Summary

This document provides comprehensive notes on red eye, covering various aspects of eye anatomy, the causes of red eye, conjunctivitis, and other related eye conditions. The information provided is useful for medical professionals.

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Comprehensive Red Eye Notes (Doctor’s notes and Additional high-yield notes) 1. Overview of Eye Anatomy Relevant to Red Eye 1.​ Conjunctiva ○​ Bulbar Conjunctiva: Covers the sclera (the “white” of the eye) up to the edge of the cornea. ○​ Palpebral...

Comprehensive Red Eye Notes (Doctor’s notes and Additional high-yield notes) 1. Overview of Eye Anatomy Relevant to Red Eye 1.​ Conjunctiva ○​ Bulbar Conjunctiva: Covers the sclera (the “white” of the eye) up to the edge of the cornea. ○​ Palpebral Conjunctiva: Lines the inside of the eyelids. ○​ Normally transparent; when inflamed (conjunctivitis), it becomes red and edematous, hiding the white sclera beneath. 2.​ Sclera ○​ The tough, white outer coat of the globe. ○​ Forms approximately 5/6 of the outer surface. 3.​ Cornea ○​ Transparent, domed structure forming about 1/6 of the outer surface of the eye. ○​ Highly innervated → extremely sensitive. 4.​ Uveal Tract (Uvea) ○​ Composed of iris, ciliary body, and choroid. ○​ Inflammation (uveitis) often causes redness, pain, photophobia. 5.​ Eyelids & Lacrimal Apparatus ○​ Eyelids: Blepharitis, styes, or trauma can produce redness/irritation. ○​ Lacrimal system issues can cause tearing and secondary irritation. 2. General Causes of Red Eye A “red eye” can arise from multiple pathologies: 1.​ Conjunctival (conjunctivitis, subconjunctival hemorrhage). 2.​ Episcleral / Scleral (episcleritis, scleritis). 3.​ Corneal (keratitis, abrasion, ulcer). 4.​ Uveal (uveitis, iritis). 5.​ Raised IOP (acute angle-closure glaucoma). 6.​ Intraocular infection (endophthalmitis). 7.​ Trauma (foreign body, hyphema, chemical injury). 8.​ Others (tumors, severe dryness, etc.). 3. Conjunctivitis (Most Common Cause) 3.1 Viral Conjunctivitis ​ Presentation: Watery or mucoid discharge, possible follicles on palpebral conjunctiva (lower lid especially). ​ Often associated with flu-like symptoms (sore throat, fever). ​ Highly contagious. ​ Management: Supportive (lubricants, topical decongestants, hygiene). Usually self-limiting over 1–2 weeks. Adenoviral Keratoconjunctivitis ​ More severe form with possible pseudomembrane formation (peels off without bleeding). ​ Can involve the cornea → subepithelial infiltrates, scarring. ​ Management: ○​ Short course of topical steroids (under ophthalmology guidance) to reduce corneal scarring/infiltrates. ○​ Lubricants, decongestants. ○​ Emphasize hygiene due to high contagion. 3.2 Bacterial Conjunctivitis ​ Presentation: Mucopurulent or purulent discharge (sticky eyelids on waking). ​ Management: ○​ Broad-spectrum topical antibiotics (e.g., fluoroquinolones: moxifloxacin, ofloxacin) QID for 5–7 days. ○​ Antibiotic ointment (e.g., fusidic acid, erythromycin) at night. Gonococcal / Chlamydial Conjunctivitis ​ Profuse purulent discharge, potential corneal involvement (especially gonococcus). ​ May see or suspect concomitant STI (urethral discharge). ​ Management: Systemic therapy (IM ceftriaxone, oral azithromycin) + topical antibiotics; treat partners if indicated. 3.3 Allergic Conjunctivitis ​ Presentation: Intense itching, bilateral redness, watery or ropy discharge. ​ Types: ○​ Simple Allergic: Seasonal/perennial triggers. ○​ Vernal Keratoconjunctivitis (VKC) / Giant Papillary Conjunctivitis: More severe form with “cobblestone papillae” on the tarsal conjunctiva, often in young males, warm climates. ​ Management: ○​ Topical antihistamines (e.g., olopatadine), mast cell stabilizers. ○​ Lubricants. ○​ Short-course topical steroids for severe cases. ○​ Cyclosporine drops in chronic/refractory cases. 