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Anisocoria After Direct Light Stimulus is Associated with Poor Outcomes Following Acute Brain Injury
Brittany R Doyle1, Venkatesh Aiyagari2, Shoji Yokobori3
1Department of Nursing, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Anisocoria (unequal pupil size) after light stimulus is a new biomarker predicting worse outcomes in neurocritically ill patients compared to anisocoria at rest. This finding may improve patient assessment and care.
Area of Science:
- Neuroscience
- Ophthalmology
- Critical Care Medicine
Background:
- Pupil size and reactivity assessment is standard for neurocritically ill patients.
- Anisocoria (unequal pupil size) in these patients often necessitates further investigation and treatment.
- This study investigates anisocoria as a predictor of discharge modified Rankin Scale (mRS) scores.
Purpose of the Study:
- To explore anisocoria at rest and after light stimulus using quantitative pupillometry.
- To determine if anisocoria predicts discharge modified Rankin Scale (mRS) scores in neurocritically ill patients.
- To compare the prognostic value of anisocoria at rest versus after light stimulus.
Main Methods:
- Analysis of an international registry including patients with paired pupillometry and discharge mRS scores.
- Anisocoria defined by pupil size difference (>0.5 mm, >1 mm, >2 mm).
- Nonparametric models used to assess outcome predictors: anisocoria at rest, after light stimulus, and persistent anisocoria.
Main Results:
- 152,905 observations from 6,654 patients analyzed.
- Anisocoria after light stimulus (using >0.5 mm cutoff) was associated with worse median mRS scores (2) than anisocoria at rest (1).
- Persistent anisocoria showed significantly worse outcomes (median mRS 3) compared to no persistent anisocoria (median mRS 1).
Conclusions:
- Anisocoria after light stimulus is a novel biomarker indicating a worse prognosis than anisocoria at rest.
- Anisocoria after light should be considered for routine clinical assessment and trending in neurocritical care.
- Further validation is recommended for incorporating this biomarker into clinical practice.
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