Prematurity Does Not Increase Early Childhood Fracture Risk
| Autor: | Elizabeth Hisle-Gorman, Apryl Susi, Gregory Gorman, Scott C. Wagner, Kari Wagner |
|---|---|
| Rok vydání: | 2019 |
| Předmět: |
Male
Pediatrics medicine.medical_specialty Time Factors Military Health Services Gestational Age Comorbidity Infant Premature Diseases Risk Assessment Fractures Bone 03 medical and health sciences 0302 clinical medicine Cholestasis Risk Factors 030225 pediatrics medicine Humans 030212 general & internal medicine Neonatal cholestasis Retrospective Studies business.industry Incidence Infant Newborn Infant Gestational age Retrospective cohort study Infant Low Birth Weight medicine.disease United States Osteopenia Low birth weight Child Preschool Pediatrics Perinatology and Child Health Necrotizing enterocolitis Gestation Female medicine.symptom business Infant Premature Follow-Up Studies |
| Zdroj: | The Journal of Pediatrics. 207:148-153 |
| ISSN: | 0022-3476 |
| DOI: | 10.1016/j.jpeds.2018.11.017 |
| Popis: | Objective To evaluate the impact of prematurity on fracture by age 5, controlling for medications and comorbidities of prematurity. Study design We performed a retrospective cohort study of infants born in Military Treatment Facilities in 2009-2010 with ≥5 years of follow-up care. Gestational age, low birth weight, comorbidities of prematurity (osteopenia, necrotizing enterocolitis, chronic lung disease, and cholestasis) and fractures were identified by International Classification of Disease, 9th Edition, codes. Pharmaceutical records identified treatment with caffeine, diuretics, postnatal corticosteroids, and antacids. Poisson regression analysis determined fracture rate by 5 years of life. Results There were 65 938 infants born in 2009-2010 who received care in the military health system for ≥5 years, including 3589 born preterm; 165 born at ≤286/7 weeks of gestation, 380 born at 29-316/7 weeks of gestation, and 3044 born at 32-366/7 weeks of gestation. Preterm birth at any gestational age was not associated with fracture rate in adjusted models. The fracture rate was increased with cholestasis, proton pump inhibitor exposure, and male sex. Conclusions Prematurity was not associated with fracture rate. Neonatal cholestasis and proton pump inhibitor treatment were associated with increased fractures by age 5. |
| Databáze: | OpenAIRE |
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