CASE
 PRESENTATION


Department of Ophthalmology
    October 13, 2010
GENERAL DATA



•ZN, 69/F
•Bauang, LU
•Filipino
•Catholic
•Date of consult-November 2008
OCULAR       PAST MEDICAL     FAMILY      PERSONAL
  HISTORY        HISTORY        HISTORY        AND
                                              SOCIAL
                                             HISTORY
2007-Cataract (+) HPN x 5 yrs (+) HPN     Previous
extraction, OU metoprolol     (-) DM      smoker
No other       (-) DM         (-) Ca      Non alcoholic
ocular disease                            beverage
                                          drinker
                                          housewife
• REVIEW OF SYSTEMS

• PHYSICAL EXAMINATION
OCULAR EXAMINATION
                              OD               OS
Visual acuity      20/70-20/30      20/200- NI

IOP                10               10
Ocular adnexae     E/N              E/N
AC                 Deep and quiet   Deep and quiet
Lens               IOL in place     IOL in place
EOM                intact           intact
pupils             3-2 mm           3-2 mm
                   (-) RAPD         (-) RAPD
Color perception   (+) RGB          (-) blue
AMSLER GRID
Dilated Fundus Exam
• Fasting blood sugar
• Fluorescein Angiography
SALIENT FEATURES
•   69 y/o
•   Blurred vision with metamorphopsia
•   History of smoking
•   hypertensive
•   Decreased color perception
•   (+) drusen, RPE atrophy
AGE- RELATED MACULAR
 DEGENERATION, NON-
    NEOVASCULAR
AGE- RELATED MACULAR
         DEGENERATION
• Leading cause of IRREVERSIBLE vision loss in
  the developed countries
• 4th common cause of vision loss in Phil
• Autosomal dominant disease affected by
  nutritional and environmental factors
• bilateral
• I. Dry/ Non- exudative/Non-
  neovascular AMD- 90%

• II. WET/Exudative/Neovascular-
      10 %
CHANGES DURING AGING




REDUCED DENSITY AND DISTRIBUTION OF
         PHOTORECEPTORS


       INVOLUTIONAL CHANGES IN THE
            CHORIOCAPILLARIES
RISK
FACTORS
FAMILY HISTORY
• Relatives w/ AMD- 50%
• (-) relatives w/ AMD- 12 %
GENETIC MUTATIONS:
• CFH gene ( Ch.1)
• BF and C2 ( Ch. 6)
• LOC ( Ch. 10 )
Framimgham Eye Study:
• 65- 74 y/o- 6.4%
• >75 y/o- 19.7 %
• >80 y/o- 6x
DRUSEN
• Most important risk
  factor
• Small, round, yellow
  lesions
• Composed of
  vitronectin, lipids,
  immune and
  inflammatory related
  proteins
CLINICAL PRESENTATION
SCREENING
•   Amsler grid
•   Macular Photostress Test
•   Color perception test
•   Kollner Rule-
    – Optic nerve- RED, GREEN
    – Retina – BLUE, YELLOW
DIAGNOSTIC
                          OPTICAL COHERENCE
FLUORESCEIN ANGIOGRAPHY   TOMOGRAPHY
CHOROIDAL NEOVASCULARIZATION


Most common cause
 of visual loss
MANAGEMENT
• NO definitive treatment
• DETERMINE PERSONS WHO WILL DEVELOP
  ADVANCED ARMD
• Goal: prevent development of
  neovascularization
Age- Related Eye Disease Study
•   Vitamin A ( Beta Carotene)- 15 mg
•   Vitamin C- 500 mg
•   Vitamin E- 400 IU
•   Zinc- 80 mg
•   Copper- 2 mg
AREDS
 Antioxidants plus   Zinc alone   Antioxidants alone
        zinc
  Reduced risk of
developing AMD by
        25%             21%              17%
  Reduced risk of
   vision loss by
        19%            11%               10%
Who will benefit from high- dose
             antioxidants?
•   Extensive intermediate drusen
•   At least 1 large druse
•   geographic atrophy
•   Advanced AMD in one eye
LUTEIN
“Dietary lutein/zeaxanthin intake was inversely
  associated with neovascular AMD”

    -The Relationship of Dietary Carotenoid and Vitamin A, E, and C Intake With Age-Related Macular Degeneration
    in a Case-Control StudyAREDS Report No. 22
•   Age-Related Eye Disease Study Research Group*

•   Arch Ophthalmol. 2007;125(9):1225-1232
“visual function is improved with lutein alone or
    lutein together with other nutrients”

