Total Live Articles: 447

Age-Related Macular Degeneration (AMD)

NICE guideline [NG82] Age-related macular degeneration. Published: Jan 2018.

NICE CKS Macular degeneration – age-related. Last revised: Oct 2025.

Age-Related Macular Degeneration (AMD)

Age-related macular degeneration (AMD) is a potentially progressive degenerative disorder of the macula that typically affects people aged over 50 years. It is a common cause of irreversible central visual loss and is the leading cause of severe irreversible visual impairment in older adults in the developed world. AMD is broadly classified into dry AMD and wet AMD.

This updated UKMLA guide to AMD is based on NICE NG82 and NICE CKS, which covers classification, risk factors, symptoms, diagnosis, and management.

Classification

There are 2 main traditional types of AMD:

Dry AMD (atrophic) Wet AMD (neovascular / exudative)
Prevalence ~90% of AMD cases ~10% of AMD cases
Pathophysiology Gradual atrophy of retinal pigment epithelium and photoreceptors Choroidal neovascularisation → leakage, haemorrhage, fibrosis

Disclaimer:

AMD is traditionally divided into dry AMD and wet AMD, which is the most useful classification for exam and non-specialist levels.

NICE uses a more detailed classification system to describe disease stage and activity, but this level of detail is mainly relevant to ophthalmology.

NICE Classification

AMD classification Definition
Normal eyes
  • No signs of age-related macular degeneration (AMD)
  • Small (‘hard’) drusen (less than 63 micrometres) only
Early AMD Low risk of progression:

  • Medium drusen (63 micrometres or more and less than 125 micrometres) or
  • Pigmentary abnormalities

Medium risk of progression:

  • Large drusen (125 micrometres or more) or
  • Reticular drusen or
  • Medium drusen with pigmentary abnormalities

High risk of progression:

  • Large drusen (125 micrometres or more) with pigmentary abnormalities or
  • Reticular drusen with pigmentary abnormalities or
  • Vitelliform lesion without significant visual loss (best-corrected acuity better than 6/18) or
  • Atrophy smaller than 175 micrometres and not involving the fovea
Late AMD (indeterminate)
  • Retinal pigment epithelial (RPE) degeneration and dysfunction (presence of degenerative AMD changes with subretinal or intraretinal fluid in the absence of neovascularisation)
  • Serous pigment epithelial detachment (PED) without neovascularisation
Late AMD (wet active)
  • Classic choroidal neovascularisation (CNV)
  • Occult (fibrovascular PED and serous PED with neovascularisation)
  • Mixed (predominantly or minimally classic CNV with occult CNV)
  • Retinal angiomatous proliferation (RAP)
  • Polypoidal choroidal vasculopathy (PCV)
Late AMD (dry) Geographic atrophy (in the absence of neovascular AMD)

Significant visual loss (6/18 or worse) associated with:

  • Dense or confluent drusen or
  • Advanced pigmentary changes and/or atrophy or
  • Vitelliform lesion
Late AMD (wet inactive)
  • Fibrous scar
  • Sub-foveal atrophy or fibrosis secondary to an RPE tear
  • Atrophy (absence or thinning of RPE and/or retina)
  • Cystic degeneration (persistent intraretinal fluid or tubulations unresponsive to treatment)

Note that eyes may still develop or have a recurrence of late AMD (wet active)

Causes and Risk Factors

Smoking is the main modifiable risk factor

  • Dose-response relationship
  • Stopping smoking reduces the risk of AMD

Other risk factors:

  • AMD in the other eye
  • Advancing age
  • Females
  • Family history
  • Certain diet patterns
    • Low in omega-3 and 6
    • Low in vitamins A, C and E
    • Low in carotenoids (e.g. lutein) and minerals (e.g. zinc)
    • High glycaemic index
    • High in saturated fat and cholesterol
  • Hypertension and history of cardiovascular disease
  • Physical inactivity

Diagnosis

Disclaimer:

This article summarises AMD for educational and exam-focused learning, focusing on the core principles most relevant to a non-specialist level.

As explained above, the traditional dry vs wet AMD classification is more appropriate for non-specialist learning. Therefore, the investigation, diagnosis and management sections have been simplified and adapted around this distinction, rather than following NICE’s full detailed classification system.

