A controlled trial of dexamethasone to prevent bronchopulmonary dysplasia in surfactant-treated infants

被引:0
|
作者
Rastogi, A
Akintorin, SM
Bez, ML
Morales, P
Pildes, RS
机构
[1] UNIV ILLINOIS,DEPT PEDIAT,CHICAGO,IL
[2] COOK CTY HOSP,DIV NEONATOL,CHICAGO,IL 60612
[3] OUR LADY LOURDES MED CTR,DIV NEONATOL,CAMDEN,NJ
[4] ROCKFORD MEM HOSP,DIV NEONATOL,ROCKFORD,IL
[5] FINCH UNIV HLTH SCI,DEPT PEDIAT,CHICAGO,IL
关键词
prevention of bronchopulmonary dysplasia; very low birth weight; respiratory distress syndrome; dexamethasone;
D O I
暂无
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background. Surfactant therapy now has a well-established role in the treatment of neonates with respiratory distress syndrome but has failed to reduce the incidence of bronchopulmonary dysplasia (BPD). We conducted a double-blind, placebo-controlled trial to test the hypothesis that dexamethasone therapy given during the first 12 days of life to very low birth weight infants would be synergistic to surfactant in preventing BPD. Methods. Seventy surfactant-pretreated infants (700-1500 g) who had severe respiratory distress syndrome (a/A ratio, 0.18 +/- 0.10; mean airway pressure, 11.1 +/- 1.9 cm H2O; fraction of inspired oxygen, 0.81 +/- 0.22) were enrolled to receive a 12-day course of dexamethasone (n = 36) or saline placebo (n = 34) starting within the first 12 hours after birth. The starting dose of dexamethasone was 0.5 mg/kg per day, and it was tapered progressively. Results. Ventilator variables at 5 to 14 days were significantly improved in those infants who received dexamethasone compared with those who received the placebo. The effect seem to be more marked in infants weighing less than 1250 g at birth. Significantly more infants could be extubated by 14 days of age in the dexamethasone group (26 of 32 vs 14 of 32). Dexamethasone therapy reduced the incidence of BPD at 28 days (odds ratio, 0.1; 95% confidence interval, 0.03 to 0.3) and eliminated BPD at 36 weeks' postconceptional age. Dexamethasone-treated infants had greater weight loss at 14 days (12.9 +/- 6.4% vs 3.7 +/- 8.6%, respectively) and higher blood pressures from days 3 to 10. However, no differences were seen in time to regain birth weight, hypertension (1 infant in each group), or incidence of intraventricular hemorrhage. Conclusions. We found an additive effect between dexamethasone and surfactant in improving pulmonary status and reducing the incidence of BPD. Compared with the placebo, dexamethasone therapy was more effective in reducing the incidence of BPD in surfactant-pretreated very low birth weight infants.
引用
收藏
页码:204 / 210
页数:7
相关论文
共 50 条
  • [41] Systemic Hydrocortisone To Prevent Bronchopulmonary Dysplasia in preterm infants (the SToP-BPD study); a multicenter randomized placebo controlled trial
    Onland, Wes
    Offringa, Martin
    Cools, Filip
    De Jaegere, Anne P.
    Rademaker, Karin
    Blom, Henry
    Cavatorta, Eric
    Debeer, Anne
    Dijk, Peter H.
    van Heijst, Arno F.
    Kramer, Boris W.
    Kroon, Andre A.
    Mohns, Thilo
    van Straaten, Henrica L.
    te Pas, Arjan B.
    Theyskens, Claire
    van Weissenbruch, Mirjam M.
    van Kaam, Anton H.
    BMC PEDIATRICS, 2011, 11
  • [42] Dexamethasone Therapy in Preterm Infants Developing Bronchopulmonary Dysplasia: Effect on Pulmonary Surfactant Disaturated-Phosphatidylcholine Kinetics
    Paola E Cogo
    Manuela Simonato
    Gianna Mariatoffolo
    Giorgio Stefanutti
    Marco Chierici
    Claudio Cobelli
    Carlo Ori
    Virgilio P Carnielli
    Pediatric Research, 2008, 63 : 433 - 437
  • [43] Dexamethasone therapy in preterm infants developing bronchopulmonary dysplasia: Effect on pulmonary surfactant disaturated-phosphatidylcholine kinetics
    Cogo, Paola E.
    Simonato, Manuela
    Mariatoffolo, Gianna
    Stefanutti, Giorgio
    Chierici, Marco
    Cobelli, Claudio
    Ori, Carlo
    Carnielli, Virgilio P.
    PEDIATRIC RESEARCH, 2008, 63 (04) : 433 - 437
  • [44] Pulmonary function at school-age in surfactant-treated preterm infants
    Gappa, M
    Berner, MM
    Hohenschild, S
    Dammann, CEL
    Bartmann, P
    PEDIATRIC PULMONOLOGY, 1999, 27 (03) : 191 - 198
  • [45] Postnatal corticosteroids to prevent or treat bronchopulmonary dysplasia in preterm infants
    Lemyre, Brigitte
    Dunn, Michael
    Thebaud, Bernard
    PAEDIATRICS & CHILD HEALTH, 2020, 25 (05) : 322 - 326
  • [46] Rationale for antioxidant therapy in premature infants to prevent bronchopulmonary dysplasia
    Welty, SE
    Smith, CV
    NUTRITION REVIEWS, 2001, 59 (01) : 10 - 17
  • [47] GASTRODUODENAL PERFORATION IN PRETERM BABIES TREATED WITH DEXAMETHASONE FOR BRONCHOPULMONARY DYSPLASIA
    SHIMIZU, T
    YAMASHIRO, Y
    YABUTA, K
    ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 1992, 67 (04): : 470 - 471
  • [48] GASTRODUODENAL PERFORATION IN PRETERM BABIES TREATED WITH DEXAMETHASONE FOR BRONCHOPULMONARY DYSPLASIA
    NG, PC
    BROWNLEE, KG
    DEAR, PRF
    ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 1991, 66 (10): : 1164 - 1166
  • [49] Stem cells for bronchopulmonary dysplasia in preterm infants: A randomized controlled phase II trial
    Ahn, So Yoon
    Chang, Yun Sil
    Lee, Myung Hee
    Sung, Se In
    Lee, Byong Sop
    Kim, Ki Soo
    Kim, Ai-Rhan
    Park, Won Soon
    STEM CELLS TRANSLATIONAL MEDICINE, 2021, 10 (08) : 1129 - 1137
  • [50] Neurodevelopmental outcomes in extremely premature infants treated with intratracheal budesonide-surfactant for the prevention of bronchopulmonary dysplasia
    Gurung, A.
    Zayek, M.
    Eyal, F.
    Dolma, K.
    AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2023, 365 : S328 - S328