Am J Perinatol 2005; 22(8): 441-448
DOI: 10.1055/s-2005-916332
Copyright © 2005 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA.

Antenatal Glucocorticoid Treatment Decreases Mortality and Chronic Lung Disease in Survivors among 23- to 28-Week Gestational Age Preterm Infants

José Figueras-Aloy1 , Manuel Moro Serrano2 , Jesús Pérez Rodríguez3 , Cristina Fernández Pérez2 , Vicente Roqués Serradilla4 , José Quero Jiménez3 , Rafael Jiménez González1 , The SEN1500 Spanish Neonatal Network5
  • 1Hospital Clínic, Institut Clínic de Ginecologia, Obstetrícia i Neonatologia, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Unidad Integrada de Pediatría, Universitat de Barcelona, Barcelona, Spain
  • 2Hospital Clínico San Carlos, Madrid, Spain
  • 3Hospital La Paz, Madrid, Spain
  • 4Hospital La Fe, Valencia, Spain
  • 5Contributors to the SEN1500 Spanish Neonatal Network (see Appendix)
Further Information

Publication History

Publication Date:
21 September 2005 (online)

ABSTRACT

The purpose of this study was to analyze the influence of antenatal glucocorticoid therapy (AGT) on mortality and chronic lung disease (CLD) in surviving preterm infants 23 to 28 weeks gestational age (WGA). This was a multicenter, prospective, observational study. A total of 2448 infants 23 to 28 WGA were born in 2002 to 2003; 27.7% did not receive AGT, 18.8% were exposed to partial AGT, and 53.5% were exposed to complete AGT. A total of 883 died and 22.9% of 1537 survivors were affected by CLD. Unadjusted univariate analysis showed AGT was associated with a reduction in mortality (p < 0.001), either with partial or complete AGT courses, and also with a reduction in CLD in survivors (p < 0.001), but only with complete AGT courses. In logistic regression analysis adjusted for confounding factors and a propensity score for AGT, AGT was significant and independently associated with a reduction of mortality, but only for complete AGT course (odds ratio [OR], 0.64; 95% confidence interval [CI], 0.47 to 0.87; p = 0.004), and with a decrease in CLD if a complete AGT course was administered (OR, 0.63; 95% CI, 0.45 to 0.89; p = 0.009). A complete course of AGT in 23 to 28 WGA pregnancies is associated with decreased rates of neonatal mortality and CLD disease in surviving infants.

