Drug-Drug Interactions in the Treatment of HCV Among People Who Inject Drugs

被引:11
|
作者
Mauss, Stefan [1 ]
Klinker, Hartwig [2 ]
机构
[1] Ctr HIV & Hepatogastroenterol, D-40237 Dusseldorf, Germany
[2] Univ Wurzburg, Med Ctr, Dept Internal Med 2, Div Infect Dis, Wurzburg, Germany
关键词
HCV; drug interactions; telaprevir; boceprevir; drugs; addiction; mental health; PROTEASE INHIBITOR BOCEPREVIR; HEPATITIS-C; PHARMACOKINETIC INTERACTION; HIV/HCV-COINFECTION; TELAPREVIR; ATORVASTATIN; CYCLOSPORINE; TACROLIMUS; VOLUNTEERS; THERAPY;
D O I
10.1093/cid/cit299
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Boceprevir and telaprevir are inhibitors and substrates of the cytochrome P450 3A4 family. With the use of these HCV protease inhibitors as part of standard therapy for chronic hepatitis C genotype 1 infection, drug-drug interactions with multiple medications being inductors, inhibitors, or substrates of cytochrome P450 3A4 can be expected. Due to the complexity of these interactions, predicting the expected magnitude and sometimes even the direction of the effect has proven to be difficult. Pharmacokinetic studies should be carried out to evaluate drugs with clinical relevance and possible interactions. This review focuses on the data available regarding drugs that are frequently used in the setting of addiction or used by patients with addiction. In addition to highlighting relevant drug-drug interactions, alternative drugs that can be safely used are suggested.
引用
收藏
页码:S125 / S128
页数:4
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