Recombinant, activated factor VII for surgery in factor VII deficiency: A prospective evaluation - the surgical STER

British Journal of Haematology

Volumn 152, Issue 3, 2011, Pages 340-346

  Mariani, Guglielmo ^a   Dolce, Alberto ^b   Batorova, Angelika ^c   Auerswald, Günter ^d   Schved, Jean Francois ^e   Siragusa, Sergio ^f   Napolitano, Mariasanta ^a   Knudsen, Jens Bjerre ^g   Ingerslev, Jørgen ^h  

^a UNIVERSITY OF L'AQUILA   (Italy)

^b ITALIAN NATIONAL INSTITUTE OF STATISTICS   (Italy)

^c UNIVERSITY HOSPITAL BRATISLAVA   (Slovakia)

^d Central Hospital   (Germany)

^e MONTPELLIER UNIVERSITY HOSPITAL   (France)

^f UNIVERSITY OF PALERMO   (Italy)

^g NOVO NORDISK A S   (Denmark)

^h AARHUS UNIVERSITY HOSPITAL   (Denmark)

Author keywords

Factor VII deficiency; Replacement therapy; Surgery

Indexed keywords

BLOOD CLOTTING FACTOR 7 ANTIBODY; PROTEIN ANTIBODY; RECOMBINANT BLOOD CLOTTING FACTOR 7A; UNCLASSIFIED DRUG;

ABSENCE OF SIDE EFFECTS; ADOLESCENT; ADULT; AGED; ARTICLE; BLEEDING; BLOOD CLOTTING FACTOR 7 DEFICIENCY; CHILD; CLINICAL ARTICLE; CONTINUOUS INFUSION; DRUG EFFICACY; ELECTIVE SURGERY; FEMALE; FOLLOW UP; HUMAN; INFANT; LOW DRUG DOSE; MAJOR SURGERY; MALE; MINOR SURGERY; MULTICENTER STUDY; OBSERVATIONAL STUDY; ORTHOPEDIC SURGERY; PRIORITY JOURNAL; PROSPECTIVE STUDY; SINGLE DRUG DOSE; THROMBOSIS; TOOTH EXTRACTION;

ADOLESCENT; ADULT; AGED; BLOOD LOSS, SURGICAL; CHILD; CHILD, PRESCHOOL; COAGULANTS; DRUG EVALUATION; EPIDEMIOLOGIC METHODS; FACTOR VII DEFICIENCY; FACTOR VIIA; FEMALE; HEMOSTASIS, SURGICAL; HUMANS; INFANT; MALE; MIDDLE AGED; PROSPECTIVE STUDIES; RECOMBINANT PROTEINS; TREATMENT OUTCOME;

EID: 78651288289     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2010.08287.x     Document Type: Article

References (16)

1. Bauer, K.A. (1996) Treatment of Factor VII deficiency with recombinant Factor VIIa. Haemostasis, 26, 155-158.
2. Bernardi, F., Dolce, A., Pinotti, M., Shapiro, A., Santagostino, E., Peyvandi, F., Botorova, A., Lapecorella, M., Schved, J., Ingerslev, J. & Mariani, G. (2009) Major differences in bleeding symptoms between Factor VII deficiency and Haemophilia B. Journal of Thrombosis and Haemostasis, 7, 774-779.
3. Brummel Ziedins, K., Rivard, G.E., Pouliot, R.L., Butenas, S., Gissel, M., Parhami-Seren, B. & Mann, K.G. (2004) Factor VIIa replacement therapy in factor VII deficiency. Journal of Thrombosis and Haemostasis, 2, 1735-1746.
4. Giansily-Blaizot, M., Biron-Andreani, C., Aguilar-Martinez, P., de Moeloose, P., Briquel, M.E., Goudemand, J., Stieltjes, N., Barrot, C., Chambost, H., Durin, A., Gay, V., Peynet, J., Pouymayou, K. & Schved, J.F. (2002) Inherited factor VII deficiency and surgery: clinical data are the best criteria to predict the risk of bleeding. British Journal Haematology, 117, 172-175.
5. Herrmann Wulff, F.K., Auerswald, G., Schulman, S., Astermark, J., Batorova, A., Kreuz, W., Pollmann, H., Ruiz-Saez, A., De Bosch, N. & Salazar-Sanchez, L.; Greifswald Factor FVII Deficiency Study Group. (2009) Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene. Haemophilia, 15, 267-280.
6. Hoffman, M., Colina, C.M., McDonald, A.G., Arepally, G.M., Pedersen, L. & Monroe, D.M. (2007) Tissue factor around dermal vessels has bound factor VII in the absence of injury. Journal of Thrombosis and Haemostasis, 5, 1403-1408.
7. Ingerslev, J., Christiansen, K. & Sørensen, B.; International Registry on Factor VII Deficiency (IRF7) Steering Committee. (2005) Inhibitor to factor VII in severe factor VII deficiency: detection and course of the inhibitory response. Journal of Thrombosis and Haemostasis, 3, 799-800.
8. Kitchens, C.S. (2002) Surgery and haemostasis. In: Consultative Hemostasis and Thrombosis (ed. by Craig S. Kitchens, Barbara M. Alving & Craig M. Kessler), pp. 463. WB Saunders Company, Philadelphia.
9. Mannucci, P.M., Duga, S. & Peyvandi, F. (2004) Recessively inherited coagulation disorders. Blood, 104, 1243-1252.
10. Mariani, G. & Dolce, A. (2005) Congenital factor VII deficiency. In: Textbook of Haemophilia (ed. by C.A. Lee, E.E. Berntorp & W.K. Hoots), pp. 313. Blackwell Publishing, Malden, MA, USA.
11. Mariani, G., Testa, M.G., DiPaolantonio, T., Molskov Bech, R. & Hedner, U. (1999) The use of Recombinant, Activated Factor VII in the Treatment of Congenital Factor VII Deficiencies. Vox Sanguinis, 77, 131-136.
12. Mariani, G., Herrmann, F.H., Schulman, S., Batorova, A., Wulff, K., Etro, D., Dolce, A., Auerswald, G., Astermark, J., Schved, J.F., Ingerslev, J. & Bernardi, F.; International Factor VII Deficiency Study Group. (2003) Thrombosis in inherited factor VII deficiency. Journal of Thrombosis and Haemostasis, 1, 2153-2158.
13. Mariani, G., Herrmann, F.H., Dolce, A., Batorova, A., Etro, D., Peyvandi, F., Wulff, K., Schved, J.F., Auerswald, G., Ingerslev, J. & Bernardi, F.; For the International Factor VII Deficiency Study Group. (2005) Clinical phenotypes and factor VII genotype in congenital factor VII deficiency. Thrombosis and Haemostasis, 93, 481-487.
14. Mariani, G., Konkle, B.A. & Ingerslev, J. (2006) Congenital factor VII deficiency: therapy with recombinant activated factor VII - a critical appraisal. Haemophilia, 12, 19-27.
15. Perry, D.J. (2002) Factor VII Deficiency. British Journal Haematology, 118, 689-700.
16. Roberts, H.R. & Escobar, M.A. (2006) Inherited disorders of prothrombin conversion. In: Haemostasis and Thrombosis. Basic Principles and Clinical Practice, 5th edn (ed. by R.W. Colman, V.J. Marder, A.W. Clowes, J.N. George & S.Z. Goldhaber), pp. 923. Lippincott Williams & Wilkins, Philadelphia.