Ophthalmology

Painless Vision Loss

The Algorithm…

  • Immediate Priorities
    • Confirm the loss, localize the problem, and identify what needs treatment now.
    • Assess retinal ischemia and GCA in parallel when both are plausible.
    • Do not delay an indicated stroke / GCA pathway to complete the eye examination.

01 Confirm / Localize

  • Confirm The Loss
    • Test acuity and fields in each eye separately.
    • Compare with baseline; establish last known well.
  • One Eye Or Both?
    • Distinguish monocular, homonymous, and bilateral loss before choosing the pathway.
    • Sudden homonymous loss → cerebral-stroke assessment.
  • Eye Examination
    • Assess pupils, red reflex, and fundus.
    • Ocular pain / redness → painful-eye assessment.
  • Vision Returned?
    • Suspected retinal TIA still requires urgent ischemia assessment.

02 R/O Emergent Diagnoses

  • CRAO / Retinal Arterial Occlusion?
    • Abrupt, painless monocular loss.
    • Stroke-center evaluation + urgent ophthalmology.
    • Use the CRAO-specific treatment pathway—not automatic thrombolysis.
  • GCA?
    • Age ≥50 + ischemic visual symptoms.
    • Assess jaw claudication, headache / scalp symptoms, and PMR.
    • Strong suspicion + acute / transient visual ischemia → steroids now.
      • Do not wait for laboratory results or biopsy.
  • Retinal Detachment?
    • New flashes / floaters + curtain or field loss.
    • Immediate retina contact / same-day assessment.
    • Preserved central vision or negative POCUS does not replace the specialist retinal examination.
  • Cerebral Stroke?
    • Sudden homonymous defect → stroke activation.
    • Do not wait for weakness or aphasia.

03 Other Urgent Diagnoses

  • CRVO / BRVO
    • Retinal hemorrhages + dilated tortuous veins.
    • Prompt ophthalmology assessment.
  • Vitreous Hemorrhage
    • Haze / floaters + obscured fundus.
    • Urgent retina assessment; a tear / detachment may be hidden.
  • NAION
    • Painless loss + swollen disc / altitudinal defect.
    • Ophthalmology assessment; assess GCA before accepting the nonarteritic label.
  • Macular Disease
    • Central distortion / scotoma → retina assessment + OCT.
  • Other Optic Neuropathy
    • Color loss / RAPD without a retinal explanation → optic-nerve assessment.
  • Resolved Loss
    • Continue the appropriate urgent assessment when ischemia is suspected.
  • Unexplained Acute Loss
    • A normal-appearing fundus does not end the evaluation.

Confirm / Localize

Acuity / Fields / Timing

  • Visual Acuity
    • Test each eye with the patient’s usual glasses.
    • Compare with baseline.
  • Pinhole
    • Repeat reduced acuity through a pinhole.
    • Improvement suggests a refractive contribution.
    • It does not explain a new field defect or another concerning finding.
  • Fields
  • Timing
    • Record last known well and symptom discovery separately.
    • Establish sudden versus progressive onset and persistent versus resolved loss.
    • Resolved Blackout / Dimming

One Eye Or Both?

  • Monocular
    • Loss remains confined to one eye when the other is covered.
    • Localize to ocular media, retina, or optic nerve.
  • Homonymous
    • The same right or left field is missing in both eyes.
    • The patient may report “one-eye blindness.”
    • This localizes behind the optic chiasm.
      • Sudden onset → cerebral-stroke assessment.
  • Bilateral

Painful Or Painless?

