Dry eye disease (KCS)
Tear-film instability/deficiency (evaporative MGD or aqueous-deficient, e.g. Sjögren)
Overview
Keratoconjunctivitis sicca — a multifactorial disease of tear-film instability causing ocular surface inflammation. Evaporative (MGD-related) is commonest; aqueous-deficient forms include Sjögren syndrome. Diagnosis and primary management are symptom-led; refer for serious causes or non-response.
Recognise
- Bilateral grittiness, burning, foreign-body sensation, fluctuating blurred vision relieved by blinking
- Paradoxical watering (reflex tearing); worse with screens, air-conditioning, low humidity
- Signs: reduced tear break-up time, punctate corneal staining, low tear meniscus; Schirmer test reduced in aqueous deficiency
Red flags
- Red flags of a serious cause (severe pain, photophobia, marked visual loss) → same-day ophthalmology
- Suspected Stevens–Johnson syndrome or ocular cicatricial pemphigoid → urgent referral
- Dry eyes + dry mouth + arthralgia → investigate for Sjögren syndrome
Differentials & how to tell them apart
Investigations
Clinical with fluorescein (tear break-up time, staining). Schirmer test. Screen for Sjögren (anti-Ro/La, salivary symptoms) if suggestive.
Management
Ocular lubricants + lid hygiene; preservative-free if used frequently
- 1Lubricants (preservative-free if used >4–6×/day), lid hygiene/warm compresses for MGD, environmental advice (screen breaks, humidity).Gate: Same-day referral for red-flag/serious causes; urgent referral if SJS or cicatricial pemphigoid suspected; investigate Sjögren if sicca symptoms
- 2No response after 4–12 weeks → ophthalmology; options include topical ciclosporin (NICE TA for severe disease), punctal plugs, autologous serum.
Key points
Common, chronic, symptom-led. The integration point: dry eye + dry mouth = Sjögren — look for the systemic disease.
Monitor & prognosis
Symptom control; corneal staining.
Chronic but manageable.
Source: NICE CKS Dry eye disease; TFOS DEWS II; College of Optometrists CMG