Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Via Pace 9, 20122, Milan, Italy.
Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy.
Intern Emerg Med. 2023 Aug;18(5):1251-1254. doi: 10.1007/s11739-023-03331-7. Epub 2023 Jul 29.
Hemophilia is an X-linked bleeding disorder, characterized by low plasma levels of coagulation factor VIII (FVIII) (hemophilia A) or FIX (hemophilia B). Because of this, hemophilia patients (HP) were considered as naturally-anticoagulated and therefore protected from thrombosis. Over the last decades hemophilia care underwent striking changes by the introduction of prophylaxis with repeated injections of standard or modified coagulation factor products that maintain steady-state trough levels of the deficient factor. Meanwhile, new medications, not based on replacement therapy, were developed (i.e., emicizumab and others). However, emicizumab (the only licensed drug) can be used only for prophylaxis; during acute bleeding or surgery, HP require additional therapies, supplementing emicizumab with FVIII/IX concentrates or with bypassing agents (e.g., recombinant activated FVII or activated prothrombin complex concentrate). Owing to the new therapeutic strategies, the hemostatic competency of HP is now much better assured than in the past and therefore their life expectancy is considerably improved. Furthermore, the combined effects of the improved life-expectancy and of the steady-state hemostatic competence achieved by prophylaxis, make HP to be near(normal). They are, therefore, liable to be affected by the circumstantial risk factors of venous thromboembolism (VTE) that are common in the general population. Furthermore, HP undergo frequent surgery/invasive procedures (especially major orthopedic surgery) when they are treated with coagulation factor concentrates or bypassing agents that may increase the risk of post-operative VTE. Therefore, one wonders if HP should be considered for perioperative antithrombotic prophylaxis to prevent postoperative VTE.Clinical data on the value of antithrombotic prophylaxis in this setting are scanty. Indeed, data from an observational multicentre prospective study of 46 HP who underwent orthopedic surgery concluded that the prevalence of postoperative symptomatic VTE was similar to that estimated in the general population. Multicenter prospective trials are warranted to address the value of antithrombotic prophylaxis to avoid post-operative VTE in HP, especially during major surgery when regular prophylaxis is supplemented with additional coagulation factor products or bypassing agents. Until this information is available, HP undergoing major surgery whilst on antihemorrhagic prophylaxis supplemented with coagulation factor concentrates or bypassing agents, should at least receive intermittent pneumatic compression.
血友病是一种 X 连锁出血性疾病,其特征是凝血因子 VIII(FVIII)(血友病 A)或 FIX(血友病 B)的血浆水平降低。正因为如此,血友病患者(HP)被认为是天然抗凝的,因此可以免受血栓形成的影响。在过去的几十年里,通过反复注射标准或改良的凝血因子产品进行预防治疗,使血友病的治疗发生了显著变化,这种方法可以维持缺乏的因子的稳定状态。与此同时,开发了一些基于替代疗法的新药物(例如,emicizumab 等)。然而,emicizumab(唯一获得许可的药物)只能用于预防;在急性出血或手术期间,HP 需要额外的治疗方法,在 emicizumab 中补充 FVIII/IX 浓缩物或旁路剂(例如,重组激活的 FVII 或激活的凝血酶原复合物浓缩物)。由于新的治疗策略,HP 的止血能力现在比过去要好得多,因此他们的预期寿命大大提高。此外,由于预期寿命的提高和通过预防治疗实现的稳定止血能力的综合作用,使得 HP 几乎(接近)正常。因此,他们可能会受到静脉血栓栓塞症(VTE)的环境危险因素的影响,这些危险因素在普通人群中很常见。此外,HP 在接受凝血因子浓缩物或旁路剂治疗时经常需要进行手术/有创手术(特别是主要的矫形手术),这可能会增加术后 VTE 的风险。因此,人们不禁要问,是否应该考虑对 HP 进行围手术期抗血栓预防,以预防术后 VTE。关于这种情况下抗血栓预防价值的临床数据很少。事实上,一项针对 46 名接受矫形手术的 HP 的多中心前瞻性观察性研究的数据表明,术后有症状性 VTE 的发生率与普通人群估计的发生率相似。需要进行多中心前瞻性试验,以确定抗血栓预防对避免 HP 术后 VTE 的价值,尤其是在大手术期间,当常规预防治疗补充额外的凝血因子产品或旁路剂时。在获得这些信息之前,接受抗出血预防治疗且补充凝血因子浓缩物或旁路剂的 HP 进行大手术时,至少应接受间歇性气动压迫。