Literature DB >> 16131530

Prenatal predictors of chronic lung disease in very preterm infants.

D J Henderson-Smart1, J L Hutchinson, D A Donoghue, N J Evans, J M Simpson, I Wright.   

Abstract

OBJECTIVE: To identify prenatal risk factors for chronic lung disease (CLD) at 36 weeks postmenstrual age in very preterm infants. POPULATION: Data were collected prospectively as part of the ongoing audit of the Australian and New Zealand Neonatal Network (ANZNN) of all infants born at less than 32 weeks gestation admitted to all tertiary neonatal intensive care units in Australia and New Zealand.
METHODS: Prenatal factors up to 1 minute of age were examined in the subset of infants born at gestational ages 22-31 weeks during 1998-2001, and who survived to 36 weeks postmenstrual age (n = 11 453). Factors that were significantly associated with CLD at 36 weeks were entered into a multivariate logistic regression model.
RESULTS: After adjustment, low gestational age was the dominant risk factor, with an approximate doubling of the odds with each week of decreasing gestational age from 31 to less than 25 weeks (trend p<0.0001). Birth weight for gestational age also had a dose-response effect: the lower the birth weight for gestational age, the greater the risk, with infants below the third centile having 5.67 times greater odds of CLD than those between the 25th and 75th centile (trend p<0.0001). There was also a significantly increased risk for male infants (odds ratio 1.51 (95% confidence interval 1.36 to 1.68), p<0.0001).
CONCLUSIONS: These population based data show that the prenatal factors low gestational age, low birth weight for gestational age, and male sex significantly predict the development of chronic respiratory insufficiency in very preterm infants and may assist clinical decision about delivery.

Entities:  

Mesh:

Year:  2005        PMID: 16131530      PMCID: PMC2672649          DOI: 10.1136/adc.2005.072264

Source DB:  PubMed          Journal:  Arch Dis Child Fetal Neonatal Ed        ISSN: 1359-2998            Impact factor:   5.747


  30 in total

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  24 in total

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Authors:  N Evans; J Hutchinson; J M Simpson; D Donoghue; B Darlow; D Henderson-Smart
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2006-07-28       Impact factor: 5.747

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7.  Extracellular superoxide dismutase overexpression can reverse the course of hypoxia-induced pulmonary hypertension.

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8.  Elective high-frequency oscillatory ventilation in preterm infants with respiratory distress syndrome: an individual patient data meta-analysis.

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9.  Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study.

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10.  Occurrence and severity of bronchopulmonary dysplasia and respiratory distress syndrome after a preterm birth.

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