Hospital Carlos III, Department of Infectious Diseases, C/Sinesio Delgado 10, Madrid, 28029, Spain.
Expert Opin Drug Saf. 2013 Sep;12(5):697-707. doi: 10.1517/14740338.2013.806480. Epub 2013 Jun 4.
The number of HIV patients receiving antiretroviral therapy is increasing worldwide, as new infections continue to occur and access to drugs is scaling up in most developing regions. Due to the efficacious nature of combination antiretroviral therapy in most drug-adherent patients, the concerns on the safety profile of these lifelong medicines have attracted great attention.
Side effects of antiretroviral agents can be clinically symptomatic or manifest only as laboratory abnormalities. Drug-related toxicities can be grouped by antiretroviral drug class or damage of distinct body organs/systems. By mechanism, antiretroviral-associated adverse events generally result from hypersensitivity reactions, direct cytopathic effect, or idiosyncratic phenomena.
A good knowledge of the toxicity profile of antiretroviral agents is warranted for HIV care providers in order to prevent and avoid unwanted complications.
随着新的感染继续发生,并且在大多数发展中地区扩大了药物获取途径,接受抗逆转录病毒疗法的艾滋病毒感染者人数在全球范围内不断增加。由于联合抗逆转录病毒疗法在大多数依从性药物的患者中的疗效,人们对这些终身药物的安全性特征的关注引起了极大的关注。
抗逆转录病毒药物的副作用可能具有临床症状,或者仅表现为实验室异常。药物相关的毒性可以按抗逆转录病毒药物类别或特定器官/系统的损害进行分组。根据机制,抗逆转录病毒相关的不良事件通常是由于过敏反应、直接细胞毒性作用或特发性现象引起的。
为了预防和避免不必要的并发症,艾滋病毒护理提供者需要充分了解抗逆转录病毒药物的毒性特征。