Rodeghiero F
Ric Clin Lab. 1985 Oct-Dec;15(4):289-303.
The therapy of hemorrhagic symptoms and the prevention of subsequent chronic disability in patients with hemophilia A and B are based on the appropriate use of specific concentrates of the deficient blood-clotting factors. The proper amount of the factor to infuse is calculated on the basis of the following parameters: patient's weight; type, location and severity of the hemorrhage to be controlled or prevented; biological half-life and yield of the infused factor. The elaboration of the therapeutic regimens to be followed in specific clinical situations is based on the above-mentioned parameters, which are fully discussed in this review. However, in the overall approach to hemophilia care, there are various other aspects, apart from strictly pathophysiological considerations. There are psychological, social and practical aspects which account for a number of specific proposals for therapeutic procedures to be used in certain circumstances (all discussed in the present report) and which should be considered separately. An example of the above is home therapy of hemophilia, which is fundamentally based on the observation that hemarthroses and hematomas account for over 90% of hemorrhagic episodes, with an average frequency of approximately 40 episodes/year/subject. It is therefore clearly understood that only early administration of specific concentrates will effectively prevent chronic joint damage, still the main cause of disability in the life of the hemophiliac. Annual average consumption of concentrates per patient is principally linked to the therapy of this type of hemorrhage and is, in turn, also influenced by the minimum effective dose for treatment of single episodes. Although this problem has not been completely solved, there is sufficient consensus that administration of 250 IU of concentrate (factor VIII or IX) in children and 500 IU in adults is effective, providing that hemarthroses and muscle hemorrhages are of a minor degree and are promptly treated. This approach leads to an average annual individual consumption of approximately 10,000 IU in children and 20,000 IU in adults, only for these episodes. A therapeutic regimen which is being increasingly used consists of treatment of acute synovitis with brief periods of prophylactic administration of concentrates (1-3 months), with the intention of interrupting the hemarthrosis-synovitis vicious circle and to allow for physiotherapy to avoid synovectomy.(ABSTRACT TRUNCATED AT 400 WORDS)
A型和B型血友病患者出血症状的治疗以及后续慢性残疾的预防,基于适当使用缺乏的凝血因子特异性浓缩物。输注因子的合适剂量根据以下参数计算:患者体重;要控制或预防的出血类型、部位和严重程度;输注因子的生物半衰期和回收率。在特定临床情况下遵循的治疗方案的制定基于上述参数,本综述将对这些参数进行充分讨论。然而,在血友病护理的整体方法中,除了严格的病理生理考虑外,还有其他各种方面。存在心理、社会和实际方面,这些方面促成了在某些情况下使用的治疗程序的一些具体建议(本报告中均有讨论),并且应分别予以考虑。上述情况的一个例子是血友病的家庭治疗,其根本依据是观察到关节积血和血肿占出血发作的90%以上,平均频率约为每年40次/患者。因此,很明显只有早期给予特异性浓缩物才能有效预防慢性关节损伤,而慢性关节损伤仍是血友病患者生活中致残的主要原因。每位患者浓缩物的年平均消耗量主要与这类出血的治疗有关,反过来也受单次发作治疗的最低有效剂量影响。尽管这个问题尚未完全解决,但人们已达成足够的共识,即儿童给予250国际单位浓缩物(因子VIII或IX)、成人给予500国际单位是有效的,前提是关节积血和肌肉出血程度较轻且得到及时治疗。仅针对这些发作,这种方法导致儿童平均每年个人消耗量约为10,000国际单位,成人约为20,000国际单位。一种越来越常用的治疗方案包括用短期预防性给予浓缩物(1 - 3个月)治疗急性滑膜炎,目的是中断关节积血 - 滑膜炎恶性循环,并允许进行物理治疗以避免滑膜切除术。(摘要截选至400字)