macular examination, jay chhablani

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    Evaluation of Macula

    Dr Jay Kumar Chhablani

    Smt. Kanuri Santhamma Retina &Vitreous Centre

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    Anatomy of macula

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    Evaluation of macula

    History Examination Investigations

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    History

    Distortion of images Blurring of images Unable to identify faces Difficulty in color vision

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    Examination

    Binocular indirect ophthalmoscpy Slit-lamp biomicroscopy

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    Slit lamp Biomicroscopy

    Slit lamp-

    Adjustable intense illumination

    Slit beam adjustable width / length 3600 rotation, variable angle

    Provides optical section Provides high magnification and stereopsis Surface contours of chorioretinal lesions better

    appreciated

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    Slit lamp biomicroscopy

    Principle-

    Use of an accessory lens to image the fundus in aposition, where it can be reimaged by slit lamp

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    Accessories-

    Contact lenses:-Neutralizes corneal power

    Noncontact lenses: use refractive power of cornea and high convex /

    concave lens to image the fundus

    Slit lamp biomicroscopy

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    Advantages

    NONCONTACT METHOD

    Quicker Examine post op. and

    infected patients

    No coupling agent No topical anaesthesia

    CONTACT METHOD

    Better stability Better quality of

    image

    Some control ofocular movements

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    Lenses used

    NON CONTACTMETHOD

    Hruby lensAspheric lenses(+60, +78, +90D)

    CONTACT METHODGoldman three mirror lensGoldman posterior lensMainster lensPanfundoscopicQuadrisphericVolk Super Quad

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    Non Contact Methods

    Hruby lens-

    Plano concave (-58.6 D) Mounted on slit lamp View: 300 vertical / 600 lateral Image : Erect / virtual / in pupillary plane

    Minification of pupil To view only post. pole

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    Non Contact Methods

    Indirect fundus biomicroscopy-

    High convex lenses (+60D, +78D, +90D) Image : Real, Inverted, High quality Magnify the pupil - wider fieldFundus scanning : Upto pre equatorial region with certain adjustments

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    Volk TransEquator

    132 Dynamic Fieldof View

    0.7x Magnification 1.44 Laser Spot

    Magnification Factor

    13

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    Volk SuperQuad 160

    160 Field of View 0.5x Magnification 2.0x Laser Spot

    Magnification Factor

    14

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    Mainster Lens

    35 - 48 Dynamic Fieldof View

    0.95 x Magnification 1.05 Laser Spot

    Magnification Factor

    15

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    Indirect fundus biomicroscopy

    Technique-

    Narrow slit width / low intensity Lowest magnification Align illumination / visualization angle straight ahead Focus the cornea with beam passing through dilated

    pupil

    Hold the lens in front of pupil Pull the slit lamp back to get fundus image

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    Indirect fundus biomicroscopy

    Increasing field of Exam-

    Shifting patients gaze Changing beam width / magnification Moving Slit Lamp

    Vertically / Horizontally Vertical tilt by 150

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    LENS

    FEATURE 60D 78D 90D

    Magnification 1.18D 0.95D 0.75

    Field of view 76 degrees 84 degrees 94 degrees

    Focal length 19mm 15mm 12mmClear lens aperture 30mm 29mm 19mm

    Indirect fundus biomicroscopy

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    Contact Lens Methods

    Needs coupling solution Topical anaesthesia cannot be used in immediate post op. period / infectionAdvantages:

    Better stability Better quality of image (less interfaces) No need to retract the lids Can control ocular movements

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    Contact Lens Methods

    3 mirror lens (Goldmann)-

    Clear central portion planoconcave (-64D)Views central 300 of an emmetropic eye

    Radially arranged 3 mirrorssmall (590) - for Gonioscopy, region anterior to oramiddle (670)-pre-equatorial partlarge (730) -post. pole to equator

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    Contact Lens Methods

    3 mirror lens (Contd.)-

    ImageCentral lens : Erect, virtualPeripheral mirrors : A-P inverted

    : Not laterally reversed

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    Contact lens methods

    3 mirror lens (Contd.)-

    Technique Position patients head on slit lamp Hold the lens in first 3 fingers Ring finger to retract lower lid Patient to look up Place the lens on cornea Patient to look straight ahead

