Experience with direct-acting antivirals in genotype 1-5 infected chronic hepatitis C patients in Turkey.

Annals of Saudi medicine Pub Date : 2023-09-01 Epub Date: 2023-10-05 DOI:10.5144/0256-4947.2023.308
Ahmet Sahin, Ozlem Akay
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Abstract

Background: Hepatitis C virus (HCV) can cause chronic liver disease, hepatic cirrhosis, hepatocellular carcinoma, liver transplantation, and death. Early diagnosis and treatment are thus vital.

Objectives: We aimed to investigate the sustained virological response (SVR) rates in chronic hepatitis C patients infected with different genotypes, receiving different direct-acting antiviral treatments (DAAs).

Design: Retrospective, observational SETTING: Clinic for infectious diseases and clinical microbiology PATIENTS AND METHODS: Patients diagnosed with chronic hepatitis C who applied to our outpatient clinic between January 2016 and November 2022 and were treated with a DAA were included in the study. Treatment responses were evaluated after each patient was treated with either ledipasvir plus sofosbuvir (LDV/SOF), LDV/SOF + ribavirin (RBV), SOF+RBV, ombitasvir/paritaprevir/ritonavir plus dasabuvir (OBV/PTV/r±DSV) ±RBV, or glecaprevir plus pibrentasvir (GLE/PIB).

Main outcome measures: Sustained virological response (SVR) rates at 12 weeks (SVR12) post-treatment.

Sample size: 360 patients.

Results: Of 360 patients who met the inclusion criteria, 218 (60.6%) were male and 142 (39.4%) were female with no statistically significant differences in SVR between sexes (P=.252). Nearly all had a SVR (n=353, 98.1%). The median (IQR) age of the patients was 56 (30.3) years. There were 42 (11.7%), 199 (55.3%), 4 (1.1%), 106 (29.4%), 8 (2.2%) and 1 (0.3%) patient with genotypes 1a, 1b, 2, 3, 4 and 5, respectively, and SVR12 did not differ significantly between genotypes (P=.066). SVR12 response was higher in 246 (68.3%) non-injecting drug users compared to 114 (31.7%) injecting drug users (P=.005). The SVR12 response was achieved in 100% of patients with genotypes 1a, 2, 4, and 5. SVR12 response could not be obtained in 1 of 199 genotype 1b patients and 6 of 106 genotype 3 patients. The common feature of 6 reinfection patients with genotype 3 was that they were using intravenous drugs. These 6 patients were reinfected due to their continued intravenous drug use.

Conclusion: In conclusion, DAAs provide high SVR12 rates in cirrhotic/non-cirrhotic, pegylated interferon-naive/experienced patient groups and in patients infected with all genotypes. DAAs have a high SVR12 rate in patients with chronic hepatitis C.

Limitations: Retrospective, single-center.

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土耳其1-5型感染的慢性丙型肝炎患者使用直接作用抗病毒药物的经验。
背景:丙型肝炎病毒(HCV)可引起慢性肝病、肝硬化、肝细胞癌、肝移植和死亡。因此,早期诊断和治疗至关重要。目的:我们旨在研究不同基因型感染的慢性丙型肝炎患者接受不同直接作用抗病毒治疗(DAAs)的持续病毒学应答(SVR)率,观察环境:传染病和临床微生物学诊所患者和方法:2016年1月至2022年11月期间申请我们门诊并接受DAA治疗的被诊断为慢性丙型肝炎的患者被纳入研究。在每位患者接受乐迪帕韦加索非布韦(LDV/SOF)、LDV/SOF+利巴韦林(RBV)、SOF+RBV、奥比他韦/帕利他韦/利托那韦加达沙布韦(OBV/PTV/r±DSV)±RBV或格列卡韦加皮布伦他韦(GLE/PIB)治疗后,评估治疗反应。主要结果指标:治疗后12周的持续病毒学反应(SVR)率(SVR12)。样本量:360名患者。结果:在符合纳入标准的360名患者中,218名(60.6%)为男性,142名(39.4%)为女性,性别间SVR无统计学显著差异(P=.252)。几乎所有患者都有SVR(n=353,98.1%)。患者的中位(IQR)年龄为56(30.3)岁。基因型1a、1b、2、3、4和5的患者分别为42例(11.7%)、199例(55.3%)、4例(1.1%)、106例(29.4%)、8例(2.2%)和1例(0.3%),不同基因型的SVR12无显著差异(P=.066),2、4和5。199例基因型1b患者中有1例和106例基因型3患者中有6例不能获得SVR12应答。6例基因型为3的再次感染患者的共同特征是他们正在使用静脉注射药物。这6名患者因持续静脉注射药物而再次感染。结论:总之,DAAs在肝硬化/非肝硬化、聚乙二醇干扰素初始/经验丰富的患者组以及所有基因型感染的患者中提供了高SVR12率。DAA在慢性丙型肝炎患者中具有较高的SVR12比率。局限性:回顾性,单中心。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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