Back to Search
Start Over
Genotypic and phenotypic resistance testing of HIV-1 in routine clinical care
- Source :
- European Journal of Clinical Microbiology & Infectious Diseases. 24:733-738
- Publication Year :
- 2005
- Publisher :
- Springer Science and Business Media LLC, 2005.
-
Abstract
- Data on genotypic and phenotypic resistance testing of HIV-1 in the routine clinical setting are lacking. In a retrospective single-center study, all patients (n = 102) for whom genotypic resistance typing (GRT) and phenotypic resistance typing (PRT) were performed during the calendar year 2002 were examined. GRT and PRT results were concordant for 79% of the drugs, being highest for nevirapine (92%) and lowest for didanosine (57%). Concordance of results for protease inhibitors was lowest for lopinavir (78%) and highest for indinavir (88%). Discordant results for lamivudine were observed in 16% of patients; 90% of these results corresponded to high-level resistance by PRT and susceptibility by GRT. Overall, HIV loads were lower and CD4+ cell counts higher after therapy following resistance testing, but a significant association with the number of active drugs as predicted by GRT or PRT could not be identified. In a subgroup of 43 patients with virological failure under antiretroviral therapy and sufficient follow-up data, HIV loads were significantly lower after 3 and 6 months. More patients with HIV loads
- Subjects :
- Adult
Male
Microbiology (medical)
medicine.medical_specialty
Nevirapine
Genotype
Anti-HIV Agents
Population
HIV Infections
Drug resistance
Biology
Ambulatory Care Facilities
Indinavir
Internal medicine
Drug Resistance, Viral
medicine
Humans
education
Didanosine
Aged
education.field_of_study
food and beverages
Lamivudine
Lopinavir
General Medicine
Middle Aged
Viral Load
Phenotype
Infectious Diseases
Immunology
HIV-1
Female
Viral load
medicine.drug
Subjects
Details
- ISSN :
- 14354373 and 09349723
- Volume :
- 24
- Database :
- OpenAIRE
- Journal :
- European Journal of Clinical Microbiology & Infectious Diseases
- Accession number :
- edsair.doi.dedup.....f92ce799bf74791aa91322302de0c513
- Full Text :
- https://doi.org/10.1007/s10096-005-0044-4