The frequency and reasons for antiretroviral switching with specific antiretroviral associations: The SWITCH study

被引:30
作者
Davidson, I. [2 ]
Beardsell, H. [2 ]
Smith, B. [2 ]
Mandalia, S. [2 ]
Bower, M. [1 ]
Gazzard, B. [2 ]
Nelson, M. [2 ]
Stebbing, J. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Sch Med, Chelsea & Westminster Hosp, London, England
[2] Chelsea & Westminster Hosp Trust, St Stephens Ctr, London, England
关键词
Adherence; Compliance; Toxicity; Switching; Antiretroviral; HAART; ADULT HIV-INFECTION; SOCIETY-USA PANEL; RECOMMENDATIONS; ADHERENCE; TENOFOVIR; THERAPY;
D O I
10.1016/j.antiviral.2010.03.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: We investigated the reasons for switching antiretroviral regimens, an issue rarely addressed in cohort studies. Methods: An observed toxicity switch rate (OTSR) was calculated by Poisson regression using the number of days individuals received each individual antiretroviral drug. Results: Of 3333 individuals receiving HAART, a total of 14% of regimens were switched, the majority occurring after 6 months of therapy. Toxicity was the major reason for switching (61%) and there were no major statistically significant differences in OTSR between the protease inhibitor (OTSR 26.4, 95% CI 18.3-37) and non-nucleoside reverse transcriptase inhibitor (OTSR 22.2,95% CI 13.6-34.4) based regimes. For individual antiretrovirals, stavudine and zidovudine had significantly higher "switch" scores than all other drugs. Conclusions: There were no differences between the major HAART classes in OTSR. We suggest that newer antiretrovirals will require differentiation in terms of longer-term toxicity, as this is the major reason for switching. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:227 / 229
页数:3
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