Kawaguchi Takumi, Kuromatsu Ryoko, Ide Tatsuya, Taniguchi Eitaro, Itou Minoru, Sakata Masahiro, Abe Mitsuhiko, Sumie Shuji, Sata Michio
Department of Digestive Disease Information & Research, Kurume University School of Medicine, Asahi-machi, Kurume, Japan.
Kurume Med J. 2009;56(1-2):9-15. doi: 10.2739/kurumemedj.56.9.
In patients with chronic liver diseases, thrombocytopenia is a common manifestation which interferes with antiviral therapy for hepatitis C virus (HCV), and with hepatocellular carcinoma (HCC) treatment. While thrombopoietin-receptor agonist is expected to improve thrombocytopenia for patients with chronic liver diseases in 2-3 weeks, there is still a lack of fundamental data about short-term variations in the natural course of platelet count in cirrhotic patients, and the impact of thrombocytopenia on antiviral therapy for HCV-infected patients and patients being treated for HCC. The aims of this study are to investigate sequential changes in platelet count and the impact of thrombocytopenia on antiviral therapy and HCC treatment in patients with chronic liver diseases. A total of 726 chronic liver disease patients were enrolled in this study. Changes of platelet count were examined during a 4-week follow-up. Risk of discontinuation or reduction of peginterferon dosage was evaluated in HCV patients with moderate thrombocytopenia (5-10x10(4)/microL). Risk of platelet transfusion or splenectomy was evaluated in HCC patients with severe thrombocytopenia (<5x10(4)/microL). No significant changes of platelet count were observed in cirrhotic patients with thrombocytopenia during a 4-week follow-up. The rate of discontinuation or reduction in dosage of peginterferon was 85.2% (23/27) in patients with moderate thrombocytopenia. Risk of discontinuation or reduction of peginterferon dosage was 3.4-times higher in HCV patients with thrombocytopenia than in those without thrombocytopenia. In HCC patients with severe thrombocytopenia, the frequency of platelet transfusion or splenectomy during HCC treatment was 57.9% (22/38). Risk of platelet transfusion or splenectomy in HCC patients with thrombocytopenia was 57.9-times higher than in those without thrombocytopenia. In conclusion, we demonstrated no significant variation in the short-term natural course of platelet count in cirrhotic patients. In chronic liver disease patients with moderate and severe thrombocytopenia, about 85% of patients treated with peginterferon, and 60% of patients receiving HCC treatments suffered from thrombocytopenia-related limitations, respectively.
在慢性肝病患者中,血小板减少是一种常见表现,会干扰丙型肝炎病毒(HCV)的抗病毒治疗以及肝细胞癌(HCC)的治疗。虽然血小板生成素受体激动剂有望在2至3周内改善慢性肝病患者的血小板减少情况,但关于肝硬化患者血小板计数自然病程的短期变化以及血小板减少对HCV感染患者抗病毒治疗和HCC治疗患者的影响,仍缺乏基础数据。本研究的目的是调查慢性肝病患者血小板计数的连续变化以及血小板减少对抗病毒治疗和HCC治疗的影响。本研究共纳入726例慢性肝病患者。在4周的随访期间检查血小板计数的变化。对中度血小板减少(5 - 10×10⁴/μL)的HCV患者评估聚乙二醇干扰素剂量中断或减少的风险。对重度血小板减少(<5×10⁴/μL)的HCC患者评估血小板输注或脾切除术的风险。在4周的随访期间,血小板减少的肝硬化患者未观察到血小板计数有显著变化。中度血小板减少的患者中,聚乙二醇干扰素剂量中断或减少的发生率为85.2%(23/27)。血小板减少的HCV患者聚乙二醇干扰素剂量中断或减少的风险比无血小板减少的患者高3.4倍。在重度血小板减少的HCC患者中,HCC治疗期间血小板输注或脾切除术的频率为57.9%(22/38)。血小板减少的HCC患者血小板输注或脾切除术的风险比无血小板减少的患者高57.9倍。总之,我们证明肝硬化患者血小板计数的短期自然病程无显著变化。在中度和重度血小板减少的慢性肝病患者中,分别约有85%接受聚乙二醇干扰素治疗的患者和60%接受HCC治疗的患者受到血小板减少相关的限制。