What is the recommended workup and treatment for dry eyes?

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Last updated: December 23, 2025View editorial policy

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Workup for Dry Eyes

Begin with a detailed symptom assessment using validated questionnaires (OSDI or NEI-VFQ25), followed by slit-lamp examination with specific diagnostic tests including tear break-up time, ocular surface staining, and tear osmolarity or MMP-9 testing to confirm the diagnosis. 1

Initial Clinical Assessment

Symptom Evaluation

  • Document specific symptoms: irritation, burning, stinging, foreign body sensation, photophobia, blurred vision, contact lens intolerance, redness, mucous discharge, eye fatigue, and diurnal fluctuation (typically worsening later in the day) 1
  • Use validated questionnaires: the Ocular Surface Disease Index (OSDI) has demonstrated good specificity (0.83) and moderate sensitivity (0.60) for distinguishing dry eye from normal subjects 1
  • Identify exacerbating factors: air travel, low humidity, air drafts from fans or air conditioner vents, prolonged screen time, reading, digital device use, and poorly fitted sleep apnea devices 1

Comprehensive History

  • Medication review: Identify systemic medications that decrease tear production (antihistamines, decongestants, antidepressants, antihypertensics, hormonal therapies) 1
  • Systemic disease screening: Ask about dry mouth, joint pain, skin rashes, thyroid symptoms, or family history of autoimmune disorders 1
  • Ocular history: Previous eye surgeries (particularly LASIK or cataract surgery), contact lens wear, and prior ocular surface disease 1
  • Environmental exposures: Screen time duration, occupational exposures, smoking status, and living/working environment humidity 1

Slit-Lamp Examination

Essential Findings to Document

  • Tear meniscus height: Reduced height suggests aqueous deficiency 1
  • Lid margin abnormalities: Meibomian gland obstruction, telangiectasia, lid margin irregularity, or signs of blepharitis 1
  • Conjunctival changes: Injection, chemosis, scarring, keratinization, or mucous plaques 1
  • Corneal findings: Punctate epithelial erosions, filaments, epithelial defects, basement membrane irregularities, thinning, infiltrates, ulceration, or neovascularization 1

Diagnostic Testing Algorithm

First-Tier Tests (Perform in All Suspected Cases)

  • Tear break-up time (TBUT): Apply fluorescein dye and measure time until first break in tear film; less than 10 seconds is abnormal 1
    • A rapid TBUT may indicate unstable tear film with normal aqueous production and minimal ocular surface staining 1
  • Ocular surface staining: Use fluorescein, lissamine green, or rose bengal to assess epithelial damage; staining of inferior cornea and bulbar conjunctiva within the palpebral fissure is typical 1

Second-Tier Tests (Select Based on Clinical Presentation)

  • Tear osmolarity: Elevated osmolarity (>308 mOsm/L) or inter-eye differences (>8 mOsm/L) confirm diagnosis 1

    • Normal subjects have exceptionally stable tear film osmolarity, whereas dry eye patients lose homeostasis quickly with environmental changes 1
    • Correlation with clinical findings over time is more informative than a single measurement 1
  • Point-of-care MMP-9 test: Binary test indicating presence of inflammation; aids in diagnosis and can assess disease state changes 1

    • Does not differentiate dry eye from other inflammatory ocular surface diseases 1
  • Schirmer test without anesthesia (Schirmer I): Measures both basic and reflex tearing; less than 5.5 mm of wetting after 5 minutes is diagnostic of aqueous tear deficiency 1

  • Meibomian gland assessment: Evaluate expressibility and quality of meibum secretions 1

Corneal Sensation Testing

  • Assess when trigeminal nerve dysfunction is suspected (history of herpes zoster, diabetes, contact lens wear, or refractive surgery) 1

Laboratory Workup for Systemic Disease

Indications for Serologic Testing

Order laboratory tests when patients have:

  • Significant dry eye with other autoimmune symptoms (particularly dry mouth) 1
  • Family history of autoimmune disorders 1
  • Severe dry eye in younger patients or males (atypical demographics) 1

Specific Testing by Suspected Condition

For Sjögren Syndrome (approximately 10% of clinically significant aqueous deficient dry eye cases) 1:

  • Anti-Sjögren syndrome A antibody (SSA/anti-Ro)
  • Anti-Sjögren syndrome B antibody (SSB/anti-La)
  • Antinuclear antibody (ANA)
  • Rheumatoid factor (RF)
  • Salivary protein 1 (SP1)
  • Carbonic anhydrase 6 (CA6)
  • Parotid secretory protein (PSP) 1

For Thyroid Eye Disease:

  • Antithyroid peroxidase antibody
  • Antithyroglobulin antibody
  • Orbital imaging (CT or MRI) if proptosis or lid retraction present 1

For Sarcoidosis:

  • Serum lysozyme
  • Angiotensin-converting enzyme (ACE)
  • Chest CT to determine disease extent
  • Consider conjunctival biopsy
  • Consult pulmonology as necessary 1

For Ocular Mucous Membrane Pemphigoid:

  • Conjunctival biopsy with light microscopy and immunofluorescent or immunohistochemical studies 1

Classification of Disease Severity

Mild Dry Eye

  • Symptoms: Intermittent irritation, itching, soreness, ocular discomfort, burning, or intermittent blurred vision 1
  • Signs: Inconsistent correlation between symptoms and clinical findings 1

Moderate Dry Eye

  • Increased discomfort and frequency of symptoms
  • More consistent negative effect on visual function 1

Severe Dry Eye

  • Constant or potentially disabling visual symptoms
  • Risk of complications: ocular surface keratinization, conjunctival fibrosis, limbal stem cell deficiency, corneal scarring, thinning, neovascularization, microbial or sterile corneal ulceration with possible perforation 1

Critical Pitfalls to Avoid

  • Don't rely on a single diagnostic test: The diagnosis is difficult because of inconsistent correlation between symptoms and signs; combine at least two tests 1, 2
  • Don't miss underlying systemic disease: Ophthalmologists should have a high index of suspicion for Sjögren syndrome (associated with increased lymphoma risk) and low threshold for serologic workup 1
  • Don't overlook meibomian gland dysfunction: Most patients have evaporative or mixed-mechanism dry eye rather than pure aqueous deficiency 1
  • Don't dismiss pediatric presentations: Children may present with chronic recurrent blepharokeratoconjunctivitis and subtle rosacea signs before cutaneous manifestations 1
  • Recognize post-surgical dry eye: All patients undergoing cataract or refractive surgery should be evaluated preoperatively, as baseline parameters predict postoperative risk 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Current Approach to Dry Eye Disease.

Clinical reviews in allergy & immunology, 2015

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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