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Jorge Cuadros OD PhD
        Tara Seymour
Significance of Broader Blindness
Prevention in Our Clinics
 Diabetic retinopathy is the main cause of
  blindness in working age adults, but not
  in all adults.
 More people will become blind from
  macular degeneration and glaucoma.
 The majority of blindness could be
  prevented with early intervention.
 Many sight-threatening conditions have
  been detected and referred through
  EyePACS
EyePACS Referrals
 8.21% of all EyePACS consults resulted in
  referral for sight-threatening diabetic retinopathy
 7.83% of all EyePACS consults resulted in
  referral for other sight-threatening conditions
     Glaucoma
     Cataract
     Maculopathy
     Papillopathy (optic nerve)
     Pigmented lesions
     Retinal degeneration
How Does Your Clinic Handle Eye
Referrals?
 No time frame given – all eye referrals
  generally treated the same
 Urgent referrals (within 2 days) made with
  sudden decreased vision or ocular pain; all
  other referrals generally treated the same
 Clinic is able to differentiate conditions
  requiring within 1 month from conditions
  requiring referral within 2 days
What Is The Average Waiting Time For
Eye Care Referrals From Your Clinic?


   Less than one week
   One week to less than one month
   One month to less than three months
   Three months to less than six months
   Six months or more
   I don’t know how long my patients wait to see
    an eye care provider.
The Challenge of Referral for
Other Conditions
 The retinal consult does not take the place
  of a full eye exam.
 Sensitivity and specificity of referral based
  on electronic consults have not been
  validated for other conditions
     Disagreement about when to treat, when to refer
     Excessive variability in consultant
      recommendations
     Less effective treatment
     Excessive over-referral
Scientific Committee
Recommendations:
 Purpose: Identify patients with sight-
  threatening conditions.
 Develop protocol for acquiring necessary
  information and images for consistent and
  easily adapted detection system.
 Retinal image interpretation protocol for
  identifying significant lesions in:
     Optic nerves
     Retinas
     Maculas
Optic Nerve Lesions
   Signs of glaucoma:
     Asymmetric cupping: greater than 0.2 dd cupping difference between the two
        eyes
       Enlarged cup: optic nerve cupping equal to or greater than 0.7
       Rim notch or thinning: notch in or thinning of optic nerve tissue extending to edge
        of the optic nerve or disproportionate thinning of rim tissue in inferior or superior
        sections of optic nerve
       Optic nerve/Splinter hemorrhage: flame shaped hemorrhage near or at the rim or
        in the substance of the cup
       Nerve fiber layer defect (NFLD): NFLD occupying greater than 10 degrees of arc
        in the inferior or superior arcuate areas
       For screening purposes, referable glaucoma is considered sight-threatening,
        well-established glaucoma that is likely to be treated immediately. Low risk
        glaucoma suspects would not be referred from this protocol.