  • Angle Closure?
    • Severe ocular pain, red eye, halos, headache, or nausea / vomiting.
    • Assess the anterior segment and IOP.
  • Inflammation / Infection?
    • Pain, photophobia, or redness.
    • Assess corneal disease, uveitis, scleritis, or intraocular infection.
    • Pain with eye movement supports optic neuritis / orbital disease.
  • Next Action
    • Slit-lamp / anterior-segment examination and IOP when appropriate.
    • Use the painful-eye pathway.
    • Open Globe Suspected: Avoid tonometry and ocular pressure. Vision-Loss Examination Review
  • Headache ≠ Ocular Pain
    • GCA may cause headache / scalp tenderness while the visual loss remains painless. BSR 2020

Pupils / Color / Red Reflex / Fundus

  • RAPD — Relative Afferent Pupillary Defect
    • Supports asymmetric optic-nerve or substantial retinal dysfunction.
    • Not specific to optic-nerve disease.
    • Swinging-Light Test
      • Move the light from the unaffected to the affected eye.
      • Both pupils constrict less or appear to dilate as afferent input falls. EM:RAP — Pupillary Defect
  • Color: Compare color perception.
  • Red Reflex
    • Compare both eyes.
    • A dim / absent reflex with an obscured fundus suggests an opacity, such as cataract or vitreous hemorrhage.
    • Assess the cornea and lens for another explanation.
    • A preserved reflex does not exclude retinal or optic-nerve disease. Stanford — Fundus Examination
  • Fundus

R/O Emergent Diagnoses

Central Retinal Artery Occlusion — CRAO

General

  • Acute Retinal Ischemic Stroke
    • Interrupted arterial flow can cause permanent visual loss.
    • CRAO is an eye emergency and a vascular warning—not an isolated ophthalmology referral. AHA 2021
  • Source
    • Usually thromboembolic, often from ipsilateral carotid disease or a cardiac source.
    • GCA Can Also Cause Arterial Occlusion
      • Assess in parallel when plausible.
      • Arteritic disease requires different immediate treatment. Dattilo Et Al., 2018

Clinical / Red Flags — What Moves The Needle?

  • Onset / Pattern
    • Abrupt, painless monocular loss over seconds to minutes, often severe.
    • Establish whether loss persists or has resolved.
    • Central Island Preserved: Cilioretinal supply may preserve central acuity despite substantial field loss.
    • BRAO: A branch retinal artery occlusion may cause a sectoral deficit; urgent ischemia assessment still applies. ASRS — Retinal Artery Occlusion
  • Vascular / Embolic Risk
    • Carotid disease, AF, valvular disease, or prior vascular events.
    • Hypertension, diabetes, dyslipidemia, or smoking.
    • Absence of known risk factors does not exclude a convincing presentation. AHA 2021
  • Prior Transient Loss
    • A preceding monocular blackout may represent retinal ischemia.
    • Ischemic transient monocular loss / amaurosis fugax is a retinal TIA.
    • Return of vision is not reassurance. Dattilo Et Al., 2018
  • RAPD / Fundus
    • RAPD, retinal whitening, a cherry-red spot, attenuated arteries, or an embolus support the diagnosis.
    • Early findings may be subtle or absent.
    • Do not require a cherry-red spot or visible embolus before stroke activation. Bénard-Séguin Et Al., 2026
  • GCA? — Age ≥50
    • Ask about jaw claudication, headache / scalp symptoms, PMR, and systemic illness.
    • No headache does not exclude arteritic disease.
    • See GCA. ACR/VF 2021

Diagnosis

  • Eye Examination
    • Document acuity, pupils / RAPD, fields, and retinal findings.
    • Confirm true monocularity.
      • Homonymous defect → cerebral-stroke assessment.
  • Ophthalmology
    • Urgent dilated examination / retinal confirmation.
    • Fundus photography or OCT may clarify subtle findings.
      • OCT can show acute inner-retinal swelling.
    • Do not delay stroke-center evaluation while awaiting confirmation. Bénard-Séguin Et Al., 2026
  • GCA Testing
    • ESR / CRP + CBC / platelets in the appropriate age / clinical context.
    • Normal markers do not independently exclude GCA.
    • Strongly suspected arteritic visual ischemia → treat while testing proceeds. ACR/VF 2021

