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Pupil Size and Reactivity in Pediatric Patients With Sickle Cell Disease
Joana M Mack1,2, Sara Frankowski3,2, Bethany Verkamp4,5
1Division of Pediatric Hematology-Oncology, Department of Pediatrics.
Insights
Pupillometry shows differences in pupil size and reactivity in children with sickle cell disease compared to white children. Further research is needed to use this for objective pain assessment in Black pediatric patients.
Area of Science:
- Ophthalmology
- Pediatrics
- Hematology
Background:
- Objective pain assessment is challenging in pediatric sickle cell disease.
- Pupillometry offers a potential tool for measuring pain objectively.
- Normative pupillometry values are needed for diverse pediatric populations.
Purpose of the Study:
- Establish normative values for pupil size and reactivity in pediatric patients with sickle cell disease.
- Investigate pupillometry as a tool for objective pain measurement and treatment response assessment.
- Compare pupillometry findings in Black pediatric patients with existing data.
Main Methods:
- Utilized the NeurOptics PLR-2000 pupillometer for measurements.
- Studied a cohort of 82 Black pediatric patients (44 males, 38 females) aged 2 to 21.
- Compared findings with a previously published study on white pediatric participants.
Main Results:
- Significant differences observed in maximum constriction velocity, maximum pupil size, and minimum pupil size when comparing study participants to white participants.
- No significant differences in pupil size and reactivity between sickle cell disease patients and Black patients without the disease compared to prior studies.
- Pupillometry data suggests potential ethnic variations in pupil dynamics.
Conclusions:
- Pupillometry may reveal ethnic differences in pupil size and reactivity in pediatric populations.
- Further investigation is warranted in Black pediatric patients with sickle cell disease during vaso-occlusive crisis and well states.
- Normative pupillometry data is crucial for objective pain assessment in diverse pediatric groups.
Abstract:
Pupil size and reactivity have been studied to objectively measure pain utilizing pupillometry measurements. Given the challenges associated with treating vaso-occlusive pain in pediatric patients with sickle cell disease, better assessment tools are needed. The objective of this study is to establish normative values for pupil size and reactivity in pediatric patients with sickle cell disease with the hope that pupillometry can be used as a tool to objectively measure pain and response to treatment with analgesic medications. Readings were performed using a NeurOptics PLR-2000 pupillometer. Forty-four males and 38 females, all black, were studied. Their median age was 11 years (range: 2 to 21). When comparing our participants with white participants in a previously published pediatric study, there was a significant difference in maximum constriction velocity ( t =3.45, P =0.009), maximum pupil size ( t =-5.57 mm, P <0.0001), and minimum pupil size ( t =-3.24, P =0.002). There was no significant difference in pupil size and reactivity between patients with sickle cell disease and black patients without the disease when compared with the previously published study. Therefore, further investigation of pupillometry within the black population during vaso-occlusive crisis and in the "well state" is warranted in pediatric patients with sickle cell disease.
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