Iniesta-Navalón Carles, Franco-Miguel Juan José, Gascón-Cánovas Juan José, Rentero-Redondo Lorena
Department of Hospital Pharmacy, Queen Sofia Hospital of Murcia, Murcia, Spain.
Department of Public Health, University of Murcia, Murcia, Spain.
Eur J Hosp Pharm. 2016 Jul;23(4):241-243. doi: 10.1136/ejhpharm-2015-000670. Epub 2015 Jun 18.
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-lowerARV) on HIV viral load.
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 'InteraccionesHIV.com'. The study focused on interactions involving at least one ARV drug and, especially, any pDDI-lowerARV.
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).
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.
大多数研究聚焦于潜在药物相互作用,而未考虑其对抗逆转录病毒(ARV)治疗反应的影响。我们评估了可能降低ARV浓度的潜在药物-药物相互作用(pDDI)对HIV病毒载量的影响。
对西班牙东南部穆尔西亚一家地区参考医院药房服务的所有HIV感染门诊患者进行回顾性观察队列研究。随后使用“InteraccionesHIV.com”数据库对完整治疗方案进行pDDI筛查。该研究重点关注涉及至少一种ARV药物的相互作用,尤其是任何可能降低ARV浓度的pDDI。
229名患者纳入研究。共识别出168种pDDI,其中62种(36.9%)有可能降低ARV浓度。在77%的病例中,参与降低血浆浓度的药物是蛋白酶抑制剂(PI),在其余药物相互作用中,受影响的ARV药物是非核苷类逆转录酶抑制剂。有pDDI且降低ARV浓度的患者中,57.1%在基线时病毒得到抑制,而无此类pDDI的患者中这一比例为61.5%(p = 0.605);在24周随访期后,这两个比例分别为85.7%和79.7%(p = 0.516)。
本研究表明,有可能降低ARV浓度的pDDI发生率较高;然而,未发现这些相互作用的存在与病毒学失败之间存在关联。这些结果证实有必要进行进一步研究,以了解现实临床实践中相互作用的后果,因为大多数药代动力学研究倾向于在受控条件下评估两种药物之间相互作用的能力。