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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.
RapidMLAMSRAGP

Monitoring adherence and progression

Essential points for quick revision.

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New symptoms override the routine review interval

Scheduled surveillance is intended for chronic disease; sudden visual loss, a painful red eye or significant new treatment-related systemic symptoms require a separate urgent assessment.

Action: Arrange same-day emergency care for acute ocular warning symptoms and urgent medical assessment for serious drug effects, rather than waiting for the booked glaucoma appointment.

Synopsis

Plan glaucoma reassessment according to control and visual risk, distinguish progression from uncertainty, and address practical treatment barriers before and alongside appropriate escalation.

  • Judge glaucoma control through pressure, optic nerve structure and visual function, while considering treatment burden and the risk of lifetime sight loss.
  • Check adherence, supply and observed instillation before declaring a pressure-lowering medicine ineffective.
  • A measured pressure at target does not exclude progression; reproducible nerve or field deterioration should trigger a review of the target and treatment plan.

Key red flags

A person reporting new painful visual deterioration needs urgent eye assessment even if the last pressure was controlled and the next routine review is months away.

Investigation priorities

01
Goldmann pressure and anterior segment reviewFirst step

Assess current pressure control and look for a change in ocular status.

Management branches

Routine reviewReassess control and set the next interval

A person attends scheduled follow-up for ocular hypertension, suspected glaucoma or established glaucoma.

  1. Confirm the diagnostic category, current treatment, functional concerns and any new ocular or systemic symptoms before interpreting the test results.
  2. Assess pressure control, the quality of structural and field data and the risk of future sight loss, separating no detected change from unresolved uncertainty.

Key medicines

Latanoprost administration when prescribed for ongoing controlFor latanoprost 50 micrograms/mL, deliver a single drop to each prescribed eye every evening and continue the agreed long-term course; resume at the next usual dose after a missed dose rather than doubling.
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Sources and review status7 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