Purpose
Preterm infants undergoing Retinopathy of Prematurity Eye Exams
(ROPEE) may experience adverse events, possibly from systemic absorption of
cyclopentolate. The purpose of this study was to analyze the association
between adverse events and drug levels found in neonates undergoing
ROPEE.
Materials and Methods
25 infants were randomized into two groups during routine ROP
screening: 5 infants for blood collection before mydriatic drops and 20 for
blood collection 1 h after eye drops. Blood was collected onto dried blood
spot cards, extracted, and analyzed for cyclopentolate and phenylephrine
using liquid chromatography and mass spectrometry. Relationships between
drug levels and adverse events were assessed.
Results
Cyclopentolate (range 6–53 ng/ml) was observed in 15 of 18
infants, while phenylephrine was not detected. Levels of cyclopentolate were
significantly higher in infants who were on oxygen (p =
0.01). There was a significant association between cyclopentolate levels and
gastric residuals in tube-fed infants not receiving oxygen
(p = 0.01).
Conclusions
Cyclopentolate levels varied among preterm infants after ROPEE.
Cyclopentolate was positively associated with increased gastric residuals.
Underlying medical conditions requiring oxygen administration may affect
absorption and metabolism of cyclopentolate. There is a need to predict
infants at risk for high blood levels of cyclopentolate in order to prevent
or treat adverse events after ROPEE.