10 Steps to a Better Slit
Lamp Examination
Brush up on this essential part of every eye examination.
By Etty Bitton, OD, MSc, FAAO
Brush up on this essential part of every eye examination.
By Etty Bitton, OD, MSc, FAAO
Are you
getting the most out of your slit lamp exam (SLE)? Like most, your slit lamp
skills have no doubt improved with time. To maximize the use of your slit lamp,
try adding the following 10 reminders to your routine.
1. Clean
Up Your View
Whether or not you cover your slit
lamp at the end of the day, dust and oils from your eyelashes will soil the
oculars. Make sure you dust the mirror of the illumination column as well as
the patient side of the oculars. You can use a small brush, which usually comes
as part of the slit lamp accessories, to dust off the mirror. Adding a routine
cleaning will keep your image sharp.
2. Adjust Your Oculars
This step may be more pertinent if you practice in a group or hospital
setting whereby several individuals share the equipment. Verifying the
interpupillary distance of the oculars prior to evaluation will maximize
three dimensional (3D) viewing of the ocular tissues. In addition, you should
also adjust the objectives to your prescription by turning the knurled ring
of the eyepiece. Daily handling can displace the interpupillary distance of the
oculars, hence a small adjustment could make a big difference with respect to
viewing comfort and rendering subtle
3D details more evident.
2. Adjust Your Oculars
This step may be more pertinent if you practice in a group or hospital
setting whereby several individuals share the equipment. Verifying the
interpupillary distance of the oculars prior to evaluation will maximize
three dimensional (3D) viewing of the ocular tissues. In addition, you should
also adjust the objectives to your prescription by turning the knurled ring
of the eyepiece. Daily handling can displace the interpupillary distance of the
oculars, hence a small adjustment could make a big difference with respect to
viewing comfort and rendering subtle
3D details more evident.
3. Follow the Anatomy A comprehensive SLE should follow a logical
sequence. It's best to begin with low magnification and observe the
external structures first, such as lids, lashes, inner and outer canthi
and tear meniscus. You can also evaluate the overall appearance of
the bulbar conjunctiva, cornea, iris and pupilBegin by sweeping the lid margin from the outer canthus towards the inner canthus. Of particular interest for contact lens (CL) wearers is a detailed examination of the lid margin, paying particular attention to the lids, lashes and tear film. Examine the lashes for signs of blepharitis, madarosis (loss of lashes) and trichiasis (misdirected lashes). Observing the tear meniscus should reveal a uniform structure with little debris and an inferior meniscus that's slightly larger than its superior counterpart. Note lid margin scars or deformities, especially if they obstruct the flow of the tears towards the punctum. Meibomian gland expression should require little force and reveal clear liquid secretions. Meibomian gland dysfunction is often underdiagnosed, leading to an unstable tear film and unexplained CL dropout. Make lid eversion a routine part of every anterior segment examination, even more so in CL wearers. Check the lids for signs of papillary response or hyperemia. Some silicone hydrogel lenses that have higher modulus have resulted in a papillary response in some patients. Switching to a lens with lower modulus may have beneficial effects.
TABLE 1
|
|||
llumination
Techniques
|
|||
ILLUMINATION
|
ILLUMINATION
ANGLE (DEGREES) |
MAGNIFICATION*
|
TISSUES
|
Diffuse
|
30-45
|
Low
|
External
overall view, lid, lashes, CL fit
|
Direct:
|
|||
• Broad
beam
|
30-45
|
Low-med
|
Conjunctiva,
cornea
|
•
Parallelepiped
|
30-45
|
Med
|
Cornea,
meniscus, iris, lens
|
•
Optical Section
|
30-60
|
Med
|
Angle
estimation, corneal layers, lenticular layers
|
•
Conical Beam
|
30-45
|
Med
|
Anterior
chamber (cells)
|
Indirect
|
45-60
|
Med
|
Cornea
|
Retroillumination
|
0
|
Low-med
|
Transillumination
of the iris, lenticular opacities
direct |
Specular
Reflection
|
90 from
microscope
|
Med-high
|
Tear
Layer, endothelium
|
Sclerotic
scatter
|
60
|
Low
|
Corneal
scars, central edema
|
Tangential
|
70-80
|
Med
|
Iris
(freckles, suspicious nevi)
|
* Low: 6X to 10X,
Med: 10X to 16X, High: 25X to 40X
|
A detailed examination
of the corneal structures (epithelium, stroma and endothelium) is next, varying
magnification and illumination as needed. Examine the iris, pupil and
crystalline lens last because the direct illumination is more bothersome for
the patient. A systematic SLE will improve efficiency, uncover reasons for CL
intolerance, reduce chair time and limit omissions of tissue anomalies.
4. Know
Your Illuminations
Can you differentiate between
specular reflection and sclerotic scatter? Most practitioners vaguely remember
learning about illuminations, but the specifics have developed cobwebs over
time. Most of us perform SLE under a somewhat automated mode. We constantly
switch from one type of illumination to another without realizing it.
