Effects of prophylactic treatment regimens in children with severe haemophilia: a comparison of different strategies

被引:36
作者
van den Berg, HM
Fischer, K
van der Bom, JG
Roosendaal, G
Mauser-Bunschoten, EP
机构
[1] Univ Med Ctr Utrecht, Van Creveldklin, NL-3584 CX Utrecht, Netherlands
[2] Univ Med Ctr, Dept Paediat, Utrecht, Netherlands
[3] Univ Med Ctr, Julius Ctr Patient Oriented Res, Utrecht, Netherlands
关键词
prophylaxis; children with severe haemophilia; outcome;
D O I
10.1046/j.1351-8216.2001.00120.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Both Sweden and the Netherlands have a long experience with primary prophylaxis in children with severe haemophilia. In these countries it has been offered to all children for the last 3-4 decades. In Sweden prophylaxis is generally started at an earlier age with a higher dosage and frequency than in the Netherlands. Patients in the Netherlands receive a more individually tailored regimen, with prophylaxis now started after the first one or two joint bleeds and dosages are increased when breakthrough bleeds occur. The current study evaluated the effect prophylaxis on long-term outcomes and the consumption of clotting factor concentrates in Dutch and Swedish cohorts. Our results show that the orthopaedic outcome in the oldest groups of patients from Sweden and the Dutch cohorts were comparable, although the Swedish patients used twice as much clotting products per year. In the youngest patients, joint status is very good and further follow-up is necessary to demonstrate the benefits of either strategy. In conclusion, more individually tailored regimens aimed at preventing bleeding prevent joint damage in children with severe haemophilia, while clotting factor consumption is about half of that in previously described regimens.
引用
收藏
页码:43 / 46
页数:4
相关论文
共 10 条
[1]   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
[2]  
BRACKMANN HH, 1992, HAEMOSTASIS, V22, P251
[3]   PROPHYLAXIS OF JOINT HEMORRHAGES IN HEMOPHILIA [J].
CREVELD, SV .
ACTA HAEMATOLOGICA, 1971, 45 (02) :120-+
[4]  
FISCHER K, 2000, THROMB HAEMOSTASIS, V83, P65
[5]   Haemophilia prophylaxis in young patients - a long-term follow-up [J].
Lofqvist, T ;
Nilsson, IM ;
Berntorp, E ;
Pettersson, H .
JOURNAL OF INTERNAL MEDICINE, 1997, 241 (05) :395-400
[6]   RESULTS OF SECONDARY PROPHYLAXIS IN CHILDREN WITH SEVERE HEMOPHILIA [J].
MANCOJOHNSON, MJ ;
NUSS, R ;
GERAGHTY, S ;
FUNK, S ;
KILCOYNE, R .
AMERICAN JOURNAL OF HEMATOLOGY, 1994, 47 (02) :113-117
[7]   25 YEARS EXPERIENCE OF PROPHYLACTIC TREATMENT IN SEVERE HEMOPHILIA-A AND HEMOPHILIA-B [J].
NILSSON, IM ;
BERNTORP, E ;
LOFQVIST, T ;
PETTERSSON, H .
JOURNAL OF INTERNAL MEDICINE, 1992, 232 (01) :25-32
[8]  
PETRINI P, 1991, AM J PEDIAT HEMATOL, V13, P280
[9]  
SCHRAMM W, 1993, SEMIN HEMATOL, V30, P12
[10]   Long-term outcome of individualized prophylactic treatment of children with severe haemophilia [J].
van den Berg, HM ;
Fischer, K ;
Mauser-Bunschoten, EP ;
Beek, FJA ;
Roosendaal, G ;
van der Bom, JG .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 112 (03) :561-565