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  • Meeting abstract
  • Open Access

Transendocardial, autologous bone-marrow cell transplant in severe, chronic ischemic heart failure

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Critical Care20037 (Suppl 3) :P12

  • Published:


  • Reversible Defect
  • Ischemic Heart Failure
  • Doppler Echocardiogram
  • Transendocardial
  • Electromechanical Mapping


This study evaluated the hypothesis that transendocardial injections of autologous mononuclear bone-marrow cells in patients with end-stage ischemic heart disease could promote neovascularization and improve perfusion and myocardial contractility.

Methods and results

Twenty-one patients were enrolled into this prospective, non-randomized, open-label, controlled study (first 14, treatment; last seven, control). Baseline evaluations included complete clinical and laboratory evaluations, exercise stress (ramp treadmill), two-dimensional Doppler echocardiogram, SPECT perfusion scan, and 24-hour Holter monitoring. Bone-marrow mononuclear cells were harvested, isolated, washed, and resuspended in saline for injection by NOGA catheter (15 injections of 0.2 cm3). Electromechanical mapping (EMM) was used to identify viable myocardium (unipolar voltage ≥ 6.9 mV) for treatment. Patients underwent 2-month noninvasive and 4-month invasive (treatment group only) follow-up using standard protocols and the same procedures as baseline. Patient population demographics and exercise test variables did not differ significantly between the treatment and control groups; only creatinine and BNP levels varied in laboratory evaluations. At 2 months, there was a significant reduction in total reversible defect within the treatment group and between the treatment and control groups (P = 0.02) on quantitative SPECT analysis. At 4 months, there was improvement in ejection fraction from a baseline of 20% to 29% (P = 0.003) and a reduction in ESV (P = 0.03) in the treated patients. EMM revealed significant mechanical improvement of the injected segments (P < 0.0005).


In patients with chronic, ischemic heart failure, EMM technology was used to target viable, hibernating myocardium for transendocardial delivery of autologous bone-marrow mononuclear cells. At follow-up, treated patients had significantly improved myocardial perfusion and contractility.

Authors’ Affiliations

Hospital Pró-Cardíaco, Rio de Janeiro, Brazil
Texas Heart Institute, 6770 Bertner Avenue, Houston, TX 77030, USA


© BioMed Central Ltd 2003