Treatment and Management of Age-Related Macular Degeneration
For an older adult with macular degeneration, immediately determine whether the disease is wet (neovascular) or dry (non-exudative), as wet AMD requires urgent intravitreal anti-VEGF therapy within days of diagnosis, while dry AMD requires AREDS2 supplementation and risk factor modification. 1
Immediate Diagnostic Classification
The first critical step is optical coherence tomography (OCT) to identify subretinal fluid, intraretinal fluid (indicating wet AMD), or geographic atrophy (indicating advanced dry AMD). 1 This distinction determines the entire treatment pathway and urgency of intervention.
Treatment Algorithm for Wet (Neovascular) AMD
If wet AMD is confirmed, initiate intravitreal anti-VEGF therapy immediately—treatment within 2 years of diagnosis significantly reduces legal blindness and visual impairment. 1
Loading Phase Protocol
- Administer three loading doses at exactly 4-week intervals using aflibercept, ranibizumab, or bevacizumab 1, 2
- Perform OCT imaging at each visit to assess for persistent subretinal or intraretinal fluid 1
- Biomicroscopic fundus examination is required at every injection visit 1
Maintenance Phase Options
After completing the loading phase, choose from evidence-based maintenance regimens: 1
- Aflibercept every 8 weeks (comparable efficacy to monthly dosing in first year) 1
- Treat-and-extend protocol (adjust intervals based on disease activity) 1
- PRN (as-needed) dosing with monthly monitoring 1
- Monthly injections if disease remains active 1
Critical pitfall: Avoid arbitrary dosing intervals (such as every 6 weeks) that lack clinical trial support—stick to established protocols of 4-week or 8-week intervals. 1
Monitoring Requirements
- OCT at every visit to detect recurrent fluid 1
- If disease activity recurs before the 8-week interval, increase frequency to every 4 weeks until stabilization 1
- Patients must report symptoms of endophthalmitis, retinal detachment, or decreased vision immediately 1
Treatment Algorithm for Dry (Non-Exudative) AMD
For intermediate or advanced dry AMD, prescribe AREDS2 supplementation immediately—this reduces progression risk by up to 36% over 10 years. 1
AREDS2 Formulation Components
The specific formulation includes: 1
- Vitamin C
- Vitamin E
- Zinc 25mg (not 80mg—lower dose has equivalent efficacy with fewer genitourinary complications) 1
- Copper (essential to prevent copper-deficiency anemia from zinc) 1
- Lutein 10mg 1
- Zeaxanthin 2mg 1
Critical safety consideration: Beta-carotene was eliminated from AREDS2 due to 18% increased cumulative incidence of lung cancer in current and former smokers (relative risk 1.28). 1 Never prescribe beta-carotene-containing formulations to smokers.
Coordination with Primary Care
Coordinate with the patient's primary care physician before initiating long-term AREDS2 supplementation due to potential adverse effects, particularly increased genitourinary hospitalizations with zinc. 1 This is non-negotiable for patient safety.
Risk Factor Modification (All AMD Types)
Smoking Cessation—Non-Negotiable Priority
Cigarette smoking is the only proven modifiable risk factor and must be addressed aggressively in all AMD patients. 3 Current smokers face 2-3 times higher AMD risk, with risk increasing proportionally to pack-years smoked. 3 Smoking cessation is mandatory and the key modifiable risk factor. 1
Additional Modifiable Factors
- Address elevated body mass index 3
- Manage cardiovascular disease and hyperlipidemia 3
- Encourage dietary intake of antioxidants and carotenoids 4
Patient Education and Counseling
Visual Prognosis
Reassure patients that while central visual loss is common, total blindness is extremely rare—peripheral vision is typically preserved. 1 Central visual acuity may range from near-normal (20/40-20/60) in early disease to severe impairment (20/200-20/400) in advanced disease. 1
Fellow Eye Monitoring
For patients with wet AMD in one eye, the fellow eye remains at exceptionally high risk and requires monitoring every 6-12 months even without symptoms. 1 Patients with advanced AMD in one eye and large drusen with retinal pigment epithelial changes in the fellow eye represent the highest risk group. 1
Home Monitoring
Provide an Amsler grid for daily self-monitoring—patients should look at the central dot and evaluate if any grid lines appear wavy or distorted (metamorphopsia). 1 Instruct patients to return immediately with any new visual symptoms in the unaffected eye. 1
Vision Rehabilitation Referral
Refer patients with reduced visual function to vision rehabilitation services immediately, including: 1
- Optical or electronic magnifying devices 1
- Bright lights and enhanced lighting 1
- Electronic reading aids 1
Important counseling point: Vision rehabilitation optimizes existing visual function rather than restoring lost vision—patients often have unrealistic expectations about this. 1
Psychosocial Considerations
- Loss of visual acuity increases risk of frequent falls 1
- Depression frequently accompanies severe central vision loss and should be screened for 1
- Charles Bonnet syndrome (visual hallucinations) frequently accompanies severe central vision loss but does not represent psychosis or mental deterioration—counsel patients about this benign phenomenon 1
Follow-Up Schedule
For Wet AMD
- Monthly visits during loading phase 1
- Every 8 weeks during maintenance (if stable on aflibercept) 1
- More frequent if disease activity recurs 1
For Dry AMD
- Regular comprehensive eye examinations for early detection of progression 1
- Monitor fellow eye every 6-12 months if unilateral advanced disease 1
- Annual examinations if bilateral early/intermediate disease 1
What NOT to Do
- Do not delay anti-VEGF therapy in wet AMD—early treatment within 2 years significantly reduces blindness 1
- Do not use beta-carotene formulations in current or former smokers 1
- Do not use 80mg zinc when 25mg provides equivalent efficacy with better safety 1
- Do not prescribe AREDS2 supplements as a substitute for anti-VEGF therapy in wet AMD 1
- Do not use arbitrary injection intervals lacking clinical trial support 1