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OPTE: Ocular Pharmacology and Diagnostic Agents

OPTE · Work through your exam, one topic at a time.

All guide sections

Ocular Pharmacology and Diagnostic Agents

This domain tests the agents you use to examine the eye: what they do, how long they last, and which patients need caution before instillation.

Classes and behaviour

  • Cycloplegic mydriatics block muscarinic receptors on the sphincter and ciliary muscle. Atropine 1% is longest acting (up to 1–2 weeks of cycloplegia), cyclopentolate 1% intermediate (roughly a day), tropicamide short (hours).
  • Phenylephrine 2.5% dilates without cycloplegia; the 10% concentration is avoided because of systemic hypertensive risk.
  • Topical anaesthetics (proparacaine, benoxinate, tetracaine) are for procedures only; chronic use causes epithelial toxicity and masks disease.
  • Dyes: sodium fluorescein for corneal and tear assessment, lissamine green and rose bengal for devitalised epithelium.
  • IOP agents: prostaglandin analogues raise uveoscleral outflow; beta-blockers and carbonic anhydrase inhibitors reduce production; pilocarpine raises trabecular outflow; alpha-2 agonists do both.

Worked example

A 64-year-old hyperope with a 2.5 mm pupil in dim light needs funduscopy. Shallow peripheral anterior chamber on van Herick grading suggests angle-closure risk. Reasoning through: gonioscopy or referral before dilation; if dilation is still required, use tropicamide with phenylephrine 2.5% rather than atropine, and warn about the signs of acute angle closure. The short-acting combination limits the duration of any risk.

Traps

Believing phenylephrine produces cycloplegia; dilating a shallow anterior chamber without grading or gonioscopy; prescribing topical steroids without monitoring IOP and corneal status; ignoring benzalkonium chloride toxicity with frequent dosing; and using fluorescein on a soft lens.