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J Thorac Cardiovasc Surg 2007;134:1347-1349
© 2007 The American Association for Thoracic Surgery
Brief Communication |
Department of Surgery and Clinical Science, Division of Cardiovascular Surgery, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.
Received for publication May 28, 2007; revisions received June 19, 2007; accepted for publication July 12, 2007. * Address for reprints: Kimikazu Hamano, MD, PhD, Department of Surgery and Clinical Science, Division of Cardiovascular Surgery, Yamaguchi University Graduate School of Medicine, 1-1-1 Minami-Kogushi, Ube, Yamaguchi, Japan 755-8505. (Email: litaoshe@yamaguchi-u.ac.jp).
| The first 20% of the full text of this article appears below. |
The delivery of autologous bone marrow–derived cells has developed as a revolutionary concept for repairing the injured heart,1
and many clinical trials have been conducted all over the world. Although there are conflicting reports about the beneficial effects of bone marrow cells for myocardial repair,2
early- and middle-phase clinical trials have not found any severe side effects of cell-based therapy. However, its long-term safety and feasibility have not yet been established. We report the results of more than 5 years follow-up of patients treated with the intramyocardial injection of autologous bone marrow mononuclear cells (BM-MNCs) after coronary artery bypass grafting (CABG).
Clinical Summary
Between November 1999 and March 2002, 8 selected patients undergoing standard CABG were given an intramyocardial injection of BM-MNCs into the ungrafted ischemic area (Table 1). The collection and separation of BM-MNCs was detailed previously.1
After the completion of CABG, 3
22 x 108 BM-MNCs were injected directly, with 6
22 injections, into the targeted area, where there was no indication for CABG or intervention therapy (Figure 1). To determine the safety and feasibility of this therapy, we monitored the
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