Effect of drug interactions involving antiretroviral drugs on viral load in HIV population

被引:1
|
作者
Iniesta-Navalon, Carles [1 ]
Jose Franco-Miguel, Juan [1 ]
Jose Gascon-Canovas, Juan [2 ]
Rentero-Redondo, Lorena [1 ]
机构
[1] Queen Sofia Hosp Murcia, Dept Hosp Pharm, Murcia 30003, Spain
[2] Univ Murcia, Dept Publ Hlth, Murcia, Spain
关键词
PREVALENCE; RISK;
D O I
10.1136/ejhpharm-2015-000670
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background Most studies focus on potential drug interactions, without considering the effect of these on the response to antiretroviral (ARV) therapy. We assess the effect of potential drug-drug interactions (pDDIs) that could have lowered the ARV concentration (pDDI-owerARV) on HIV viral load. Methods Retrospective observational cohort study was conducted on all HIV-infected outpatients attending the Pharmacy Service of a regional reference hospital in Murcia (south-eastern Spain). The complete treatment was subsequently screened for pDDIs using the database 'Interacciones HIV.com'. The study focused on interactions involving at least one ARV drug and, especially, any pDDI-lowerARV. Results Two hundred and twenty-nine patients were included in the study. A total of 168 pDDIs were identified, of which 62 (36.9%) had the potential to lower ARV concentrations. In 77% of cases, the drug involved in the reduction of plasma concentrations was a protease inhibitor (PI), and in the rest of the drug interactions the ARV drug affected was a non-nucleoside reverse-transcriptase inhibitor. Baseline viral suppression was noted in 57.1% of patients with pDDI-lowerARV compared with 61.5% of patients without pDDI-lowerARV (p=0.605), and in 85.7% versus 79.7%, respectively, after a 24-week follow-up period (p=0.516). Conclusions This study shows that prevalence of pDDI-lowerARV was high; however, no association was found between the presence of these interactions and virological failure. These results confirm the need for further studies to understand the consequences of interactions in real-life clinical practice, since most pharmacokinetic studies tend to evaluate the ability of interaction between two drugs under controlled conditions.
引用
收藏
页码:241 / 243
页数:3
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