Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders

被引:363
作者
Peyvandi, F. [1 ]
Palla, R. [1 ]
Menegatti, M. [1 ]
Siboni, S. M. [1 ]
Halimeh, S. [2 ]
Faeser, B. [2 ]
Pergantou, H. [3 ]
Platokouki, H. [3 ]
Giangrande, P. [4 ]
Peerlinck, K. [5 ]
Celkan, T.
Ozdemir, N. [6 ]
Bidlingmaier, C. [7 ,8 ]
Ingerslev, J.
Giansily-Blaizot, M. [9 ]
Schved, J. F. [9 ]
Gilmore, R. [10 ]
Gadisseur, A. [11 ]
Benedik-Dolnicar, M. [12 ]
Kitanovski, L. [12 ,13 ]
Mikovic, D.
Musallam, K. M. [1 ]
Rosendaal, F. R. [14 ,15 ]
机构
[1] Univ Milan, Fdn IRCCS, Ca Granda Osped Maggiore Policlin, UOS Dipartimentale Diagnosi Terapia Coagulopatie, I-20122 Milan, Italy
[2] MVZ Labor Duisburg GmbH, Duisburg, Germany
[3] Agia Sofia Children s Hosp, Haemostasis Unit, Haemophillia Ctr, Athens, Greece
[4] Univ Oxford, Nuffield Dept Clin Med, Oxford Haemophilia & Thrombosis Ctr, Oxford, England
[5] Katholieke Univ Leuven, Hemofilie Ctr Leuven, Louvain, Belgium
[6] Istanbul Univ, Cerrahpasa Med Fac, Dept Pediat Hematol Oncol, Istanbul, Turkey
[7] Dr von Hauners Childrens Univ Hosp, Pediat Hemophilia & Thrombosis Ctr, Munich, Germany
[8] Univ Hosp Skejbi, Dept Clin Biochem, Ctr Hemophilia & Thrombosis, Aarhus, Denmark
[9] Hop St Eloi, Montpellier, France
[10] St James Hosp, Natl Ctr Hereditary Coagulat Disorders, Dublin 8, Ireland
[11] Univ Antwerp, Hosp UZA, Edegem, Belgium
[12] Univ Med Ctr, Dept Pediat, Natl Haemophilia Ctr, Ljubljana, Slovenia
[13] Blood Transfus Inst Serbia, Haemostasis Dept & Haemophilia Ctr, Belgrade, Serbia
[14] Leiden Univ, Med Ctr, Dept Thrombosis & Hemostasis, Leiden, Netherlands
[15] Leiden Univ, Med Ctr, Dept Clin Epidemiol, Leiden, Netherlands
关键词
bleeding episode; coagulant activity; phenotype; rare bleeding disorder; FACTOR-V DEFICIENCY; FACTOR-VIII; FACTOR-XI; HEMOPHILIA; SYMPTOMS; SUBCOMMITTEE; PHENOTYPES; FIBRINOGEN; INHIBITOR; MUTATION;
D O I
10.1111/j.1538-7836.2012.04653.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The European Network of Rare Bleeding Disorders (EN-RBD) was established to bridge the gap between knowledge and practise in the care of patients with RBDs. Objectives: To explore the relationship between coagulation factor activity level and bleeding severity in patients with RBDs. Patients/Methods: Cross-sectional study using data from 489 patients registered in the EN-RBD. Coagulation factor activity levels were retrieved. Clinical bleeding episodes were classified into four categories according to severity. Results: The mean age of patients at data collection was 31 years (range, 7 months to 95 years), with an equal sex distribution. On linear regression analysis, there was a strong association between coagulation factor activity level and clinical bleeding severity for fibrinogen, factor (F) X, FXIII, and combined FV and FVIII deficiencies. A weaker association was present for FV and FVII deficiencies. There was no association between coagulation factor activity level and clinical bleeding severity for FXI. The coagulation factor activity levels that were necessary for patients to remain asymptomatic were: fibrinogen, > 100 mg dL(-1); FV, 12 U dL(-1); combined FV + VIII, 43 U dL(-1); FVII, 25 U dL(-1); FX, 56 U dL(-1); FXI, 26 U dL(-1); FXIII, 31 U dL(-1). Moreover, coagulation factor activity levels that corresponded with Grade III bleeding were: undetectable levels for fibrinogen, FV and FXIII, < 15 U dL(-1) for combined FV + VIII; < 8 U dL(-1) for FVI; < 10 U dL(-1) for FX; and < 25 U dL(-1) for FXI. Conclusions: There is a heterogeneous association between coagulation factor activity level and clinical bleeding severity in different RBDs. A strong association is only observed in fibrinogen, FX and FXIII deficiencies.
引用
收藏
页码:615 / 621
页数:7
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