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DOI 10.1111/j.1365-2516.2007.01473.x

Медицинская библиотека · Haemophilia : the official journal of the World Federation of Hemophilia · 2007

Long-term major joint outcomes in young adults with haemophilia: interim data from the HGDS.

Su Y, Wong W-Y, Lail A, Donfield S M, Konzal S, Gomperts E, Hemophilia Growth And Development Study

СтатьяМногоцентровое исследованиеПеревод в очереди

Аннотация

A study of major joint outcomes, specifically range of motion and synovitis, was conducted with data from a subset of adolescents enrolled in the prospective Hemophilia Growth and Development Study (HGDS). Clinical observations were carried out over a 7-year period from 1989 to 1996. A secondary aim was to gain insight into factors that might influence decisions regarding maintaining or discontinuing prophylaxis during early adulthood. Twenty-nine participants (median age 17.4 at entry) were included. Median follow-up was 7 years (range: 4.8-7.7). Range of motion (ROM) and synovitis in six major joints (knees, elbows and ankles), were evaluated by physical examination every 6-12 months. At the baseline observation, 73.6% of joints showed no ROM abnormalities or synovitis, and all joints were normal in 11 patients. Of the 11 participants, 54.5% developed abnormalities and 28.1% of normal joints at baseline became abnormal during the follow-up. Ankles were the most severely affected and had persistent progression during late adolescence and adulthood. Elbows and knees did not show progression after the first few years of the follow-up. The progression of haemophilic arthropathy in adolescents and young adults varies from individual to individual and also in the site of affected joints. In view of this, the decision regarding discontinuation of prophylaxis in patients with haemophilia should be individualized.

Для цитирования: Su Y, Wong W-Y, Lail A, Donfield S M, Konzal S, Gomperts E, Hemophilia Growth And Development Study. Long-term major joint outcomes in young adults with haemophilia: interim data from the HGDS.. Haemophilia : the official journal of the World Federation of Hemophilia. 2007. DOI: 10.1111/j.1365-2516.2007.01473.x.

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