TEG ® - or ROTEM ® -based individualized goal-directed coagulation algorithms: don’t wait - act now!

Donat R Spahn

doi:10.1186/s13054-014-0637-3

Commentary

Open Access

TEG^®- or ROTEM^®-based individualized goal-directed coagulation algorithms: don’t wait - act now!

Donat R Spahn¹Email author

Critical Care201418:637

https://doi.org/10.1186/s13054-014-0637-3

Published: 24 November 2014

Abstract

In trauma patients, TEG^® and ROTEM^® allow prediction of massive transfusion requirement and mortality, and creation of goal-directed, individualized coagulation algorithms that may improve patient outcome. This outcome benefit has been shown for cardiac surgery in prospective randomized trials. For trauma, only non-randomized studies have been performed. Nevertheless, TEG^® and ROTEM^® are highly promising monitoring techniques to guide coagulation management in all types of major bleeding, including trauma.

The review by Da Luz and colleagues in this issue of Critical Care highlights the progress provided by thrombelastography (TEG^®) and thrombelastometry (ROTEM^®) in diagnosing and monitoring the coagulation system in trauma patients [1]. Their systematic review includes 55 studies and over 12,000 patients and they find that early abnormalities in TEG^®/ROTEM^® predict massive transfusion need and mortality. However, they conclude that 'Effects on blood product transfusion, mortality and other patient-important outcomes remain unproven in randomized trials' [1]. Formalistically this is of course correct; however, which monitoring system or laboratory value in medicine has ever improved relevant patient outcomes such as length of ICU or hospital stay, complications, treatment costs or even mortality? The answer is none, simply because a monitoring system or a laboratory value provides information allowing risk assessment but lacks any therapeutic potential.

TEG^®/ROTEM^® information, however, allows creation of goal-directed, individualized treatment algorithms that may improve patient outcome. This has been shown for TEG^®/ROTEM^®-based algorithms in prospective randomized studies in cardiac surgery [2],[3]. In liver transplantation such algorithms have even become standard. And the benefits are impressive: reduced transfusion needs, less complications, shorter length of ICU and hospital stay, better survival and reduced treatment costs [2],[3]. TEG^®/ROTEM^®-based algorithms have also been successful in improving patient outcome in trauma, although these studies were not prospective and randomized [4]-[6]. Nevertheless, the recommendation to use TEG^®/ROTEM^® in the treatment of severely injured trauma patients was upgraded in the 2013 European Trauma Treatment Guidelines from 2C to 1C with a plea to implement goal-directed, individualized treatment algorithms and to monitor treatment adherence [4].

TEG^®, and even more so ROTEM^®, point to the most critical element of coagulation within approximately 5 to 10 minutes [7] (compared with traditional laboratory analyses with turnaround times of consistently 60 minutes or more [1]), and allow diagnosis of even mild forms of hyperfibrinolysis that are not detectable by standard laboratory tests but are associated with increased mortality [8]. In the modern emergency room the first blood from a severely injured patient thus goes immediately into a ROTEM^® device, the blood gas analyser, the central laboratory and the blood bank, and 1 gram of tranexamic acid is administered immediately thereafter. This provides within 10 minutes a baseline analysis of the coagulation situation and allows goal-directed specific treatment of the most critical deficit with coagulation factor concentrates [4]-[6]. The ROTEM^® analysis is repeated again soon after to assess treatment success and to capture the dynamic evolution of the coagulation situation. This concept allows the patient to be treated sufficiently with the lowest dose of coagulation factors aiming at low normal coagulability and avoiding hypercoagulability. This is important for limiting treatment costs as well as avoiding thrombotic complications.

The success of the above concept has been shown in many studies [1]-[6],[9], although a 'perfectly' designed prospective randomized double-blind multicentre study has not yet been performed to formalistically 'prove' its superiority. Is this a problem? My personal answer is: maybe. Sure, it would be nice to have such a study that would satisfy experts on a theoretical level. However, having served on numerous study-design committees of such studies, I have to admit that the ideal study design is extremely difficult to find. One crucial question is the definition of the control group. Is the control group also treated according to an individualized goal-directed algorithm or simply by a 1:1(:1) (red blood cell:plasma(:platelet)) transfusion regimen? Does the control group receive only labile blood products or also factor concentrates to treat coagulation abnormalities if present? The choice between a simple 1:1:1 transfusion regimen versus any individualized goal-directed algorithm has become particularly difficult after the recent prospective randomized study showing a more than two-fold increased mortality (32%) in the 1:1:1 transfusion regimen compared with a traditional laboratory-based individualized goal-directed treatment algorithm (14%) [9].

