Debnath Prasanta, Chandnani Sanjay, Rathi Pravin, Nair Sujit, Pawar Vinay, Contractor Qais
T.N.M.C & B.Y.L Nair Charitable Hospital, Gastroenterology, Mumbai, India.
Arq Gastroenterol. 2020 Jan-Mar;57(1):39-44. doi: 10.1590/S0004-2803.202000000-08.
Hepatitis C virus (HCV) infection is the most common hepatotropic viral infection affecting the patients on maintenance hemodialysis. Treatment of chronic HCV infection in stage 4 and 5 CKD includes a combination of elbasvir/grazoprevir and glecaprevir/pibrentasvir, which are not available in many countries.
Hence, we have conducted this study to look for the safety and efficacy of sofosbuvir combination therapy in this difficult to treat population.
We conducted a single-center, prospective, open-label study in which Stage 5 CKD patients on maintenance hemodialysis with HCV infection. Total of 18 patients was included. sofosbuvir with daclatasvir or ledipasvir was used according to genotype for 12 weeks. HCV RNA, genotype, transient elastography (TE) was considered for every patient. HCV RNA was quantified at 4th week, 12th week and 12 weeks post-treatment to look for sustained virologic response (SVR 12).
Infection due to genotype 1 was seen in 12 (66.7%) patients followed by genotype 3 in 4 (22.3%) with each patient of genotype 2 and 5. The median value of HCV RNA was 2,35,000 IU/mL. On TE, all had liver stiffness of <9.4 KPa. All patients had HCV RNA of <15 IU/mL at 4th and 12th week of treatment and 12 weeks post-treatment. No significant change in hemoglobin, eGFR and liver stiffness was observed.
Full dose sofosbuvir i.e. 400 mg, in combination with NS5A inhibitors daclatasvir or ledipasvir is found to be safe and effective in patients with end stage renal disease, who are on maintenance hemodialysis.
丙型肝炎病毒(HCV)感染是影响维持性血液透析患者的最常见嗜肝病毒感染。4期和5期慢性肾脏病患者慢性HCV感染的治疗包括艾尔巴韦/格拉瑞韦和格卡瑞韦/哌仑他韦联合用药,但许多国家没有这些药物。
因此,我们开展了这项研究,以探寻索磷布韦联合疗法在这一难治性人群中的安全性和疗效。
我们进行了一项单中心、前瞻性、开放标签研究,纳入维持性血液透析的5期慢性肾脏病合并HCV感染患者。共纳入18例患者。根据基因型,使用索磷布韦联合达卡他韦或来迪派韦治疗12周。对每位患者检测HCV RNA、基因型、瞬时弹性成像(TE)。在治疗第4周、第12周以及治疗后12周对HCV RNA进行定量检测,以评估持续病毒学应答(SVR 12)。
12例(66.7%)患者为1型感染,4例(22.3%)为3型感染,各有1例2型和5型感染患者。HCV RNA的中位数为235,000 IU/mL。在TE检测中,所有患者的肝脏硬度均<9.4 KPa。所有患者在治疗第4周、第12周以及治疗后12周时HCV RNA均<15 IU/mL。未观察到血红蛋白、估算肾小球滤过率和肝脏硬度有显著变化。
对于接受维持性血液透析的终末期肾病患者,发现全剂量索磷布韦(即400 mg)联合NS5A抑制剂达卡他韦或来迪派韦是安全有效的。