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dc.contributor.authorGatt, Alexander-
dc.contributor.authorRiddell, A.-
dc.contributor.authorCalvaruso, V.-
dc.contributor.authorTuddenham, E. G.-
dc.contributor.authorMakris, M.-
dc.contributor.authorBurroughs, A. K.-
dc.date.accessioned2022-11-07T06:56:40Z-
dc.date.available2022-11-07T06:56:40Z-
dc.date.issued2010-
dc.identifier.citationGatt, A., Riddell, A., Calvaruso, V., Tuddenham, E. G., Makris, M., & Burroughs, A. K. (2010). Enhanced thrombin generation in patients with cirrhosis‐induced coagulopathy. Journal of Thrombosis and Haemostasis, 8(9), 1994-2000.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar/handle/123456789/103422-
dc.description.abstractBackground: Prothrombin time (PT) and the international normalized ratio (INR) are still routinely measured in patients with liver cirrhosis to ‘assess’ their bleeding risk despite the lack of correlation with the two. Thrombin generation (TG) assays are global assays of coagulation that are showing promise in assessing bleeding and thrombosis risks. Aim: To study the relationship between the INR and TG profiles in cirrhosis-induced coagulopathy. Methods: Seventy-three patients with cirrhosis were studied. All TG parameters were compared with those from a normal control group. Contact activation was prevented using corn trypsin inhibitor. TG was also assayed in the presence of Protac®. The endogenous thrombin potential (ETP) ratio was derived by dividing the ETP with Protac® by the ETP without Protac®. Results: The INR (mean 1.7) did not correlate with the ETP and the velocity of TG (P > 0.05). There was no difference between the lag time and ETP of the two groups (P > 0.05). The velocity of TG was increased in cirrhosis (67.95 ± 34.8 vs. 45.05 ± 25.9 nM min−1; P = 0.016) especially in patients with INRs between 1.21 and 2.0. Both the ETP with Protac® and the ETP ratio were increased in cirrhosis (mean 1074 ± 461.4 vs. 818 ± 357.9 nM min, P = 0.004 and 0.80 ± 0.21 vs. 0.44 ± 0.15, P ≤ 0.0001, respectively). Conclusion: Despite a raised INR, TG parameters are consistent with a hypercoagulable profile in cirrhosis-related coagulopathy. This confirms that the PT or INR should not be used to assess bleeding risk in these patients, and other parameters, such as TG, need to be explored as clinical markers of coagulopathy.en_GB
dc.language.isoenen_GB
dc.publisherWileyen_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectThrombin -- Physiological effecten_GB
dc.subjectBlood coagulation factorsen_GB
dc.subjectBlood coagulation testsen_GB
dc.subjectLiver -- Diseases -- Case studiesen_GB
dc.subjectLiver -- Cirrhosisen_GB
dc.titleEnhanced thrombin generation in patients with cirrhosis-induced coagulopathyen_GB
dc.typearticleen_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holder.en_GB
dc.description.reviewedpeer-revieweden_GB
dc.identifier.doi10.1111/j.1538-7836.2010.03937.x-
dc.publication.titleJournal of Thrombosis and Haemostasisen_GB
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