In addition, even if such a 'perfect' study were to be performed, its interpretation would be extremely difficult. In the case of lack of a significant outcome difference, the discussion would be that too few patients were included and thus the study would have been underpowered or the two treatment regimens were not sufficiently different from one another. In the case of a significant difference, the interpretation would be even more difficult and controversial: is the difference due to a different delay in the specific treatment of coagulopathy, or the fact that in one of the arms coagulation factors were used whereas in the other more blood products were used, or very generally because one of the algorithms was not good enough to provide a good outcome. This is by no means to say that we should stop doing outcomes research on coagulation management in severely injured patients, but that we should not dismiss existing evidence in favour of TEG^®/ROTEM^®-based goal-directed individualized coagulation algorithms on the basis that we lack the ultimate 'perfect' study. As a matter of fact, today all hospitals should have an individualized and goal-directed coagulation algorithm [4]: don’t wait - act now!

Declarations

Competing interests

DRS's academic department receives grant support from the Swiss National Science Foundation, Berne, Switzerland, the Ministry of Health (Gesundheitsdirektion) of the Canton of Zurich, Switzerland for Highly Specialized Medicine, the Swiss Society of Anesthesiology and Reanimation (SGAR), Berne, Switzerland, the Swiss Foundation for Anesthesia Research, Zurich, Switzerland, Bundesprogramm Chancengleichheit, Berne, Switzerland, CSL Behring, Berne, Switzerland, Vifor SA, Villars-sur-Glâne, Switzerland. DRS was chairman of the ABC Faculty and is the co-chairman of the ABC-Trauma Faculty, which both are managed by Physicians World Europe GmbH, Mannheim, Germany and sponsored by unrestricted educational grants from Novo Nordisk Health Care AG, Zurich, Switzerland, CSL Behring GmbH, Marburg, Germany and LFB Biomédicaments, Courtaboeuf Cedex, France. In the past 5 years, DRS has received honoraria or travel support for consulting or lecturing from the following companies: Abbott AG, Baar, Switzerland, AMGEN GmbH, Munich, Germany, AstraZeneca AG, Zug, Switzerland, Bayer (Schweiz) AG, Zürich, Switzerland, Baxter AG, Volketswil, Switzerland, Baxter S.p.A., Roma, Italy, B Braun Melsungen AG, Melsungen, Germany, Boehringer Ingelheim (Schweiz) GmbH, Basel, Switzerland, Bristol-Myers-Squibb, Rueil-Malmaison Cedex, France and Baar, Switzerland, CSL Behring GmbH, Hattersheim am Main, Germany and Berne, Switzerland, Curacyte AG, Munich, Germany, Ethicon Biosurgery, Sommerville, New Jersey, USA, Fresenius SE, Bad Homburg v.d.H., Germany, Galenica AG, Bern, Switzerland (including Vifor SA, Villars-sur-Glâne, Switzerland), GlaxoSmithKline GmbH & Co. KG, Hamburg, Germany, Janssen-Cilag AG, Baar, Switzerland, Janssen-Cilag EMEA, Beerse, Belgium, Merck Sharp & Dohme AG, Luzern, Switzerland, Novo Nordisk A/S, Bagsvärd, Denmark, Octapharma AG, Lachen, Switzerland, Organon AG, Pfäffikon/SZ, Switzerland, Oxygen Biotherapeutics, Costa Mesa, CA, Photonics Healthcare GmbH, Munich, Germany, ratiopharm Arzneimittel Vertriebs-GmbH, Vienna, Austria, Roche Diagnostics International Ltd, Reinach, Switzerland, Roche Pharma (Schweiz) AG, Reinach, Switzerland, Schering-Plough International, Inc., Kenilworth, New Jersey, USA, Tem International GmbH, Munich, Germany, Verum Diagnostica GmbH, Munich, Germany, Vifor Pharma Deutschland GmbH, Munich, Germany, Vifor Pharma Österreich GmbH, Vienna, Austria, Vifor (International) AG, St. Gallen, Switzerland. None of the above listed companies and/or entities have been directly or indirectly involved in discussing and/or developing this manuscript or parts thereof. None of them have financially contributed to this endeavor in whatever form, either directly or indirectly. Therefore, it is beyond my capacity to tell whether any of the above listed companies and/or entities do or do not have a direct financial interest in the subject matter or materials discussed in this manuscript. Statement regarding support for the work: support was provided solely from institutional and/or departmental sources.