Critical Actions

  • Stroke Activation
    • Establish exact last known well—not discovery time alone.
    • Involve stroke / neurology and ophthalmology together.
  • Stroke Workup — Cerebral Ischemia / Embolic Source
    • Brain Imaging
      • Follow the acute stroke pathway.
      • MRI-DWI may identify cerebral infarction without another obvious deficit.
    • CTA Head / Neck Or Equivalent
      • Assess carotid and upstream arterial disease, including dissection.
      • Routine CTA generally does not show the retinal occlusion itself.
      • Normal CTA does not exclude CRAO.
    • Cardiac Assessment
  • Strong GCA Suspicion + Visual Ischemia
  • IV Thrombolysis? — Within 4.5 Hours
    • Immediately discuss the CRAO-specific protocol with the stroke team.
    • AHA/ASA 2026 describes benefit as uncertain in otherwise eligible disabling nonarteritic CRAO.
    • Retinal stroke does not automatically mean IV thrombolysis. AHA/ASA 2026 — CRAO
  • Traditional Maneuvers
    • Ocular massage, anterior chamber paracentesis, and hemodilution have no established benefit and may cause harm.
    • Do not delay stroke / GCA assessment for these measures. AHA 2021

Reassessment / Prevention

  • Late Presentation / Vision Returned
    • Complete the urgent vascular assessment.
    • Prevention and antithrombotic selection follow the mechanism, bleeding risk, and stroke-team plan. Dattilo Et Al., 2018
  • Ophthalmic Follow-Up
    • Surveillance for retinal / iris neovascularization and glaucoma.
    • Support for persistent visual impairment.
    • New pain or redness after an initially painless event → reassessment. ASRS — Retinal Artery Occlusion

In The Pit

  • Sudden Painless Monocular Loss Concerning For CRAO
    • Last known well + stroke activation + urgent ophthalmology.
    • Do not require a classic fundus.
    • Normal CTA does not exclude CRAO.
  • Age ≥50
    • Assess GCA.
    • Strong suspicion + visual ischemia → steroids now.
  • Within 4.5 Hours
    • Immediate CRAO-specific treatment discussion.
    • Not automatic thrombolysis or ocular massage.
  • Resolved / Late
    • Urgent vascular assessment and prevention still apply.

Must-Read References

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Additional Cited Guidance

Giant Cell Arteritis — Arteritic Optic Neuropathy / Retinal Ischemia

General

  • GCA
    • Large- and medium-vessel vasculitis, predominantly in adults ≥50.
    • A normal temporal artery examination does not exclude it. ACR/VF 2021
  • Why Vision Is Lost
    • Posterior ciliary artery involvement may infarct the optic nerve head.
      • Arteritic anterior ischemic optic neuropathy — AAION.
    • GCA may also cause retinal arterial occlusion.
    • This is inflammatory arterial disease—not simply another embolic CRAO.
  • Immediate Threat
    • Established ischemic loss is often permanent.
    • Treat to limit further loss and protect remaining vision—especially the fellow eye. Hayreh — Iowa Ophthalmology

Clinical / Red Flags — What Moves The Needle?

  • Vision
    • Sudden painless monocular loss, often profound.
    • Transient monocular loss or new diplopia may precede permanent loss.
  • Jaw / Tongue Claudication
    • Pain or fatigue with chewing that improves with rest.
    • Not simply jaw tenderness.
  • Head / Scalp
    • New headache or scalp tenderness.
    • A tender / thickened temporal artery with reduced pulse.
  • PMR / Systemic Clues
    • Polymyalgia rheumatica: shoulder / hip-girdle pain and morning stiffness.
    • Fever, fatigue, or weight loss.
    • These support the pattern but do not establish GCA alone. Van Der Geest Et Al., 2020
  • No Headache?
    • Ocular GCA may lack headache, scalp symptoms, and constitutional illness.
    • Do not require systemic symptoms before pursuing the diagnosis. Hayreh Et Al., 1998

