Preventing graft restenosis after coronary artery bypass grafting with tissue-type plasminogen activator

Eur J Med Res. 2017 Jun 12;22(1):18. doi: 10.1186/s40001-017-0259-8.

Abstract

Objective: To explore the feasibility and safety of using tissue-type plasminogen activator (t-PA) to prevent graft restenosis after coronary artery bypass grafting (CABG).

Methods: In this prospective observational study, 37 patients underwent CABG between June 2009 and May 2013. These patients were grouped according to the anti-coagulation strategy after surgery: t-PA (n = 12) and conventional treatments (n = 25). In the t-PA group, the patients received acetylsalicylic acid (ASA) and clopidogrel plus intravenous infusion of t-PA (0.25 mg/kg/day) starting at 24 h after surgery and that lasted for 3 days. In the conventional group, the patients received only ASA and clopidogrel. 64-row spiral computed tomographic coronary angiography was performed at 1 week, 1, and 3 months after surgery to evaluate the patency of the graft vessel.

Results: The mean stenosis severity of the saphenous vein grafts was lower in the t-PA group compared with the conventional group at 3 months after surgery (p < 0.05), but there was no significant difference at 1 week and 1 month (p > 0.05). The patency rate of the grafts was not significantly different between the two groups at 1 week, 1, and 3 months after surgery (p > 0.05).

Conclusion: Early application of t-PA after CABG was feasible and safe, and might help prevent early restenosis of SV grafts. Additional clinical randomized trials are necessary to address this issue.

Keywords: Coronary artery bypass grafting; Restenosis; Tissue-type plasminogen activator.

MeSH terms

  • Aged
  • Aspirin / administration & dosage
  • Blood Coagulation / drug effects
  • Clopidogrel
  • Coronary Angiography
  • Coronary Artery Bypass / adverse effects*
  • Female
  • Graft Occlusion, Vascular / drug therapy*
  • Graft Occlusion, Vascular / etiology
  • Graft Occlusion, Vascular / genetics
  • Graft Occlusion, Vascular / prevention & control*
  • Humans
  • Male
  • Middle Aged
  • Prospective Studies
  • Ticlopidine / administration & dosage
  • Ticlopidine / analogs & derivatives
  • Ticlopidine / chemistry
  • Tissue Plasminogen Activator / administration & dosage*
  • Tissue Plasminogen Activator / chemistry
  • Treatment Outcome

Substances

  • Clopidogrel
  • PLAT protein, human
  • Tissue Plasminogen Activator
  • Ticlopidine
  • Aspirin