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RapidMLAMSRAGP

Bitemporal, homonymous and monocular field defects

Essential points for quick revision.

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Sudden field loss needs emergency localisation

An abrupt persistent homonymous defect can be a stroke even without weakness. Sudden monocular loss may reflect retinal ischaemia, while severe headache with bitemporal loss can indicate pituitary apoplexy.

Action: Arrange immediate emergency assessment for a new persistent deficit. Record the last-known-well time, examine each eye separately and activate the appropriate stroke, retinal or pituitary pathway without delaying referral for formal perimetry.

Synopsis

Use the distribution and time course of visual-field loss to localise disease, recognise vascular and pituitary emergencies, and guide investigation and rehabilitation.

  • Monocular field loss usually localises to the retina or optic nerve before the chiasm.
  • Bitemporal loss suggests optic-chiasm dysfunction and requires assessment for a sellar or suprasellar lesion.
  • A homonymous defect affects the same side of visual space in both eyes and localises behind the chiasm on the opposite side.

Key red flags

Abrupt persistent loss of one side of the visual world requires emergency stroke assessment even when speech and limb strength are normal.

Investigation priorities

01
Immediate bedside visual and neurological examinationFirst step

Localise the deficit and identify emergency pathways without waiting for formal testing.

Management branches

EmergencySudden persistent visual-field loss

A new monocular or homonymous deficit remains present or accompanies acute neurological symptoms.

  1. Activate emergency assessment, document symptom timing and ensure the patient does not drive to hospital.
  2. Distinguish monocular from homonymous loss at the bedside while preserving rapid access to stroke and ophthalmic expertise.

Key medicines

Aspirin for suspected TIAGive 300 mg orally once daily immediately unless contraindicated, pending urgent specialist assessment and the resulting secondary-prevention plan.
Hydrocortisone for emergency pituitary apoplexyThe Society for Endocrinology emergency guidance includes 100 mg intramuscularly immediately, followed by 50–100 mg intramuscularly every six hours; continued route and dosing are directed by the emergency endocrine team.
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Sources and review status6 sources · checked 7 Sept 2026 · clinical review pending
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 7 Sept 2026; clinical approval remains outstanding.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom