Open Access

Thrombelastography and sepsis

Critical Care200711:409

https://doi.org/10.1186/cc5712

Published: 19 April 2007

We read with great interest the recent report by Gonano et al. [1] describing the effects of antithrombin versus placebo in the coagulation profile of a group of patients with severe sepsis. However, we thought that several important issues needed to be addressed in regards to hypercoagulability and thrombelastography (TEG). First, hypercoagulability was not clearly defined in the study. Second, neither Coagulation Index (CI) nor Thrombodynamic Potential Index (an alternative TEG index of hypercoagulability) [2] were calculated or reported. Third, conventional studies of hypercoagulability were not performed in parallel. Fourth, Table 2 in the paper shows that some patients had low fibrinogen, platelets, and prolonged activated partial thromboplastin time with a probably 'hypocoagulable' thrombelastogram (CI lower than -3) profile.

Contrary to the authors' statements, there are previously described studies of hypercoagulability in sepsis using TEG.

A decade ago, Grant and Hadley [3] described the coagulation changes of 27 neonates with sepsis and found a 'hypocoagulability' profile in 85% of the neonates studied. These findings are also supported in animal data for which our lab has shown similar hypocoagulable patterns in a porcine model of sepsis using TEG [4].

Hypercoagulability is defined in thromboelastography as a CI greater than +3 [2]. This means that patients with reaction time (r), coagulation time (k), alpha angle, or maximum amplitude on the 'hypercoagulable side' may still fall within a normal CI range and not meet criteria to be called 'hypercoagulable'. We believe that it would have been of great interest if the authors had provided the actual CI values, as well as the percentage of patients with hypercoagulable and hypocoagulable profiles.

Authors' response

Stephan C Kettner and Christopher Gonano

We appreciate the interest of Dr Puana and Dr Nates in our article and their comments. Standard TEG parameters have been described as they are most commonly used by clinicians. Calculated indexes, however, add limited information. No patient with severely altered coagulation was included in our study, due to the complex inclusion and exclusion criteria of the KyberSept trial. We actually excluded patients with severe coagulation abnormalities, who might have benefited most from antithrombin therapy. A recent analysis of the KyberSept trial showed that high-dose antithrombin in septic patients with disseminated intravascular coagulation resulted in decreased mortality rates [5]. We agree that hypercoagulation may not be present in septic patients with disseminated intravascular coagulation, as hyperfibrinolysis may cause straight line TEG.

We knowingly did not cite the study by Grant and Hadley [3], for several reasons. First, the coagulation system in neonates is profoundly different compared to adults [6], and normal values for TEG have not been established in neonates [7]. Second, causes and incidence of sepsis in neonates are completely different compared to adults [8]. Third, the immune system in neonates is immature [9]. Fourth, we feel Grant's interpretation that TEG has a 96% sensitivity of and a 96% specificity for sepsis is inappropriate, as if every abnormal TEG in neonates should be associated with sepsis. Of course there are other causes for abnormal TEGs in neonates.

Abbreviations

CI: 

Coagulation Index

TEG: 

thrombelastography.

Declarations

Authors’ Affiliations

(1)
Department of Critical Care, Division of Anesthesiology and Critical Care, The University of Texas M. D. Anderson Cancer Center

References

  1. Gonano C, Sitzwohl C, Meitner E, Weinsrabl C, Kettner SC: Four-day antithrombin therapies do not seem to attenuate hypercoagulability in patients suffering from sepsis. Crit Care 2006, 10: R160. 10.1186/cc5098PubMed CentralView ArticlePubMedGoogle Scholar
  2. Haemoscope Corporation: TEG Hemostasis Analyzer User Manual. Niles, IL: Haemoscope Corporation; 1999.Google Scholar
  3. Grant HW, Hadley GP: Prediction of neonatal sepsis by thrombelastography. Pediatr Surg Int 1997, 12: 289-292.View ArticlePubMedGoogle Scholar
  4. Nates JL, Doursout MF, Weavind L, Chelly JE: A thrombelastographic study of lipopolysaccharide induced coagulation abnormalities in a pig endotoxemic shock model. Crit Care Med 1999, 27: A102. 10.1097/00003246-199912001-00274View ArticleGoogle Scholar
  5. Kienast J, Juers M, Wiedermann CJ, Hoffmann JN, Ostermann H, Strauss R, Keinecke HO, Warren BL, Opal SM: Treatment effects of high-dose antithrombin without concomitant heparin in patients with severe sepsis with or without disseminated intravascular coagulation. J Thromb Haemost 2006, 4: 90-97. 10.1111/j.1538-7836.2005.01697.xView ArticlePubMedGoogle Scholar
  6. Andrew M, Paes B, Milner R, Johnston M, Mitchell L, Tollefsen DM, Powers P: Development of the human coagulation system in the full-term infant. Blood 1987, 70: 165-172.PubMedGoogle Scholar
  7. Kettner SC, Pollak A, Zimpfer M, Seybold T, Prusa AR, Herkner K, Kuhle S: Heparinase-modified thrombelastography in term and preterm neonates. Anesth Analg 2004, 98: 1650-1652. 10.1213/01.ANE.0000115149.25496.DDView ArticlePubMedGoogle Scholar
  8. Watson RS, Carcillo JA, Linde-Zwirble WT, Clermont G, Lidicker J, Angus DC: The epidemiology of severe sepsis in children in the United States. Am J Respir Crit Care Med 2003, 167: 695-701. 10.1164/rccm.200207-682OCView ArticlePubMedGoogle Scholar
  9. Fadel S, Sarzotti M: Cellular immune responses in neonates. Int Rev Immunol 2000, 19: 173-193.View ArticlePubMedGoogle Scholar

Copyright

© BioMed Central Ltd 2007

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