Literature DB >> 11585480

Single vs weekly courses of antenatal corticosteroids for women at risk of preterm delivery: A randomized controlled trial.

D A Guinn1, M W Atkinson, L Sullivan, M Lee, S MacGregor, B V Parilla, J Davies, K Hanlon-Lundberg, L Simpson, J Stone, D Wing, K Ogasawara, J Muraskas.   

Abstract

CONTEXT: The practice of administering weekly courses of antenatal corticosteroids to pregnant women at risk of preterm delivery is widespread, but no randomized trial has established the efficacy or safety of this practice.
OBJECTIVES: To evaluate the efficacy of weekly administration of antenatal corticosteroids compared with a single course in reducing the incidence of neonatal morbidity and to evaluate potential complications of weekly treatment. DESIGN AND
SETTING: Randomized, double-blind, placebo-controlled intention-to-treat trial conducted in 13 academic centers in the United States from February 1996 through April 2000. PARTICIPANTS: A total of 502 pregnant women between 24 and 32 completed weeks' gestation who were at high risk of preterm delivery. INTERVENTION: All patients received a complete single course of antenatal corticosteroids (either betamethasone, 12 mg intramuscularly repeated once in 24 hours for 2 doses, or dexamethasone, 6 mg intramuscularly repeated every 12 hours for 4 doses). Participants who had not delivered 1 week after receipt of the single course were randomly assigned to receive either betamethasone, 12 mg intramuscularly repeated once in 24 hours for 2 doses every week until 34 weeks' gestation or delivery, whichever came first (n = 256), or a similarly administered placebo (n = 246). MAIN OUTCOME MEASURE: Composite neonatal morbidity (including severe respiratory distress syndrome, bronchopulmonary dysplasia, severe intraventricular hemorrhage, periventricular leukomalacia, proven sepsis, necrotizing enterocolitis, or perinatal death).
RESULTS: Composite morbidity occurred in 22.5% of the weekly-course group vs 28.0% of the single-course group (unadjusted relative risk, 0.80; 95% confidence interval, 0.59-1.10). Neither group assignment nor the number of treatment courses was associated with a reduction in composite morbidity.
CONCLUSIONS: Weekly courses of antenatal corticosteroids did not reduce composite neonatal morbidity compared with a single course of treatment. Weekly courses of antenatal corticosteroids should not be routinely prescribed for women at risk of preterm delivery.

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Year:  2001        PMID: 11585480     DOI: 10.1001/jama.286.13.1581

Source DB:  PubMed          Journal:  JAMA        ISSN: 0098-7484            Impact factor:   56.272


  36 in total

Review 1.  Decline in effectiveness of antenatal corticosteroids with time to birth: real or artefact?

Authors:  Simon Gates; Peter Brocklehurst
Journal:  BMJ       Date:  2007-07-14

Review 2.  Repeat doses of prenatal corticosteroids for women at risk of preterm birth for improving neonatal health outcomes.

Authors:  Caroline A Crowther; Christopher Jd McKinlay; Philippa Middleton; Jane E Harding
Journal:  Cochrane Database Syst Rev       Date:  2011-06-15

Review 3.  Antenatal corticosteroids in the management of preterm birth: are we back where we started?

Authors:  Clarissa Bonanno; Ronald J Wapner
Journal:  Obstet Gynecol Clin North Am       Date:  2012-03       Impact factor: 2.844

4.  Angiotensin-(1-7) deficiency and baroreflex impairment precede the antenatal Betamethasone exposure-induced elevation in blood pressure.

Authors:  Hossam A Shaltout; James C Rose; Mark C Chappell; Debra I Diz
Journal:  Hypertension       Date:  2012-01-03       Impact factor: 10.190

5.  [Systemic drug treatment during pregnancy].

Authors:  Maximilian Riedel; Bettina Kuschel
Journal:  Hautarzt       Date:  2020-04       Impact factor: 0.751

6.  Histochemical analyses of altered fetal lung development following single vs multiple courses of antenatal steroids.

Authors:  Zarah J Pua; Barbara S Stonestreet; Anne Cullen; Aliakbar Shahsafaei; Grazyna B Sadowska; Mary E Sunday
Journal:  J Histochem Cytochem       Date:  2005-06-13       Impact factor: 2.479

7.  Bronchopulmonary dysplasia in preterm infants: pathophysiology and management strategies.

Authors:  Carl T D'Angio; William M Maniscalco
Journal:  Paediatr Drugs       Date:  2004       Impact factor: 3.022

8.  Gestational age-specific risks vs benefits of multicourse antenatal corticosteroids for preterm labor.

Authors:  Laurie C Zephyrin; Kimberly N Hong; Ronald J Wapner; Alan M Peaceman; Yoram Sorokin; Donald J Dudley; Jay D Iams; Margaret Harper; Steve N Caritis; Brian M Mercer; John M Thorp; Susan M Ramin; Dwight J Rouse; Baha Sibai
Journal:  Am J Obstet Gynecol       Date:  2013-06-13       Impact factor: 8.661

9.  Pessaries in multiple pregnancy as a prevention of preterm birth: the ProTwin Trial.

Authors:  Maud A Hegeman; Dick J Bekedam; Kitty Wm Bloemenkamp; Anneke Kwee; Dimitri Nm Papatsonis; Joris Am van der Post; Arianne C Lim; Hubertina Cj Scheepers; Christine Willekes; Johannes J Duvekot; Marc Spaanderman; Martina Porath; Jim van Eyck; Monique C Haak; Marielle G van Pampus; Hein W Bruinse; Ben Willem J Mol
Journal:  BMC Pregnancy Childbirth       Date:  2009-09-17       Impact factor: 3.007

10.  The links between prenatal stress and offspring development and psychopathology: disentangling environmental and inherited influences.

Authors:  F Rice; G T Harold; J Boivin; M van den Bree; D F Hay; A Thapar
Journal:  Psychol Med       Date:  2009-05-29       Impact factor: 7.723

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