PEDIATRICS Vol. 111 No. 3 March 2003, pp. 483-487
Chronic Lung Disease of Prematurity and Intrauterine Growth Retardation: A Population-Based Study



* Neonatal Unit, Leicester Royal Infirmary, University Hospitals of Leicester, Leicester, United Kingdom
Department of Epidemiology and Public Heath, University of Leicester Medical School, Leicester, United Kingdom
Department of Child Health, Robert Kilpatrick Clinical Sciences Building, University of Leicester, Leicester, United Kingdom
--> Objective. To determine the risk of chronic lung disease (CLD) in small for gestational age (SGA) preterm infants in comparison to appropriately grown and large for gestational age (LGA) infants.
Methods. Observational study derived from a geographically defined population (Trent Health Region, United Kingdom). All preterm infants of
32 completed weeks gestation born to Trent resident mothers admitted to neonatal units between 1995 and 1999 (inclusive) were included. Birth weight percentiles were created for the whole population, and infants were classified as SGA infants (if <10th percentile), appropriately grown (if between 25th and 75th percentilesreference group), and LGA infants (if
90th centile). Both mortality and CLD rates (using both 28 days and 36 weeks postmenstrual age [PMA] definitions) were determined for these groups of infants.
Results. Four thousand fifty-one preterm infants
32 weeks gestation were identified. SGA infants showed higher mortality before 28 days postnatal age and 36 weeks PMA as compared with reference group infants (odds ratio [OR]: 2.01, 95% confidence interval [CI]: 1.492.72; and OR: 2.00, 95% CI: 1.492.69), respectively.
SGA infants showed a significantly greater risk of developing CLD, both at 28 days and 36 weeks PMA as compared with the reference group infants (OR: 1.34, 95% CI: 1.031.74; and OR: 1.87, 95% CI: 1.392.51), respectively. LGA infants showed a trend toward a reduced incidence of CLD in comparison to the reference group, which was statistically significant for the 36 weeks definition (OR: 0.7628 weeks, 95% CI: 0.571.01; and OR: 0.5536 weeks, 95% CI: 0.370.81).
Conclusions. Fetal growth seems to influence mortality in general and morbidity, attributable to CLD, in particular in preterm infants. SGA preterm infants are at higher risk of death before 28 days and 36 weeks PMA and CLD by both definitions. LGA infants show reduced risk of CLD.
Key Words: prematurity chronic lung disease intrauterine growth retardation small for gestational age bronchopulmonary dysplasia
Abbreviations: CLD, chronic lung disease PMA, postmenstrual age VLBW, very low birth weight SGA, small for gestational age LGA, large for gestational age OR, odds ratio CI, confidence interval
Received for publication Sep 12, 2002; Accepted Sep 12, 2002.
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