Thorac Cardiovasc Surg 2009; 57(8): 455-459
DOI: 10.1055/s-0029-1186067
Original Cardiovascular

© Georg Thieme Verlag KG Stuttgart · New York

Aprotinin-Associated Risks in Off-Pump Coronary Artery Bypass Grafting[*]

H. B. Bittner1 , M. Lange1 , J. Lemke1 , A. Rastan1 , F. W. Mohr1
  • 1Cardiovascular and Thoracic Surgery, Heart Center Leipzig, Leipzig, Germany
Further Information

Publication History

received January 31, 2009

Publication Date:
14 December 2009 (online)

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Abstract

Background: Little data is available regarding the safety of using the serine protease inhibitor aprotinin in off-pump cardiac surgery. We retrospectively assessed the risks of administering the drug to adult patients undergoing off-pump coronary artery bypass grafting (OPCABG). Methods: Aprotinin was administered as a bolus of 1 or 2 million kallikrein inhibiting units to 391 patients following median sternotomy; 370 control patients underwent surgery during the same time period without receiving aprotinin. No other antifibrinolytic agents were administered. Results: Preoperative characteristics, length of ICU and hospital stay were similar between the mostly medium-risk aprotinin and the control patients. Postoperative cardiac, renal, neurological, and respiratory complications and hospital mortality occurred with comparable frequencies in both groups. Levels of myocardial enzymes during the first 72 h after surgery also did not differ significantly. Conclusion: Use of aprotinin in OPCABG was not associated with a higher incidence of hospital mortality, cardiovascular, renal, or other complications. Given the good safety profile in this large patient population we suggest that aprotinin could still be a valid antifibrinolytic treatment option in OPCABG.

1 Presented in part at the 36th Annual Meeting of the German Society for Thoracic and Cardiovascular Surgery, Hamburg, February 11–14, 2007.

References

1 Presented in part at the 36th Annual Meeting of the German Society for Thoracic and Cardiovascular Surgery, Hamburg, February 11–14, 2007.

Dr. MD, PhD Hartmuth B. Bittner

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