Hörnfeldt Erika, Gjertsen Henrik, Weiland Ola
Department of Medicine, Division of Infectious Diseases, Karolinska University Hospital Huddinge, Karolinska Institute, Stockholm, Sweden.
Scand J Infect Dis. 2008;40(3):259-65. doi: 10.1080/00365540701633020. Epub 2007 Sep 6.
Patients with recurrent hepatitis C after liver transplantation often cannot tolerate full dose of pegylated interferon (peg-IFN) and ribavirin (RBV) and are often withdrawn prematurely from treatment. We chose a low initial RBV dose, later increased due to tolerance to a mean dose of 600 mg daily (range 200-1000 mg daily) in combination with a peg-IFN alpha-2a 180 mcg weekly in an effort to improve tolerance and minimize withdrawals. 16 patients with hepatitis C recurrence and 1 with de novo HCV infection with a mean age of 54 y (range 43-66 y), 71% males, were treated. All patients completed the intended treatment schedule 24 weeks for genotype 2 and 3 and 48 weeks for genotype 1 and 4. Early viral response was achieved in 12 (71%), non-response in 1 patient with genotype 4, and sustained viral response in 4/5 (80%) patients with genotype 2 or 3 and 3/11 (27%) with genotype 1, p<0.05. To conclude, we found that utilizing a low initial daily RBV dose, later increased due to tolerance in combination with peg-IFN alpha-2a 180 microg weekly, was successful. Hence, all patients completed a full treatment course, which also offered a reasonable efficacy.
肝移植后丙型肝炎复发的患者通常无法耐受全剂量的聚乙二醇化干扰素(peg-IFN)和利巴韦林(RBV),并且常常过早停止治疗。我们选择了较低的初始RBV剂量,随后根据耐受性增加至平均每日600毫克(范围为每日200 - 1000毫克),并联合每周一次180微克的聚乙二醇化干扰素α-2a,以提高耐受性并尽量减少停药情况。对16例丙型肝炎复发患者和1例新发丙型肝炎病毒感染患者进行了治疗,患者平均年龄54岁(范围43 - 66岁),男性占71%。所有患者均完成了预定的治疗疗程,2型和3型疗程为24周,1型和4型疗程为48周。12例(71%)患者实现了早期病毒学应答,1例4型患者无应答,2型或3型患者中有4/5(80%)、1型患者中有3/11(27%)实现了持续病毒学应答,p<0.05。总之,我们发现采用低初始每日RBV剂量,随后根据耐受性增加,并联合每周一次180微克的聚乙二醇化干扰素α-2a是成功的。因此,所有患者均完成了整个治疗疗程,且疗效也较为合理。