrand’s device in 1911 by creating an adjustable slit-lamp by combining Czapski’s microscope with Gullstrand’s slit-lamp illumination.
  • 7. Basic design of slit lamp • The three main components of the modern slit-lamp are: 1) Illumination system 2)Observation system 3) Mechanical system
  • 8. Mechanical system • It is mainly concerned with: • Positioning of patient. • Adjustment for observer and patient. • Adjustment of illumination and observations system. • It generally contains following hard ware.
  • 9. Fixation light Head rest Canthal alignment mark Chin rest Lock for slit lamp base Joy stick Power unit
  • 10. Chinrest adjust -ment knob Height adjustment switch
  • 11. • Mechanical coupling: Mechanical system provides coupling of microscope and illumination system along a common axis of rotation that coincides their focal planes. • This arrangement ensures that light falls on the point where microscope is focused.
  • 12. Illumination System It is based on Kohler illumination •The light source L is imaged in the objective O by the collector system K. The objective in turn produces an image at S in the mechanical slit located next to the collector system. The image of the light source at O is the exit pupil of the system. •The filament is imaged on to the objective lens but the mechanical slit is imaged on to the patient’s eye.
  • 13. • Köhler illumination provides a very homogeneous slit image.
  • 14. Illumination System • The illumination system of most slit-lamps consists of two different designs. • The first design: the Haag-Streit type illumination, allows de-coupling in the vertical meridian. • Such vertical de-coupling is particularly useful when performing gonioscopy to minimize reflections and for indirect fundus examination to gain increased peripheral views.
  • 15.
  • 16. In the Zeiss type the illumination comes from below. The second design: the Zeiss type illumination system, does not allow decoupling in the vertical meridian.
  • 17. Illumination system control • Angle • Width • Type 1.Neutral density2.Red free 3.Cobalt blue • Height • Intensity
  • 18. Observation system • Should have following Characteristics : • Optimum stereoscopic observation. • Selectable magnification. • Large field of view. • Large depth of field. • Enough space in front of the microscope for manipulations on the eye.
  • 19. Observation system is composed of • An objective lens: Two planoconvex lenses with their convexities put together. • Magnifying lenses • Telescope • Pair of prisms: To reinvert the image. • Eyepiece • Converging tubes: They are converged at an angle of 10-15 degree, to provide good stereopsis.
  • 20. • The object is located at the object side focal point of the magnifying lens that magnifies the object image projecting it virtually to infinity. • The image is than viewed with respective magnification through telescope.
  • 21. Change in magnification • Grenough type: • Galilean changer type: • Czapskiscope with rotating objective: • Zoom system:
  • 22. The Grenough type(Classical Haag Streit) Flip lever to change magnification
  • 23. • The Galilean Magnification changer
  • 24.
  • 25. The Galilean Magnification changer • It utilises the Galilean telescopes to alter the magnification. • It has two optical components: • 1)Positive lens 2)Negative lens • Lenses are arranged in turret arrangement. • It provides large range of magnifications, typically five.
  • 27. The Galilean Magnification changer Knob to change magnification (3 or 5step)
  • 28. Czapskiscope with rotating objectives • The different objectives are usually placed on a turret type of arrangement that allows them to be fairly rapidly changed during examination.
  • 29. Zoom System • Zoom system allows continuously various degree of magnification. • E.g, Nikon photo slit lamp &Zeiss-75 Sl
  • 30. Magnification can also be changed by changing the eyepiece power
  • 31. Clinical Procedure • Before using the slit-lamp, it is important to ensure that the instrument is correctly set up. • The eyepieces should be focused for the observer for his/her own refractive error. • Often a little more minus correction is required than the observer’s actual refractive error due to accommodation and proximal convergence. • The Pupillary distance (pd) is adjusted for the observer (perhaps the pd should be slightly less than that usually measured to account for proximal convergence).
  • 32. • Check that the observation and illumination systems are coupled, and the slit-beam is of even illumination and has sharply demarcated edge (otherwise irregularity of the beam may be falsely interpreted as irregularity of tissues). • The slit-lamp examination is conducted in a semi dark room.
  • 33. • Patient is seated in front of slit-lamp on an adjustable stool and his/her head is steadied by placing chin on chin-rest and his forehead rests on the bar of head-rest. • Adjust the chin-rest so that the patient’s eyes are approximately level with the black marker on the side of the head rest. • Focus the slit-beam on the eye by moving the joystick either towards or away from the patient.
