Exposure to repeat doses of antenatal glucocorticoids is associated with altered cardiovascular status after birth. Issue 1 (20th September 2005)

• Record Type: Journal Article
• Authors: Mildenhall, L F J; Battin, M R; Morton, S M B; Bevan, C; Kuschel, C A; Harding, J E
• Is Part Of: Archives of disease in childhood. Volume 91:Issue 1(2006)
• Page Start: F56
• Page End: F60
• Publication Date: 2005-09-20
• Subjects: EDIVS, end diastolic interventricular septal -- EDLVPW, end diastolic left ventricular posterior wall; corticosteroids -- premature -- blood pressure -- cardiac hypertrophy; Infants -- Diseases -- Periodicals; Newborn infants -- Diseases -- Periodicals; Fetus -- Diseases -- Periodicals; 618.920105
• DOI: 10.1136/adc.2004.065300
• Languages: English
• ISSNs: 1359-2998

Abstract

Abstract : Objective: To determine if exposure to more than one course of antenatal glucocorticoids is associated with changes in infant blood pressure and myocardial wall thickness in the first month after birth. Design: Prospective cohort study. Setting: Tertiary neonatal intensive care unit. Participants: Mothers who were eligible for but declined to enter a randomised trial of repeated doses of antenatal glucocorticoids (ACTORDS)—that is, who had a singleton, twin, or triplet pregnancy at <32 weeks gestation, had received an initial course of glucocorticoids seven or more days previously, and were considered to be at continued risk of preterm birth. Main outcome measures: Blood pressure daily for the first week then weekly until 4 weeks of age. End diastolic interventricular septal and left ventricular posterior wall (EDIVS and EDLVPW) thickness at 48–72 hours after birth. Results: Thirty seven women were enrolled and delivered 50 infants. Thirty mothers (39 infants) were exposed to one course of glucocorticoids, and seven mothers (11 infants) to more than one course. Blood pressures were higher in the first week after birth in infants exposed to multiple courses of glucocorticoids, and in infants with a latency between last exposure and delivery of less than seven days. Systolic blood pressure on day 1 was >2SD above published normal ranges in 67% of babies exposed to multiple courses and 24% of babies exposed to a single course of glucocorticoids (p = 0.04). There was no difference between groups in thickness of the EDIVS or EDLVPW. However, 44/50 (88%) babies had EDIVS and 49/50 (98%) babies had EDLVPW thickness >2 SD above the expected mean for birth weight and gestation. EDIVS but not EDLVPW thickness increased with increasing latency (mean 0.02 mm/day, p = 0.03). Conclusion: Future randomised trials should assess the long term effects of exposure to antenatal glucocorticoids, particularly multiple courses, on the cardiovascular status of the infant.