Division of Nephrology, Johns Hopkins University , Baltimore, MD, US.
Division of Pediatric Nephrology, Johns Hopkins University , Baltimore, MD, US.
Expert Opin Pharmacother. 2021 Jan;22(1):69-82. doi: 10.1080/14656566.2020.1817383. Epub 2020 Sep 21.
Since the developmentof combined antiretroviral therapy (cART), HIV-associated mortality and the incidence of HIV-associated end-stage kidney disease (ESKD) has decreased. However, in the United States, an increase in non-HIV-associated kidney diseases within the HIV-positive population is expected.
In this review, the authors highlight the risk factors for kidney disease within an HIV-positive population and provide the current recommendations for risk stratification and for the monitoring of its progression to chronic kidney disease (CKD), as well as, treatment. The article is based on literature searches using PubMed, Medline and SCOPUS.
The authors recommend clinicians (1) be aware of early cART initiation to prevent and treat HIV-associated kidney diseases, (2) be aware of cART side effects and discriminate those that may become more nephrotoxic than others and require dose-adjustment in the setting of eGFR ≤ 30ml/min/1.73m, (3) follow KDIGO guidelines regarding screening and monitoring for CKD with a multidisciplinary team of health professionals, (4) manage other co-infections and comorbidities, (5) consider changing cART if drug induced toxicity is established with apparent eGFR decline of ≥ 10ml/min/1.73m or rising creatinine (≥0.5mg/dl) during drug-drug interactions, and (6) strongly consider kidney transplant in appropriately selected individuals with end stage kidney failure.
自联合抗逆转录病毒疗法(cART)发展以来,HIV 相关死亡率和 HIV 相关终末期肾病(ESKD)的发病率有所下降。然而,预计在美国,HIV 阳性人群中非 HIV 相关肾脏疾病的发病率将会增加。
在这篇综述中,作者强调了 HIV 阳性人群中肾脏疾病的危险因素,并提供了目前用于风险分层以及监测其进展为慢性肾脏病(CKD)的建议,以及治疗方法。本文基于使用 PubMed、Medline 和 SCOPUS 进行的文献检索。
作者建议临床医生(1)了解早期 cART 启动以预防和治疗 HIV 相关肾脏疾病,(2)了解 cART 的副作用,并区分那些可能比其他药物更具肾毒性且需要在 eGFR ≤ 30ml/min/1.73m 时调整剂量的药物,(3)遵循 KDIGO 指南,由多学科卫生专业人员团队进行 CKD 的筛查和监测,(4)管理其他合并感染和合并症,(5)如果药物相互作用导致明显 eGFR 下降≥10ml/min/1.73m 或肌酐升高(≥0.5mg/dl)时,考虑更换 cART,如果药物诱导的毒性已经确立,(6)在适当选择的终末期肾衰竭患者中强烈考虑进行肾脏移植。