Löfqvist T, Nilsson I M, Berntorp E, Pettersson H
Department of Coagulation Disorders, University of Lund, Malmö, Sweden.
J Intern Med. 1997 May;241(5):395-400. doi: 10.1046/j.1365-2796.1997.130135000.x.
To review long-term prophylactic factor treatment in young patients with severe haemophilia A and B, focusing on the orthopaedic and radiological outcome.
We received 34 patients with severe haemophilia A (n = 29) and B (n = 5), aged 7-22 years. Age at start of treatment was 1-4.5 years. Dosages of factor concentrate (F VIII and F IX, respectively) were 25-40 IU/kg body weight, three times a week for haemophilia A and twice a week for haemophilia B. The patients had been checked annually over a 5-year period (1990-95). Orthopaedic and radiological joint scores were evaluated according to recommendations by the World Federation of Haemophilia.
All results were obtained at the Department for Coagulation Disorders, University of Lund, Malmö University Hospital, Malmö, Sweden.
Orthopaedic and radiological joint scores were found to have remained unchanged during follow-up in almost all patients and to be still zero (i.e. no unaffected joints) in 79% (n = 27) of the patients.
There is a growing international consensus haemophilic arthropathy can be prevented by administering early high-dose prophylaxis. The results of the present investigation strongly support this opinion.
回顾重度甲型和乙型血友病年轻患者的长期预防性因子治疗,重点关注骨科和放射学结果。
我们纳入了34例重度甲型血友病患者(n = 29)和乙型血友病患者(n = 5),年龄在7至22岁之间。开始治疗的年龄为1至4.5岁。因子浓缩物(分别为F VIII和F IX)的剂量为25至40 IU/kg体重,甲型血友病每周3次,乙型血友病每周2次。在5年期间(1990 - 95年)对患者进行每年一次的检查。根据世界血友病联盟的建议评估骨科和放射学关节评分。
所有结果均在瑞典马尔默大学医院隆德大学凝血障碍科获得。
几乎所有患者在随访期间骨科和放射学关节评分均保持不变,79%(n = 27)的患者评分仍为零(即无未受影响的关节)。
国际上越来越多的人达成共识,即通过早期高剂量预防可以预防血友病性关节病。本研究结果有力地支持了这一观点。