Diagnosis

Eye Examination
  • Both Eyes: Record acuity, pupils / RAPD, fields, and fundus findings.
  • Pale, Swollen Disc
    • Profound loss + pallid disc edema supports AAION.
    • The examination may be nonclassic.
    • Pallor alone is not acute pallid disc swelling. Hayreh — Iowa Ophthalmology
ESR / CRP + CBC / Platelets
  • Obtain Promptly
  • Before Steroids?
    • Draw blood first when immediately feasible.
    • Do not delay indicated treatment or wait for results. BSR 2020
  • Normal ESR / CRP
    • Lower probability but do not exclude strongly suspected GCA.
Biopsy / Expert Vascular Ultrasound
  • Confirm While Treating
    • Arrange biopsy and/or expert vascular ultrasound.
    • Neither should delay vision-protecting treatment. BSR 2020
  • Temporal Artery Biopsy
    • Arrange promptly—ideally within two weeks of starting steroids.
    • ACR/VF conditionally favors biopsy in U.S. practice, partly because ultrasound expertise varies.
    • Biopsy may remain informative later; treatment does not immediately erase its diagnostic value. ACR/VF 2021
  • Expert Vascular Ultrasound
    • Examine temporal and axillary arteries when suitable expertise is available.
    • EULAR recommends ultrasound first.
    • This is a dedicated vascular study—not routine ocular POCUS.
    • Timing
      • Ideally before steroids without delaying treatment, or within approximately 72 hours afterward.
      • Treatment may reduce sensitivity. EULAR 2023 Update
  • Negative Test + Strong Suspicion
    • Specialist reassessment / further testing.
    • A negative biopsy can miss segmental disease. ACR/VF 2021

Critical Actions

  • Strongly Suspected GCA + Acute / Transient Visual Ischemia
    • Start systemic glucocorticoids immediately.
    • Do not wait for persistent loss, laboratory results, biopsy, or ultrasound. BSR 2020 — Executive Summary
  • Threatened / Established Visual Loss
    • Methylprednisolone: 500–1,000 mg IV daily, commonly for three consecutive days.
    • Follow with high-dose oral therapy under the specialist plan.
    • IV Unavailable
      • Start high-dose oral glucocorticoids under the urgent specialist protocol.
      • Arrange IV treatment / transfer without leaving the patient untreated. BSR 2020
  • Ophthalmology + Rheumatology
    • Contact urgently while initiating treatment.
    • Suspected GCA + new transient / permanent visual loss or diplopia → ophthalmic assessment as soon as possible that day.
    • Not routine outpatient referral. BSR 2020

Reassessment / Disposition

  • Both Eyes
    • Repeat acuity / fields and assess new symptoms.
    • Further visual loss after the first steroid dose → immediate reassessment.
    • Treatment does not guarantee immediate protection. Hayreh — Iowa Ophthalmology
Monitored Admission
  • IV Pulses / Evolving Loss / No Immediate Specialist-Directed Care
    • Arrange admission or transfer for treatment and reassessment.
    • Start treatment before transfer.
  • Ongoing Plan
    • Confirm steroid continuation, specialist follow-through, and diagnostic testing.
    • A resolved visual episode or normal ESR / CRP alone does not justify discharge. BSR 2020

In The Pit

  • Age ≥50 + New Painless Visual Loss
    • Assess GCA—even without headache.
    • Jaw claudication or profound loss with a pale, swollen disc increases concern.
  • Strong GCA Suspicion + Persistent / Transient Visual Ischemia
    • Steroids now.
    • Urgent ophthalmology / rheumatology.
  • ESR / CRP + CBC / Platelets
    • Obtain promptly.
    • Do not wait for results or biopsy before indicated treatment.
  • Both Eyes
    • Reassess vision and arrange ongoing treatment / admission.
    • Further deterioration → immediate reassessment.