•   Double-masked, placebo-controlled, randomized trial of lutein and antioxidant supplementation in the intervention of
    atrophic age-related macular degeneration: the Veterans LAST study (Lutein Antioxidant Supplementation Trial).
•   Richer S, Stiles W, Statkute L, Pulido J, Frankowski J, Rudy D, Pei K, Tsipursky M, Nyland J.
•   Department of Veterans'Affairs, Medical Center Eye Clinic, North Chicago, Illinois 60064-3095, USA.
    stuart.richer1@med.va.gov
PROPHYLACTIC LASER
PROPHYLACTIC TREATMENT OF AMD TRIAL (PTAMD):
̋ Patients treated wih prophylactic laser were more likely to have
  a CNV event ( 21%) than were the observed patients at 18
  months ( 14%) ̋


COMPLICATIONS OF AGE- RELATED MACULAR
  DEGENERATION PREVENTION TRIAL ( CAPT)
Incidence of late AMD was 19.7% in treated eyes and 20.4 % in
   untreated eyes, incidence of CNV was 13.3% for both groups
RHEOPHERESIS
• - An extracorporeal blood filtration procedure that
  removes circulating macromolecules from the blood

MULTICENTER INVESTIGATION OF RHEOPHERESIS OF
 AMD( MIRA-1)
‘No statistically significant benefit of rheopheresis over sham
  treatment’
TREATMENT OF NEOVASCULAR
         ARMD
Laser Photocoagulation
           MACULAR
            PHOTOCOAGULATION
            STUDY
           • Treatment did not decrease
             the chance of maintaining
             good VA or vision within 1.5
             lines of VA before the
             treatment
Photodynamic therapy
          TREATMENT OF AMD
            WITH PHOTODYNAMIC
            THERAPY
          -‘59 % of PDT treated eyes
             versus 31% (placebo)
             avoided moderate vision
             loss’
          • Visudyne in Minimally
             Classic Trial
          • Vertoporfin in
             Photodynamic Therapy
             study
Anti- VEGF
     • MARINA Study
            ANCHOR STUDY
     • 95% of Ranibizumab
       -95% vs 64% of PDT
        treated patients
       treated patients
        experienced visual
       maintained/ improved
       vision- 12 mos vs 62% of
        improvement
       -90% vstreated patients
        sham 65.7 % after 24
      mos
      -41% of patients improved
      3 lines after 24 mos
• After a year…
• VA- 20/100, OD   HM, OS
“Age is an issue of mind
       over matter.
   If you don't mind, it
      doesn't matter.

