Begovac Josip
Klinika za infektivne bolesti "Dr. Fran Mihaljević", Zagreb, Hrvatska.
Acta Med Croatica. 2005;59(5):473-8.
Treatment of chronic hepatitis C in patients infected with the human immunodeficiency virus (HIV) is recommended when: 1) aminotransferase levels are repeatedly elevated; 2) CD4+ blood cell counts are above 350 per microl; and 3) HIV RNA plasma levels are less than 50 000 copies per milliliter. Treatment is not recommended for patients who inject illegal drugs, consume large amount of alcohol, or have a severe psychiatric disorder. Treatment of patients with normal aminotransferase levels can be considered in the context of a clinical trial or if stage F2 or worse has been histologically confirmed on a liver biopsy specimen. Liver biopsy is generally recommended prior to treatment. However, because of faster progression to fibrosis in HIV and hepatitis C virus (HCV) coinfected patients, if the patient declines liver biopsy it should not exclude him from treatment. Treatment with interferon and ribavirin (800 mg/day orally) is recommended. Pegylated interferon is preferred (180 microg of alfa-2a form and 1.5 mg/kg of alfa-2b form once weekly subcutaneously) because of poor results with the conventional form of interferon, however, treatment with conventional interferon (3 times weekly 3 million units subcutaneously) can be considered in HCV genotype 2 or 3 infection. All genotypes should be treated for 48 weeks. Since only patients who have a decline of HCV viremia of at least 2 logarithms after 12 weeks of treatment have a chance of cure, treatment should be discontinued in patients who do not achieve this target. Concurrent treatment with zidovudine and didanosine should be avoided because of additive toxicity. One should also be cautious when antiretroviral drugs with a greater potential for hepatotoxicity (nevirapine, ritonavir) are concurrently administered.
在以下情况下,建议对感染人类免疫缺陷病毒(HIV)的慢性丙型肝炎患者进行治疗:1)氨基转移酶水平反复升高;2)CD4 +血细胞计数高于每微升350;3)HIV RNA血浆水平低于每毫升50000拷贝。不建议对注射非法药物、大量饮酒或患有严重精神疾病的患者进行治疗。在临床试验背景下,或肝活检标本经组织学证实为F2期或更严重时,可考虑对氨基转移酶水平正常的患者进行治疗。一般建议在治疗前进行肝活检。然而,由于HIV和丙型肝炎病毒(HCV)合并感染患者的纤维化进展更快,如果患者拒绝肝活检,不应将其排除在治疗之外。建议使用干扰素和利巴韦林(口服800毫克/天)进行治疗。由于传统形式的干扰素效果不佳,聚乙二醇化干扰素更受青睐(α-2a形式180微克和α-2b形式1.5毫克/千克,每周一次皮下注射),但是,对于HCV基因型2或3感染,可考虑使用传统干扰素(每周三次,皮下注射300万单位)。所有基因型均应治疗48周。由于只有在治疗12周后HCV病毒血症下降至少2个对数的患者才有治愈的机会,因此未达到该目标的患者应停止治疗。应避免同时使用齐多夫定和去羟肌苷,因为会产生累加毒性。同时使用具有更大肝毒性潜力的抗逆转录病毒药物(奈韦拉平、利托那韦)时也应谨慎。