Korean J Perinatol.
1999 Mar;10(1):10-16.
Cardiac Effect of Pulse Dexamethasone Therapy in Infants with Bronchopulmonary Dysplasia
Abstract
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PURPOSE: To examine the cardiac function, incidence and natural history of cardiac
hypertrophy (CH) and the association of side effects with CH after pulse dexamethasone
therapy in infants with bronchopulmonary dysplasia.
METHODS
Twelve infants, gestational age 28.6+/-1.6(26-31)weeks, birth weight 1243+/-186
(1010- 1620)g, received a pulse course of dexamethasone, starting at 0.5mg/kg/d for three
days and readministered ten days thereafter at a median of 19 days of age. Serial
echocardiographic measurement of septal thickness(ST), left ventricular(LV) posterior wall
thickness(PWT), LV diameter(LVD), LV length(LVL), LV mass, ejection fraction(EF) and
acceleration time to right ventricular ejection time ratio(AT/RVET) were taken before,
and 4, 11 days after starting dexamethasone. For infants diagnosed as CH, echocardiography
was performed weekly until the parameters were normalized. Side effects of dexamethasone
such as leukocytosis, hypertension, hyperglycemia and insulin therapy were recorded and
compared.
RESULTS
CH occurred in 5 of 12 infants(47%). ST, PWD, and AT/RVET increased
significantly at 4 days and 11 days after starting dexamethasone than baseline. LVD
decreased significantly at 4 days and 11 days after the administration of dexamethasone
than before. Other parameter such as LVL, LV mass and EF were not changed and the evidence
of left ventricular outflow obstruction was not observed. The incidence of hyperglycemia
and insulin therapy were higher in CH group than in no CH group(p<0.05). Five infants with
CH recovered until five weeks after starting dexamethasone on serial echocardiography,
CONCLUSION
Infants receiving a pulse course of dexamethasone developed evidence of septal
hypertrophy, thickened left ventricular wall and impaired filling of left ventricle
immediately after starting dexamethasone but always resolved within five weeks Serial
echocardiography is not probably routinely required in preterm infants with bronchopulmonary
dysplasia receiving pulse dexamethasone therapy.