Baradhi K M, Aure R L, El-Amm J-M
Division of Nephrology, University of Oklahoma, Tulsa, Oklahoma.
Division of Nephrology, University of Oklahoma, Tulsa, Oklahoma.
Transplant Proc. 2018 Jan-Feb;50(1):142-144. doi: 10.1016/j.transproceed.2017.11.013.
We report the first case of a ganciclovir-resistant cytomegalovirus (CMV) involving the gastrointestinal tract that was successfully treated with high-dose valganciclovir. A kidney transplant recipient developed drug-resistant CMV colitis which was initially treated with valganciclovir, but his CMV was found to have major resistance to ganciclovir and cidofovir due to UL97 and UL54 mutations. The patient was switched to intravenous foscarnet 40 mg/kg given every twelve hours. However, foscarnet had to be discontinued after 4 days of treatment due to acute kidney injury. Patient was restarted on valganciclovir at a higher target dose of 1800 mg twice a day based on the creatinine clearance. CMV became undetectable 2 weeks after valganciclovir treatment was completed. High-dose valganciclovir along with immune suppression reduction may be a treatment option for CMV colitis with ganciclovir resistance due to dual UL97 and UL54 gene mutations.
我们报告了首例涉及胃肠道的耐更昔洛韦巨细胞病毒(CMV)病例,该病例通过高剂量缬更昔洛韦成功治愈。一名肾移植受者发生了耐药性CMV结肠炎,最初接受缬更昔洛韦治疗,但由于UL97和UL54突变,其CMV被发现对更昔洛韦和西多福韦具有主要耐药性。该患者改为每12小时静脉注射40mg/kg膦甲酸钠。然而,由于急性肾损伤,治疗4天后不得不停用膦甲酸钠。根据肌酐清除率,患者以更高的目标剂量1800mg每天两次重新开始使用缬更昔洛韦。缬更昔洛韦治疗完成2周后,CMV检测不到。对于因UL97和UL54双基因突变导致对更昔洛韦耐药的CMV结肠炎,高剂量缬更昔洛韦联合降低免疫抑制可能是一种治疗选择。