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PEDIATRICS Vol. 111 No. 3 March 2003, pp. 469-476

Pulmonary Outcome at 1 Year Corrected Age in Premature Infants Treated at Birth With Recombinant Human CuZn Superoxide Dismutase

Jonathan M. Davis, MD*,§, Richard B. Parad, MD, MPH,#, Theresa Michele, MD{ddagger}{ddagger}, Elizabeth Allred, PhD#,**, Anita Price, MD{ddagger}, Warren Rosenfeld, MD* for the North American Recombinant Human CuZnSOD Study Group

* Department of Pediatrics (Neonatology)
{ddagger} Radiology
§ CardioPulmonary Research Institute, Winthrop University Hospital, SUNY Stony Brook School of Medicine, Mineola, New York
|| Department of Newborn Medicine, Brigham and Women’s Hospital
Divisions of Newborn Medicine
# Biostatistics, Children’s Hospital
** Harvard Medical School and Harvard School of Public Health, Boston, Massachusetts
{ddagger}{ddagger} Bio-Technology General Corporation, Iselin, New Jersey

--> Objective. To examine whether treatment of premature infants with intratracheal recombinant human CuZn superoxide dismutase (r-h CuZnSOD) reduces bronchopulmonary dysplasia and improves pulmonary outcome at 1 year corrected age.

Design. Three hundred two premature infants (600–1200 g birth weight) treated with exogenous surfactant at birth for respiratory distress syndrome were randomized to receive either intratracheal r-h CuZnSOD (5 mg/kg in 2 mL/kg saline) or placebo every 48 hours (as long as intubation was required) for up to 1 month of age. Short-term, as well as longer-term pulmonary outcome was assessed.

Results. There were no differences between groups in the incidence of death or the development of bronchopulmonary dysplasia (oxygen requirement with an Edwards chest radiograph score of >=3) at 28 days of life or 36 weeks’ postmenstrual age. r-h CuZnSOD was well-tolerated and not associated with significant increases in any adverse event. At a median of 1 year corrected age, health assessments and physical examinations were performed on 209 (80%) surviving infants, with complete data available on 189 infants. Thirty-seven percent of placebo-treated infants had repeated episodes of wheezing or other respiratory illness severe enough to require treatment with asthma medications such as bronchodilators and/or corticosteroids compared with 24% of r-h CuZnSOD-treated infants, a 36% reduction. In infants <27 weeks’ gestation, 42% treated with placebo received asthma medications compared with 19% of r-h CuZnSOD-treated infants, a 55% decrease. Infants <27 weeks’ gestation who received r-h CuZnSOD also had a 55% decrease in emergency department visits and a 44% decrease in subsequent hospitalizations. Growth measurements and the results of physical examinations were comparable between groups.

Conclusions. These data indicate that treatment at birth with r-h CuZnSOD may reduce early pulmonary injury, resulting in improved clinical status when measured at 1 year corrected age. r-h CuZnSOD appears to be a safe and effective therapy that improves pulmonary outcome in high-risk premature infants.

Key Words: bronchopulmonary dysplasia • oxygen • antioxidant • superoxide dismutase • asthma • chronic lung disease

Abbreviations: BPD, bronchopulmonary dysplasia • CLD, chronic lung disease • PMA, postmenstrual age • SOD, superoxide dismutase • r-h CuZnSOD, recombinant human CuZnSOD • RDS, respiratory distress syndrome • IT, intratracheal(ly) • DSMC, Data Safety Monitoring Committee • ROS, reactive oxygen species


Received for publication Jul 22, 2002; Accepted Nov 20, 2002.


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