Initial Management of New Onset Mydriasis
The initial management of new onset mydriasis should focus on rapidly identifying and treating life-threatening causes, particularly uncal herniation due to increased intracranial pressure, which requires immediate aggressive intervention with hyperosmolar therapy, hyperventilation, and neurosurgical consultation. 1
Immediate Assessment
Vital Signs and Neurological Examination
- Check vital signs (blood pressure, heart rate, respiratory rate, temperature)
- Assess level of consciousness
- Evaluate for other neurological deficits:
- Motor responses
- Pupillary light reflexes
- Extraocular movements
- Contralateral Babinski sign (may indicate brainstem compression)
Key Differentiating Features
- Unilateral vs. bilateral mydriasis
- Associated symptoms (headache, altered mental status, focal neurological deficits)
- Pupillary reactivity (reactive vs. non-reactive to light)
- Onset (sudden vs. gradual)
Emergency Management Algorithm
Step 1: Rule Out Life-Threatening Causes
If patient shows signs of increased intracranial pressure (decreased level of consciousness, ipsilateral pupillary dilation, abnormal motor responses):
- Elevate head of bed 20-30° to facilitate venous drainage 1
- Administer hyperosmolar therapy:
- Consider hyperventilation to PaCO₂ of 30-35 mmHg (temporary measure only) 1
- Urgent neuroimaging (CT scan)
- Neurosurgical consultation
Step 2: Assess for Drug/Toxin Exposure
Common causes of pharmacologic mydriasis:
- Anticholinergic agents (atropine, scopolamine)
- Sympathomimetics (phenylephrine, epinephrine)
- Serotonergic drugs (may cause serotonin syndrome with mydriasis) 2
- Recreational drugs (cocaine, amphetamines)
For suspected serotonin syndrome:
- Consider cyproheptadine (serotonin2A antagonist) if severe 2
- Adult dosage: 12 mg initially, followed by 2 mg every 2 hours for continuing symptoms 2
- Pediatric dosage: 0.25 mg/kg per day 2
Step 3: Consider Benign Causes
If neurological examination is otherwise normal and vital signs are stable:
- Benign episodic unilateral mydriasis - typically self-limited, may be associated with migraine or anxiety 3, 4
- Physiologic anisocoria - difference in pupil size <1 mm, both pupils reactive to light
- Local ocular causes - direct trauma, eye drops, or medications
Special Considerations
Intraoperative Mydriasis
Pediatric Considerations
- Consider non-accidental injury in well-appearing children with unexplained mydriasis 7
- Carefully assess for other signs of trauma or concerning parental behavior
Follow-up Management
- For benign causes: Reassurance and observation
- For serious neurological causes: Continued monitoring of intracranial pressure, neurological status, and response to interventions
- For drug-induced causes: Discontinuation of offending agent when possible
Pitfalls and Caveats
- Do not delay treatment of suspected increased intracranial pressure while waiting for neuroimaging
- Avoid prolonged hyperventilation as it can cause cerebral ischemia 1
- Do not miss subtle signs of deterioration in patients with supratentorial ischemic stroke (ipsilateral pupillary dysfunction is often an early sign) 2
- Beware of hypoactive presentations of delirium that may be accompanied by mydriasis but missed due to less obvious clinical manifestations 2
- Monitor serum osmolality (<320 mOsm/L), electrolytes, and renal function when using mannitol 1
Remember that new onset mydriasis, particularly when unilateral and accompanied by neurological deficits, should be treated as a neurological emergency until proven otherwise.