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长期使用活化凝血酶原复合物浓缩剂进行预防并不能阻止现有关节疾病的进展。

Long-term FEIBA prophylaxis does not prevent progression of existing joint disease.

作者信息

Hilgartner M W, Makipernaa A, Dimichele D M

机构信息

New York Presbyterian Hospital--Weill Medical College of Cornell University, New York, NY, USA.

出版信息

Haemophilia. 2003 May;9(3):261-8. doi: 10.1046/j.1365-2516.2003.00771.x.

Abstract

Activated prothrombin complex concentrates have been used to treat bleeding episodes for patients who have developed an inhibitor to factor VIII (FVIII). FEIBA-Vh (FVIII bypassing activity, FEIBA) has been used since 1970 for this purpose and with FVIII for immune tolerance programmes. Studies have not been presented to show the safety and efficacy of FEIBA when given over a long period of time to prevent haemophilic arthropathy with bleeding into the joints of these patients. This study was undertaken to ascertain the outcome of haemophilic arthropathy with FEIBA prophylaxis. Data were collected on seven patients with known long-standing high-titre FVIII inhibitors given FEIBA prophylaxis for 3-6(1/2) years. Patients were given 50-100 units of FEIBA three to four times weekly. A functional joint evaluation revealed some degree of arthropathy already present in all patients at time of prophylaxis initiation. Safety was measured by medical status, evidence of thrombosis, life-threatening bleeding and inhibitor titre. Efficacy was measured for joint outcome by a functional physical therapeutic scale. At the conclusion of the study, efficacy was mixed as all of the joints for which the patients were placed on prophylaxis had progressed and developed synovitis. Two patients had a functional improvement in their arthropathy, and all were functional enough to attend regular school. The product was deemed safe for long-term use, as there were no complications of therapy with no thrombosis, no life-threatening bleeding episodes and no anamnesis caused by FEIBA alone. Inhibitor titres fell in all patients over the course of the study. Total product usage ranged from approximately 9373-15,571 U kg(-1) year(-1). FEIBA is safe for long-term prophylaxis when given in the recommended dosage for an extended period of time. Efficacy to prevent arthropathy could not be seen as all patients had some degree of arthropathy at time of prophylaxis initiation. An additional study needs to be performed using FEIBA before arthropathy has developed.

摘要

活化凝血酶原复合物浓缩剂已被用于治疗已产生凝血因子 VIII(FVIII)抑制剂的患者的出血发作。自 1970 年以来,FEIBA-Vh(FVIII 旁路活性,FEIBA)一直用于此目的,并与 FVIII 一起用于免疫耐受方案。尚未有研究表明长期给予 FEIBA 以预防这些患者关节出血导致的血友病性关节病的安全性和有效性。本研究旨在确定 FEIBA 预防血友病性关节病的结果。收集了 7 例已知长期存在高滴度 FVIII 抑制剂且接受 FEIBA 预防 3 - 6(1/2)年的患者的数据。患者每周接受 3 - 4 次 50 - 100 单位的 FEIBA。功能性关节评估显示,在开始预防时所有患者均已存在一定程度的关节病。通过医疗状况、血栓形成证据、危及生命的出血和抑制剂滴度来衡量安全性。通过功能性物理治疗量表来衡量关节结局的疗效。在研究结束时,疗效不一,因为所有接受预防的关节均已进展并出现滑膜炎。2 例患者的关节病有功能改善,且所有患者功能良好,足以正常上学。该产品被认为长期使用安全,因为治疗没有并发症,没有血栓形成,没有危及生命的出血发作,且单独使用 FEIBA 没有引起回忆反应。在研究过程中所有患者的抑制剂滴度均下降。产品总用量范围约为 9373 - 15571 U kg(-1) 年(-1)。当长时间给予推荐剂量的 FEIBA 进行长期预防时是安全的。由于在开始预防时所有患者均有一定程度的关节病,因此未观察到预防关节病的疗效。需要在关节病发生之前使用 FEIBA 进行另一项研究。

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