Comparing Death or Neurodevelopmental Outcomes of Haemodynamically Significant Patent Ductus Arteriosus in Very Low Birth Weight Preterm Infants

crossref(2021)

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Abstract BackgroundOptimal management of haemodynamically significant patent ductus arteriosus (HsPDA) remains controversial for premature infants. Treatment options include conservative treatment with fluid restriction and diuretics, medical treatment with cyclo-oxygenase (COX) inhibitors or surgical ligation. Our primary objective is to compare the death and/or adverse neurodevelopmental outcomes among very low birth weight (VLBW) infants with HsPDA who were managed with conservative, medical and/or surgical treatment. The secondary objectives are to examine antenatal factors predisposing to surgical treatment and the neonatal short-term morbidities between three groups.MethodsThis was a retrospective, gestational age-stratified study of VLBW infants born in National University Hospital (NUH) in Singapore and admitted to the intensive care unit from 2007–2016.. Perinatal variables, short-term neonatal outcomes and neurodevelopmental outcomes were studied. Statistical analysis were performed with chi square and t-test.. Results124 infants were included. 17 VLBW infants managed conservatively [C] were identified and compared with 83 VLBW infants managed medically [M] and 24 VLBW infants managed surgically [S]. The main group analysis compared outcomes between infants managed [C] and those who received either medical or surgical treatment [M+S]. The subgroup analysis compared outcomes between infants managed [C] vs [M] and [C] vs [S]. The main group analysis found group M+S infants had a higher incidence of chronic lung disease (CLD) (p=0.005) than group C. The odds ratio (OR) of group M+S developing CLD was significant (OR 6.83). They were significantly shorter (p=0.017) and had a smaller head circumference (p=0.039) at discharge. Group S infants were older at discharge, due to a longer NICU stay , and were lighter , shorter and had a smaller head circumference (p<0.05). No significant differences in death, composite outcome of death and global development delay and neurological outcomes such as hearing loss, cerebral palsy (CP) and speech delay were found. Conclusions: Comparing the management, infants requiring surgical treatment for hsPDA were more likely to have short-term complications such as CLD, longer hospitalization, and poorer growth. Despite a more turbulent postnatal course, death and/or adverse neurodevelopmental outcomes were not worse in these infants. Further randomized control studies will be useful to verify these findings.
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