rdf:type |
|
lifeskim:mentions |
umls-concept:C0003451,
umls-concept:C0012655,
umls-concept:C0013227,
umls-concept:C0019704,
umls-concept:C0030946,
umls-concept:C0040808,
umls-concept:C0205314,
umls-concept:C0205466,
umls-concept:C0231174,
umls-concept:C0441655,
umls-concept:C0442967,
umls-concept:C0679622,
umls-concept:C1274040,
umls-concept:C1442488,
umls-concept:C1707520
|
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 |
http://linkedlifedata.com/resource/pubmed/chemical/Dideoxynucleosides,
http://linkedlifedata.com/resource/pubmed/chemical/HIV Protease Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Indinavir,
http://linkedlifedata.com/resource/pubmed/chemical/Nelfinavir,
http://linkedlifedata.com/resource/pubmed/chemical/Nevirapine,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Viral,
http://linkedlifedata.com/resource/pubmed/chemical/Reverse Transcriptase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Ritonavir,
http://linkedlifedata.com/resource/pubmed/chemical/Saquinavir,
http://linkedlifedata.com/resource/pubmed/chemical/abacavir
|
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
|