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    Contact lens methods

    3 mirror lens (Contd.)-

    Slit lamp Slit beam along the radial axis of mirror

    Evaluate fundus by Rotation of mirrors Readjusting the slit beam Redirecting the patients gaze

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    Contact lens methods

    Panfundoscope lens (Rodenstock)-

    Meniscus lens coupled with spherical lens (+81 D)

    Image : Real, inverted Within the lens Minification (0.7X)

    Wide angle view (upto equator) More useful for Laser photocoagulation

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    Contact lens methods

    Mainster lens-

    Meniscus lens with double aspheric lens Image

    Inverted, real High lateral and axial magnification Excellent resolution

    Image plane is very anterior - Difficult focusing Used for examination / Laser treatment

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    Contact lens methods

    Mainster lens: Modifications-

    View Magnification

    (degrees) Standard 90 0.96x Ultrafield 140 0.53x Widefield 125 0.68x High mag. 75 1.25x

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    Care of Lenses

    Sterilization : ETO gas (520 C) Cleaning:

    Rinse in cold / tepid water Clean with dishwashing liquid Rinse and blot dry with lint free cloth

    Disinfection: 2% Glutaraldehyde - (20 min.) Rinse in cool water dry 1:10 sol. of Na. hypochlorite (10 min) Rinse Dry

    Never boil or Autoclave

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    Investigations

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    Visual acuity measurement Color visionContrast sensitivity

    Amsler charts Visual discrimination tests (Two point

    discrimination) Entoptic imagery tests

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    Fundus fluorescein angiogram ICG angiogramOCT

    Elecrophysiology

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    Pinhole visual acuity Clinical interferometersGuyton-Minkowski Potential Acuity Meter(PAM)

    Visual acuity measurement

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    Blue field entoptoscopy

    penlight ortransilluminator

    To observe the flowof white blood cells in

    the parafoveal

    capillaries.

    Blue light is absorbedby the red blood cells

    but not the white

    blood cells.

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    Two-point discrimination

    Two light sources of equal intensity About 25 inches (or 62 cm)No information is learned about macularpotential.

    Fully mature cataracts or otherwise denseocular media.

    Gross color perception

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    Potential acuity

    PAM Reducedsnellen chart

    Laser inferometry

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    Contrast sensitivity

    Terry Acuity Pelli-Robson

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    Amsler: Set-up

    Pt holds grid 28cm-30cm Grid should be brightly illuminatedPt should be wearing best-corrected Rx fornear

    10 degree of the visual field10 cm square

    AMLSER GRID: Charts

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    1: Standard grid (mostcommon)

    black lines on whitebackground or white lines onblack background

    central fixation spot

    AMLSER GRID: Charts

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    AMLSER GRID: Charts

    2: chart 1 with diagonal lines" Use on pt w/

    central scotoma fixation problems

    " Help maintain fixation

    pt fixate at intersection ofdiagonals lines

    AMLSER GRID Ch t

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    AMLSER GRID: Charts

    3: Red grid on black background acts like a Red desaturation test

    toxic amblyopic pts better for relative scotomas

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    AMLSER GRID: Charts

    4: Random dots Pt with paracentral

    relative scotomas

    can delineate defectsbetter due to no linedistortion

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    AMLSER GRID: Charts

    5: Parallel horizontallines

    Sensitive tometamorphopsi

    a b/c lines

    adjusted to

    defects

    orientation

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    AMLSER GRID: Charts

    6: chart 5 w/additional horizontal

    lines 1 degree

    above & belowfixation

    " Helpful for evaluation

    complaints ofmetamorphopsia @

    the reading level

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    AMLSER GRID: Charts

    7: breaks horizontalcentral area

    3cm X 4cm square more sensitive to

    subtle defects in the

    fovea

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    Color vision

    Ishihara pseudo isochromatic charts FM 100 hue test D 15 test

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    Farnsworth D-15 Color Vision Test

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    Fransworth Munsell 100 hue test

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    Photo Sttress Test

    BCVA checked Pen torch / indirect about 3 cm away for abou

    10 seconds

    Photostress recovery time - to read any threeletters of the pre-test acuity line (15-30

    seconds)

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    Optical Coherence Tomogram(OCT)

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    Central Serous Retinopathy

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    Pigment Epithelial Detachment

    M l h l

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    Macular hole

    T i

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    Traction

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