Thromb Haemost 2009; 102(04): 765-771
DOI: 10.1160/TH08-12-0826
Cardiovascular Biology and Cell Signalling
Schattauer GmbH

Repletion of factor XIII following cardiopulmonary bypass using a recombinant A-subunit homodimer

A preliminary report
Jerrold H. Levy
1   Department of Cardiothoracic Anesthesiology and Critical Care, Emory University School of Medicine, Emory Healthcare, Atlanta, Georgia, USA
,
Ravi Gill
2   Southampton Hospital, Southampton, UK
,
Nancy A. Nussmeier
3   Department of Anesthesiology, SUNY Upstate Medical University, Syracuse, New York, USA
,
Peter Skov Olsen
4   Department of Cardiothoracic Surgery, Rigshospitalet, University of Copenhagen, Denmark
,
Henning F. Andersen
5   Novo Nordisk A/S, Bagsvaerd, Denmark
,
Frank V. McL. Booth
6   Novo Nordisk, Princeton, NJ, USA
,
Christian M. Jespersen
5   Novo Nordisk A/S, Bagsvaerd, Denmark
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Publikationsverlauf

Received: 18. Dezember 2008

Accepted after major revision: 02. Juli 2009

Publikationsdatum:
24. November 2017 (online)

Summary

Bleeding following cardiac surgery involving cardiopulmonary bypass (CPB) remains a major concern. Coagulation factor XIII (FXIII) functions as a clot-stabilising factor by cross-linking fibrin. Low post-operative levels of FXIII correlate with increased post-operative blood loss. To evaluate preliminary safety and pharmacokinetics of recombinant FXIII (rFXIII-A2) in cardiac surgery, patients scheduled for coronary artery bypass grafting were randomised to receive a single dose of either rFXIII-A2 (11.9,25,35 or 50 IU/kg) or placebo in a 4:1 ratio.Study drug was given post-CPB within 10 to 20 minutes after first protamine dose. Patients were evaluated until day 7 or discharge, with a follow-up visit at weeks 5–7.The primary end-point was incidence and severity of adverse events.Thirty-five patients were randomised to rFXIII-A2 and eight to placebo. Eighteen serious adverse events were reported.These were all complications well recognised during cardiac surgery. Although one patient required an implantable defibrillator, all recovered without sequelae. One myocardial infarction in a patient receiving 35 IU/ kg rFXIII-A2 was identified by the Data Monitoring Committee after reviewing ECGs and cardiac enzymes. No other thromboembolic events were seen. Dosing with 25–50 IU/kg rFXIII-A2 restored levels of FXIII to pre-operative levels, with a tendency towards an overshoot in receiving 50 IU/kg. rFXIII-A2, in doses from 11.9 IU/kg up to 50 IU/kg, was well tolerated. For postoperative FXIII replenishment, 35 IU/kg of rFXIII-A2 may be the most appropriate dose.

Footnote: Jerrold H. Levy, Ravi Gill, and Nancy A. Nussmeier serve as consultants to Novo Nordisk; Henning F. Andersen, Frank V. Booth, and Christian M. Jespersen are employees of Novo Nordisk.