Buchanan G R, Kevy S V
Pediatrics. 1978 Nov;62(5):767-74.
Nine patients with severe classic hemophilia and inhibitors against factor VIII were treated for 156 bleeding episodes with 503 infusions of Proplex, Konyne, or Auto-Factor IX, three preparations of prothrombin complex concentrates (PCCs). Approximately two thirds of the bleeding episodes were managed successfully. Although the prothrombin time (PT) and partial thromboplastin time (PTT) were shortened after most PCC infusions, there was no evidence of disseminated intravascular coagulation. The degree of shortening of PT or PTT was not related to the particular PCC preparation used, dose, or cessation of hemorrhage. All PCC preparations contained activated clotting factors, as manifested by their ability to shorten the PTT of normal plasma, factor-VIII-deficient plasma, and factor-IX-deficient plasma. Shortening, which was greater with Auto-Factor IX than with the other products, was inhibited partially by a factor IX antibody and blocked completely by prolonged incubation with plasma. Although the nature of the procoagulant material in PCCs is uncertain, these products are of proven benefit to hemophilic patients with high-titer inhibitors. Side effects have been minimal and inhibitor titers have not risen.
9例患有严重典型血友病且体内存在抗凝血因子VIII抑制剂的患者,因156次出血发作接受了503次凝血酶原复合物浓缩剂(PCC)输注治疗,使用的三种PCC制剂分别为Proplex、Konyne或自动凝血因子IX。约三分之二的出血发作得到成功处理。尽管大多数PCC输注后凝血酶原时间(PT)和部分凝血活酶时间(PTT)缩短,但未发现弥散性血管内凝血的证据。PT或PTT的缩短程度与所用的特定PCC制剂、剂量或出血停止情况无关。所有PCC制剂均含有活化凝血因子,这可通过它们缩短正常血浆、缺乏凝血因子VIII的血浆和缺乏凝血因子IX的血浆的PTT的能力得以体现。自动凝血因子IX引起的缩短程度大于其他产品,这种缩短部分被凝血因子IX抗体抑制,并通过与血浆长时间孵育而完全被阻断。尽管PCC中促凝物质的性质尚不确定,但这些产品已被证明对高滴度抑制剂的血友病患者有益。副作用极小,且抑制剂滴度未升高。