Key result
Low-dose anthracycline exposure in asymptomatic pediatric cancer survivors was associated with significantly reduced septal systolic and diastolic strain rates compared to healthy controls, indicating early regional wall dysfunction.
Why the study?
Does vector velocity imaging detect early regional wall dysfunction in asymptomatic children treated with low-dose anthracyclines compared to healthy controls?
Cross-Sectional (n=28)
No
Does vector velocity imaging detect early regional wall dysfunction in asymptomatic children treated with low-dose anthracyclines compared to healthy controls?
Absolute Event Rate: -1.66% vs -1.89%
p-value: p=0.042
Vector velocity imaging can detect early subclinical regional wall dysfunction in children exposed to low-dose anthracyclines before global ejection fraction declines.
Strain imaging may detect early septal dysfunction in anthracycline survivors; leaves open prognostic value and need for prospective validation.
BACKGROUND AND OBJECTIVES: Anthracyclines are effective drugs that are widely used in pediatric cancer treatment. Previous studies have demonstrated that exposure to low-dose anthracyclines (<300 mg/m(2)) induces a progressive decrease in cardiac function during long-term follow-up. The goal of this study was to assess left ventricular function using vector velocity imaging (VVI) in children undergoing low-dose anthracycline therapy. SUBJECTS AND METHODS: We examined 14 asymptomatic patients who had been treated with anthracyclines and had normal fractional shortening (FS) and ejection fraction (EF). In all of the patients, standard two-dimensional (2D) pulsed and tissue Doppler echocardiographic measurements were taken from an apical 4-chamber view. The peak myocardial velocity, peak strain rate (SR), peak strain, and displacement were obtained from VVI. Data were compared with 14 age-matched healthy controls. RESULTS: From the regional wall motion analysis using VVI in the left ventricle, the peak myocardial velocity and displacement of the lateral wall were increased significantly more than the septum, and there were no significant differences between the patients and the controls. Although systolic strain, and the systolic and diastolic SRs showed no significant differences between the septum and lateral wall in the controls, those of septum, in the patients, were decreased significantly more than those of lateral wall (p<0.05). In comparison with the controls, these changes in septal strain and SRs of patients were significant (p<0.05). CONCLUSION: Anthracycline therapy, even low-dose, can induce changes in regional wall function before global dysfunction. Also, the strain and SR obtained from VVI may be useful for early detection of these changes.
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Park et al. (2009) conducted a cross-sectional in Pediatric cancer survivors treated with anthracyclines (n=28). Low-dose anthracycline therapy vs. Age-matched healthy controls was evaluated on Septal systolic strain rate (s-1) (p=0.042). Low-dose anthracycline exposure in asymptomatic pediatric cancer survivors was associated with significantly reduced septal systolic and diastolic strain rates compared to healthy controls, indicating early regional wall dysfunction.
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