3.4 Subconjunctival Hemorrhage ​ Bright red patch on sclera beneath conjunctiva. ​ Often spontaneous (Valsalva from coughing/sneezing) or due to trauma. ​ Exclude systemic issues (hypertension, coagulopathy, anticoagulant use). ​ Typically self-limiting; reassure patient once serious causes are excluded. 4. Episcleritis & Scleritis 4.1 Episcleritis ​ Inflammation of the episcleral tissue. ​ Mild discomfort; redness often sectoral. ​ Blanches with phenylephrine 10%. ​ Management: Often self-limited; NSAIDs, lubricants, mild topical steroids can speed resolution. 4.2 Scleritis ​ Severe, boring pain, can disturb sleep. ​ Does not blanch with phenylephrine. ​ Often associated with connective tissue disease (e.g., rheumatoid arthritis). ​ Management: ○​ Systemic workup (rheumatology). ○​ Systemic steroids (and possibly immunosuppressants). ○​ Can threaten vision if untreated. 5. Corneal Pathologies (Keratitis, Ulcers, Abrasions) 5.1 Corneal Abrasion ​ Severe pain, photophobia, foreign-body sensation. ​ Fluorescein staining reveals epithelial defect. ​ Management: ○​ Topical antibiotic prophylaxis. ○​ Bandage contact lens + cycloplegic for pain if needed. 5.2 Infectious Keratitis (Corneal Ulcer) ​ Causes: Bacteria, viruses, fungi, protozoa (Acanthamoeba). ​ Risk Factors: Contact lens misuse, immunosuppression, corneal trauma. ​ Signs: Corneal infiltrate, possible hypopyon (pus in anterior chamber). ​ Management: ○​ Corneal scraping for gram stain/culture. ○​ High-frequency topical antimicrobials (e.g., fluoroquinolone or fortified vancomycin + ceftazidime) around-the-clock. ○​ Referral to ophthalmology urgently. Herpes Simplex Keratitis ​ Dendritic ulcers on fluorescein. ​ Management: ○​ Topical antivirals (acyclovir or ganciclovir) 5 times/day for ~2 weeks. ○​ Avoid steroids unless guided by a specialist. Herpes Zoster Ophthalmicus ​ Rash in trigeminal (V1) distribution; can involve cornea. ​ Management: Oral antivirals (acyclovir, valacyclovir), topical antibiotic cover if corneal epithelial breakdown. 6. Uveitis (Iritis, Iridocyclitis, Choroiditis) ​ Inflammation of the uveal tract (iris, ciliary body, choroid). ​ Signs: Deep aching pain, photophobia, possible irregular pupil (due to posterior synechiae), “cells & flare” in the anterior chamber on slit-lamp exam. ​ Causes: Autoimmune disorders, infections, trauma, or idiopathic. ​ Management: ○​ Topical or systemic steroids. ○​ Cycloplegic drops (e.g., atropine) to reduce pain and prevent synechiae. ○​ Investigate for underlying systemic disease. 7. Acute Angle-Closure Glaucoma ​ Presentation: Sudden severe eye pain, nausea/vomiting, blurred vision, red eye, mid-dilated pupil. ​ Elevated intraocular pressure (IOP can be 40–70 mmHg). ​ Management: 1.​ Decrease IOP: IV/oral acetazolamide, topical beta-blockers, alpha-agonists, pilocarpine (after initial pressure reduction). 2.​ Definitive: Laser peripheral iridotomy to open drainage pathway. ​ Ophthalmic Emergency: Delayed treatment can lead to permanent vision loss. 8. Endophthalmitis ​ Infection within the eye (vitreous, aqueous). ​ Post-surgical, post-trauma, or hematogenous spread in immunocompromised individuals. ​ Presentation: Severe pain, profound vision loss, marked redness. ​ Management: Intravitreal antibiotics, possible vitrectomy. Urgent referral required. 9. Ocular Trauma 1.​ Foreign Body / Abrasion ○​ Check for corneal scratch with fluorescein. ○​ Remove foreign body if superficial; cover with topical antibiotic. 2.​ Penetrating Injury / Ruptured Globe ○​ Sight-threatening. ○​ Protective shield, IV antibiotics, urgent surgical repair. ○​ Avoid pressurizing the globe (no tonometry if obvious rupture). 