Must-Read References

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Additional Cited Guidance

Retinal Detachment

General

  • Detachment
    • Retina separates from its underlying support layer.
    • Most acute detachments follow a tear that allows fluid underneath—rhegmatogenous detachment. ASRS — Retinal Detachment

Clinical / Red Flags — What Moves The Needle?

  • Pattern
    • New flashes / floaters followed by a curtain, shadow, or field loss.
    • Loss may advance centrally; not every patient has the full sequence.
  • Risk: High myopia, prior cataract / intraocular surgery, trauma, or previous detachment.
  • Posterior Vitreous Detachment — PVD
    • Vitreous separates from the retina—not retina from the eye wall.
    • PVD can cause similar symptoms and a retinal tear.
    • Symptoms alone do not establish harmless PVD. AAO 2025 — PVD / Retinal Breaks

Diagnosis

  • Eye Examination
    • Record acuity, pupils, and fields.
    • Arrange a dilated peripheral retinal examination.
    • Preserved central acuity does not exclude peripheral detachment. AAO 2025
  • Ocular POCUS
    • An elevated echogenic membrane tethered to the optic disc supports detachment.
    • Useful when hemorrhage obscures the fundus.
    • Negative Scan: Does not exclude a retinal tear or replace the dilated examination.
    • Macular Status: Do not rely on ED POCUS alone to distinguish macula-on from macula-off.
    • Open Globe Suspected: Avoid ocular ultrasound / pressure. ACEP — Ocular Emergencies

Critical Actions

  • Suspected Detachment
    • Immediate ophthalmology / retina contact for same-day assessment.
    • Arrange direct evaluation or transfer—not routine follow-up.
  • Macular Status
    • Determines repair urgency and prognosis.
    • Macula-On: Central Retina Attached
      • Urgent repair planning to preserve central vision.
    • Macula-Off: Central Retina Detached
      • Prompt assessment / repair planning.
      • Reduced vision is not permission to delay.
      • The retina surgeon determines timing. ACEP — Ocular Emergencies
  • Definitive Treatment
    • Retinal tears may require laser / cryotherapy.
    • Established detachment usually requires retinal repair.
    • Procedure and timing follow the specialist examination. ASRS — Retinal Detachment

In The Pit

  • Flashes / Floaters + Curtain
    • Suspect detachment → immediate retina contact / same-day assessment.
  • Central Vision Preserved
    • The macula may still be attached.
    • Do not downgrade urgency.
  • Negative POCUS
    • Does not exclude a retinal tear.
    • A concerning presentation still needs a dilated examination.

Must-Read References

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Additional Cited Guidance

Cerebral Stroke — Redirect From Field Testing

  • Homonymous Defect
    • The same right or left field is missing in both eyes.
    • This localizes behind the optic chiasm—not to isolated monocular retinal loss.
  • Sudden Onset

Reference

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Other Urgent Diagnoses

Central Retinal Vein Occlusion — CRVO

Deep Dive CorePendium — Central Retinal Vein Occlusion

  • Pattern
    • Impaired venous drainage causes retinal hemorrhage and edema.
    • Painless monocular blur / loss varies in severity.
    • Ischemic CRVO may cause profound loss. ASRS — CRVO
  • Fundus
    • Widespread hemorrhages, dilated tortuous veins, and disc edema.
    • Classic “blood-and-thunder” appearance.
    • BRVO: Branch retinal vein occlusion produces a sectoral rather than diffuse pattern. RCOphth 2022
  • Next Action
    • Prompt ophthalmology / retina assessment.
    • Review BP, diabetes, and other vascular risks.
    • Macular edema is commonly treated with intravitreal anti-VEGF. ASRS — CRVO
  • Confirmed Isolated CRVO
    • Not a CRAO reperfusion indication.
    • Systemic anticoagulation is not routine solely for CRVO. RCOphth 2022
  • Pain / Redness / Elevated IOP
    • Assess for neovascular glaucoma, particularly after ischemic CRVO.
    • Urgent ophthalmic treatment. ASRS — CRVO

