Lysis Timer: a new sensitive tool to diagnose hyperfibrinolysis in liver transplantation.

Stéphanie Roullet, Sylvie Labrouche, Christine Mouton, Alice Quinart, Karine Nouette-Gaulain, Christophe Laurent, Geneviève Freyburger

Journal: Journal of clinical pathology 2018;72(1):58-65

PMID: 30282673

Abstract

AIMS

Diagnosis of hyperfibrinolysis in orthotopic liver transplantation (OLT) remains challenging. Euglobulin clot lysis time (ECLT) is not adapted to clinical situations. ROTEM is specific but seldom sensitive to hyperfibrinolysis. The Lysis Timer assesses 'Global Fibrinolytic Capacity' in citrated plasma (GFC/LT). GFC/LT associates reagents for in vitro triggering of the clot (thrombin and calcium) and its lysis (tissue-plasminogenactivator (t-PA)), turbidity signal acquisition by the Lysis Timer, and dedicated software converting the digital signal into an optical curve. A visual check of the curves was systematic to ascertain the lysis time values calculated by the software. The primary aim of this prospective observational study was to evaluate the ability of GFC/LT to recognise hyperfibrinolysis during OLT. The secondary aim was to compare its results with ROTEM maximum lysis (EXTEM ML) and with standard laboratory tests.

METHODS

Thirty consecutive adult patients undergoing OLT were included (NCT03012633). Standard laboratory tests, ROTEM, GFC/LT, ECLT and fibrinolysis parameters were assayed at five sample times.

RESULTS

GFC/LT was correlated with ECLT, plasmin activator inhibitor 1 antigen and activity and t-PA activity (r=0.490, 0.681, 0.643 and -0.359, respectively). Hyperfibrinolysis was defined as ECLT ≤60 min. Receiver operating characteristic curve analysis showed that GFC/LT with a threshold of 31 min detected hyperfibrinolysis with a sensitivity of 0.88 (95% CI 0.73 to 0.96), a specificity of 0.68 (95% CI 0.56 to 0.78) and an area under the curve (AUC) of 0.85 (95% CI 0.74 to 0.94). EXTEM ML >12% did not detect hyperfibrinolysis (sensitivity 0.38 (95% CI 0.24 to 0.55), specificity 0.95 (95% CI 0.86 to 0.99) and AUC 0.60 (95% CI 0.46 to 0.75)).

CONCLUSIONS

GFC/LT recognised hyperfibrinolysis during OLT with a significant agreement with the other tests of fibrinolysis.

TRIAL REGISTRATION NUMBER

NCT03012633.

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Address: CHU Bordeaux, Service d'Anesthésie-Réanimation Pellegrin, Bordeaux, France [email protected].; Université de Bordeaux, INSERM U 12-11, Maladies rares: Génétique et Métabolisme, Bordeaux, France.; CHU Bordeaux, Laboratoire d'Hématologie - PTRR, Hôpital Pellegrin, Bordeaux, France.; Université de Bordeaux, INSERM U 10-34, Biologie des Maladies Cardio-Vasculaires, Pessac, France.; CHU Bordeaux, Service d'Hématologie Biologique, Bordeaux, France.; CHU Bordeaux, Service d'Anesthésie-Réanimation Sud, Pessac, France.; CHU Bordeaux, Service d'Anesthésie-Réanimation Pellegrin, Bordeaux, France.; CHU Bordeaux, Service de Chirurgie Hépato-biliaire et Transplantation Hépatique, Pessac, France.
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