Literature DB >> 8049446

Activation of the coagulation cascade after infusion of a factor XI concentrate in congenitally deficient patients.

P M Mannucci1, K A Bauer, E Santagostino, E Faioni, S Barzegar, R Coppola, R D Rosenberg.   

Abstract

Virally inactivated, high-purity factor XI concentrates are available for treatment of patients with factor XI deficiency. However, preliminary experience indicates that some preparations may be thrombogenic. We evaluated whether a highly purified concentrate produced signs of activation of the coagulation cascade in two patients with severe factor XI deficiency infused before and after surgery. Signs of heightened enzymatic activity of the common pathway of coagulation (elevated plasma levels of prothrombin fragment 1 + 2 and fibrinopeptide A) developed in the early post-infusion period, accompanied by more delayed signs of fibrin formation with secondary hyperfibrinolysis (elevated D-dimer and plasmin-antiplasmin complex). These changes occurred in both patients, but were more severe in the older patient with breast cancer when she underwent surgery, being accompanied by fibrinogen and platelet consumption. There were no concomitant signs of heightened activity of the factor VII-tissue factor mechanism on the factor Xase complex (plasma levels of activated factor VII and of factor IX and X activation peptides did not increase). The observed changes in biochemical markers of coagulation activation indicate that concentrate infusions increased thrombin generation and activity and that such changes were magnified by malignancy and surgery. Because some factor XI concentrates may be thrombogenic, they should be used with caution, especially in patients with other risk factors for thrombosis.

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Year:  1994        PMID: 8049446

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  7 in total

1.  Allosteric inhibition of factor XIa. Sulfated non-saccharide glycosaminoglycan mimetics as promising anticoagulants.

Authors:  Rami A Al-Horani; David Gailani; Umesh R Desai
Journal:  Thromb Res       Date:  2015-04-22       Impact factor: 3.944

Review 2.  Rare bleeding disorders - bleeding assessment tools, laboratory aspects and phenotype and therapy of FXI deficiency.

Authors:  P James; O Salomon; D Mikovic; F Peyvandi
Journal:  Haemophilia       Date:  2014-05       Impact factor: 4.287

3.  Evidence for factor IX-independent roles for factor XIa in blood coagulation.

Authors:  A Matafonov; Q Cheng; Y Geng; I M Verhamme; O Umunakwe; E I Tucker; M-F Sun; V Serebrov; A Gruber; D Gailani
Journal:  J Thromb Haemost       Date:  2013-12       Impact factor: 5.824

4.  A proposal for managing bleeding in patients on therapeutic factor XI(a) inhibitors.

Authors:  Ophira Salomon; David Gailani
Journal:  J Thromb Haemost       Date:  2021-11-21       Impact factor: 16.036

5.  Uneventful cesarean delivery with administration of factor XI concentrate in a patient with severe factor XI deficiency.

Authors:  Georgios Mavromatidis; Konstantinos Dinas; Dimitrios Delkos; Fotios Goutzioulis; Christos Vosnakis; Emmanouel Hatzipantelis; Vassilia Garipidou; David Rousso
Journal:  Int J Hematol       Date:  2007-10       Impact factor: 2.490

6.  Sulfated pentagalloylglucoside is a potent, allosteric, and selective inhibitor of factor XIa.

Authors:  Rami A Al-Horani; Pooja Ponnusamy; Akul Y Mehta; David Gailani; Umesh R Desai
Journal:  J Med Chem       Date:  2013-01-28       Impact factor: 7.446

7.  Factor XI replacement for inherited factor XI deficiency in routine clinical practice: results of the HEMOLEVEN prospective 3-year postmarketing study.

Authors:  F Bauduer; E de Raucourt; C Boyer-Neumann; M Trossaert; P Beurrier; A Faradji; J Peynet; J-Y Borg; P Chamouni; C Chatelanaz; C Henriet; F Bridey; J Goudemand
Journal:  Haemophilia       Date:  2015-03-26       Impact factor: 4.287

  7 in total

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