   Prominent pallor:
     pale optic nerve without cupping not previously identified
     pale swelling of segment of optic nerve with or without hemorrhage
   Papilledema:
     swollen, hyperemic disc with blurred margins in one or both eyes
Retinal Lesions
   Moderate/Severe nonproliferative diabetic
    retinopathy (NPDR), as defined by the
    International Clinical Diabetic Retinopathy
    Disease Severity Scale
   Neovascularization
     New vessels or diabetes-related fibrous proliferation
      anywhere
     Vitreous hemorrhage or pre-retinal hemorrhage
   Invasive lesions: eg melanomas
   Neovascularization of the iris
   Active retinitis: active retinal inflammation
   Retinal detachment (recent onset)
Lesions of the Macula
   High-risk drusen (large, soft drusen) especially
    associated with:
     Pigment migration
     Geographic atrophy not involving the foveal center
     Disciform scar or prior chorodial neovascularization
 Macular edema, not clinically significant: hard
  exudates within 2 disc diameters but more than one
  disc diameter from the fovea
 Clinically Significant Macular Edema (CSME): hard
  exudates within one disc diameter of fovea
 Subretinal neovascularization
     subretinal hemorrhage or lipid exudate with hemorrhage
      within the arcades
     wet macular edema-intraretinal hemorrhage involving the
      fovea
     cystoid macular edema with blood in cysts
     subretinal pigment epithelial blood (drusen visible over the
      hemorrhage)
Other Referral Criteria
 Visual Acuity < 20/40
 Acute onset of pain and/or vision loss
 *Intraocular pressures
 *Initiation of systemic treatments
  associated with vision loss:
     Hepatitis C treatment
     Plaquenil / quinine derivatives
     Steroids
         *    Not part of the Prevent Blindness Northern
          California Protocol
PBNC Referral Guideline
   Emergency Referral – 1-2 days:
     papilledema
     recent onset retinal detachment
     neovascularization of the iris
     active retinitis
     subretinal neovascularization
     acute vision loss
     acute onset of pain
PBNC Referral Guideline
   Urgent Referral (within 1 month)
     pale swelling of optic nerve or segment of optic
      nerve (with or without hemorrhage)
     neovascularization
     clinically significant macular edema
     possibly invasive lesion
   Moderately Urgent Referral (within 6 months)
     retinal and optic nerve features blurred in all views,
      with VA less than 20/40
     obvious glaucoma
     moderate to severe non-proliferative diabetic
      retinopathy
     high-risk drusen
PBNC Referral Guideline
   Pass
     clear media; retinal and optic nerve features clear
     optic nerve margins sharp, vessels easily visible,
      pink rim, less than 0.5 dd cup in both eyes
     retinal vessels visible and sharp, normal diameters,
      no hemorrhages or pigmented lesions, minimal
      microanerysms
     foveal reflex present, minimal drusen, no
      hemorrhages, flat or pitted
   Non-Readable
     Unreadable photos will not be used to initiate
      referrals; other screening results will be used instead
Future Efforts
   Validation of protocol
   Primary care provider certification for triage
    purposes
   Automation and integration into electronic
    medical records and referral systems
   Connect treating clinicians with EyePACS
    cases
   Automated patient alerts
   Using retinal images for identification of risk
    factors and biomarkers of systemic disease
   Validation of new technology and automated
    algorithms

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LC 09-2011-Broader Blindness Prevention

  • 1. Jorge Cuadros OD PhD Tara Seymour
  • 2. Significance of Broader Blindness Prevention in Our Clinics  Diabetic retinopathy is the main cause of blindness in working age adults, but not in all adults.  More people will become blind from macular degeneration and glaucoma.  The majority of blindness could be prevented with early intervention.  Many sight-threatening conditions have been detected and referred through EyePACS
  • 3. EyePACS Referrals  8.21% of all EyePACS consults resulted in referral for sight-threatening diabetic retinopathy  7.83% of all EyePACS consults resulted in referral for other sight-threatening conditions  Glaucoma  Cataract  Maculopathy  Papillopathy (optic nerve)  Pigmented lesions  Retinal degeneration
  • 4. How Does Your Clinic Handle Eye Referrals?  No time frame given – all eye referrals generally treated the same  Urgent referrals (within 2 days) made with sudden decreased vision or ocular pain; all other referrals generally treated the same  Clinic is able to differentiate conditions requiring within 1 month from conditions requiring referral within 2 days
  • 5. What Is The Average Waiting Time For Eye Care Referrals From Your Clinic?  Less than one week  One week to less than one month  One month to less than three months  Three months to less than six months  Six months or more  I don’t know how long my patients wait to see an eye care provider.
