Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1999-6-21
pubmed:databankReference
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124541, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124542, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124543, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124544, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124545, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124546, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124547, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124548, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124549, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124550, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124551, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124552, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124553, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124554, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124555, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF124556
pubmed:abstractText
Twenty human immunodeficiency virus-infected patients experiencing virologic failure of an indinavir- or ritonavir-containing treatment regimen were evaluated in a prospective, open-label study. Subjects received nelfinavir, saquinavir, abacavir, and either another nucleoside analog (n=10) or nevirapine (n=10). Patients treated with the nevirapine-containing regimen experienced significantly greater virologic suppression at week 24 than those not treated with nevirapine (P=.04). Baseline phenotypic drug susceptibility was strongly correlated with outcome in both treatment arms. Subjects with baseline virus phenotypically sensitive to 2 or 3 drugs in the salvage regimen experienced significantly greater virus load suppression than those with baseline virus sensitive to 0 or 1 drug (median week-24 change=-2.24 log and -0.35 log, respectively; P=.01). In conclusion, non-nucleoside reverse transcriptase inhibitors may represent a potent drug in salvage therapy regimens after failure of an indinavir or ritonavir regimen. Phenotypic resistance testing may provide a useful tool for selecting more effective salvage regimens.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0022-1899
pubmed:author
pubmed:issnType
Print
pubmed:volume
179
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1375-81
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:10228057-Adult, pubmed-meshheading:10228057-Dideoxynucleosides, pubmed-meshheading:10228057-Drug Resistance, Microbial, pubmed-meshheading:10228057-Drug Therapy, Combination, pubmed-meshheading:10228057-Female, pubmed-meshheading:10228057-HIV Infections, pubmed-meshheading:10228057-HIV Protease Inhibitors, pubmed-meshheading:10228057-HIV-1, pubmed-meshheading:10228057-Humans, pubmed-meshheading:10228057-Indinavir, pubmed-meshheading:10228057-Male, pubmed-meshheading:10228057-Nelfinavir, pubmed-meshheading:10228057-Nevirapine, pubmed-meshheading:10228057-Phenotype, pubmed-meshheading:10228057-Prospective Studies, pubmed-meshheading:10228057-RNA, Viral, pubmed-meshheading:10228057-Reverse Transcriptase Inhibitors, pubmed-meshheading:10228057-Ritonavir, pubmed-meshheading:10228057-Salvage Therapy, pubmed-meshheading:10228057-Saquinavir
pubmed:year
1999
pubmed:articleTitle
Novel four-drug salvage treatment regimens after failure of a human immunodeficiency virus type 1 protease inhibitor-containing regimen: antiviral activity and correlation of baseline phenotypic drug susceptibility with virologic outcome.
pubmed:affiliation
University of California, San Francisco, AIDS Program. San Francisco General Hospital, San Francisco General Hospital, San Francisco, CA 94110, USA. sdeeks@sfaids.ucsf.edu
pubmed:publicationType
Journal Article, Clinical Trial, Research Support, U.S. Gov't, P.H.S., Controlled Clinical Trial, Research Support, Non-U.S. Gov't