首页|减量索磷布韦联合全量达卡他韦治疗终末期肾病合并急性丙型肝炎患者临床疗效研究

减量索磷布韦联合全量达卡他韦治疗终末期肾病合并急性丙型肝炎患者临床疗效研究

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目的 应用半量索磷布韦联合全量达卡他韦治疗长期血液透析的终末期肾病(ESRD)合并急性丙型肝炎(AHC)患者的临床效果。方法 2020 年6 月~2022 年1 月我院诊治的长期接受血液透析的ESRD合并AHC患者49 例,被随机分为观察组25 例和对照组24 例,分别接受半量索磷布韦联合全量达卡他韦治疗或全量索磷布韦联合全量的达卡他韦治疗12 周。使用全自动病毒载量分析系统检测血清HCV RNA载量。使用流式细胞仪检测外周血T淋巴细胞亚群。结果 观察组获得早期病毒学应答、治疗结束病毒学应答、随访12 周和24 周持续病毒学应答率分别为 72。0%、96。0%、88。0%和88。0%,与对照组的70。8%、95。8%、87。5%和87。5%比,差异无统计学意义(P>0。05);在治疗结束时,观察组估算的肾小球滤过率(eGFR)为(12。5±1。0)ml/min·1。73m2,显著高于对照组[(9。0±1。0)ml/min·1。73m2,P<0。05],而血清肌酐(sCr)水平为(448。5±11。7)μmol/L,显著低于对照组[(477。4±12。6)μmol/L,P<0。05];治疗前后两组外周血CD4+细胞和CD8+细胞百分比及CD4+/CD8+细胞比值均无显著性差异(P>0。05);观察组不良反应发生率为4。0%,显著低于对照组的25。0%(P<0。05)。结论 应用半量索磷布韦联合全量达卡他韦治疗长期血液透析的ESRD合并AHC患者不影响抗病毒疗效,但可减轻肾功能损伤,值得进一步研究,优化治疗方案。
Similar virological response to half-dose of sofosbuvir and full-dose of daclatasvir therapy in patients with end-stage renal disease and acute hepatitis C
Objective The aim of this study was to observe the virological response to half-dose of sofosbuvir and full-dose of daclatasvir therapy in patients with end-stage renal disease(ESRD)and acute hepatitis C(AHC).Methods 49 patients with ESRD and AHC who underwent long-term hemodialysis in our hospital were enrolled between June 2020 and January 2022,and were randomly divided into observation(n=25)and control(n=24)groups,receiving half-dose of sofosbuvir and full-dose of daclatasvir or full-dose of sofosbuvir and full-dose of daclatasvir antiviral therapy for 12 weeks.Serum HCV RNA load was detected by RT-PCR,and the peripheral blood T lymphocyte subsets were detected by flow cytometry.Results The rapid virological response,end-of-treatment virological response,12-week sustained virological response(SVR12)and SVR24 in the observation group were 72.0%,96.0%,88.0%and 88.0%,not significantly different compared to 70.8%,95.8%,87.5%and 87.5%in the control group(P>0.05);at the end of antiviral treatment,the estimated glomerular filtration ratein the observation group was(12.5±1.0)ml/min·1.73m2,much higher than[(9.0±1.0)ml/min·1.73m2,P<0.05],while serum creatinine level was(448.5±11.7)μmol/L,much lower than[(477.4±12.6)μmol/L,P<0.05]in the control;there were no significant differences as respect to the percentages of peripheral blood CD4+cells and CD8+cell as well as the CD4+/CD8+cell ratio between the two groups at the end of antiviral treatment or of the follow-up(P>0.05);the incidence of untoward effects in the observation group during the antiviral therapy was 4.0%,much lower than 25.0%(P<0.05)in the control group.Conclusion The modified half-dose of sofosbuvir and full-dose of daclatasvirin treating patients with ESRD and AHC is relatively efficacious,which might meet the request of antiviral therapy and the reduction of renal function injury,and needs multi-central verification.

Hepatitis CEnd-stage renal diseaseSofosbuvirDaclatasvirTherapy

于欣欣、付朝霞、薛莉

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266100 山东省青岛市第八人民医院肾内科

266100 山东省青岛市第八人民医院消化内科

青岛大学附属医院健康管理中心

丙型肝炎 终末期肾病 索磷布韦 达卡他韦 治疗

青岛市科技局科研基金资助项目

2021LK03140

2024

实用肝脏病杂志
中华医学会安徽分会

实用肝脏病杂志

CSTPCD
影响因子:1.362
ISSN:1672-5069
年,卷(期):2024.27(2)
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