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在临床实践中,HIV/丙型肝炎病毒合并感染患者中直接作用抗病毒药物与伴随治疗之间潜在相互作用的高发生率。

High frequency of potential interactions between direct-acting antivirals and concomitant therapy in HIV/hepatitis C virus-coinfected patients in clinical practice.

作者信息

Macías J, Monge P, Mancebo M, Merchante N, Neukam K, Real L M, Pineda J A

机构信息

Infectious Diseases and Microbiology Unit, Hospital Universitario de Valme, Seville, Spain.

Instituto de Biomedicina de Sevilla (IBiS), Seville, Spain.

出版信息

HIV Med. 2017 Aug;18(7):445-451. doi: 10.1111/hiv.12471. Epub 2016 Nov 24.

Abstract

OBJECTIVES

The aim of the study was to analyse the frequency and degree of potential drug-drug interactions (DDIs) between direct-acting antivirals (DAAs) and concomitant medication used by HIV/hepatitis C virus (HCV)-coinfected patients, including antiretroviral therapy (ART) and other drugs.

METHODS

All patients with HIV infection and viraemic HCV genotype 1, 3 or 4 coinfection attending a tertiary care centre in Spain (November 2014 to November 2015) were included in the study. DDIs were classified as major, i.e. drugs should not be co-administered, or minor, i.e. close monitoring, dosage alteration or change in timing may be required if drugs are co-administered, following the http://www.hep-druginteractions.org database recommendations.

RESULTS

A total of 244 patients were included in the study, of whom 224 (92%) were previous injecting drug users. Major DDIs were found for: paritaprevir-r/ombitasvir plus dasabuvir (3D), in 60 (44%) of 138 individuals with genotype 1; paritaprevir-r/ombitasvir (2D), in 22 (37%) of 60 individuals with genotype 4; sofosbuvir/ledipasvir (SOF/LDV), in four (2%) of 198 patients with genotype 1 or 4; simeprevir (SMV) plus SOF, in 160 (81%) of 198 patients with genotype 1 or 4; daclatasvir (DCV) plus SOF, in seven (3%) of 244 patients with genotype 1, 3 or 4 (P < 0.001). Minor DDIs were found for: 3D, in 123 (89%) individuals with genotype 1; 2D, in 52 (87%) individuals with genotype 4; SOF/LDV, in 154 (78%) patients with genotype 1 or 4; SMV plus SOF, in 129 (65%) patients with genotype 1 or 4; DCV plus SOF, in 149 (61%) patients with genotype 1, 3 or 4 (P < 0.001).

CONCLUSIONS

Drug-drug interactions between DAAs and ART or other commonly prescribed medications are frequently found among HIV/HCV-coinfected patients. Potential major and minor DDIs are more frequent with 3D, 2D and SMV plus SOF regimens.

摘要

目的

本研究旨在分析直接作用抗病毒药物(DAA)与人类免疫缺陷病毒(HIV)/丙型肝炎病毒(HCV)合并感染患者所使用的伴随用药(包括抗逆转录病毒疗法(ART)和其他药物)之间潜在药物相互作用(DDI)的频率和程度。

方法

纳入在西班牙一家三级护理中心就诊的所有HIV感染且HCV 1、3或4型病毒血症合并感染患者(2014年11月至2015年11月)。根据http://www.hep-druginteractions.org数据库的建议,DDI被分类为主要相互作用(即药物不应联合使用)或次要相互作用(即如果联合使用药物,可能需要密切监测、调整剂量或改变用药时间)。

结果

本研究共纳入244例患者,其中224例(92%)曾是注射吸毒者。发现主要DDI的情况如下:对于138例1型基因型个体中的60例(44%),帕利瑞韦-r/奥比他韦加达沙布韦(3D);对于60例4型基因型个体中的22例(37%),帕利瑞韦-r/奥比他韦(2D);对于198例1型或4型基因型患者中的4例(2%),索磷布韦/来迪派韦(SOF/LDV);对于198例1型或4型基因型患者中的160例(81%),simeprevir(SMV)加SOF;对于244例1型、3型或4型基因型患者中的7例(3%),达卡他韦(DCV)加SOF(P<0.001)。发现次要DDI的情况如下:对于1型基因型的123例个体中的123例(89%)为3D;对于4型基因型的52例个体中的52例(87%)为2D;对于1型或4型基因型的154例患者中的154例(78%)为SOF/LDV;对于1型或4型基因型的129例患者中的129例(65%)为SMV加SOF;对于1型、3型或4型基因型的149例患者中的149例(61%)为DCV加SOF(P<0.001)。

结论

在HIV/HCV合并感染患者中,经常发现DAA与ART或其他常用处方药之间存在药物相互作用。3D、2D以及SMV加SOF方案出现潜在主要和次要DDI的频率更高。

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