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Colombian experience in the treatment of hepatitis C with direct-acting antiviral agents

机译:哥伦比亚在使用直接作用抗病毒药治疗丙型肝炎方面的经验

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There are few published real-world studies on hepatitis C in Latin America. This paper describes a cohort of Colombian subjects treated with direct-acting antiviral agents. A total of 195 patients from 5 hepatology centers in 4 Colombian cities were retrospectively studied. For each patient, serum biomarkers were obtained, and Child-Pugh, MELD, cirrhosis and fibrosis stage were calculated. Additionally, viral load was quantified at initiation, end of treatment and at 12 weeks of completion. Adverse effects were recorded. Patients with liver transplant were compared with non-transplanted patients in terms of serum biomarkers. The patients had received 9 different regimes. The most prevalent viral genotype was 1b (81.5%). Overall, 186 patients (95.4%) attained sustained virologic response. When comparing transplanted vs. non-transplanted patients, those in the non-transplanted group were more likely to have cirrhosis (52.6% vs. 12.5%, p = 0.0004). Pre-treatment viral load was higher in the transplant group (1 743 575 IQR = 1 038 062-4 252 719 vs. 345 769 IQR = 125 806-842 239; p 0.0001) as well as ALT and AST levels (82.5 IQR 43.5-115.5 vs. 37.0 IQR = 24.7-73.3; p = 0.0009 and 70 IQR = 41-140 vs. 37 IQR = 24-68; p = 0.004 respectively). Adverse events were reported by 28.7% of the patients; asthenia (5.6%) was the most prevalent. Our results are comparable with those from other countries in terms of therapy and biomarkers. However, our cohort reported less adverse events. Further research is needed in the region.
机译:在拉丁美洲,很少有公开的关于丙型肝炎的现实研究。本文描述了一组用直接作用抗病毒药治疗的哥伦比亚受试者。回顾性研究了来自哥伦比亚4个城市的5个肝病中心的195名患者。为每位患者获取血清生物标志物,并计算Child-Pugh,MELD,肝硬化和纤维化分期。另外,在开始,治疗结束和完成12周时对病毒载量进行定量。记录不良反应。就血清生物标志物而言,将肝移植患者与非移植患者进行了比较。患者接受了9种不同的治疗方案。最流行的病毒基因型是1b(81.5%)。总体而言,有186例患者(95.4%)获得了持续的病毒学应答。在比较移植患者与未移植患者时,未移植组的患者更容易发生肝硬化(52.6%vs. 12.5%,p = 0.0004)。移植组的治疗前病毒载量较高(1 743 575 IQR = 1 038 062-4 252 719与345 769 IQR = 125 806-842 239; p <0.0001)以及ALT和AST水平(82.5 IQR) 43.5-115.5与37.0 IQR = 24.7-73.3; p = 0.0009和70 IQR = 41-140与37 IQR = 24-68; p = 0.004)。 28.7%的患者报告了不良事件;乏力(5.6%)是最普遍的。就治疗和生物标志物而言,我们的结果可与其他国家的结果相媲美。但是,我们的队列报道不良事件较少。该地区需要进一步的研究。

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