The Journal of Pediatrics
Volume 152, Issue 2 , Pages 270-275, February 2008

Betamethasone Impairs Cerebral Blood Flow Velocities in Very Premature Infants with Severe Chronic Lung Disease

  • Gilles Cambonie, MD, PhD

      Affiliations

    • Neonatal Intensive Care Unit, Arnaud de Villeneuve Hospital, University Hospital of Montpellier, France
    • Corresponding Author InformationReprint requests: Gilles Cambonie, MD, PhD, Unité de Réanimation Néonatale, Pédiatrie II, Hôpital Arnaud de Villeneuve, 371 Avenue du Doyen G. Giraud, 34295 Montpellier Cedex 5, France.
  • ,
  • Renaud Mesnage, MD

      Affiliations

    • Neonatal Intensive Care Unit, Arnaud de Villeneuve Hospital, University Hospital of Montpellier, France
  • ,
  • Christophe Milési, MD

      Affiliations

    • Neonatal Intensive Care Unit, Arnaud de Villeneuve Hospital, University Hospital of Montpellier, France
  • ,
  • Odile Pidoux, MD

      Affiliations

    • Neonatal Intensive Care Unit, Arnaud de Villeneuve Hospital, University Hospital of Montpellier, France
  • ,
  • Corinne Veyrac, MD

      Affiliations

    • Department of Pediatric Radiology, Arnaud de Villeneuve Hospital, University Hospital of Montpellier, France.
  • ,
  • Jean-Charles Picaud, MD, PhD

      Affiliations

    • Neonatal Intensive Care Unit, Arnaud de Villeneuve Hospital, University Hospital of Montpellier, France

Received 25 September 2006; received in revised form 27 February 2007; accepted 3 July 2007. published online 29 October 2007.

Objective

To assess betamethasone (BM) effects on the cerebral hemodynamics of neonates with severe chronic lung disease (CLD).

Study design

Intravenous BM was given once daily for 6 consecutive days to 12 infants (birth weight: 698 g [range, 650-884 g], gestational age: 25.3 weeks [range, 25-26.4 weeks]) at a postnatal age of 34 days (range, 28-36 days). Cerebral blood flow velocities (CBFVs) were recorded prospectively in the anterior cerebral artery (ACA) and the lenticulostriate artery (LSA) before, during, and after treatment, using Doppler flowmetry.

Results

The decrease in systolic and diastolic velocities was maximum on the 5th day, reaching 32% (95% confidence interval [CI], 23%-42%) and 58% (95% CI, 39%-64%) from baseline in the ACA, and 44% (95% CI, 29%-50%) and 57% (95% CI, 33%-66%) in the LSA, respectively. The resistance index (RI) increased significantly in both arteries during treatment. Return to baseline values was observed after BM was stopped. The change in velocities and RI was independent of arterial blood gas and blood pressure variations.

Conclusions

BM decreased the CBFVs of premature infants, suggesting a vasoconstrictor effect in both superficial and deep arterial vessels. Caution is recommended when BM is used to treat preterm infants with severe CLD.

Abbreviations: ACA, Anterior cerebral artery, ANOVA, Analysis of variance, BM, Betamethasone, CBFV, Cerebral blood flow velocity, CLD, Chronic lung disease, DEX, Dexamethasone, EDV, End diastolic velocity, LSA, Lenticulostriate artery, MAP, Mean airway pressure, PSV, Peak systolic velocity, RI, Resistance index, Tc, Transcutaneous

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PII: S0022-3476(07)00659-2

doi:10.1016/j.jpeds.2007.07.007

The Journal of Pediatrics
Volume 152, Issue 2 , Pages 270-275, February 2008