The effects of postponing prophylactic treatment on long-term outcome in patients with severe hemophilia

被引:208
作者
Fischer, K
van der Bom, JG
Mauser-Bunschoten, EP
Roosendaal, G
Prejs, R
de Kleijn, P
Grobbee, DE
van den Berg, M
机构
[1] Univ Utrecht, Med Ctr, Van Creveldklin HP C01 425,Dept Radiol, Julius Ctr Gen Practice & Patient Oriented Res, NL-3508 GA Utrecht, Netherlands
[2] Univ Utrecht, Med Ctr, Dept Rehabil & Nutr Sci, Utrecht, Netherlands
关键词
D O I
10.1182/blood.V99.7.2337
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To prevent hemophilic arthropathy, prophylactic treatment of children with severe hemophilia should be started before joint damage has occurred. However, treatment is expensive, and the burden of regular venipunctures in young children is high. With the aim of providing information on starting prophylaxis on the basis of individual patient characteristics, the effect of postponing prophylaxis on long-term arthropathy was studied in a cohort of 76 patients with severe hemophilia born between 1965 and 1985. The median age at first joint bleed was 2.2 years (range, 0.2-5.8). Prophylaxis was started at a median age of 6 years: (interquartile range [IQR], 4-9), and the median annual clotting factor use on prophylaxis was 1750 IU/kg/y (31 Iu=U/kg/wk). Hemophilic arthropathy was measured by the Pettersson score (maximum, 78 points). At a median: age of 19 years, the median Pettersson score was 7 points (IQR, 0-17). After 2 decades of follow-up, the Pettersson score was 8% higher (95% confidence interval,: 1%-16%) for every year prophylaxis was postponed after the first joint bleed. This effect was independent of age at Pettersson score, age at first joint bleed, and prophylactic dose used. In conclusion, most patients have their first joint bleed after the age of 2 years. Patients who start prophylaxis soon after the first joint bleed show little arthropathy in adulthood. The longer the start of prophylaxis is postponed after the first joint bleed, the higher the risk of developing arthropathy. (C) 2002 by The American Society of Hematology.
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页码:2337 / 2341
页数:5
相关论文
共 24 条
[1]   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
[2]   Primary prophylaxis in severe haemophilia should be started at an early age but can be individualized [J].
Astermark, J ;
Petrini, P ;
Tengborn, L ;
Schulman, S ;
Ljung, R ;
Berntorp, E .
BRITISH JOURNAL OF HAEMATOLOGY, 1999, 105 (04) :1109-1113
[3]  
Berntorp E, 1995, B WORLD HEALTH ORGAN, V73, P691
[4]  
ERLEMANN R, 1989, ACTA RADIOL, V30, P147
[5]  
GILBERT MS, 1993, SEMIN HEMATOL, V30, P3
[6]   RADIOLOGICAL EVALUATION OF CHRONIC HEMOPHILIC ARTHROPATHY BY THE PETTERSSON SCORE - PROBLEMS IN CORRELATION IN ADULT PATIENTS [J].
HAMEL, J ;
POHLMANN, H ;
SCHRAMM, W .
SKELETAL RADIOLOGY, 1988, 17 (01) :32-36
[7]   When should prophylactic treatment in patients with haemophilia A and B start? - The German experience [J].
Kreuz, W ;
Escuriola-Ettingshausen, C ;
Funk, M ;
Schmidt, H ;
Kornhuber, B .
HAEMOPHILIA, 1998, 4 (04) :413-417
[8]   LONGITUDINAL DATA-ANALYSIS USING GENERALIZED LINEAR-MODELS [J].
LIANG, KY ;
ZEGER, SL .
BIOMETRIKA, 1986, 73 (01) :13-22
[9]   The impact of prophylactic treatment on children with severe haemophilia [J].
Liesner, RJ ;
Khair, K ;
Hann, IM .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 92 (04) :973-978
[10]   Treatment of children with haemophilia in Europe: a survey of 20 centres in 16 countries [J].
Ljung, R ;
Aronis-Vournas, S ;
Kurnik-Auberger, K ;
Van den Berg, M ;
Chambost, H ;
Claeyssens, S ;
Van Geet, C ;
Glomstein, A ;
Hann, I ;
Hill, F ;
Kobelt, R ;
Kreuz, W ;
Mancuso, G ;
Muntean, W ;
Petrini, P ;
Rosado, L ;
Scheibel, E ;
Siimes, M ;
Smith, O ;
Tusell, J .
HAEMOPHILIA, 2000, 6 (06) :619-624