  • 34. • The examination should be commenced using the X10 eyepieces and the lower powered objective to locate the pathology and higher magnification should then be used to examine it. • Use the lowest voltage setting on the transformer. • Select the longest slit-length by means of the appropriate lever. • The angulation between the observation arm and the illumination arm is adjusted.
  • 35. Examination methods – Types of Illumination. • Slit lamp Provides three basic types of Illuminations. • 1)Focal Illumination: Achieved by narrowing the slit horizontally or vertically, provides isolation of the specific areas of eye /cornea for observation. • 2) Oblique illumination: It is essential for detecting and examining findings in different layers of the cornea. • 3)The Optical Section: The narrow slit beam slices through the eye revealing the internal details of the tissue at all layers.
  • 36. Types of Illumination • Dffuse Illumination: Terminology :It is the type encountered in everyday life. For example light from sun or a light bulb that diffusely illuminate one’s surroundings. Principle :It is a Initial survey examination of the face, eyelids and ocular surface. If one directly proceeds with the magnified examination one is likely to miss skin disorders( such as acne rosacea), eyelid lesions ( such as molluscum contagiosum, small chalasion, mild ptosis). Technique: It can be done with torch light ,
  • 37. Diffuse illumination with slit lamp 1)Swing the microscope aside or keep it at 30- 40’ of angle. 2)Opening the slit beam to full height and width. 3)Dialing in the neutral density filter. • Beam is only 8-14 mm diameter and therefore must be moved over the eyelids and ocular surface. • It can reveal location and general pattern of eyelid, conjunctival, corneal lesions.
  • 38.
  • 39.
  • 40. Sclerotic Scatter • Terminology :In this technique for illuminating cornea, the slit beam is directed at the scleral limbus and illumination is transmitted into cornea by total internal reflection. • Opacities within the cornea scatter the light back to the observer. • Principle: Opaque sclera scatters the light at the point of illumination, some of the light is directed in to corneal stroma, where it travels through the entire cornea by repeatedly reflecting from its anterior and posterior surfaces. • The light emerges around circumference of the cornea, where it encounters the opaque sclera and create a glowing halo.
  • 41.
  • 42. • Should be used early in the examination because, 1) The patient acclimates to bright light of the slit lamp before it is directed in to the pupil. 2) It accurately reveals the presence and pattern of corneal opacities. 3) It helps to identify faint opacities that are difficult to see in direct illumination.
  • 43. • Technique: • SLIT BEAM : Moderate width, Directed at the 3- or 9-o’clock scleral limbus • MICROSCOPE: Independently focused onto the cornea.
  • 44.
  • 45. Direct focal slit illumination • Terminology : Projection , of a narrow slit beam at an angle, to the corneal surface, producing an optical section that slices through the cornea and eye. • Principle: A direct narrow slit beam optically cuts through the cornea , providing a cross sectional view that reveals its contour and its internal structure. • It forms two parallel curved surface, one that follows anterior corneal surface and one that posterior corneal surface. • Two surfaces are joined by a block of light scattered in the stroma to create a geometric figure that resembles an elongated ice cube. • This is known as parallelepiped/ optical block/optical section.
  • 46. • Technique: • Best used after the lesion is located by sclerotic scatter, diffuse illumination. • Examiner than focuses narrow slit of light over this lesion. • SLIT BEAM: Narrow • Approximately 30’ angle between slit beam and microscope, can be increased up to 90’.
  • 47.
  • 48.
  • 49.
  • 50. Broad tangential illumination • Terminology: A wide beam is oriented at an extremely oblique illumination angle, causing it to project tangentially across the corneal surface. • Principle : Extreme angle of incidence of the slit beam results in decrease of light reflected and scattered by the cornea, this in turn reduces background glare causes surface abnormalities to stand out. • It is most useful for examining corneal surface.
  • 51.
  • 52. • Technique: • SLIT BEAM: wide • ANGLE between slit beam and microscope: 70-80’. • This highlights irregularities of corneal surface such as epithelial defect, PEES etc.
  • 53.
  • 54.
