San Francisco General Hospital, University of California San Francisco, 1001 Potrero Avenue, Ward 93/95, San Francisco, CA 94110, USA.
Curr HIV/AIDS Rep. 2010 Aug;7(3):152-60. doi: 10.1007/s11904-010-0048-2.
While street drugs appear unlikely to alter the metabolism of antiretroviral (ARV) medications, several ARVs may induce or inhibit metabolism of various street drugs. However, research on these interactions is limited. Case reports have documented life-threatening overdoses of ecstasy and gamma-hydroxybutyrate after starting ritonavir, an ARV that inhibits several metabolic enzymes. For opioid addiction, methadone or buprenorphine are the treatments of choice. Because a number of ARVs decrease or increase methadone levels, patients should be monitored for methadone withdrawal or toxicity when they start or stop ARVs. Most ARVs do not cause buprenorphine withdrawal or toxicity, even if they alter buprenorphine levels, with rare exceptions to date including atazanavir/ritonavir associated with significant increases in buprenorphine and adverse events related to sedation and mental status changes in some cases. There are newer medications yet to be studied with methadone or buprenorphine. Further, there are many frequently used medications in treatment of complications of HIV disease that have not been studied. There is need for continuing research to define these drug interactions and their clinical significance.
虽然街头毒品不太可能改变抗逆转录病毒(ARV)药物的代谢,但几种 ARV 可能会诱导或抑制各种街头毒品的代谢。然而,关于这些相互作用的研究有限。有病例报告记录了在开始使用利托那韦(一种抑制多种代谢酶的 ARV)后,摇头丸和γ-羟基丁酸的致命过量。对于阿片类药物成瘾,美沙酮或丁丙诺啡是首选的治疗方法。由于一些 ARV 会降低或增加美沙酮的水平,因此当患者开始或停止使用 ARV 时,应监测其是否出现美沙酮戒断或毒性。大多数 ARV 不会引起丁丙诺啡戒断或毒性,即使它们改变了丁丙诺啡的水平,到目前为止,只有少数例外,包括与丁丙诺啡显著增加以及一些情况下与镇静和精神状态改变相关的不良事件相关的阿扎那韦/利托那韦。还有一些与美沙酮或丁丙诺啡相关的新药尚未研究。此外,在治疗 HIV 疾病并发症的常用药物中,还有许多药物尚未进行研究。需要继续研究以确定这些药物相互作用及其临床意义。