Dose and response in haemophilia - optimization of factor replacement therapy

被引:45
作者
Srivastava, A [1 ]
机构
[1] Christian Med Coll & Hosp, Dept Haematol, Vellore 632004, Tamil Nadu, India
关键词
haemophilia; clotting factor; dose; response;
D O I
10.1111/j.1365-2141.2004.05110.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The mainstay of the management of haemophilia is the replacement of clotting factors, using clotting factor concentrates (CFC) in a way that prevents bleeding and its complications. Beginning with small doses, as whole blood and plasma over 50 years ago, highly purified CFCs are now administered frequently in large doses to effectively treat this condition so that even people with severe haemophilia can lead near normal lives. However, with such regimens, compliance and expense have both become significant issues. The question therefore is whether the current models of clotting factor replacement are optimal. This article reviews the literature on the dose-response relationship in haemophilia, with particular reference to management of musculoskeletal bleeding and surgical haemostasis. Current practices are based on uncontrolled observational data. Less intensive protocols could achieve similar outcomes. Large multi-centre prospective studies are needed to provide comparative data on unresolved issues so that factor replacement therapy can be optimized, based on evidence.
引用
收藏
页码:12 / 25
页数:14
相关论文
共 114 条
[1]  
ABILDGAARD CF, 1975, SEMIN HEMATOL, V12, P223
[2]  
Abshire TC, 2000, THROMB HAEMOSTASIS, V83, P811
[3]  
ADELOYE A, 1972, TROP GEOGR MED, V24, P23
[4]   A LONGITUDINAL-STUDY OF ORTHOPEDIC OUTCOMES FOR SEVERE FACTOR-VIII-DEFICIENT HEMOPHILIACS [J].
ALEDORT, LM ;
HASCHMEYER, RH ;
PETTERSSON, H ;
EIBL, H ;
GILBERT, M ;
HILGARTNER, M ;
KUNSHACK, M ;
LARRIEU, MJ ;
LEVINE, P .
JOURNAL OF INTERNAL MEDICINE, 1994, 236 (04) :391-399
[5]  
ALLAIN JP, 1979, THROMB HAEMOSTASIS, V42, P825
[6]  
ARONSTAM A, 1983, CLIN LAB HAEMATOL, V5, P157
[7]  
ARONSTAM A, 1980, LANCET, V1, P169
[8]   LOW-DOSES OF FACTOR-VIII FOR SELECTED ANKLE BLEEDS IN SEVERE HEMOPHILIA-A [J].
ARONSTAM, A ;
WASSEF, M ;
HAMAD, Z .
BRITISH MEDICAL JOURNAL, 1982, 284 (6318) :790-790
[9]   THE IDENTIFICATION OF HIGH-RISK ELBOW HEMORRHAGES IN ADOLESCENTS WITH SEVERE HEMOPHILIA-A [J].
ARONSTAM, A ;
WASSEF, M ;
HAMAD, Z ;
ASTON, DL .
JOURNAL OF PEDIATRICS, 1981, 98 (05) :776-778
[10]   PROPHYLAXIS IN HEMOPHILIA - DOUBLE-BLIND CONTROLLED TRIAL [J].
ARONSTAM, A ;
ARBLASTER, PG ;
RAINSFORD, SG ;
TURK, P ;
SLATTERY, M ;
ALDERSON, MR ;
HALL, DE ;
KIRK, PJ .
BRITISH JOURNAL OF HAEMATOLOGY, 1976, 33 (01) :81-90