Lifelong prophylaxis in a large cohort of adult patients with severe haemophilia: a beneficial effect on orthopaedic outcome and quality of life

被引:83
作者
Khawaji, Mohammed [1 ,2 ]
Astermark, Jan [1 ,2 ]
Berntorp, Erik [1 ,2 ]
机构
[1] Skane Univ Hosp, Malmo Ctr Thrombosis & Haemostasis, SE-20502 Malmo, Sweden
[2] Lund Univ, Dept Clin Sci, Malmo, Sweden
关键词
haemophilia; prophylaxis; health-related quality of life; joint status;
D O I
10.1111/j.1600-0609.2012.01750.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In the 1950s, Sweden initiated prophylaxis as a lifelong treatment for haemophilia. It was the first country to do so. Objective: To describe and evaluate dosing and outcome of prophylactic treatment in a large cohort of adult people with severe haemophilia who have been using prophylaxis most of their lives. Methods: Eighty-one patients born between 1932 and1992 were divided into two groups (Group A started prophylaxis at the age of <= 3 yr; Group B at three or more years of age) and evaluated retrospectively. Outcome was evaluated using the Hemophilia Joint Health Score (HJHS) and SF-36, a measure of quality of life. Results: The median number of joint bleeds per year was 0 in both study groups; however, the annual number of joint bleeds during the final 3 yr of observation was higher in group B than in group A (P < 0.006). Twenty-five of 30 patients in group A and 27 / 51 patients in group B had no joint bleeds in that period. Group A had significantly better joint outcomes than group B. Patients in group A experienced better physical and social health than those in group B. Conclusions: This follow-up has provided for the first time more extensive and detailed information regarding the practice of prophylactic treatment in a large cohort of adults with severe haemophilia. The present study confirms that early start of prophylaxis continuing throughout the lifespan has been successful in virtually eliminating joint bleeds, preserving a close to normal joint status, and keeping patients healthy and able to live normal lives.
引用
收藏
页码:329 / 335
页数:7
相关论文
共 22 条
[1]   A 6-year follow-up of dosing, coagulation factor levels and bleedings in relation to joint status in the prophylactic treatment of haemophilia [J].
Ahnström, J ;
Berntorp, E ;
Lindvall, K ;
Björkman, S .
HAEMOPHILIA, 2004, 10 (06) :689-697
[2]   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
[3]   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
[4]   Guidelines on treatment of haemophilia in Sweden [J].
Berntorp, E .
HAEMOPHILIA, 1998, 4 (04) :425-426
[5]  
Berntorp E, 1995, B WORLD HEALTH ORGAN, V73, P691
[6]   HEMOPHILIC ARTHROPATHY - A 10-YEAR RADIOLOGICAL AND CLINICAL-STUDY [J].
BROWN, IS ;
TOOLIS, F ;
PRESCOTT, RJ .
SCOTTISH MEDICAL JOURNAL, 1982, 27 (04) :279-283
[7]   On-demand vs. prophylactic treatment for severe haemophilia in Norway and Sweden:: differences in treatment characteristics and outcome [J].
Carlsson, KS ;
Höjgård, S ;
Glomstein, A ;
Lethagen, S ;
Schulman, S ;
Tengborn, L ;
Lindgren, A ;
Berntorp, E ;
Lindgren, B .
HAEMOPHILIA, 2003, 9 (05) :555-566
[8]   Prophylactic treatment for severe haemophilia: comparison of an intermediate-dose to a high-dose regimen [J].
Fischer, K ;
Astermark, J ;
Van der Bom, JG ;
Ljung, R ;
Berntorp, E ;
Grobbee, DE ;
Van den Berg, HM .
HAEMOPHILIA, 2002, 8 (06) :753-760
[9]   The effects of postponing prophylactic treatment on long-term outcome in patients with severe hemophilia [J].
Fischer, K ;
van der Bom, JG ;
Mauser-Bunschoten, EP ;
Roosendaal, G ;
Prejs, R ;
de Kleijn, P ;
Grobbee, DE ;
van den Berg, M .
BLOOD, 2002, 99 (07) :2337-2341
[10]   Hemophilia joint health score reliability study [J].
Hilliard, P. ;
Funk, S. ;
Zourikian, N. ;
Bergstrom, B. -M. ;
Bradley, C. S. ;
Mclimont, M. ;
Manco-Johnson, M. ;
Petrini, P. ;
Van den Berg, M. ;
Feldman, B. M. .
HAEMOPHILIA, 2006, 12 (05) :518-525