  • 55. Proximal( indirect) illumination • Terminology: It requires that the slit beam is directed adjacent (proximal) to the area of interest to illuminate it indirectly. • Principle: It combines the Principle of Sclerotic Scatter and Retro illumination. • When directed adjacent to opaque area of the cornea, the illumination of the slit beam is internally reflected within the cornea causing light to spread throughout the stroma, light striking the opacity is scattered and some of the scattered light is reflected back to the observer. • It is used to define the an opaque area of the cornea and to identify details within the opacity.
  • 56. • Technique: • SLIT Beam: • Short: 2-3 mm • Slightly broad: 0.2 mm • Directed adjacent to area of interest. • Angle between microscope and slit lamp is 15 degree.
  • 57.
  • 58.
  • 59. Retroillumination from Iris • Terminology: It is a technique of illuminating an area of cornea using light reflected from structure posterior to cornea such as iris. • Direct type: Cornea illuminated by light is viewed directly. • Indirect type: Cornea viewed adjacent to area of illuminated by the reflected light.
  • 60. Direct type of Retro illumination
  • 61.
  • 62. Indirect type of Retro illumination from Iris
  • 63. • Principle: When light of direct illumination strikes a corneal opacity, it scatters and some of the light is reflected back towards the examiner. This form of illumination often washes out and obscures details of the lesion and provide little information about optical qualities and internal structure of small lesion. • When retroillumination is used these details stands out more prominently because the lesion is less likely to scatter and more likely to obstruct and refract the reflected light.
  • 64. • Observer looks for three optical phenomena in retroillumination. • 1) Obstruction of light by densely opaque abnormalities appear black against the light beam. e.g, pigment deposit. • 2)Substructure of the droplets or refractile material in retroillumination. • 3)Distortion of light especially near the edge of the abnormality by refractile lesions that have different refractive index than the media in which they are contained.
  • 65. Technique: Slit beam: narrow to medium, slit height is reduced, area of corneal pathology is positioned directly over the slit beam light reflected from the iris, either by moving the instrument or by altering the patient’s gaze.
  • 68. Retroillumination from the fundus: • Terminology : Light entering the pupil is reflected from RPE and choroid and emerges from the pupil with orange red glow, commonly called as red reflex. • When examiner views the cornea against this reflex he/she is able to detect lesions that are to subtle for visualization by other techniques.
  • 69. • Principle: Same that of the Retroillumination from iris. • Dense scars : Obstructs the reflected and they appear as dark silhouettes. • Translucent/transparent objects: Corneal guttae, DM Folds, Lattice corneal dystrophy, epithelial oedema stands out as brightly refractile contours.
  • 70. • Technique: Slit lamp is aligned coaxial with microscope. Then decentered to the edge of the pupil. • Slit width: Medium and curved at one edge to fit in pupil. • Slit height: Reduced to 1/3 .
  • 71.
  • 72.
  • 73.
  • 74. Specular reflection • Terminology: The smooth surfaces of cornea reflect incident light like a plain mirror following SNELL’S LAW. • When angle of incidence is equal to angle of reflection as measured from line drawn perpendicular to the surface. THIS IS KNOWN AS SPECULAR REFLECTION.
  • 75. • Principle: Surface light reflex from the tear air interface is brightest specular reflection emanating from the cornea, but this does not permit examination of individual epithelial cells, because the light is reflected from tear film. • Intensity of anterior reflection is great because the difference in refractive index between air and tears is large. • Intensity of posterior reflection from endothelial surface is much less because the difference in index of refraction between aqueous humor and endothelium is much less.
  • 76. • Light Reflected from the endothelium is 0.22% of total incident light. • Because cornea is curved , only a small part of the incident light beam is reflected in a specular manner which forces the observer to narrow the slit beam in to eliminate the surrounding glare. • Mirror smooth posterior surface of endothelium is broken by the intercellular spaces, which do not reflect the light, thus appears dark boundaries outlining a regular mosaic.
  • 77. • The regular endothelial mosaic pattern can be disrupted by various pathologic entities. • 1) large and small cells may form a heterogeneous population. • 2)Irregularities in Descemet’s membrane e.g., cornea guttata , ridges, folds may displace the endothelial cells from the plane of reflected light so that they can not be clearly visualised and localised black area is viewed. • 3)Pigment deposits/ keratic precipitates on the posterior surface of the endothelium may reflect light and may be seen as focal bright spots.