REFERENCES

  • 1 Crowley P. Prophylactic corticosteroids for preterm birth (Cochrane Review). In: the Cochrane Library. Issue 3 2004 Chichester, United Kingdom; John Wiley & Sons Ltd
  • 2 Gunkel J H, Mitchell B R. Observational evidence for the efficacy of antenatal steroids from randomized studies of surfactant replacement.  Am J Obstet Gynecol. 1995;  173 281-285
  • 3 Horbar J D. Antenatal corticosteroid treatment and neonatal outcomes for infants 501 to 1500 gm in the Vermont-Oxford Trials Network.  Am J Obstet Gynecol. 1995;  173 275-281
  • 4 Kari M A, Hallman M, Eronen M et al.. Prenatal dexamethasone treatment in conjunction with rescue therapy of human surfactant: a randomized placebo-controlled multicenter study.  Pediatrics. 1994;  93 730-736
  • 5 Tarnow-Mordi W. Scottish Neonatal Consultants' Collaborative Study Group . Trends and variation in use of antenatal corticosteroids to prevent neonatal respiratory distress syndrome: recommendations for national and international comparative audit.  Br J Obstet Gynecol. 1996;  103 534-540
  • 6 Wright L L, Verter J, Younes N et al.. Antenatal corticosteroid administration and neonatal outcome in very low birthweight infants: the NICHD Neonatal Research Network.  Am J Obstet Gynecol. 1995;  173 269-274
  • 7 Wells L R, Papile L A, Gardner M O, Hartenberger C R, Merker L. Impact of antenatal corticosteroid therapy in very low birthweight infants on chronic lung disease and other morbidities of prematurity.  J Perinatol. 1999;  19 578-581
  • 8 Van Marter L J, Allred E N, Leviton A et al.. Antenatal glucocorticoid treatment does not reduce chronic lung disease among surviving preterm infants.  J Pediatr. 2001;  138 198-204
  • 9 Salhab W A, Hynan L S, Perlman J M. Partial or complete antenatal steroids treatment and neonatal outcome in extremely low birthweight infants ≤ 1000 g: is there a dose-dependent effect?.  J Perinatol. 2003;  23 668-672
  • 10 The International Neonatal Network . The CRIB (clinical risk index for babies) score: a tool for assessing initial neonatal risk and comparing performance of neonatal intensive care.  Lancet. 1993;  342 193-198
  • 11 Rubin D B. Estimating causal effects from large data sets using propensity scores.  Ann Intern Med. 1997;  127 757-763
  • 12 Dales L G, Ury H K. An improper use of statistical significance testing in studying covariables.  Int J Epidemiol. 1978;  7 373-375
  • 13 Liggins G C, Howie R N. A controlled trial of antepartum glucocorticoid treatment for prevention of the respiratory distress syndrome in premature infants.  Pediatrics. 1972;  50 515-525
  • 14 Guinn D A, Atkinson M W, Sullivan L et al.. Single versus weekly courses of antenatal corticosteroids for women at risk of preterm delivery: a randomized controlled trial.  JAMA. 2001;  286 1581-1587
  • 15 Baud O. Antenatal corticosteroid therapy: benefits and risks.  Acta Paediatr. 2004;  444 6-10
  • 16 Maher J E, Cliver S P, Goldenberg R L, Davis R O, Copper R L. The effect of corticosteroid therapy in the very premature infant.  Am J Obstet Gynecol. 1994;  170 869-873
  • 17 Jobe A H, Mitchell B R, Gunkel J H. Beneficial effects of the combined use of prenatal corticosteroids and postnatal surfactant on preterm infants.  Am J Obstet Gynecol. 1993;  168 508-513
  • 18 Kaaresen P I, Dohlen G, Fundingsrud H P, Dahl L B. The use of CRIB (clinical risk index for babies) score in auditing the performance of one neonatal intensive care unit.  Acta Paediatr. 1998;  87 195-200
  • 19 Silver R K, Vyskocil C, Solomon S L, Ragin A, Neerhof M G, Farrell E E. Randomized trial of antenatal dexamethasone in surfactant-treated infants delivered before 30 weeks' gestation.  Obstet Gynecol. 1996;  87 683-691
  • 20 Del Moral T, Claure N, Van Buskirk S, O'Sullivan M J, Bancalari E. Perinatal interventions associated with a decreased incidence of intraventricular hemorrhage in extremely low birthweight infants.  Pediatr Res. 1999;  45 920
  • 21 Agarwal R, Chiswick M L, Rimmer S et al.. Antenatal steroids are associated with a reduction in the incidence of cerebral white matter lesions in very low birthweight infants.  Arch Dis Child Fet Neonat Ed. 2002;  86 F96-F101
  • 22 Figueras-Aloy J, Carbonell-Estrany X, Krauel X. Antenatal glucocorticoid treatment increases the rate of “survival without chronic lung disease” among 25-29 week preterm infants.  J Pediatr. 2002;  140 486-487
  • 23 Dammann O, Allred E N, Van Marter L J, Dammann C EL, Leviton A. for the Developmental Epidemiology Network Investigators . Bronchopulmonary dysplasia is not associated with ultrasound-defined cerebral white matter damage in preterm newborns.  Pediatr Res. 2004;  55 319-325

J. Figueras-AloyM.D. Ph.D. 

Servicio Neonatología, Hospital Clínic (sede Maternitat), C/ Sabino de Arana 1

08028 Barcelona, Spain

    >