Pulmonary outcome at 1 year corrected age in premature infants treated at birth with recombinant human CuZn superoxide dismutase

被引:175
作者
Davis, JM
Parad, RB
Michele, T
Allred, E
Price, A
Rosenfeld, W
机构
[1] SUNY Stony Brook, Winthrop Univ Hosp, Dept Pediat Neonatol, Sch Med, Mineola, NY 11501 USA
[2] SUNY Stony Brook, Winthrop Univ Hosp, Dept Radiol, Sch Med, Mineola, NY 11501 USA
[3] SUNY Stony Brook, Winthrop Univ Hosp, CardioPulm Res Inst, Sch Med, Mineola, NY 11501 USA
[4] Brigham & Womens Hosp, Dept Newborn Med, Boston, MA 02115 USA
[5] Childrens Hosp, Div Newborn Med, Boston, MA 02115 USA
[6] Childrens Hosp, Div Biostat, Boston, MA 02115 USA
[7] Harvard Med Sch, Boston, MA USA
[8] Harvard Sch Publ Hlth, Boston, MA USA
[9] Biotechnol Gen Corp, Iselin, NJ USA
关键词
bronchopulmonary dysplasia; oxygen; antioxidant; superoxide dismutase; asthma; chronic lung disease;
D O I
10.1542/peds.111.3.469
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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. Shortterm, 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 greater than or equal to3) 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 CuZn-SOD-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.
引用
收藏
页码:469 / 476
页数:8
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