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Dexamethasone may affect the occurrence of parenteral nutrition-associated cholestasis in preterm neonates
Saizhi Jiang1, Qingqing Hu1, Jing Zhang1
1Department of Pediatrics, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Insights
Late postnatal dexamethasone may protect preterm neonates from parenteral nutrition-associated cholestasis. This study found dexamethasone treatment reduced the incidence of this condition in vulnerable infants.
Area of Science:
- Neonatology
- Pediatric Gastroenterology
- Pharmacology
Background:
- Glucocorticoids manage autoimmune hepatitis and cholestatic diseases.
- The efficacy of glucocorticoids for parenteral nutrition-associated cholestasis is unknown.
- Bronchopulmonary dysplasia treatment with dexamethasone may impact cholestasis.
Purpose of the Study:
- To investigate if late postnatal dexamethasone influences parenteral nutrition-associated cholestasis in preterm neonates.
- To analyze the protective effect of dexamethasone on cholestasis development.
Main Methods:
- Retrospective study of 78 preterm neonates (<30 weeks gestation, birthweight ≤1000g).
- Bilirubin levels monitored bi-weekly.
- Data on dexamethasone, intravenous nutrition, and enteral feeding collected via audits.
Main Results:
- 15 neonates diagnosed with parenteral nutrition-associated cholestasis.
- Prolonged parenteral nutrition was a risk factor.
- Late postnatal dexamethasone treatment was a protective factor.
Conclusions:
- Dexamethasone treatment may decrease the incidence of parenteral nutrition-associated cholestasis.
- Further research into dexamethasone's role in neonatal cholestasis is warranted.
Introduction:
Glucocorticoids are currently used for the co-therapeutic management of autoimmune hepatitis and some cholestatic diseases. Thus far, we do not know the efficacy of glucocorticoids in the treatment of parenteral nutrition-associated cholestasis. We aimed to analyze whether the administration of late postnatal dexamethasone for treating bronchopulmonary dysplasia influence the occurrence of parenteral nutrition-associated cholestasis in preterm neonates.
Methods:
A retrospective study was conducted for 78 preterm neonates without major anomalies (gestational age was <30 weeks, and birthweight was ≤1000 g) hospitalized in a neonatal unit. Total and direct serum bilirubin levels were measured about every two weeks for all neonates. Data including the administration of dexamethasone, intravenous nutrition, and enteral feeding were collected by at least three audits.
Results:
A total of 15 preterm neonates were diagnosed with parenteral nutrition-associated cholestasis, and after stopping parenteral nutrition, the direct bilirubin value decreased to the normal level for no longer than 150 days. The prolonged duration of parenteral nutrition was a risk factor, and late postnatal dexamethasone treatment was a protective factor in reducing the incidence of parenteral nutrition-associated cholestasis.
Conclusion:
Dexamethasone treatment may reduce the occurrence of parenteral nutrition-associated cholestasis in preterm neonates.
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