Authors’ Affiliations

(1)

Institute of Anesthesiology and Head Medical, Section Anesthesiology, Intensive Care Medicine and OR-Management, University and University Hospital Zurich

References

Da Luz LT, Nascimento B, Shankarakutty AK, Rizoli S, Adhikari NKJ: Effect of thromboelastography (TEG^®) and rotational thromboelastometry (ROTEM^®) on diagnosis of coagulopathy, transfusion guidance and mortality in trauma: descriptive systematic review. Crit Care. 2014, 18: 518-10.1186/s13054-014-0518-9.PubMed CentralView ArticleGoogle Scholar
Weber CF, Gorlinger K, Meininger D, Herrmann E, Bingold T, Moritz A, Cohn LH, Zacharowski K: Point-of-care testing: a prospective, randomized clinical trial of efficacy in coagulopathic cardiac surgery patients. Anesthesiology. 2012, 117: 531-547. 10.1097/ALN.0b013e318264c644.View ArticleGoogle Scholar
Rahe-Meyer N, Solomon C, Hanke A, Schmidt DS, Knoerzer D, Hochleitner G, Sorensen B, Hagl C, Pichlmaier M: Effects of fibrinogen concentrate as first-line therapy during major aortic replacement surgery: a randomized, placebo-controlled trial. Anesthesiology. 2013, 118: 40-50. 10.1097/ALN.0b013e3182715d4d.View ArticleGoogle Scholar
Spahn DR, Bouillon B, Cerny V, Coats TJ, Duranteau J, Fernandez-Mondejar E, Filipescu D, Hunt BJ, Komadina R, Nardi G, Neugebauer E, Ozier Y, Riddez L, Schultz A, Vincent JL, Rossaint R: Management of bleeding and coagulopathy following major trauma: an updated European guideline. Crit Care. 2013, 17: R76-10.1186/cc12685.PubMed CentralView ArticleGoogle Scholar
Schochl H, Nienaber U, Maegele M, Hochleitner G, Primavesi F, Steitz B, Arndt C, Hanke A, Voelckel W, Solomon C: Transfusion in trauma: thromboelastometry-guided coagulation factor concentrate-based therapy versus standard fresh frozen plasma-based therapy. Crit Care. 2011, 15: R83-10.1186/cc10078.PubMed CentralView ArticleGoogle Scholar
Schoechl H, Nienaber U, Hofer G, Voelckel W, Jambor C, Scharbert G, Kozek-Langenecker S, Solomon C: Goal-directed coagulation management of major trauma patients using rotation thromboelastometry (ROTEM)-guided administration of fibrinogen and prothrombin complex concentrate. Crit Care. 2010, 14: R55-10.1186/cc8948.View ArticleGoogle Scholar
Theusinger OM, Nurnberg J, Asmis LM, Seifert B, Spahn DR: Rotation thromboelastometry (ROTEM) stability and reproducibility over time. Eur J Cardiothorac Surg. 2010, 37: 677-683. 10.1016/j.ejcts.2009.07.038.View ArticleGoogle Scholar
Chapman MP, Moore EE, Ramos CR, Ghasabyan A, Harr JN, Chin TL, Stringham JR, Sauaia A, Silliman CC, Banerjee A: Fibrinolysis greater than 3% is the critical value for initiation of antifibrinolytic therapy. J Trauma Acute Care Surg. 2013, 75: 961-967. 10.1097/TA.0b013e3182aa9c9f. discussion 967PubMed CentralView ArticleGoogle Scholar
Nascimento B, Callum J, Tien H, Rubenfeld G, Pinto R, Lin Y, Rizoli S: Effect of a fixed-ratio (1:1:1) transfusion protocol versus laboratory-results-guided transfusion in patients with severe trauma: a randomized feasibility trial. CMAJ. 2013, 185: E583-E589. 10.1503/cmaj.121986.PubMed CentralView ArticleGoogle Scholar

Copyright

This article is published under license to BioMed Central Ltd. The licensee has exclusive rights to distribute this article, in any medium, for 12 months following its publication. After this time, the article is available under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

TEG®- or ROTEM®-based individualized goal-directed coagulation algorithms: don’t wait - act now!