Patil A Jayaprakash, Sharma Ashish, Kenney M Cristina, Kuppermann Baruch D
Department of Ophthalmology, Gavin S Herbert Eye Institute,University of California, Irvine, Irvine, CA, USA.
Clin Ophthalmol. 2010 Mar 4;4:111-9. doi: 10.2147/opth.s3248.
Oral valganciclovir is a new and highly efficacious alternative to the chronic administration of ganciclovir in the treatment of cytomegalovirus (CMV) retinitis in HIV-infected patients. In addition to its excellent bioavailability and favorable pharmacokinetic profile, valganciclovir has also proved cost effective and is the most widely used drug in the armamentarium for the treatment of CMV retinitis. Valganciclovir is a prodrug of ganciclovir, the erstwhile commonly used therapy. In March 2001, the US Food and Drug Administration approved valganciclovir for the induction and maintenance treatment of CMV disease, including CMV retinitis. Valganciclvoir has compared favorably with both oral and intravenous treatments for induction and maintenance therapy with ganciclovir. The reduced pill burden and the ease of oral administration has helped avoid the risks associated with intravenous therapy. The most serious adverse event is neutropenia, which makes the patient susceptible to infections. In the current review, we have compiled all the available evidence-based information on valganciclovir.
口服缬更昔洛韦是在治疗HIV感染患者的巨细胞病毒(CMV)视网膜炎时,一种可替代长期使用更昔洛韦的新型高效药物。除了具有出色的生物利用度和良好的药代动力学特征外,缬更昔洛韦还被证明具有成本效益,并且是治疗CMV视网膜炎的药物库中使用最广泛的药物。缬更昔洛韦是更昔洛韦的前体药物,更昔洛韦是以前常用的治疗方法。2001年3月,美国食品药品监督管理局批准缬更昔洛韦用于CMV疾病(包括CMV视网膜炎)的诱导和维持治疗。缬更昔洛韦在诱导和维持治疗方面与更昔洛韦的口服和静脉治疗相比具有优势。减少的服药负担和口服给药的便利性有助于避免与静脉治疗相关的风险。最严重的不良事件是中性粒细胞减少症,这使患者易受感染。在本综述中,我们汇编了所有关于缬更昔洛韦的现有循证信息。