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Outcomes in extremely preterm neonates after the introduction of early low-dose hydrocortisone treatment: A
Ellie Purcell1, Pooja Sachdev2, Dushyant Batra3
1School of Medicine, University of Nottingham, United Kingdom of Great Britain and Northern Ireland.
Insights
Early low-dose hydrocortisone (ELDH) did not improve survival without bronchopulmonary dysplasia (BPD) in extremely preterm infants. ELDH was linked to increased sepsis and longer respiratory support needs.
Area of Science:
- Neonatal Medicine
- Pediatric Critical Care
- Pharmacology
Background:
- Extremely preterm neonates face high risks of bronchopulmonary dysplasia (BPD).
- Early low-dose hydrocortisone (ELDH) is explored as a potential intervention.
- The PREMILOC study protocol guides ELDH administration within 24 hours of birth.
Purpose of the Study:
- To assess the association between ELDH use and BPD-free survival at 36 weeks completed gestational age (CGA).
- To evaluate secondary outcomes, including mortality, sepsis, and respiratory support duration.
Main Methods:
- Retrospective, matched case-control study involving 188 extremely preterm neonates.
- Cases received ELDH (8.5 mg/kg over 10 days) within 24 hours of life.
- Controls did not receive ELDH; data collected from tertiary neonatal intensive care units.
Main Results:
- No significant association between ELDH and improved BPD-free survival (p=0.153) or reduced mortality (p=0.814).
- ELDH use was significantly associated with increased culture-positive late-onset sepsis (p=0.006).
- Higher non-invasive respiratory support days (p=0.032) and longer total length of stay (p=0.004) were observed with ELDH.
Conclusions:
- ELDH did not enhance BPD-free survival in extremely preterm neonates.
- ELDH use correlated with increased sepsis incidence and prolonged respiratory support.
- Further research is needed to identify preterm neonates who may benefit from ELDH.
Objective:
Assess the association between use of early low-dose hydrocortisone (ELDH) in extremely preterm neonates, and bronchopulmonary dysplasia (BPD)-free survival at 36 weeks completed gestational age (CGA), as well as additional secondary outcomes.
Design:
Retrospective, matched, case-control study.
Setting:
Tertiary neonatal intensive care units in Nottingham University Hospitals NHS Trust (Queens Medical Centre and Nottingham City Hospital).
Patients:
188 extremely preterm neonates. 94 historical controls born between 1 October 2017 and 30 September 2019. 94 cases born between 1 January 2020 and 31 December 2021.
Interventions:
ELDH using the published PREMILOC study protocol (total dose of 8.5 mg/kg over 10 days) initiated within the first 24 h of life.
Primary Outcome Measure:
Survival without BPD at 36 weeks CGA.
Results:
There were no statistically significant associations between the sex, gestational age or birthweight of the groups. There was no significant association between the use of ELDH and increased survival without BPD at 36 weeks CGA (p = 0.153) or reduction in mortality (p = 0.814). Using ELDH was significantly associated with an increased incidence of culture positive late-onset sepsis (p = 0.006), higher non-invasive respiratory support days (p = 0.032) and a longer total length of stay (p = 0.004).
Conclusions:
ELDH use was not associated with an improvement in BPD free survival in extremely preterm neonates. The cases had a higher incidence of culture positive late-onset sepsis and longer duration of respiratory support. Further research exploring stratification of preterm neonates that will benefit from ELDH is needed.
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