The document discusses the importance of broader blindness prevention through early detection and intervention of sight-threatening eye conditions. It presents referral data from EyePACS retinal screening, showing that over 8% of scans detected diabetic retinopathy and nearly 8% detected other conditions like glaucoma and macular degeneration. Recommendations are provided for a protocol to standardized detection and referral of optic nerve, retinal, and macular lesions. Guidelines establish timeframes for emergency, urgent, and moderately urgent referrals for different conditions. Future efforts include validating the protocol, integrating it into electronic records, and connecting treating clinicians.
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