  • 78. • Technique: It requires a more systematic, stepwise, careful approach. • Patient is asked to look straight ahead. • Slit beam is projected on the central cornea from the temporal side. • The height of beam : 3 to 4 mm • Width of beam: Moderately wide (0.5mm) • Angle of slit beam and microscope should be same from the perpendicular to the corneal surface. • With this settings observer sees three lights:
  • 79. • 1. Slit beam parallelepiped in the cornea. • 2) Beam reflected from the iris nasal to the parallelepiped. • 3) The corneal light reflex( First Catoptric image) temporal to parallelepiped. • Examiner focuses the slit beam at the level of the endothelium and slowly moves it temporally towards the first catoptric image.
  • 80. • As this being done entire corneal parallelepiped changes in appearance from grey black to lighter and brighter structure. • When the corneal parallelepiped passes in front of the catoptric reflection, the bright surface reflex from the tear air interface dazzles the examiner and faint mosaic pattern of the endothelium becomes apparent, at this point magnification is changed to high power.
  • 81.
  • 82.
  • 83.
  • 84. Aqueous flare and cells • Conical beam: is a small circular beam used to examine the presence of cells and flare. • Beam: Small circular pattern. • Light Source:45-60’ Temporally and directed in to the pupil. • Biomicroscope: Directly in front of the eye. • Magnification: High • Focusing: Beam is focused between cornea and anterior lens surface.
  • 85.
  • 86. Filters • Sodium fluorescein is applied gently to the bulbar conjunctiva. • The patient should blink once or twice for the dye to be dispersed over the eye. • If the epithelium of the conjunctiva or the cornea is damaged, the fluorescein stains the underlying tissue. • The remaining dye fluoresces a yellow green colour when excited by the blue light. • Healthy epithelium does not stain. • Uses: • Contact lens fitting, • Marginal tear film height measurement, • Tear film break up time, • Jone’s dye disappearance test
  • 87.
  • 88. Red free filter • The Red-free (green) filter to differentiate vascular from pigmented lesions. • Blood vessels and small haemorrhages will take on a dark appearance with the use of the red-free filter, whereas pigmented lesions will remain dark. • It makes the detail better by improving contrast.
  • 89.
  • 90. Clinical Slit Lamp Microscopy • Examiner must integrate various types of illuminations in to flowing examination of cornea that permits rapid and accurate observations of corneal disease. • An example for sequence of illuminations in which the corneal lesion is to be seen: • 1)Flash light/ diffuse illumination: To locate the pathology. • 2)Sclerotic scatter: To see the pattern of abnormality. • 3)Focal slit: To know the depth at which the lesion is located. • 4)Proximal illumination : For internal details of the lesion. • 5)Tangential illumination: For surface characteristics of the lesion. • 6)Retroillumination from iris & fundus: For optical qualities of the lesion.
  • 91. Clinical Drawings of Corneal Pathology Colour coding: • Black: • Corneal limbus, • Scars , • Degenerations, • Foreign Bodies, • Suture, • Contact lens.
  • 92. • Blue: Designates oedema 1)Shading: Diffuse stromal oedema. 2)Small circles: Epithelial Oedema. 3)Wavy Lines: DM Folds.
  • 93. • Brown: Indicates Melanin or Iron Pigmentations 1)Pupil 2)Iris 3)Deposits of Melanocytes on Posterior cornea. 4)Sundry Iron lines on the epithelium.
  • 94. • Red 1) Blood vessels: i) Wavy lines: Begin outside the limbus indicates subepithelial vessels. ii) Straight lines : Begin inside the limbus indicates stromal vessels. 2) Rose bengal stain: RED DOTS indicates area stained by rose bengal. 3)Solid red shades: Indicates haemorrhage.
  • 95. • Yellow: indicates presence of white blood cells. • Hypopyon • Stromal infiltrate • Keratic precipitates
  • 96. • Green: fluorescein staining of the cornea • Green coloured dots: PEES • Small Lines: Filaments • Shaded Outlines: Epithelial Defect.
  • 97.
  • 98.
  • 99. Accessory Devices: • Gonioscopy. • Pachymetry. • Applanation tonometry. • Slit lamp photography. • Slit lamp as a delivery system for argon, diode,and YAG laser.