Aguilar Carlos
Department of Haematology, Hospital General Santa Bárbara, Paseo Santa Bárbara s/n, Soria, Spain.
Blood Coagul Fibrinolysis. 2013 Apr;24(3):231-6. doi: 10.1097/MBC.0b013e3283606a0b.
New thrombopoietin receptor agonists (TPO-RA) eltrombopag and romiplostin were initially used for refractory immune thrombocytopaenic purpura, but more recently reported experience shows that they may also be applied to patients with thrombocytopaenia secondary to hepatitis C virus (HCV)-related chronic liver disease (CLD) in certain clinical situations; in haemophilic patients these drugs are always part of a therapeutic approach involving other haemostatic resources required to cover the joint congenital and acquired bleeding diathesis found in these patients. Platelet count elevation before invasive procedures or surgery or prior to and during antiviral therapy involving interferon are the main clinical applications of these drugs; they might also be useful in cases with advanced CLD and severe thrombocytopaenia in order to prevent recurrent bleeding episodes (namely articular and muscular in haemophilic individuals) or reduce bleeding risk in patients with multiple haemorrhagic risk factors. Long-term prophylactic treatment with factor concentrates in such cases is mandatory. There have been some reports of portal or splanchnic thromboses in patients on TPO-RA with CLD, especially in cases undergoing invasive procedures who reach platelet counts at least 200×10/l and often with additional risk factors for thrombosis. For this reason, and although haemophilic patients have an important protection against thrombosis, platelet counts should ideally be maintained between 50 and 100×10/l with dose adjustments carried out as required and initial doses of eltrombopag in patients with moderate or severe CLD, especially in prolonged treatments, should be reduced to 25 g once daily. These new drugs can be a useful adjuvant tool in patients with thrombocytopaenia secondary to CLD.
新型血小板生成素受体激动剂(TPO-RA)艾曲泊帕和罗米司亭最初用于治疗难治性免疫性血小板减少性紫癜,但最近的报道经验表明,在某些临床情况下,它们也可应用于丙型肝炎病毒(HCV)相关慢性肝病(CLD)继发血小板减少的患者;在血友病患者中,这些药物始终是治疗方法的一部分,该治疗方法还涉及其他止血资源,以应对这些患者出现的先天性和后天性关节出血素质。在侵入性操作或手术前,或在涉及干扰素的抗病毒治疗之前及期间提高血小板计数是这些药物的主要临床应用;它们可能对晚期CLD和严重血小板减少的病例也有用,以预防复发性出血事件(即血友病患者的关节和肌肉出血)或降低具有多种出血风险因素患者的出血风险。在这种情况下,长期使用因子浓缩物进行预防性治疗是必要的。有报道称,接受TPO-RA治疗的CLD患者出现门静脉或内脏血栓形成,尤其是在侵入性操作的病例中,这些患者的血小板计数至少达到200×10⁹/L,且通常伴有其他血栓形成风险因素。因此,尽管血友病患者对血栓形成有重要的保护作用,但理想情况下血小板计数应维持在50至100×10⁹/L之间,并根据需要调整剂量,对于中度或重度CLD患者,尤其是长期治疗时,艾曲泊帕的初始剂量应减至每日25mg。这些新药对于CLD继发血小板减少的患者可能是一种有用的辅助工具。