A review of illuminations may be
helpful in reminding us of those used less frequently but with inherent
advantages. Table 1 offers a quick overview of different illuminations and which
structures are best viewed under these illumination techniques. Some slit lamp
models have the ability to tilt the illumination column (towards the patient)
up to 20 degrees (in 5 degree increments). This oblique illumination is useful
in reducing reflections during gonioscopy. In modern slit lamps, manufacturers
have replaced most tungsten type bulbs, which have a redder light, with more
efficient halogen illumination, which provides a bluer light. Fluorescein is
also useful in performing the Seidel test, which identifies aqueous leaking.
5. Enhance
Your View
Adding ophthalmic dyes to your SLE
will improve your diagnostic evaluation. Sodium fluorescein highlights areas of
corneal stress while lissamine green is best at highlighting conjunctival problems.
Better tolerated than rose bengal, lissamine green is observed in white light
and provides additional insight for patients presenting with dry eye
symptomology or CL intolerance.
Document staining, noting the form,
depth and extent. The shape of staining can be micropunctate (resembling small
dots), macropunctate (larger dots) or coalescent staining (a patch). Its depth
can be limited to the epithelium or it may enter the stromal layers. You can
approximate the extent in percentage of the surface area affected by the
staining. Improving your documentation of staining will facilitate your
observation for any progression or regression at follow-up visits.
Table 2
|
|
Effect of
Magnification on Field of View*
|
|
MAGNIFICATION
|
FIELD OF VIEW
|
6X
|
35.1mm
|
10X
|
22.5mm
|
16X
|
14.1mm
|
25X
|
8.8mm
|
40X
|
5.6mm
|
* Using a 12.5X eyepiece
|
6. Filters
We perform most of a SLE using white
light. When using fluorescein, use a yellow (Wratten #12) barrier filter in
conjunction with a cobalt (blue) filter to maximize viewing of the
fluorescence. Positioning the yellow barrier filter in the path of the
returning light and not in the path of the incident light will enhance the
contrast significantly. Newer slit lamps have integrated the yellow barrier
filter in the ocular housing, as its use is becoming more commonplace.
You can use the red-free (green)
filter to differentiate vascular from pigmented lesions. Blood vessels and
small hemorrhages will take on a dark appearance with the use of the red-free
filter, whereas pigmented lesions will remain dark. Some slit lamps can also be
equipped with a neutral density filter and/or a heat-absorbing filter to
increase patient comfort.
7. Magnification
Most slit lamp models offer 10X, 16X
and 25X magnification, although some models extend to 40X. Most use eyepieces
of 10X or 12.5X. As magnification increases, it limits the depth of focus,
hence small adjustments with the joystick of the slit lamp will keep the image
in sharp focus. Furthermore, increased magnification reduces the field of view
(Table 2), allowing for greater detail of structures. Depending on the model,
magnification drums can have specified click stops or be continuous. The
continuous option, also called zoom system, has the advantage of a smoother
transition with no image loss.
If upgrading your biomicroscope is
not in your immediate plans, then try extending the magnification by simply
purchasing an additional set of oculars (for example, 20X). Returning the
magnification to the lowest setting at the end of the examination will reduce
prep time for the next patient.
8. Illumination
Intensity
Novice users have a tendency to use
the highest illumination intensity during the entire examination. The problem
is that these habits are hard to break. The examination should begin under the
lowest intensity to examine external tissues and to allow the patient to adapt
to the illumination, which is even more important if the patient has undergone
pupillary dilation. The slit width is often decreased to examine details of
ocular tissues under higher magnification. Reserve higher intensity
illumination for examining details and use it for a shorter amount of time to
conserve energy. You can equally reduce the slit beam height to increase
patient comfort during the use of higher illumination intensity.
9. Viewing
Angle
During most of the SLE, the
observation arm of the slit lamp is directly in front of the patient. You can
move the illumination arm to obtain different illumination angles to assess
different tissues. Large illumination angles allow you to determine the depth
of corneal and lenticular lesions with greater accuracy because the distance
between layers of these tissues is increased under these conditions.
To increase the distance between
layers even further, make the illumination angle even larger. One way of
achieving this is to displace the observation arm from its habitual central
position to a more nasal one while extending the illumination column more
temporal (Figure 2b). This will enhance your view of the individual layers of
the cornea or lens and allow you to determine the depth of lesions with
enhanced accuracy.
10. Measuring
Eyepiece
Practitioners have traditionally
made a subjective evaluation of the height and width of lesions, nevi,
staining, meniscus and neovascularization. A measuring eyepiece or graticule
can replace a traditional eyepiece to considerably improve this measurement.
The eyepiece has a linear and an angular scale, the latter being useful for
evaluating toric lens rotation with improved accuracy. With the advent of
ocular photography, many offices photograph lesions to properly document
problems and to allow for future comparisons. If this capability isn't
available in your office, then a measuring eyepiece may considerably enhance
your documentation. You can subsequently store the eyepiece for safekeeping and
future use.
Final Pearls
SLEs are dynamic. You should have
one hand on the joystick and the other available to adjust the illumination
arm, magnification, lighting intensity, slit width or even to hold an accessory
instrument.
Locking your biomicroscope following
examination will prevent unnecessary swinging and possible damage to the
mechanics of the slit lamp during positioning towards or away from the patient.
Using a dust cover over the slit lamp at the end of the day will help protect
your investment.
Knowing the different options
(filters; illumination width, height and intensity; magnification) your slit
lamp has to offer, coupled with proper maintenance, will ensure a high image
quality and help you perform a more efficient SLE.