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Multicenter Study
. 2005 Dec 10;331(7529):1368.
doi: 10.1136/bmj.38665.534595.55. Epub 2005 Nov 18.

Time trends in primary resistance to HIV drugs in the United Kingdom: multicentre observational study

Multicenter Study

Time trends in primary resistance to HIV drugs in the United Kingdom: multicentre observational study

Patricia Cane et al. BMJ. .

Abstract

Objective: To examine whether the level of primary resistance to HIV drugs is increasing in the United Kingdom.

Design: Multicentre observational study.

Setting: All virology laboratories in the United Kingdom carrying out tests for HIV resistance as part of routine clinical care.

Participants: 2357 people infected with HIV who were tested for resistance before receiving antiretroviral therapy.

Main outcome measure: Prevalence of drug resistance on basis of the Stanford genotypic interpretation system.

Results: Over the study period (February 1996 to May 2003), 335 (14.2%, 95% confidence interval 12.8% to 15.7%) samples had mutations that conferred resistance to one or more antiretroviral drugs (9.3% high level resistance, 5.9% medium level resistance). The prevalence of primary resistance has increased markedly over time, although patterns are specific to drug class; the largest increase was for non-nucleoside reverse transcriptase inhibitors. In 2002-3, the prevalence of resistance to any antiretroviral drug to nucleoside or nucleotide reverse transcriptase inhibitors, to non-nucleoside reverse transcriptase inhibitors, or to protease inhibitors was 19.2% (15.7% to 23.2%), 12.4% (9.5% to 15.9%), 8.1% (5.8% to 11.1%), and 6.6% (4.4% to 9.3%), respectively. The risk of primary resistance was only weakly related to most demographic and clinical factors, including ethnicity and viral subtype.

Conclusions: The United Kingdom has one of the highest reported rates of primary resistance to HIV drugs worldwide. Prevalence seems still to be increasing and is high in all demographic subgroups.

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Figures

Fig 1
Fig 1
Prevalence of resistance to individual drugs
Fig 2
Fig 2
Prevalence of medium or high level drug resistance and high level drug resistance by calendar time. Values are number of samples tested at each time point

Comment in

References

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