                ~Mark Twain
age related macular degeneration

age related macular degeneration

  • 1.
    CASE PRESENTATION Department ofOphthalmology October 13, 2010
  • 4.
    GENERAL DATA •ZN, 69/F •Bauang,LU •Filipino •Catholic •Date of consult-November 2008
  • 6.
    OCULAR PAST MEDICAL FAMILY PERSONAL HISTORY HISTORY HISTORY AND SOCIAL HISTORY 2007-Cataract (+) HPN x 5 yrs (+) HPN Previous extraction, OU metoprolol (-) DM smoker No other (-) DM (-) Ca Non alcoholic ocular disease beverage drinker housewife
  • 7.
    • REVIEW OFSYSTEMS • PHYSICAL EXAMINATION
  • 8.
    OCULAR EXAMINATION OD OS Visual acuity 20/70-20/30 20/200- NI IOP 10 10 Ocular adnexae E/N E/N AC Deep and quiet Deep and quiet Lens IOL in place IOL in place EOM intact intact pupils 3-2 mm 3-2 mm (-) RAPD (-) RAPD Color perception (+) RGB (-) blue
  • 9.
  • 10.
  • 11.
    • Fasting bloodsugar • Fluorescein Angiography
  • 12.
    SALIENT FEATURES • 69 y/o • Blurred vision with metamorphopsia • History of smoking • hypertensive • Decreased color perception • (+) drusen, RPE atrophy
  • 13.
    AGE- RELATED MACULAR DEGENERATION, NON- NEOVASCULAR
  • 14.
    AGE- RELATED MACULAR DEGENERATION • Leading cause of IRREVERSIBLE vision loss in the developed countries • 4th common cause of vision loss in Phil • Autosomal dominant disease affected by nutritional and environmental factors • bilateral
  • 15.
    • I. Dry/Non- exudative/Non- neovascular AMD- 90% • II. WET/Exudative/Neovascular- 10 %
  • 16.
    CHANGES DURING AGING REDUCEDDENSITY AND DISTRIBUTION OF PHOTORECEPTORS INVOLUTIONAL CHANGES IN THE CHORIOCAPILLARIES
  • 18.
  • 19.
    FAMILY HISTORY • Relativesw/ AMD- 50% • (-) relatives w/ AMD- 12 % GENETIC MUTATIONS: • CFH gene ( Ch.1) • BF and C2 ( Ch. 6) • LOC ( Ch. 10 )
  • 20.
    Framimgham Eye Study: •65- 74 y/o- 6.4% • >75 y/o- 19.7 % • >80 y/o- 6x
  • 21.
    DRUSEN • Most importantrisk factor • Small, round, yellow lesions • Composed of vitronectin, lipids, immune and inflammatory related proteins
  • 22.
  • 25.
    SCREENING • Amsler grid • Macular Photostress Test • Color perception test • Kollner Rule- – Optic nerve- RED, GREEN – Retina – BLUE, YELLOW
  • 26.
    DIAGNOSTIC OPTICAL COHERENCE FLUORESCEIN ANGIOGRAPHY TOMOGRAPHY
  • 27.
  • 28.
    MANAGEMENT • NO definitivetreatment • DETERMINE PERSONS WHO WILL DEVELOP ADVANCED ARMD • Goal: prevent development of neovascularization
  • 29.
    Age- Related EyeDisease Study • Vitamin A ( Beta Carotene)- 15 mg • Vitamin C- 500 mg • Vitamin E- 400 IU • Zinc- 80 mg • Copper- 2 mg
  • 30.
    AREDS Antioxidants plus Zinc alone Antioxidants alone zinc Reduced risk of developing AMD by 25% 21% 17% Reduced risk of vision loss by 19% 11% 10%
  • 31.
    Who will benefitfrom high- dose antioxidants? • Extensive intermediate drusen • At least 1 large druse • geographic atrophy • Advanced AMD in one eye
  • 32.
    LUTEIN “Dietary lutein/zeaxanthin intakewas inversely associated with neovascular AMD” -The Relationship of Dietary Carotenoid and Vitamin A, E, and C Intake With Age-Related Macular Degeneration in a Case-Control StudyAREDS Report No. 22 • Age-Related Eye Disease Study Research Group* • Arch Ophthalmol. 2007;125(9):1225-1232
  • 33.
    “visual function isimproved with lutein alone or lutein together with other nutrients” • Double-masked, placebo-controlled, randomized trial of lutein and antioxidant supplementation in the intervention of atrophic age-related macular degeneration: the Veterans LAST study (Lutein Antioxidant Supplementation Trial). • Richer S, Stiles W, Statkute L, Pulido J, Frankowski J, Rudy D, Pei K, Tsipursky M, Nyland J. • Department of Veterans'Affairs, Medical Center Eye Clinic, North Chicago, Illinois 60064-3095, USA. stuart.richer1@med.va.gov
  • 34.
    PROPHYLACTIC LASER PROPHYLACTIC TREATMENTOF AMD TRIAL (PTAMD): ̋ Patients treated wih prophylactic laser were more likely to have a CNV event ( 21%) than were the observed patients at 18 months ( 14%) ̋ COMPLICATIONS OF AGE- RELATED MACULAR DEGENERATION PREVENTION TRIAL ( CAPT) Incidence of late AMD was 19.7% in treated eyes and 20.4 % in untreated eyes, incidence of CNV was 13.3% for both groups
  • 35.
    RHEOPHERESIS • - Anextracorporeal blood filtration procedure that removes circulating macromolecules from the blood MULTICENTER INVESTIGATION OF RHEOPHERESIS OF AMD( MIRA-1) ‘No statistically significant benefit of rheopheresis over sham treatment’
  • 36.
  • 37.
    Laser Photocoagulation MACULAR PHOTOCOAGULATION STUDY • Treatment did not decrease the chance of maintaining good VA or vision within 1.5 lines of VA before the treatment
  • 38.
    Photodynamic therapy TREATMENT OF AMD WITH PHOTODYNAMIC THERAPY -‘59 % of PDT treated eyes versus 31% (placebo) avoided moderate vision loss’ • Visudyne in Minimally Classic Trial • Vertoporfin in Photodynamic Therapy study
  • 39.
    Anti- VEGF • MARINA Study ANCHOR STUDY • 95% of Ranibizumab -95% vs 64% of PDT treated patients treated patients experienced visual maintained/ improved vision- 12 mos vs 62% of improvement -90% vstreated patients sham 65.7 % after 24 mos -41% of patients improved 3 lines after 24 mos
  • 40.
    • After ayear… • VA- 20/100, OD HM, OS
  • 41.
    “Age is anissue of mind over matter.   If you don't mind, it doesn't matter. ~Mark Twain