pubmed-article:21515757 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:21515757 | lifeskim:mentions | umls-concept:C2349001 | lld:lifeskim |
pubmed-article:21515757 | lifeskim:mentions | umls-concept:C0681850 | lld:lifeskim |
pubmed-article:21515757 | lifeskim:mentions | umls-concept:C1706203 | lld:lifeskim |
pubmed-article:21515757 | lifeskim:mentions | umls-concept:C2697811 | lld:lifeskim |
pubmed-article:21515757 | lifeskim:mentions | umls-concept:C0132326 | lld:lifeskim |
pubmed-article:21515757 | lifeskim:mentions | umls-concept:C0384228 | lld:lifeskim |
pubmed-article:21515757 | lifeskim:mentions | umls-concept:C0596545 | lld:lifeskim |
pubmed-article:21515757 | lifeskim:mentions | umls-concept:C0909839 | lld:lifeskim |
pubmed-article:21515757 | lifeskim:mentions | umls-concept:C1550501 | lld:lifeskim |
pubmed-article:21515757 | lifeskim:mentions | umls-concept:C0040808 | lld:lifeskim |
pubmed-article:21515757 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
pubmed-article:21515757 | lifeskim:mentions | umls-concept:C0205195 | lld:lifeskim |
pubmed-article:21515757 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:21515757 | pubmed:dateCreated | 2011-4-25 | lld:pubmed |
pubmed-article:21515757 | pubmed:abstractText | We retrospectively evaluated the durability and reasons for discontinuation of nevirapine (NVP) in combination with a tenofovir (TDF) and emtricitabine (FTC) or lamivudine (3TC)-containing antiretroviral therapy (ART) regimen in an Australian outpatient setting. Between January 2003 and June 2009, 64 patients (29 naïve and 35 treatment-experienced) received NVP/TDF-based regimens. The median exposure was 13.0 months (interquartile range [IQR] 6.0-20.0 months). The two- and three-year probability of continuing a NVP/TDF with FTC or 3TC regimen was 76% and 70%, respectively. Thirteen (20.3%) patients discontinued their regimen during the observation period. Reasons for discontinuation included virological failure in four (6.3%), rash in three (4.7%), lost to follow-up in three (4.7%), liver toxicity in two (3.1%) and HIV-1-related encephalopathy in one (1.6%). Long-term follow-up with a NVP/TDF-based regimen showed a low rate of discontinuation and enabled physicians to extend the use of ART over a long period, often with simplified (once-daily) regimens. | lld:pubmed |
pubmed-article:21515757 | pubmed:language | eng | lld:pubmed |
pubmed-article:21515757 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21515757 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:21515757 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21515757 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21515757 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21515757 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21515757 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21515757 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21515757 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21515757 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21515757 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21515757 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:21515757 | pubmed:month | Apr | lld:pubmed |
pubmed-article:21515757 | pubmed:issn | 1758-1052 | lld:pubmed |
pubmed-article:21515757 | pubmed:author | pubmed-author:CharD FDF | lld:pubmed |
pubmed-article:21515757 | pubmed:author | pubmed-author:SmithD EDE | lld:pubmed |
pubmed-article:21515757 | pubmed:author | pubmed-author:JeganathanSS | lld:pubmed |
pubmed-article:21515757 | pubmed:author | pubmed-author:MaruszakHH | lld:pubmed |
pubmed-article:21515757 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:21515757 | pubmed:volume | 22 | lld:pubmed |
pubmed-article:21515757 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:21515757 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:21515757 | pubmed:pagination | 228-30 | lld:pubmed |
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pubmed-article:21515757 | pubmed:year | 2011 | lld:pubmed |
pubmed-article:21515757 | pubmed:articleTitle | Clinical experience with nevirapine combined with tenofovir plus emtricitabine or lamivudine-containing regimens in HIV-infected subjects. | lld:pubmed |
pubmed-article:21515757 | pubmed:affiliation | Albion Street Centre, Surry Hills, Australia. Don.Smith@sesiahs.health.nsw.gov.au | lld:pubmed |
pubmed-article:21515757 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:21515757 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |