Evaluation of cardiac reserved function by high-dose dobutamine-stress echocardiography in asymptomatic anthracycline-treated survivors of childhood cancer

Pediatr Int. 2006 Jun;48(3):313-20. doi: 10.1111/j.1442-200X.2006.02210.x.

Abstract

Background: The aim of this study was to evaluate cardiac function and cardiac reserved function in asymptomatic anthracycline-treated long-time survivors of childhood cancer using dobutamine (DOB) stress echocardiography.

Methods: A total of 26 patients (19 males and 7 females) were divided into four groups according to cumulative dose of anthracycline (ATC): non-anthracycline group (N group), seven cases; low anthracycline cumulative dose group (L group), five cases (<or=200 mg/m(2)); medium anthracycline cumulative dose group (M group), seven cases (200-<400 mg/m(2)); high anthracycline group (H group), seven cases (>or=400 mg/m(2)). DOB infusion was begun at 5 microg/kg per min (gamma) and increased up to 30 gamma. Cardiac function and cardiac reserved function at rest, after low-dose and high-dose DOB stress, were estimated.

Results: In the H group, % left ventricular posterior wall thickening (%PWT) at rest and ratio of maximum early filling peak velocity (E) and atrial contraction peak velocity (A) from the left ventricular transmitral flow wave (E/A) and %PWT at DOB 5 gamma stress were significantly lower than in other groups (P<0.05). After DOB 30 gamma stress in groups given>00 mg/m(2) end-systolic wall stress was significantly higher and E/A and %PWT were significantly lower than those of other groups (P<0.05). ATC cumulative dose strongly correlated with %PWT after DOB 30 gamma stress (P<0.001).

Conclusions: Subclinical ATC cardiotoxicity was detected by high-dose DOB stress echocardiography at lower cumulative doses than with other methods. %PWT appears to be a useful index for detection of ATC cardiotoxicity.

MeSH terms

  • Adolescent
  • Adult
  • Anthracyclines / administration & dosage*
  • Antibiotics, Antineoplastic / administration & dosage*
  • Child
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Echocardiography, Stress
  • Female
  • Heart / physiopathology*
  • Hemodynamics / physiology*
  • Humans
  • Leukemia / drug therapy
  • Leukemia / physiopathology*
  • Lymphoma / drug therapy
  • Lymphoma / physiopathology*
  • Male

Substances

  • Anthracyclines
  • Antibiotics, Antineoplastic