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Randomized Controlled Trial
. 2016 Dec;41(12):1601-1607.
doi: 10.3109/02713683.2015.1136419. Epub 2016 May 9.

Systemic Absorption of Cyclopentolate and Adverse Events After Retinopathy of Prematurity Exams

Affiliations
Randomized Controlled Trial

Systemic Absorption of Cyclopentolate and Adverse Events After Retinopathy of Prematurity Exams

Anita Mitchell et al. Curr Eye Res. 2016 Dec.

Erratum in

  • Corrigendum.
    [No authors listed] [No authors listed] Curr Eye Res. 2018 Aug;43(8):1065. doi: 10.1080/02713683.2018.1489450. Epub 2018 Jul 9. Curr Eye Res. 2018. PMID: 29985656 No abstract available.

Abstract

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.

Keywords: Adverse events; cyclopentolate; preterm infant; retinopathy of prematurity; screening exams.

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Conflict of interest statement

Declaration of interest The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

Figures

Figure 1
Figure 1
Adverse events the day before ROPEE compared to the day of ROPEE, grouped by cyclopentolate concentration ranges.
Figure 2
Figure 2
Cyclopentolate concentrations by patient-on-respiratory-support. Boxplot is overlaid. Cyclopentolate concentrations for patients on respiratory support are significantly higher than those not (p = 0.01, two-sample t-test).
Figure 3
Figure 3
Scatterplots of three adverse outcomes vs. cyclopentolate concentration, stratified by patient-on-respiratory-support.

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