Tiered management strategies.
Based on the TEFOS DEWS2 Report.
TFOS DEWS – Staged Management & Therapy of Dry Eye Disease
Dry Eye Disease (DED) management follows a stepwise (staged) approach, beginning with lifestyle and environmental measures, progressing to prescription and procedural therapies when needed.
This ensures treatments are targeted, evidence-based, and appropriate to disease severity.
🔹 Stage 1 — Foundational Management
(For mild, early, or intermittent symptoms)
Patient education – explain the chronic nature of DED and treatment goals.
Environmental modification – optimise humidity, avoid drafts, reduce screen time, manage airflow.
Dietary advice – increase omega-3 intake or supplementation.
Medication review – identify and adjust systemic or topical drugs contributing to dryness.
Lid hygiene – daily cleaning of lid margins to control blepharitis.
Warm compresses – promote meibomian gland oil flow and improve tear stability.
Lubricants/artificial tears – preservative-free formulations for symptomatic relief.
🔹 Stage 2 — Targeted Medical Therapy
(For persistent or moderate disease)
Continue Stage 1 measures.
Tear conservation: punctal plugs or moisture chamber glasses.
Anti-inflammatory therapy:
Topical corticosteroids (short course)
Cyclosporine (Restasis/Ikervis)
Lifitegrast (where available)
Secretagogues / Tear stimulants: diquafosol or oral pilocarpine (selected cases).
In-office gland therapies:
Meibomian gland expression (manual or device-assisted)
Thermal pulsation systems (e.g. LipiFlow)
Intense Pulsed Light (IPL) for MGD-related inflammation
🔹 Stage 3 — Advanced / Refractory Disease Management
(For chronic, moderate–severe DED unresponsive to earlier measures)
Continue Stage 1–2 strategies.
Systemic medications: tetracyclines or macrolides for MGD; immunomodulators for autoimmune causes.
Autologous serum or platelet-rich tear substitutes.
Scleral or PROSE lenses to protect and hydrate the ocular surface.
Advanced meibomian gland treatment (combined IPL + expression series).
Low-dose topical corticosteroids under close monitoring.
🔹 Stage 4 — Severe / Resistant or Structural Disease
(For severe, sight-threatening, or non-responsive DED)
Continue supportive care from previous stages.
Amniotic membrane grafts for epithelial healing and inflammation control.
Punctal cautery for permanent tear retention.
Tarsorrhaphy (partial lid closure) to reduce exposure.
Systemic immunosuppressants for severe inflammatory or autoimmune cases (in collaboration with rheumatology).
Surgical lid correction if anatomical abnormalities contribute to exposure or incomplete closure.
Key Principle
At every stage:
We re-evaluate underlying causes and contributing factors.
Adjust treatment intensity gradually.
Combine ocular surface protection, anti-inflammatory control, and tear film restoration for optimal outcomes.