Rare bleeding disorders and invasive procedures;Déficits rares de la coagulation et gestes invasifs

Annales Francaises d'Anesthesie et de Reanimation

Volumn 32, Issue 3, 2013, Pages 198-205

  Bonhomme, F ^a   Schved, J F ^b   Giansily Blaizot, M ^b   Samama, C M ^c   De Moerloose, P ^a  

^a GENEVA UNIVERSITY HOSPITALS   (Switzerland)

^b HÔPITAL SAINT ELOI   (France)

^c HÔTEL DIEU   (France)

Author keywords

Invasive procedure; Rare bleeding disorders; Surgery

Indexed keywords

BLOOD CLOTTING FACTOR 10; BLOOD CLOTTING FACTOR 11; BLOOD CLOTTING FACTOR 13; BLOOD CLOTTING FACTOR 5; BLOOD CLOTTING FACTOR 7; PROTHROMBIN;

AUTOSOMAL RECESSIVE DISORDER; BLEEDING; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE SEVERITY; HUMAN; INVASIVE PROCEDURE; PATIENT ASSESSMENT; PERINATAL PERIOD; RARE DISEASE; RISK ASSESSMENT; SHORT SURVEY;

BLOOD COAGULATION DISORDERS, INHERITED; BLOOD COAGULATION FACTORS; COAGULATION PROTEIN DISORDERS; DISEASE MANAGEMENT; EMERGENCIES; FEMALE; GENES, RECESSIVE; HEMORRHAGE; HUMANS; MALE; POSTOPERATIVE HEMORRHAGE; POSTPARTUM HEMORRHAGE; PREGNANCY; PREVALENCE; RISK ASSESSMENT; SYMPTOM ASSESSMENT; THROMBOSIS;

EID: 84875810094     PISSN: 07507658     EISSN: 17696623     Source Type: Journal    
DOI: 10.1016/j.annfar.2013.01.019     Document Type: Short Survey

References (29)

