Therapeutic angiogenesis with basic fibroblast growth factor: technique and early results

Ann Thorac Surg. 1998 Jun;65(6):1540-4. doi: 10.1016/s0003-4975(98)00340-3.

Abstract

Background: Patients not amenable to complete myocardial revascularization by conventional methods present a difficult clinical problem. Here we present the early results and technical considerations of the administration of basic fibroblast growth factor for the induction of collateral growth using heparin-alginate slow-release devices in patients undergoing coronary artery bypass grafting.

Methods: Eight patients were enrolled. Patients were candidates if they had at least one graftable obstructed coronary artery and at least one major arterial distribution not amenable to revascularization, a serum creatinine level less than 3 mg/dL, ejection fraction greater than 0.20, and estimated operative mortality of less than 25%. During conventional coronary artery bypass grafting, 10 heparin-alginate devices, each containing either 1 microg or 10 microg of basic fibroblast growth factor, were implanted in the epicardial fat in multiple regions of the unrevascularizable territory and also in the distal distribution of a grafted or patent artery.

Results: There was no mortality and no evidence of renal, hematologic, or hepatic toxicity during follow-up. Three months after the operation, all patients remain free of angina. Seven patients were examined with stress perfusion scans. Three patients had clear enhancement of perfusion to the unrevascularized myocardium, 1 patient had a new fixed defect, and 3 had minimal overall change but had evidence of new small, fixed perfusion defects. Seven patients had improved or similar myocardial contractile function (ejection fraction at 3-month follow-up = 0.53 +/- 0.22 versus 0.47 +/- 0.14 preoperatively). One patient suffered a perioperative myocardial infarction in the area of basic fibroblast growth factor administration.

Conclusions: This preliminary study demonstrates the safety and technical feasibility of therapeutic angiogenesis with basic fibroblast growth factor delivered by heparin-alginate slow-release devices. Further studies examining the safety, clinical efficacy, and long-term results are ongoing.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase I
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Alginates
  • Angina Pectoris / surgery
  • Collateral Circulation / drug effects
  • Coronary Artery Bypass
  • Coronary Artery Disease / drug therapy*
  • Coronary Artery Disease / surgery
  • Coronary Circulation / drug effects
  • Coronary Vessels / drug effects
  • Creatinine / blood
  • Delayed-Action Preparations
  • Drug Carriers
  • Feasibility Studies
  • Female
  • Fibroblast Growth Factor 2 / administration & dosage
  • Fibroblast Growth Factor 2 / blood
  • Fibroblast Growth Factor 2 / therapeutic use*
  • Follow-Up Studies
  • Glucuronic Acid
  • Heparin
  • Hexuronic Acids
  • Humans
  • Male
  • Middle Aged
  • Myocardial Contraction / physiology
  • Myocardial Infarction / etiology
  • Neovascularization, Physiologic*
  • Pericardium / surgery
  • Safety
  • Stroke Volume / physiology
  • Survival Rate

Substances

  • Alginates
  • Delayed-Action Preparations
  • Drug Carriers
  • Hexuronic Acids
  • Fibroblast Growth Factor 2
  • Glucuronic Acid
  • Heparin
  • Creatinine