Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Randomized Controlled Trial
. 2007 Jun;39(2):66-70.

Autotransfusion management during and after cardiopulmonary bypass alters fibrin degradation and transfusion requirements

Affiliations
Randomized Controlled Trial

Autotransfusion management during and after cardiopulmonary bypass alters fibrin degradation and transfusion requirements

Alice Wiefferink et al. J Extra Corpor Technol. 2007 Jun.

Abstract

The coagulation-fibrinolytic profile during cardiopulmonary bypass (CPB) has been widely documented. However, less information is available on the possible persistence of these alterations when autotransfusion is used in management of perioperative blood loss. This study was designed to explore the influence of autotransfusion management on intravascular fibrin degradation and postoperative transfusions. Thirty patients, undergoing elective primary isolated coronary bypass grafting, were randomly allocated either to a control group (group A; n=15) or an intervention group (group B; n=15) in which mediastinal and residual CPB blood was collected and processed by a continuous autotransfusion system before re-infusion. Intravascular fibrin degradation as indicated by D-dimer generation was measured at five specific intervals and corrected for hemodilution. In addition, chest tube drainage and need for homologous blood were monitored. D-dimer generation increased significantly during CPB in group A, from 312 to 633 vs. 291 to 356 ng/mL in group B (p = .001). The unprocessed residual blood (group A) revealed an unequivocal D-dimer elevation, 4131 +/- 1063 vs. 279 +/- 103 ng/mL for the processed residual in group B (p < .001). Consequently, in the first post-CPB period, the intravascular fibrin degradation was significantly elevated in group A compared with group B (p = .001). Twenty hours postoperatively, no significant difference in D-dimer levels was detected between both groups. However, a significant intra-group D-dimer elevation pre- vs. postoperative was noticed from 312 to 828 ng/mL in group A and from 291 to 588 ng/mL in group B (p < .01 for both). Postoperative chest tube drainage was higher in the patients from group A, which also had the highest postoperative D-dimer levels. Patients in group A perceived a higher need for transfusions of red cells suspensions postoperatively. These data clearly indicate that autotransfusion management during and after CPB suppresses early postoperative fibrin degradation.

Keywords: cardiopulmonary bypass, cardiotomy suction, coronary surgery, autotransfusion, fibrin degradation.

PubMed Disclaimer

Conflict of interest statement

The senior author has stated that authors have reported no material, financial or other relationship with any healthcare-related business or other entity whose products or services are discussed in this paper.

Figures

Figure 1.
Figure 1.
Plasma concentration (mean ± SE) of cross-linked fibrin degradation products (D-dimer) during and after CPB in group A (bars) and group B (cross-hatched bars). *Statistically significant difference between the two groups (p < .001). ΔIntra-group statistically significant difference compared with baseline values (p < .01).
Figure 2.
Figure 2.
Relationship between plasma D-dimer levels and postoperative chest tube drainage. Plasma D-dimer levels were arbitrary subdivided into four groups. Each bar represents the amount of patients (in percentage) from group A and group B (cross-hatched).

Similar articles

Cited by

References

    1. Paparella D, Brister SJ, Buchanan MR.. Coagulation disorders of cardiopulmonary bypass: A review. Intensive Care Med. 2004;30:1873–81. - PubMed
    1. Weerwind PW, Lindhout T, Caberg NEH, De Jong DS.. Thrombin generation during cardiopulmonary bypass: The possible role of retransfusion of blood aspirated from the surgical field. Thromb J. 2003;1:3. - PMC - PubMed
    1. Gunaydin S.. Clinical significance of coated extracorporeal circuits: A review of novel technologies. Perfusion. 2004;19:S33–41. - PubMed
    1. Wan S, LeClerc J-L, Vincent J-L.. Inflammatory response to cardiopulmonary bypass: Mechanisms involved and possible therapeutic strategies. Chest. 1997;112:676–92. - PubMed
    1. Aldea GS, Soltow LO, Chandler WL, et al. . Limitation of thrombin generation, platelet activation, and inflammation by elimination of cardiotomy suction in patients undergoing coronary artery bypass grafting treated with heparin-bonded circuits. J Thorac Cardiovasc Surg. 2002;123:742–55. - PubMed

Publication types

Substances

LinkOut - more resources