1. Peyvandi F., Palla R., Menegatti M., Siboni S.M., Halimeh S., Faeser B., et al. Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders. J Thromb Haemost 2012, 10:615-621.
2. Mannucci P.M., Duga S., Peyvandi F. Recessively inherited coagulation disorders. Blood 2004, 104:1243-1252.
3. de Moerloose P., Neerman-Arbez M. Congenital fibrinogen disorders. Semin Thromb Hemost 2009, 35:356-366.
4. Lancellotti S., De Cristofaro R. Congenital prothrombin deficiency. Semin Thromb Hemost 2009, 35:367-381.
5. Huang J.N., Koerper M.A. Factor V deficiency: a concise review. Haemophilia 2008, 14:1164-1169.
6. Acharya S.S., Coughlin A., Dimichele D.M. Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias. J Thromb Haemost 2004, 2:248-256. North American Rare Bleeding Disorder Study Group.
7. Asselta R., Tenchini M.L., Duga S. Inherited defects of coagulation factor V: the hemorrhagic side. J Thromb Haemost 2006, 4:26-34.
8. Herrmann F.H., Wulff K., Auerswald G., Schulman S., Astermark J., Batorova A., et al. Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene. Haemophilia 2009, 15:267-280.
9. Mariani G., Herrmann F.H., Dolce A., Batorova A., Etro D., Peyvandi F., et al. Clinical phenotypes and factor VII genotype in congenital factor VII deficiency. Thromb Haemost 2005, 93:481-487.
10. Peyvandi F., Mannucci P.M., Lak M., Abdoullahi M., Zeinali S., Sharifian R., et al. Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients. Br J Haematol 1998, 102:626-628.
11. Herrmann F.H., Auerswald G., Ruiz-Saez A., Navarrete M., Pollmann H., Lopaciuk S., et al. Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene. Haemophilia 2006, 12:479-489.
12. Karimi M., Menegatti M., Afrasiabi A., Sarikhani S., Peyvandi F. Phenotype and genotype report on homozygous and heterozygous patients with congenital factor X deficiency. Haematologica 2008, 93:934-938.
13. Duga S., Salomon O. Factor XI deficiency. Semin Thromb Hemost 2009, 35:416-425.
14. Bolton-Maggs P.H. Factor XI deficiency and its management. Haemophilia 2000, 6(Suppl. 1):100-109.
15. Mansouritorgabeh H., Rezaieyazdi Z., Pourfathollah A.A., Rezai J., Esamaili H. Haemorrhagic symptoms in patients with combined factors V and VIII deficiency in north-eastern Iran. Haemophilia 2004, 10:271-275.
16. Brenner B., Kuperman A.A., Watzka M., Oldenburg J. Vitamin K-dependent coagulation factors deficiency. Semin Thromb Hemost 2009, 35:439-446.
17. Tosetto A., Castaman G., Plug I., Rodeghiero F., Eikenboom J. Prospective evaluation of the clinical utility of quantitative bleeding severity assessment in patients referred for hemostatic evaluation. J Thromb Haemost 2011, 9:1143-1148.
18. Bolton-Maggs P.H.B., Perry D.J., Chalmers E.A., Parapia L.A., Wilde J.T., Williams M.D., et al. The rare coagulation disorders - review with guidelines for management from the United-Kingdom Haemophilia Centre Doctors' Organisation. Haemophilia 2004, 10:593-628.
19. Keeling D., Tait C., Makris M. Guideline on the selection and use of therapeutic products to treat haemophilia and other hereditary bleeding disorders. A United-Kingdom Haemophilia Center Doctors' Organisation (UKHCDO) guideline approved by the British Committee for Standards in Haematology. Haemophilia 2008, 14:671-684.
20. Hewson I., Makhmalbaf P., Street A., McCarthy P., Walsh M. Dental surgery with minimal factor support in the inherited bleeding disorder population at the Alfred Hospital. Haemophilia 2011, 17:e185-e188.
21. Kenet G., Lubetsky A., Luboshitz J., Ravid B., Tamarin I., Varon D., et al. Lower doses of rFVIIa therapy are safe and effective for surgical interventions in patients with severe FXI deficiency and inhibitors. Haemophilia 2009, 15:1065-1073.
22. Livnat T., Tamarin I., Mor Y., Winckler H., Horowitz Z., Korianski Y., et al. Recombinant activated factor VII and tranexamic acid are haemostatically effective during major surgery in factor XI-deficient patients with inhibitor antibodies. Thromb Haemost 2009, 102:487-492.
23. Castaman G. Prophylaxis of bleeding episodes and surgical interventions in patients with rare inherited coagulation disorders. Blood Transfus 2008, 6(Suppl. 2):39-44.
24. Benlakhal F., Mura T., Schved J.F., Giansily-Blaizot M. A retrospective analysis of 157 surgical procedures performed without replacement therapy in 83 unrelated factor VII-deficient patients. J Thromb Haemost 2011, 9:1149-1156. French Study Group of Factor VII Deficiency.
25. Kadir R., Chi C., Bolton-Maggs P. Pregnancy and rare bleeding disorders. Haemophilia 2009, 15:990-1005.
26. Huq F.Y., Kadir R.A. Management of pregnancy, labour and delivery in women with inherited bleeding disorders. Haemophilia 2011, 17(Suppl. 1):20-30.
27. Salomon O., Steinberg D.M., Tamarin I., Zivelin A., Seligsohn U. Plasma replacement therapy during labor is not mandatory for women with severe factor XI deficiency. Blood Coagul Fibrinolysis 2005, 16:37-41.
28. Seligsohn U. Factor XI deficiency in humans. J Thromb Haemost 2009, 7(Suppl. 1):84-87.
29. Peyvandi F., Palla R., Menegatti M., Mannucci P.M. Introduction. Rare bleeding disorders: general aspects of clinical features, diagnosis, and management. Semin Thromb Hemost 2009, 35:349-355.