Source:http://linkedlifedata.com/resource/pubmed/id/20335191
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2010-5-13
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pubmed:abstractText |
Recent advances in the development of agents that act specifically to inhibit hepatitis C virus (HCV) are set to fundamentally change the way that patients will be treated. New directly acting anti-HCV agents such as protease and polymerase inhibitors will initially be added to standard of care with pegylated interferon-alpha and ribavirin. However, future therapy is likely to constitute combinations of agents which act at distinct stages of viral replication and have differing resistance profiles. While directly acting anti-HCV agents will undoubtedly improve treatment outcomes, the introduction of combination therapy may not be without complications in some patient groups. HIV-positive patients who are receiving antiretrovirals (ARVs) are relatively highly represented among those with HCV infection, and are at high risk of drug-drug interactions (DDIs). As combination anti-HCV treatment gradually evolves to resemble anti-HIV therapy, it is essential to consider the increased potential for DDIs in patients receiving combination anti-HCV therapy, and particularly in HCV/HIV-co-infected individuals. Therapeutic drug monitoring is likely to play a role in the clinical management of such interactions.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/2'-deoxy-2'-fluoro-2'-C-methylcytidi...,
http://linkedlifedata.com/resource/pubmed/chemical/Anti-HIV Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Antiviral Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Deoxycytidine,
http://linkedlifedata.com/resource/pubmed/chemical/N-(3-amino-1-(cyclobutylmethyl)-2,3-...,
http://linkedlifedata.com/resource/pubmed/chemical/Oligopeptides,
http://linkedlifedata.com/resource/pubmed/chemical/Proline,
http://linkedlifedata.com/resource/pubmed/chemical/telaprevir
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1460-2091
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
65
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1079-85
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pubmed:meshHeading |
pubmed-meshheading:20335191-Anti-HIV Agents,
pubmed-meshheading:20335191-Antiviral Agents,
pubmed-meshheading:20335191-Clinical Trials as Topic,
pubmed-meshheading:20335191-Deoxycytidine,
pubmed-meshheading:20335191-Drug Interactions,
pubmed-meshheading:20335191-Drug Monitoring,
pubmed-meshheading:20335191-Drug Therapy, Combination,
pubmed-meshheading:20335191-HIV Infections,
pubmed-meshheading:20335191-Hepatitis C,
pubmed-meshheading:20335191-Humans,
pubmed-meshheading:20335191-Oligopeptides,
pubmed-meshheading:20335191-Proline
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pubmed:year |
2010
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pubmed:articleTitle |
New directly acting antivirals for hepatitis C: potential for interaction with antiretrovirals.
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pubmed:affiliation |
NIHR Biomedical Research Centre, Royal Liverpool & Broadgreen University Hospitals Trust, and Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK. kseden@liverpool.ac.uk
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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