Clinical Features

Typically presents as a >50 y/o with:

  • Blurring of vision
  • Scotoma – mainly affecting the central vision
  • Metamorphopsia (straight lines appear bent / wavy / crooked)

Wet AMD presents with rapidly progressing visual deterioration.

Other symptoms:

  • Light glare
  • Loss of or decreased contrast sensitivity (the ability to discern between different shades)
  • Size or colour of objects appears different with each eye
  • Abnormal dark adaptation (difficulty adjusting from bright to dim lighting)
  • Photopsia (perception of flickering or flashing light)

Advanced AMD can cause Charles Bonnet syndrome (visual hallucinations secondary to visual impairment, despite having intact insight and no underlying psychosis, delirium, or dementia)

Investigation and Diagnosis

Primary Care

Test Findings suggestive of AMD
Amsler grid
  • Metamorphopsia (straight lines appear wavy or distorted)
  • Scotomas (parts of the lines missing)
Fundoscopy Dry AMD:

  • Drusen – main finding
  • Changes to the macula (pigmentary / exudative / haemorrhagic / atrophic changes)

Wet AMD is indicated by signs of choroidal neovascularisation, in addition to dry AMD findings

  • Subretinal / intraretinal fluid
  • Subretinal haemorrhage
  • Retinal pigment epithelial detachment

If AMD is suspected, refer urgently to ophthalmology

Secondary Care

Initial investigation: slit lamp fundus examination (findings are similar to those of fundoscopy)

  • Dry AMD:
    • Drusen – main finding
    • Changes to the macula (pigmentary / exudative / haemorrhagic / atrophic changes)
  • Wet AMD is indicated by signs of choroidal neovascularisation, in addition to dry AMD findings
    • Subretinal / intraretinal fluid
    • Subretinal haemorrhage
    • Retinal pigment epithelial detachment

Dry AMD can usually be diagnosed by slit-lamp fundus examination alone, with no further imaging required

Further imaging is necessary to diagnose wet AMD:

  • 1st line: OCT – to detect neovascularisation and subretinal / intraretinal fluid
  • 2nd line: fundus fluorescein angiography (FFA) – to confirm neovascularisation if OCT is inconclusive / cannot exclude it

Management

Dry AMD

There are no pharmacological treatments for dry AMD

Mainstay of management is active observation and conservative management:

  • Smoking cessation (to reduce risk of progression – see the Smoking Cessation article for more information)
  • Consider antioxidant vitamin and mineral supplementation (AREDS2 formula: vitamin C, vitamin E, zinc, copper, lutein, and zeaxanthin)
  • Advise on a healthy, balanced diet (low glycaemic index, rich in fruits, green leafy vegetables and fish high in omega-3 fatty acids)

Wet AMD

Mainstay of management: intravitreal anti-VEGF therapy (e.g. ranibizumab, aflibercept, bevacizumab)

Laser photocoagulation is NOT routinely used in wet AMD. It is generally reserved for rare cases of extrafoveal choroidal neovascularisation where anti-VEGF therapy is not feasible or effective.

Do NOT offer photodynamic therapy and intravitreal corticosteroids as an adjunct to anti-VEGF therapy.

References


Related Articles

Diabetic Retinopathy

Chronic Open-Angle Glaucoma

Retinal Vein Occlusion (RVO)

Retinal Arterial Occlusion (RAO)

Share Your Feedback Below

Disclaimer

We’re actively expanding Guideline Genius to cover the full UKMLA content map. Therefore, you may notice some conditions not uploaded yet, or articles that currently focus on diagnosis and management for now.

We are also continuously reviewing and updating existing content to ensure accuracy and alignment with current guidelines. Some earlier articles are undergoing revision as part of this process. Once all content has been fully reviewed, this will be clearly communicated on the platform.

For updates, follow us on Instagram @guidelinegenius.

We welcome any feedback or suggestions via the anonymous feedback box at the bottom of each article and will do our best to respond promptly.

Thank you for your support.
The Guideline Genius Team

UK medical guidelines made easy. From guidelines to genius in minutes!

Quick Links

Cookie Policy

Social Media

© 2026 GUIDELINE GENIUS LTD

Stay Updated withGuideline Genius

Sign up to be notified when our newsletter launches, covering major guideline updates, article updates, and future UKMLA resources.