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Dose, Timing, and Type of Infant Antibiotic Use and the Risk of Childhood Asthma
Brittney M Donovan1, Andrew Abreo1, Tan Ding2
1Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Insights
Infant antibiotic use increases childhood asthma risk in a dose-dependent way. Each additional prescription raises asthma odds by 20%, highlighting the need for careful antibiotic stewardship in early life.
Area of Science:
- Pediatric Health
- Epidemiology
- Pharmacology
Background:
- Infant antibiotic exposure is linked to childhood asthma development.
- Previous studies have explored this association with varying results.
- Comprehensive evaluation of dose, timing, and type of infant antibiotic use is needed.
Purpose of the Study:
- To investigate the impact of infant antibiotic exposure on childhood asthma risk.
- To analyze the dose-dependent relationship between antibiotic prescriptions and asthma.
- To assess the influence of antibiotic timing and type on asthma development.
Main Methods:
- Analysis of data from singleton, term-birth, healthy infants in the Tennessee Medicaid Program.
- Ascertainment of infant antibiotic use and childhood asthma diagnoses via prescription fills and healthcare claims.
- Application of multivariable logistic regression models to examine associations.
Main Results:
- A dose-dependent association was observed between infant antibiotic use and childhood asthma.
- Each additional antibiotic prescription increased asthma odds by 20% (aOR, 1.20).
- Broad-spectrum antibiotic use was linked to higher asthma odds compared to narrow-spectrum use.
Conclusions:
- A consistent dose-dependent relationship exists between infant antibiotic prescriptions and subsequent childhood asthma.
- Infant antibiotic stewardship requires critical assessment to prevent adverse outcomes.
- This study provides crucial insights into infant antibiotic exposure and asthma risk.
Background:
Aspects of infant antibiotic exposure and its association with asthma development have been variably explored. We aimed to evaluate comprehensively and simultaneously the impact of dose, timing, and type of infant antibiotic use on the risk of childhood asthma.
Methods:
Singleton, term-birth, non-low-birth-weight, and otherwise healthy children enrolled in the Tennessee Medicaid Program were included. Infant antibiotic use and childhood asthma diagnosis were ascertained from prescription fills and healthcare encounter claims. We examined the association using multivariable logistic regression models.
Results:
Among 152 622 children, 79% had at least 1 antibiotic prescription fill during infancy. Infant antibiotic use was associated with increased odds of childhood asthma in a dose-dependent manner, with a 20% increase in odds (adjusted odds ratio [aOR], 1.20 [95% confidence interval {CI}, 1.19-1.20]) for each additional antibiotic prescription filled. This significant dose-dependent relationship persisted after additionally controlling for timing and type of the antibiotics. Infants who had broad-spectrum-only antibiotic fills had increased odds of developing asthma compared with infants who had narrow-spectrum-only fills (aOR, 1.10 [95% CI, 1.05-1.19]). There was no significant association between timing, formulation, anaerobic coverage, and class of antibiotics and childhood asthma.
Conclusions:
We found a consistent dose-dependent association between antibiotic prescription fills during infancy and subsequent development of childhood asthma. Our study adds important insights into specific aspects of infant antibiotic exposure. Clinical decision making regarding antibiotic stewardship and prevention of adverse effects should be critically assessed prior to use during infancy.
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