3.​ Hyphema ○​ Blood in anterior chamber. ○​ Risk of increased IOP, re-bleeding. ○​ Management: Rest, cycloplegics, monitor IOP. 4.​ Chemical Burn ○​ Alkali worse than acid. ○​ Immediate copious irrigation before any other step. ○​ Then evaluate corneal damage, potential for steroid drops (supervised), antibiotics, lubricants. 5.​ Sympathetic Ophthalmia (rare) ○​ Autoimmune inflammation in both eyes after severe trauma to one eye. ○​ Can be prevented by enucleation of a hopelessly damaged eye within ~5–7 days if indicated. 10. Steven Johnson Syndrome (SJS) / Toxic Epidermal Necrolysis (TEN) ​ Severe mucocutaneous reaction, often to medications or infections. ​ Ocular Involvement: Corneal erosions, conjunctival membranes, scarring, severe dry eye. ​ Management: ICU admission, multidisciplinary approach (dermatology, ophthalmology). ○​ Systemic steroids/immunosuppressives, aggressive lubrication, possible amniotic membrane grafting to mitigate scarring. High-Yield Additional Pearls to consider A. Clues for Conjunctivitis Subtypes 1.​ Viral ○​ Discharge: Watery or mucoid. ○​ Often follicular pattern on lids. ○​ Highly contagious, self-limited. 2.​ Bacterial ○​ Discharge: Purulent (yellow/green). ○​ “Sticky eyelids,” typically worse on waking. ○​ Broad-spectrum topical antibiotics if simple; systemic coverage if gonococcal/chlamydial. 3.​ Allergic ○​ Intense itching + watery/ropy discharge. ○​ Often bilateral with history of atopy (e.g., eczema, allergic rhinitis). Pearl: Follicles often signal viral or chlamydial etiology; papillae suggest allergic or bacterial cause. B. Distinguishing Superficial vs. Deep Inflammation ​ Episcleritis: Sectoral redness, mild discomfort, phenylephrine blanching → typically benign. ​ Scleritis: Severe pain, deeper vessels, no blanching, systemic associations → vision-threatening. C. Corneal Infections ​ Contact lens use + corneal ulcer → suspect Pseudomonas or Acanthamoeba. ​ Herpes Simplex → dendritic ulcer on fluorescein; avoid topical steroids unless guided by specialist. ​ Always do corneal scraping for culture if suspicion of microbial keratitis. D. Red Eye + Severe Pain + Vision Changes = Emergency ​ Could be scleritis, acute angle-closure glaucoma, microbial keratitis, or uveitis. ​ Prompt referral is vital to prevent permanent damage. E. Subconjunctival Hemorrhage: Exclude Systemic Causes ​ If recurrent or extensive, check blood pressure, coagulation profile, and medication history (anticoagulants). ​ Often benign but sometimes the first sign of an underlying condition (e.g., hypertension). F. Chemical Eye Injuries ​ Immediate and copious irrigation (use normal saline or balanced solution) is paramount. ​ Check and recheck pH until normalized. ​ Only after thorough irrigation do you proceed with history and further exam. G. Steven Johnson Syndrome / TEN ​ Aggressive ocular care (lubrication, topical antibiotics, steroids if indicated) can help prevent scarring and symblepharon. ​ Early ophthalmology involvement improves outcomes. H. Tips 1.​ Always Check: ○​ Visual acuity, pupil reactivity, IOP, slit-lamp exam, fundus check (if the media is clear). 2.​ Discharge Types: ○​ Watery → often viral/allergic. ○​ Mucopurulent → bacterial. ○​ Ropy → allergic. 3.​ Pain Severity & Photophobia: ○​ Mild discomfort → often superficial (conjunctivitis, episcleritis). ○​ Severe pain or marked photophobia → deeper structures (cornea, sclera, uvea, acute glaucoma). 4.​ Mnemonics: ○​ “Painful Red Eye” → S (Scleritis), C (Corneal ulcer), G (Glaucoma), U (Uveitis). 5.​ Contagious Etiologies: ○​ Viral and bacterial conjunctivitis can spread. Recommend hygiene, not sharing towels, etc.. By Abdulaziz Alnufaei - B18

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