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Efficacy of a Cycloplegic Agent Administered as a Spray in the Pediatric Population
Insights
Cyclopentolate 1% spray reduced distress in pediatric patients compared to drops, but may be less effective for cycloplegia in children with dark irises.
Area of Science:
- Ophthalmology
- Pediatric Medicine
- Pharmacology
Background:
- Accurate refractive error assessment in young children is crucial for timely intervention.
- Traditional methods of administering cycloplegic eye drops can cause distress in pediatric patients.
- Cyclopentolate 1% is a commonly used anticholinergic agent for inducing cycloplegia.
Purpose of the Study:
- To assess the efficacy and tolerability of cyclopentolate 1% delivered as a spray versus traditional drops in children aged 3-6 years.
- To compare patient distress levels between the spray and drop administration methods.
- To evaluate the adequacy of cycloplegia for refraction in both groups.
Main Methods:
- A prospective, randomized, parallel-group study involving healthy pediatric volunteers aged 3-6 years.
- Participants were assigned to receive either a single drop or a single puff of cyclopentolate 1% into closed eyes.
- Distress levels and pupil diameter were measured; cycloplegia adequacy was assessed for refraction.
Main Results:
- The spray group experienced significantly lower distress levels than the drop group (P < .0001), except in 6-year-olds.
- No significant difference in pupil diameter was observed between the spray and drop groups (P = .51).
- 16.6% of patients with dark irises in the spray group did not achieve adequate cycloplegia for accurate refraction.
Conclusions:
- Cyclopentolate 1% spray offers a less distressing alternative for inducing cycloplegia in uncooperative children.
- However, reduced efficacy in achieving adequate cycloplegia for refraction in children with dark irises necessitates caution.
- Physicians should consider iris pigmentation when choosing the administration method for cyclopentolate 1% in pediatric patients.
Purpose:
To evaluate the efficacy and tolerability of cyclopentolate 1% administered as a spray in pediatric patients between 3 and 6 years old.
Methods:
In this prospective, randomized, parallel group study, healthy volunteers were randomly assigned to receive cyclopentolate 1% as a single drop or a single puff into closed eyes.
Results:
There were 61 patients included in the study; 31 received cyclopentolate 1% as drops and 30 received cyclopentolate 1% as spray. The mean age at presentation was 4.5 ± 1.07 years (range: 3 to 6 years) and 4.2 ± 1.06 years (range: 3 to 6 years) in the drops and spray groups, respectively. The distress level was significantly lower at the time of receiving cyclopentolate as a spray (P < .0001), with the exception of patients aged 6 years. There were no significant differences in pupil diameter between the two groups (P = .51), whereas 5 of 30 patients (16.6%) with dark irises who received cyclopentolate spray did not have adequate cycloplegia to allow for accurate refraction.
Conclusions:
Cycloplegia achieved with cyclopentolate 1% administered as a spray may be an option in uncooperative children because it is less distressing compared to cyclopentolate 1% drops. However, physicians should be aware that cycloplegia obtained is only partially effective in children with dark irises. [J Pediatr Ophthalmol Strabismus. 2020;57(5):301-304.].
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