  • 6. The Challenge of Referral for Other Conditions  The retinal consult does not take the place of a full eye exam.  Sensitivity and specificity of referral based on electronic consults have not been validated for other conditions  Disagreement about when to treat, when to refer  Excessive variability in consultant recommendations  Less effective treatment  Excessive over-referral
  • 7. Scientific Committee Recommendations:  Purpose: Identify patients with sight- threatening conditions.  Develop protocol for acquiring necessary information and images for consistent and easily adapted detection system.  Retinal image interpretation protocol for identifying significant lesions in:  Optic nerves  Retinas  Maculas
  • 8. Optic Nerve Lesions  Signs of glaucoma:  Asymmetric cupping: greater than 0.2 dd cupping difference between the two eyes  Enlarged cup: optic nerve cupping equal to or greater than 0.7  Rim notch or thinning: notch in or thinning of optic nerve tissue extending to edge of the optic nerve or disproportionate thinning of rim tissue in inferior or superior sections of optic nerve  Optic nerve/Splinter hemorrhage: flame shaped hemorrhage near or at the rim or in the substance of the cup  Nerve fiber layer defect (NFLD): NFLD occupying greater than 10 degrees of arc in the inferior or superior arcuate areas  For screening purposes, referable glaucoma is considered sight-threatening, well-established glaucoma that is likely to be treated immediately. Low risk glaucoma suspects would not be referred from this protocol.  Prominent pallor:  pale optic nerve without cupping not previously identified  pale swelling of segment of optic nerve with or without hemorrhage  Papilledema:  swollen, hyperemic disc with blurred margins in one or both eyes
  • 9. Retinal Lesions  Moderate/Severe nonproliferative diabetic retinopathy (NPDR), as defined by the International Clinical Diabetic Retinopathy Disease Severity Scale  Neovascularization  New vessels or diabetes-related fibrous proliferation anywhere  Vitreous hemorrhage or pre-retinal hemorrhage  Invasive lesions: eg melanomas  Neovascularization of the iris  Active retinitis: active retinal inflammation  Retinal detachment (recent onset)
  • 10. Lesions of the Macula  High-risk drusen (large, soft drusen) especially associated with:  Pigment migration  Geographic atrophy not involving the foveal center  Disciform scar or prior chorodial neovascularization  Macular edema, not clinically significant: hard exudates within 2 disc diameters but more than one disc diameter from the fovea  Clinically Significant Macular Edema (CSME): hard exudates within one disc diameter of fovea  Subretinal neovascularization  subretinal hemorrhage or lipid exudate with hemorrhage within the arcades  wet macular edema-intraretinal hemorrhage involving the fovea  cystoid macular edema with blood in cysts  subretinal pigment epithelial blood (drusen visible over the hemorrhage)
  • 11. Other Referral Criteria  Visual Acuity < 20/40  Acute onset of pain and/or vision loss  *Intraocular pressures  *Initiation of systemic treatments associated with vision loss:  Hepatitis C treatment  Plaquenil / quinine derivatives  Steroids  * Not part of the Prevent Blindness Northern California Protocol
  • 12. PBNC Referral Guideline  Emergency Referral – 1-2 days:  papilledema  recent onset retinal detachment  neovascularization of the iris  active retinitis  subretinal neovascularization  acute vision loss  acute onset of pain
  • 13. PBNC Referral Guideline  Urgent Referral (within 1 month)  pale swelling of optic nerve or segment of optic nerve (with or without hemorrhage)  neovascularization  clinically significant macular edema  possibly invasive lesion  Moderately Urgent Referral (within 6 months)  retinal and optic nerve features blurred in all views, with VA less than 20/40  obvious glaucoma  moderate to severe non-proliferative diabetic retinopathy  high-risk drusen
  • 14. PBNC Referral Guideline  Pass  clear media; retinal and optic nerve features clear  optic nerve margins sharp, vessels easily visible, pink rim, less than 0.5 dd cup in both eyes  retinal vessels visible and sharp, normal diameters, no hemorrhages or pigmented lesions, minimal microanerysms  foveal reflex present, minimal drusen, no hemorrhages, flat or pitted  Non-Readable  Unreadable photos will not be used to initiate referrals; other screening results will be used instead
  • 15. Future Efforts  Validation of protocol  Primary care provider certification for triage purposes  Automation and integration into electronic medical records and referral systems  Connect treating clinicians with EyePACS cases  Automated patient alerts  Using retinal images for identification of risk factors and biomarkers of systemic disease  Validation of new technology and automated algorithms