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肝脏失代偿可预测接受直接抗病毒药物治疗的丙型肝炎病毒患者的利巴韦林暴露过量。

Liver decompensation predicts ribavirin overexposure in hepatitis C virus patients treated with direct-acting antivirals.

作者信息

Guardigni Viola, Badia Lorenzo, Conti Matteo, Rinaldi Matteo, Mancini Rita, Viale Pierluigi, Verucchi Gabriella

机构信息

Department of Medical and Surgical Sciences, University of Bologna, S. Orsola-Malpighi Hospital, Bologna 40138, Italy.

Metropolitan Laboratory, Maggiore Hospital, Bologna 40133, Italy.

出版信息

World J Hepatol. 2017 Dec 8;9(34):1270-1277. doi: 10.4254/wjh.v9.i34.1270.

Abstract

AIM

To determine whether ribavirin (RBV) concentrations differ according to cirrhosis stage among cirrhotic patients treated with interferon-free regimens.

METHODS

We included patients with hepatitis C virus and cirrhosis [Child-Pugh (CP) A or B], Glomerular Filtration Rate ≥ 60 mL/min, who started therapy with DAAs and weight-based RBV between October 2014 and February 2016. RBV plasma levels were assessed during the treatment. We focused our analysis on the first 8 wk of therapy.

RESULTS

We studied 68 patients: 54 with compensated (CP-B) and 14 with decompensated (CP-A) cirrhosis. Patients with decompensated cirrhosis displayed significantly higher RBV concentrations than those with compensated cirrhosis at week 1, 2, 4 and 8 ( < 0.035). RBV levels were positively correlated with Hb loss over the treatment ( < 0.04). Majority (71%) of CP-B patients required a RBV dosage reduction during the treatment. After adjustment for confounders, Child-Pugh class remained significantly associated (95%CI: 35, 348, = 0.017) to RBV levels, independently from baseline per-Kg RBV dosage.

CONCLUSION

Liver decompensation might affect RBV clearance leading to an overexposure and increased related toxicities in decompensated cirrhosis. Our findings underscore the importance of an early ribavirin therapeutic drug monitoring and suggest that an initial lower RBV dose, rather than weight-based, might be considered in those with advanced liver disease (CP-B) treated with direct-acting antivirals.

摘要

目的

确定在接受无干扰素方案治疗的肝硬化患者中,利巴韦林(RBV)浓度是否因肝硬化阶段而异。

方法

我们纳入了丙型肝炎病毒和肝硬化患者[Child-Pugh(CP)A或B级],肾小球滤过率≥60 mL/分钟,于2014年10月至2016年2月开始接受直接抗病毒药物(DAA)和基于体重的RBV治疗。在治疗期间评估RBV血浆水平。我们将分析重点放在治疗的前8周。

结果

我们研究了68例患者:54例为代偿期(CP-B级)肝硬化患者,14例为失代偿期(CP-A级)肝硬化患者。在第1、2、4和8周时,失代偿期肝硬化患者的RBV浓度显著高于代偿期肝硬化患者(<0.035)。治疗期间RBV水平与血红蛋白降低呈正相关(<0.04)。大多数(71%)CP-B级患者在治疗期间需要降低RBV剂量。在对混杂因素进行校正后,Child-Pugh分级仍与RBV水平显著相关(95%CI:35,348,=0.017),独立于基线每千克RBV剂量。

结论

肝脏失代偿可能会影响RBV清除,导致失代偿期肝硬化患者药物暴露过量及相关毒性增加。我们的研究结果强调了早期进行利巴韦林治疗药物监测的重要性,并表明对于接受直接抗病毒药物治疗的晚期肝病(CP-B级)患者,可能应考虑初始使用较低而非基于体重的RBV剂量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ff9/5740096/f4d6eba68ea4/WJH-9-1270-g002.jpg

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