Related Experiment Videos
Cardiac adverse effects of early dexamethasone treatment in preterm infants: a randomized clinical trial
1Division of Neonatology, Catholic University of the Sacred Heart, Rome, Italy.
Insights
Early dexamethasone treatment in preterm infants can lead to significant left ventricular myocardial hypertrophy. Close echocardiographic monitoring is crucial for detecting this side effect in future studies.
Area of Science:
- Neonatal Medicine
- Pediatric Cardiology
- Pharmacology
Background:
- Dexamethasone is frequently used in preterm infants to manage respiratory distress syndrome.
- Potential cardiac side effects of early dexamethasone administration require thorough investigation.
Purpose of the Study:
- To evaluate the impact of early dexamethasone on left ventricle dimensions in preterm infants.
- To assess the clinical significance and echocardiographic changes associated with dexamethasone-induced left ventricular hypertrophy.
Main Methods:
- A randomized controlled trial involving 50 preterm infants (birth weight <= 1250g, gestational age <= 30 weeks).
- Infants received either dexamethasone or a placebo, with serial echocardiographic measurements taken throughout the study period.
- Left ventricle dimensions, septal thickness, and posterior wall thickness were analyzed.
Main Results:
- Dexamethasone-treated infants showed significantly increased septal and left posterior wall thickness.
- Left ventricle diameter was significantly smaller in the dexamethasone group.
- 20% of treated neonates developed symptomatic left ventricular myocardial hypertrophy.
Conclusions:
- Early, short-course dexamethasone in preterm infants can cause clinically significant left ventricular myocardial hypertrophy.
- Strict echocardiographic monitoring is recommended for preterm infants receiving dexamethasone to detect cardiac side effects.
Abstract:
This study evaluates the effects of early administration of dexamethasone on left ventricle dimensions and their clinical significance in preterm infants. Fifty preterm infants with birth weight < or = 1250 g and gestational age < or = 30 weeks were randomly assigned after 72 hours of life to the dexamethasone group (n = 25) or to the control group (n = 25). The treated infants received dexamethasone intravenously from the 4th day of life for 7 days (0.5 mg/kg/day for the first 3 days, 0.25 mg/kg/day for the next 3 days, and 0.125 mg/kg/day for the 7th day). Serial echocardiographic measurements of end systolic interventricular septum thickness, end diastolic interventricular septum thickness, end systolic left ventricle posterior wall thickness, end diastolic left ventricle posterior wall thickness, left ventricle end diastolic diameter, and left ventricle end systolic diameter were taken before starting dexamethasone, on days 3 and 7 of treatment, 7 days after the interruption of treatment, and at the 28th day of life. Five infants of each group were excluded by the final analysis because of the lack of a complete cardiac evaluation, leaving 20 treated and 20 control infants. Infants receiving dexamethasone had a significantly larger increase in mean septal and left posterior wall thickness during the treatment and 7 days after the dexamethasone weaning. The mean left ventricle diameter of treated infants was significantly lower than that of control infants from the 7th day of treatment to the 28th day of life. Four neonates (20%) in the dexamethasone group developed left ventricular myocardial hypertrophy without left ventricle outflow tract obstruction, showing signs of decreased cardiac output and ischemic changes on ECG. The daily fluid intake was increased to 200 ml/kg to ensure an adequate preload volume, and the complete resolution of left ventricle hypertrophy was obtained within the 2nd to 3rd week after dexamethasone weaning. Preterm infants receiving an early (< 96 hours of life) short course of dexamethasone develop a left ventricular myocardial hypertrophy that can be symptomatic and clinically significant. Preterm infants included in future studies with the goal to find the minimum dose and duration of dexamethasone treatment should be strictly monitored echocardiographically for this side effect.
Related Concept Videos
Drug Dosing: Infants and Children
Diphtheria
Skeletal Muscle Relaxants: Adverse Effects
Unlike...
Cardiomyopathy II: Dilated Cardiomyopathy
Adrenergic Antagonists: Pharmacological Actions of β-Receptor Blockers