Skip Navigation



BJA Advance Access published online on December 17, 2004

British Journal of Anaesthesia, doi:10.1093/bja/aei052
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
94/3/324    most recent
aei052v1
Right arrow E-Letters: Submit a response to the article
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Fenger-Eriksen, C.
Right arrow Articles by Sørensen, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fenger-Eriksen, C.
Right arrow Articles by Sørensen, B.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Board of Management and Trustees of the British Journal of Anaesthesia 2004
Accepted October 12, 2004

Laboratory Investigation

Thrombelastographic whole blood clot formation after ex vivo addition of plasma substitutes: improvements of the induced coagulopathy with fibrinogen concentrate

C. Fenger-Eriksen 1, E. Anker-Møller 2, J. Heslop 2, J. Ingerslev 3*, and B. Sørensen 3

1 Department of Anaesthesiology, Aarhus University Hospital, Aarhus Sygehus, Denmark; Center for Haemophilia and Thrombosis, Department of Clinical Biochemistry, Aarhus University Hospital, Skejby Sygehus, Denmark
2 Department of Anaesthesiology, Aarhus University Hospital, Aarhus Sygehus, Denmark
3 Center for Haemophilia and Thrombosis, Department of Clinical Biochemistry, Aarhus University Hospital, Skejby Sygehus, Denmark

* To whom correspondence should be addressed.
J. Ingerslev, E-mail: ingerslev{at}ki.au.dk


   Abstract

Background. Plasma substitutes such as hydroxyethyl starch (HES) and various dextrans may compromise the haemostatic system, thereby causing potentially dangerous bleeding. Whilst several mechanisms have been advanced to explain the nature of the coagulopathy induced by this colloid, there has been comparably little interest in devising ways to optimize haemostasis after a relative colloid overdose.

Methods. Real-time whole blood (WB) clot formation profiles were recorded using a thrombelastographic method employing activation with tissue factor. The coagulation tracings were transformed into dynamic velocity profiles of WB clot formation. WB from healthy individuals (n=20) was exposed to haemodilution of ~55% with isotonic saline, HES 200/0.5, HES 130/0.4, and dextran 70, respectively. Possible modalities for improvement of the induced coagulopathy were explored, in particular ex vivo addition of a fibrinogen concentrate.

Results. WB coagulation profiles changed significantly with decreased clot strength, and a compromised propagation phase of clot formation. The duration of the initiation phase of WB coagulation was unchanged. No statistical differences were detected amongst the HES solutions and dextran 70. However, dextran 70 returned a more suppressed clot development and strength compared with the HES solutions. Ex vivo haemostatic addition of washed platelets (75 x 109 litre-1) and factor VIII (0.6 IU ml-1) produced insignificant changes in clot initiation, propagation, and in the clot strength. In contrast, ex vivo addition of a fibrinogen concentrate (1 g litre-1) improved the coagulopathy induced by all of the three individual plasma expanders tested.

Conclusion. Coagulopathy induced by haemodilution with either HES 200/0.5, HES 130/0.4, and dextran 70 may be improved by fibrinogen supplementation.

Keywords: blood, coagulation; blood, haemodilution; blood, replacement; measurement techniques, thrombelastograph.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Br J AnaesthHome page
D. Bolliger, F. Szlam, R. J. Molinaro, N. Rahe-Meyer, J. H. Levy, and K. A. Tanaka
Finding the optimal concentration range for fibrinogen replacement after severe haemodilution: an in vitro model
Br. J. Anaesth., June 1, 2009; 102(6): 793 - 799.
[Abstract] [Full Text] [PDF]


Home page
Br J AnaesthHome page
P. Moor, T. Woolley, M. Midwinter, C. Fenger-Eriksen, J. Ingerslev, and B. Sorensen
Coagulation tests in future studies: what to use?
Br. J. Anaesth., May 1, 2009; 102(5): 716 - 717.
[Full Text] [PDF]


Home page
Br J AnaesthHome page
C. Fenger-Eriksen, M. Lindberg-Larsen, A. Q. Christensen, J. Ingerslev, and B. Sorensen
Fibrinogen concentrate substitution therapy in patients with massive haemorrhage and low plasma fibrinogen concentrations
Br. J. Anaesth., December 1, 2008; 101(6): 769 - 773.
[Abstract] [Full Text] [PDF]


Home page
Anesth. Analg.Home page
T. Haas, D. Fries, C. Velik-Salchner, C. Reif, A. Klingler, and P. Innerhofer
The In Vitro Effects of Fibrinogen Concentrate, Factor XIII and Fresh Frozen Plasma on Impaired Clot Formation After 60% Dilution
Anesth. Analg., May 1, 2008; 106(5): 1360 - 1365.
[Abstract] [Full Text] [PDF]


Home page
TraumaHome page
V. McDonald and K. Ryland
Coagulopathy in trauma: optimising haematological status
Trauma, April 1, 2008; 10(2): 109 - 123.
[Abstract] [PDF]


Home page
Anesth. Analg.Home page
V. G. Nielsen and J. H. Levy
Fibrinogen and Bleeding: Old Molecule New Ideas
Anesth. Analg., October 1, 2007; 105(4): 902 - 903.
[Full Text] [PDF]


Home page
Anesth. Analg.Home page
M. Mittermayr, W. Streif, T. Haas, D. Fries, C. Velik-Salchner, A. Klingler, E. Oswald, C. Bach, M. Schnapka-Koepf, and P. Innerhofer
Hemostatic Changes After Crystalloid or Colloid Fluid Administration During Major Orthopedic Surgery: The Role of Fibrinogen Administration
Anesth. Analg., October 1, 2007; 105(4): 905 - 917.
[Abstract] [Full Text] [PDF]


Home page
Br J AnaesthHome page
D. Fries, T. Haas, A. Klingler, W. Streif, G. Klima, J. Martini, H. Wagner-Berger, and P. Innerhofer
Efficacy of fibrinogen and prothrombin complex concentrate used to reverse dilutional coagulopathy--a porcine model
Br. J. Anaesth., October 1, 2006; 97(4): 460 - 467.
[Abstract] [Full Text] [PDF]


Home page
Anesth. Analg.Home page
T. T. Niemi, R. T. Suojaranta-Ylinen, S. I. Kukkonen, and A. H. Kuitunen
Gelatin and hydroxyethyl starch, but not albumin, impair hemostasis after cardiac surgery.
Anesth. Analg., April 1, 2006; 102(4): 998 - 1006.
[Abstract] [Full Text] [PDF]


Home page
Anesth. Analg.Home page
C. De Lorenzo, A. Calatzis, U. Welsch, and B. Heindl
Fibrinogen concentrate reverses dilutional coagulopathy induced in vitro by saline but not by hydroxyethyl starch 6%.
Anesth. Analg., April 1, 2006; 102(4): 1194 - 1200.
[Abstract] [Full Text] [PDF]


Home page
Anesth. Analg.Home page
D. Fries, P. Innerhofer, C. Reif, W. Streif, A. Klingler, W. Schobersberger, C. Velik-Salchner, and B. Friesenecker
The Effect of Fibrinogen Substitution on Reversal of Dilutional Coagulopathy: An In Vitro Model
Anesth. Analg., February 1, 2006; 102(2): 347 - 351.
[Abstract] [Full Text] [PDF]


Home page
Br J AnaesthHome page
B. Sorensen, C. Fenger-Eriksen, and J. Ingerslev
Recombinant factor VIIa fails to correct coagulopathy induced by haemodilution with colloid
Br. J. Anaesth., June 1, 2005; 94(6): 862 - 863.
[Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.