What is the effect of atropine on intraocular pressure?

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Last updated: November 17, 2025View editorial policy

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Effect of Atropine on Intraocular Pressure

Atropine should be avoided in patients with increased intraocular pressure or glaucoma, as it poses a risk of elevating IOP through pupillary dilation and potential angle closure, despite some evidence suggesting it may not significantly raise IOP in most myopic children. 1

Contraindication in Acute Settings

  • The American Academy of Pediatrics explicitly states that ketamine (and by extension, anticholinergics like atropine) should be avoided in patients with increased IOP or increased intracranial pressure 1
  • This contraindication is based on the mechanism that pupillary dilation from muscarinic antagonists is a predisposing factor for angle-closure glaucoma 2

Evidence from Myopia Treatment Studies

Safety Profile in Children

  • A prospective study of 186 myopic children receiving various concentrations of atropine showed no significant IOP elevation with long-term use; in fact, both low- and high-cumulative atropine dosage groups experienced a smaller increase in IOP compared to untreated controls 3
  • A larger retrospective review of 621 myopic children (ages 6-15 years) treated with atropine for up to 3 years found no statistical association between cumulative dose or duration of atropine therapy and risk of elevated IOP 2
  • Neither the cumulative dose nor duration of atropine therapy correlated with IOP elevation risk in these pediatric myopia populations 2

Important Risk Factors

  • Age and severity of myopia (more negative spherical equivalent) were positively associated with elevated IOP risk, independent of atropine use 2
  • Older myopic children and those with more severe myopia require careful IOP monitoring regardless of atropine therapy 2

Case Reports of IOP Elevation

  • A case report documented significant IOP elevation (36 mmHg OD, 32 mmHg OS) in a 9-year-old boy using 0.125% atropine eye drops combined with orthokeratology lenses; IOP normalized to 18/20 mmHg within 2 days of discontinuation 4
  • This suggests that combination therapy with orthokeratology and atropine may carry higher risk than atropine alone 4

Mechanism Considerations

  • Atropine causes pupillary dilation, which can precipitate angle closure in predisposed individuals 2
  • The theoretical concern is that mydriasis may reduce aqueous outflow through the trabecular meshwork in susceptible eyes 1

Clinical Algorithm for Atropine Use

Pre-treatment Assessment:

  • Measure baseline IOP in all patients before initiating atropine 4, 2
  • Perform gonioscopy to assess angle anatomy in patients at risk for angle closure 1
  • Identify high-risk patients: those with narrow angles, family history of glaucoma, or pre-existing elevated IOP 1, 2

Monitoring Protocol:

  • Check IOP within 3-7 days after initiating atropine therapy, especially in children using concurrent orthokeratology 4
  • Monitor IOP more frequently in older children and those with higher myopia (>-4.00 D) 2
  • Discontinue atropine immediately if IOP rises above 21 mmHg or increases >5 mmHg from baseline 4

Contraindications:

  • Absolute: Known angle-closure glaucoma, increased IOP, or increased intracranial pressure 1
  • Relative: Narrow angles on gonioscopy, family history of angle-closure glaucoma 1

Common Pitfalls

  • Assuming all anticholinergics are safe for IOP: While studies in myopic children show relative safety, this does not apply to patients with pre-existing glaucoma or anatomically narrow angles 1, 2
  • Failing to monitor IOP in combination therapy: The risk appears higher when atropine is combined with orthokeratology lenses 4
  • Ignoring age and refractive error as independent risk factors: Older children with higher myopia need closer IOP surveillance regardless of atropine use 2

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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