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Published on: June 9, 2023
Progression of Right Ventricular Systolic Dysfunction Detected by Myocardial Deformation Imaging in Asymptomatic
Soo Jung Kang1, Mira Kim1, Seo Jung Hwang2
1Department of Pediatrics, CHA Bundang Medical Center, CHA University School of Medicine, Seongnam, Korea.
Insights
Velocity Vector Imaging (VVI) can detect evolving right ventricular systolic dysfunction (RVSD) in preterm infants. This screening method identifies RVSD progression from 4 to 24 months corrected age in asymptomatic children.
Area of Science:
- Pediatric Cardiology
- Neonatology
- Echocardiography
Background:
- Right ventricular systolic dysfunction (RVSD) is a concern in preterm infants.
- Early detection of RVSD progression is crucial for long-term outcomes.
- Velocity Vector Imaging (VVI) offers advanced echocardiographic assessment.
Purpose of the Study:
- To assess the progression of RVSD in preterm children using VVI.
- To evaluate RV longitudinal peak systolic strain (LPSS) from infancy to 24-month corrected age.
- To compare preterm infants with term controls.
Main Methods:
- Retrospective study of 24 preterm infants (<33 weeks GA) and 10 term controls.
- Sequential RV LPSS measurements at 4 and 24 months corrected age.
- VVI used for detailed echocardiographic analysis.
Main Results:
- RVSD (RV LPSS < 16%) detected in 29.2% of preterm children by 24 months.
- 5/7 preterm children with RVSD at 24 months showed improvement from 4 months.
- Only 2/7 with RVSD had a history of moderate/severe bronchopulmonary dysplasia.
Conclusions:
- Routine VVI screening can detect RVSD progression in asymptomatic preterm children.
- RVSD can evolve between 4 and 24 months corrected age.
- VVI is a valuable tool for monitoring RV function in this population.
Background:
To detect progression of right ventricular (RV) systolic dysfunction (RVSD) in asymptomatic preterm children from infancy to 24-month corrected age, using velocity vector imaging (VVI).
Methods:
Retrospective study comparing sequential RV longitudinal peak systolic strain (LPSS) from 24 children born at < 33 weeks of gestational age and 10 term infants recruited as controls, obtained at a mean of 4-month (first exam) and 24-month corrected age (second exam).
Results:
In 7/24 (29.2%) of preterm children, RV LPSS of < 16%, defined as RVSD, was detected at the second exam; 5/7 of these children had RV LPSS > 16% at the first exam, and only 2/7 of these children had a history of moderate or severe bronchopulmonary dysplasia.
Conclusion:
In asymptomatic preterm children, routine echocardiographic screening using VVI could detect RVSD which could progress from 4-24 month corrected age.
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