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Ophthalmology · RSSDI

Diabetic retinopathy

RSSDI
B
Source:RSSDI-VRSI Position Statement on Diabetic Retinopathy Screening and Management (2023)ICO Guidelines for Diabetic Eye Care (2023)AAO Diabetic Retinopathy Preferred Practice Pattern (2023)
Verified Apr 2026
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Red Flags

  • Sudden vision loss or new floaters with diabetes — emergency ophthalmology; suspect vitreous haemorrhage or tractional retinal detachment[1]
  • Severe non-proliferative diabetic retinopathy (NPDR), proliferative DR, or diabetic macular oedema — same-week retinal specialist for laser, intravitreal therapy, or vitrectomy[1]
  • Pregnancy with pre-existing diabetes — screen at booking and trimester progression; risk of rapid worsening[1]
  • Severe hypoglycaemia or rapid HbA1c reduction in T1DM with established DR — early worsening of retinopathy ('treatment-induced retinopathy')[1]

First-line treatment

Interventions

  • Glycaemic, BP, lipid optimisation[1]
    HbA1c <7% (individualised), BP <130/80, statin therapy; tight control reduces incidence and progression of DR; rapid intensification can transiently worsen — counsel and ophthalmology liaison
  • Diabetic retinopathy screening pathway[1]
    Annual digital fundus photography with grading by trained reader/AI tool; refer to ophthalmology for any DR more advanced than mild NPDR or any maculopathy
  • Pan-retinal photocoagulation (PRP)[1]
    Proliferative diabetic retinopathy; severe NPDR in selected high-risk patients; multiple sessions; transient peripheral vision loss; may combine with anti-VEGF for centre-involving DME
  • Intravitreal anti-VEGF therapy[1]
    Diabetic macular oedema (centre-involving) and high-risk PDR; ranibizumab, bevacizumab (off-label), aflibercept, faricimab; monthly loading × 5 then variable per response
  • Vitrectomy[1]
    Non-clearing vitreous haemorrhage, tractional retinal detachment, fibrovascular proliferation threatening macula; combined with PRP and intraoperative anti-VEGF where indicated

First-line drug therapy

DrugClassAdultPaediatricNotes
Ranibizumab (intravitreal)[1]Anti-VEGF Fab fragment0.5 mg intravitreal injection monthly × 4–5 doses then variable (PRN, treat-and-extend)—First-line for centre-involving DME; ophthalmology specialist administration; monitor IOP, endophthalmitis risk
Aflibercept (intravitreal)[1]Anti-VEGF fusion protein2 mg intravitreal monthly × 5 doses then every 8 weeks; high-dose 8 mg with extended interval emerging—Comparable efficacy to ranibizumab; longer durability allowing extended intervals; durable PDR control in Protocol S
Bevacizumab (intravitreal — off-label)[1]Anti-VEGF monoclonal antibody1.25 mg intravitreal monthly × 5 doses then variable—Cost-effective alternative widely used in resource-limited settings; off-label for ophthalmic use; comparable efficacy in Protocol T
Intravitreal triamcinolone or dexamethasone implant (refractory DME)[1]Intravitreal corticosteroidTriamcinolone 4 mg intravitreal; dexamethasone 0.7 mg sustained-release implant every 4–6 months—Refractory DME or anti-VEGF non-response; cataract progression and IOP rise; consider after multiple anti-VEGF failures or pseudophakic eye
Fenofibrate (selected)[1]PPAR-alpha agonist200 mg PO daily—Adjunct for DR progression in patients with elevated triglycerides per FIELD trial; not a substitute for ophthalmic therapy
Ranibizumab (intravitreal)[1]
Anti-VEGF Fab fragment
Adult
0.5 mg intravitreal injection monthly × 4–5 doses then variable (PRN, treat-and-extend)
Paediatric
—
First-line for centre-involving DME; ophthalmology specialist administration; monitor IOP, endophthalmitis risk
Aflibercept (intravitreal)[1]
Anti-VEGF fusion protein
Adult
2 mg intravitreal monthly × 5 doses then every 8 weeks; high-dose 8 mg with extended interval emerging
Paediatric
—
Comparable efficacy to ranibizumab; longer durability allowing extended intervals; durable PDR control in Protocol S
Bevacizumab (intravitreal — off-label)[1]
Anti-VEGF monoclonal antibody
Adult
1.25 mg intravitreal monthly × 5 doses then variable
Paediatric
—
Cost-effective alternative widely used in resource-limited settings; off-label for ophthalmic use; comparable efficacy in Protocol T
Intravitreal triamcinolone or dexamethasone implant (refractory DME)[1]
Intravitreal corticosteroid
Adult
Triamcinolone 4 mg intravitreal; dexamethasone 0.7 mg sustained-release implant every 4–6 months
Paediatric
—
Refractory DME or anti-VEGF non-response; cataract progression and IOP rise; consider after multiple anti-VEGF failures or pseudophakic eye
Fenofibrate (selected)[1]
PPAR-alpha agonist
Adult
200 mg PO daily
Paediatric
—
Adjunct for DR progression in patients with elevated triglycerides per FIELD trial; not a substitute for ophthalmic therapy

Safety-net

  1. Annual eye check is essential even when vision feels normal — diabetic retinopathy is silent until advanced[1]
  2. Sudden vision loss, new floaters, flashes, or sudden blurry vision — same-day ophthalmology assessment[1]
  3. Tight control of blood sugar and BP slows or prevents progression — but rapid HbA1c drops can transiently worsen retinopathy; coordinate with eye team[1]

Referral criteria

  • Any DR more advanced than mild NPDR; any diabetic macular oedemaOphthalmology / retina specialist[1]
  • Sudden vision loss, vitreous haemorrhage, tractional retinal detachment, neovascular glaucomaEmergency ophthalmology[1]
  • Pregnancy with pre-existing diabetesScreen at booking and trimester progression[1]
  • Failure of anti-VEGF or refractory DMETertiary retinal service for combined therapy or alternative agent[1]

Clinical summary

Screening, staging, and treatment pathway for diabetic retinopathy and diabetic macular oedema in adults with type 1 and type 2 diabetes.

References

  1. 1.RSSDI-VRSI Position Statement on Diabetic Retinopathy Screening and Management (2023); ICO Guidelines for Diabetic Eye Care; AAO Diabetic Retinopathy Preferred Practice Pattern (2023)

On this page

  • Red flags
  • First-line treatment
  • Safety-net
  • Referral
  • References