References

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Vitreous Hemorrhage

Deep Dive CorePendium — Vitreous Hemorrhage

  • Pattern
    • Painless haze, cobwebs, floaters, or variable visual loss.
    • Blood may obscure the fundus.
    • Blood explains the obscured view—not why the eye bled. ASRS — Retinal Tears
  • Red Reflex / Fundus
    • A dim reflex and hazy fundus support an opacity, including hemorrhage.
    • Assess the cornea and lens for another explanation.
    • An abnormal reflex is not diagnostic of hemorrhage. Stanford — Fundus Examination
  • Retina Obscured
    • Urgent ophthalmology / retina assessment.
    • A retinal tear / detachment may be hidden.
    • Specialist ophthalmic ultrasound may be needed.
    • Do not wait for the blood to clear. See Retinal Detachment. ASRS — Retinal Tears
  • Ocular POCUS
    • Mobile vitreous echoes swirling with eye movement support hemorrhage.
    • Assess for associated detachment.
    • Negative Scan: Does not exclude a tear or replace specialist examination.
    • Open Globe Suspected: Avoid ocular ultrasound / pressure. ACEP — Ocular Emergencies

References

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Nonarteritic Anterior Ischemic Optic Neuropathy — NAION

  • Pattern
    • Optic-nerve-head ischemia causes painless monocular loss and disc swelling.
    • Altitudinal Defect: Upper or lower field loss supports the pattern but is not required.
  • GCA First — Age ≥50
    • Assess arteritic disease before accepting “nonarteritic.”
    • Concerning symptoms / findings → urgent GCA assessment / treatment.
    • No headache does not exclude GCA.
  • Next Action
    • Prompt ophthalmology / neuro-ophthalmology confirmation.
    • No proven acute vision-restoring treatment.
    • Do not automatically apply CRAO reperfusion or GCA steroids.
  • Follow-Up

Reference

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  • NANOS — NAION
    • Arteritic differential, treatment limitations, and risk assessment.

Macular Disease

Deep Dive CorePendium — Acute Maculopathy

  • Central Distortion / Scotoma
    • Wavy lines, impaired reading, or a central dark patch.
    • Relatively preserved peripheral vision supports a macular source.
    • Consider neovascular age-related macular degeneration (AMD), macular edema, or macular / submacular hemorrhage.
  • New Central Loss
    • Prompt retina assessment + optical coherence tomography (OCT).
    • Suspected acute hemorrhage → urgent discussion.
    • Do not attribute sudden deterioration to chronic AMD without reassessment. ASRS — AMD

Reference

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  • ASRS — AMD
    • Central visual symptoms, specialist treatment, and complications.

Other Optic Neuropathies

Deep Dive CorePendium — Optic Neuritis

  • Optic Neuritis
    • Color desaturation and pain with eye movement support the diagnosis.
    • Painless presentations occur.
    • Ophthalmology / neuro-ophthalmology assessment.
    • Appropriate brain / orbital MRI. NANOS — Optic Neuritis
  • Compressive / Infiltrative Disease

References

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Vision Loss Resolved — Retinal TIA?

  • Pattern
    • Sudden monocular dimming, blackout, or a curtain that clears may be retinal ischemia.
    • Return of vision and a normal examination do not exclude retinal TIA.
  • Clarify The Episode
    • Establish onset, duration, recovery, and one eye versus both.
    • Not every transient visual symptom is ischemic.
  • Ischemia Suspected

Reference

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Acute Loss Still Unexplained?


General References — Examination / Localization

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Other Retinal / Optic-Nerve References

References for CRVO, vitreous hemorrhage, NAION, macular disease, other optic neuropathies, and retinal TIA appear beneath their respective sections.

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