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Risk factors for metabolic bone disease among preterm infants less than 32 weeks gestation with Bronchopulmonary
Wenwen Chen1, Zhenhai Zhang2, Shuzhen Dai2
1Zhangzhou Hospital Affiliated to Fujian Medical University, Shengli W Rd, Xiangcheng District, Zhangzhou, Fujian, China. pipixiu@163.com.
Insights
Metabolic bone disease (MBD) is common in infants with bronchopulmonary dysplasia (BPD). Risk factors include fetal growth restriction, low birth weight, poor feeding volume, cholestasis, sepsis, and diuretic use.
Area of Science:
- Neonatal Medicine
- Pediatric Endocrinology
- Critical Care Pediatrics
Background:
- Infants with bronchopulmonary dysplasia (BPD) exhibit a higher prevalence of metabolic bone disease (MBD).
- The specific contributing factors to MBD development in BPD infants remain largely undetermined.
- This study aimed to identify key risk factors for MBD in this vulnerable population.
Purpose of the Study:
- To investigate and identify significant risk factors associated with the development of metabolic bone disease (MBD) in infants diagnosed with bronchopulmonary dysplasia (BPD).
- To provide insights into potential predictive markers for MBD in BPD infants.
- To inform clinical practice and future research directions.
Main Methods:
- A retrospective analysis of medical records for BPD infants admitted to Zhangzhou Hospital's Neonatal Intensive Care Unit from June 2016 to May 2020.
- Cases of MBD were identified and matched with controls (BPD infants without MBD) based on gestational age and gender.
- Statistical analysis, including univariate and multivariate models, was employed to determine the association between various factors and MBD.
Main Results:
- Fetal growth restriction (OR 6.00), extremely low birth weight (OR 3.10), and feeding volume < 80 mL/kg/d by week 4 (OR 14.98) were significant risk factors.
- Cholestasis (OR 4.44), late-onset sepsis (OR 3.95), and prolonged diuretic use (> 2 weeks) (OR 5.45) also emerged as significant risk factors for MBD.
- A total of 156 infants were analyzed, with 52 cases of MBD and 104 controls.
Conclusions:
- Fetal growth restriction, extremely low birth weight, inadequate feeding volume, cholestasis, and late-onset sepsis are significant risk factors for MBD in BPD infants.
- Prolonged diuretic use is also identified as a risk factor.
- These findings highlight potential predictive factors for MBD in BPD infants, necessitating prospective validation.
Background:
Bronchopulmonary dysplasia (BPD) infants present an increased incidence of metabolic bone disease (MBD), but it is unknown which factors contribute to this. The aim of this study was to determine the risk factors for developing MBD in BPD infants.
Methods:
A retrospective review of the medical records of BPD infants admitted to the Neonatal intensive care unit at Zhangzhou Hospital between Jun 2016 and May 2020 was performed. BPD infants with MBD were identified, two contemporaneous without MBD matched by gestational age and gender were randomly selected as controls for each case of MBD. The association between putative risk factors and MBD was estimated with ORs and 95% CIs. A P-value threshold ≤0.2 was used in univariate analysis for inclusion into a multivariate (adjusted) model with a P-value of < 0.05 as statistically significant.
Results:
A total of 156 BPD infants were enrolled with 52 cases of MBD and 104 controls. Fetal growth restriction (OR 6.00, 95% CI, 1.81-19.84), extremely low birth weight (OR 3.10, 95% CI, 1.07-8.94), feeding volume < 80 mL/kg/d at the end of the 4th week after birth (OR 14.98, 95% CI, 4.04-55.58), cholestasis (OR 4.44, 95% CI, 1.59-12.40), late onset sepsis (OR 3.95, 95% CI, 1.12-13.98) and prolonged (> 2 weeks) diuretics application (OR 5.45, 95% CI, 1.25-23.84) were found to be statistically significant risk factors for MBD in BPD infants.
Conclusion:
In BPD infants of homogeneous gestational age, fetal growth restriction, extremely low birth weight, feeding volume < 80 mL/kg/d at the end of the 4th week after birth, cholestasis and late onset sepsis are significant risk factors for MBD. These findings provide potential predictive factors for MBD in BPD infants and warrant prospective validation.
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