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Published on: August 25, 2014
Serum caffeine concentrations in preterm infants: a retrospective study
Masashiro Sugino1, Toru Kuboi2, Yuta Noguchi3
1Division of Neonatology, NHO Shikoku Medical Center for Children and Adults, 2-1-1 Senyu Cho, Zentsuji City, Kagawa, 765-8507, Japan. rmasashirod@yahoo.co.jp.
Insights
Therapeutic drug monitoring for caffeine in preterm infants is usually not needed. However, doses of 8 mg/kg/day or higher may lead to toxic caffeine levels, requiring further study on neurological effects.
Area of Science:
- Neonatal Medicine
- Pharmacology
Background:
- Therapeutic drug monitoring for caffeine in apnea of prematurity is often deemed unnecessary due to typically low serum concentrations.
- Despite this, some preterm infants have experienced caffeine toxicity.
Purpose of the Study:
- To evaluate the relationship between caffeine maintenance dose and serum concentrations in preterm infants.
- To identify the specific maintenance dose associated with potentially toxic serum caffeine levels.
Main Methods:
- A retrospective observational study involving 24 preterm infants treated with caffeine citrate for apnea of prematurity.
- Analysis of 272 serum samples to correlate caffeine dose with serum concentrations.
Main Results:
- A significant positive correlation was observed between caffeine dose and serum caffeine concentrations (r=0.72, p<0.05).
- Approximately 15% of infants receiving doses of 8 mg/kg/day or higher had serum caffeine concentrations exceeding suggested toxic levels.
Conclusions:
- Caffeine doses of 8 mg/kg/day or more increase the risk of reaching suggested toxic serum caffeine levels in preterm infants.
- The neurological impact of these elevated caffeine concentrations requires further investigation, including long-term neurodevelopmental follow-up.
Abstract:
Therapeutic drug monitoring is generally unnecessary in caffeine treatment for apnea of prematurity, as serum caffeine concentrations in preterm infants are normally markedly lower than those at which caffeine intoxication occurs. However, several studies have reported preterm infants having developed toxicity. This retrospective observational study, conducted at a tertiary center in Kagawa, Japan, aimed to evaluate the correlation between the maintenance dose and serum caffeine concentrations and determine the maintenance dose leading to suggested toxic caffeine levels. We included 24 preterm infants (gestational age, 27 ± 2.9 weeks; body weight, 991 ± 297 g) who were treated with caffeine citrate for apnea of prematurity between 2018 and 2021, and 272 samples were analyzed. Our primary outcome measure was the maintenance dose leading to suggested toxic caffeine levels. We found a positive correlation between caffeine dose and serum caffeine concentrations (p < 0.05, r = 0.72). At doses of ≥ 8 mg/kg/day, 15% (16/109) of patients had serum caffeine concentrations above the suggested toxic levels. Patients who receive doses ≥ 8 mg/kg/day risk reaching the suggested toxic serum caffeine levels. It remains unclear whether suggested toxic caffeine concentrations are detrimental to neurological prognosis. Further investigation is required to understand the clinical effects/outcomes of high serum levels of caffeine and to obtain long-term neurodevelopmental follow-up data.
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