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首页> 外文期刊>Transplantation Proceedings >The role of valacyclovir on Epstein-Barr virus viral loads in pediatric liver transplantation patients.
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The role of valacyclovir on Epstein-Barr virus viral loads in pediatric liver transplantation patients.

机译:伐昔洛韦对小儿肝移植患者爱泼斯坦-巴尔病毒载量的作用。

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INTRODUCTION: Epstein-Barr virus (EBV) infection occurring in the postoperative period represents a significant risk for pediatric transplant recipients. It presents in various manners, including a mononucleosis-like syndrome, hepatitis, encephalopathy, or posttransplant lymphoproliferative disease (PTLD). Valacyclovir has in vitro activity against EBV. We sought to review our experience with valacyclovir on peripheral blood EBV viral loads among a group of EBV-infected patients after liver transplantation (OLT). PATIENTS AND METHODS: Twelve children of ages 6-36 months (median, 12 months), underwent OLT. Eight (66%) were EBV immunoglobulin (Ig)G seronegative at the time of the operation. Eight patients developed primary infection and 4 patients developed reactivation of a post primary infection. Valacyclovir was prescribed immediately to 3 patients when we detected an acute-primary EBV infection. Valacyclovir was prescribed for 2 patients who had primary EBV infections followed by PTLD. Three patients who had primary EBV infection were administered valacyclovir after they became chronically EBV PCR positive for more than 1 year. Four out of 12 cases (33%) were EBV seropositive at the time of OLT, and underwent postprimary EBV reactivation displaying chronic EBV carrier state for 8-10 months before valacyclovir treatment. Peripheral blood EBV viral loads were tested every 2 months. The primary outcome was the proportion of subjects with EBV viremia who had a >or=2 log 10 decrease in EBV copies/mL after valacyclovir treatment. The duration of valacyclovir treatment was a median of 10 months (range, 8-11 months). At the beginning of the treatment period the median level of EBV viral load was 1.1 x 10(4) (range, 1 x 10(4) to 1 x 10(7)). EBV virus was cleared in only 1 patient with primary acute EBV infection. EBV viral loads did not change in 7 of 12 patients and decreased only 1 log 10 (n = 2) or 2 log 10 (n = 2). CONCLUSION: In this small, non-placebo-controlled study, valacyclovir treatment was not effective to decrease peripheral blood EBV viral loads.
机译:简介:术后发生的爱泼斯坦-巴尔病毒(EBV)感染对小儿移植受者构成重大风险。它以多种方式出现,包括单核细胞增多症样综合征,肝炎,脑病或移植后淋巴增生性疾病(PTLD)。伐昔洛韦对EBV具有体外活性。我们试图回顾我们使用伐昔洛韦治疗肝移植(OLT)后一组EBV感染患者外周血EBV病毒载量的经验。患者与方法:对12例6-36个月(中位数为12个月)的儿童进行了OLT。手术时八(66%)人为EBV免疫球蛋白(Ig)G血清阴性。八名患者发生了原发感染,四名患者发生了原发感染后的再激活。当我们检测到急性原发性EBV感染时,立即对3名患者开具了伐昔洛韦处方。对2例原发性EBV感染并随后PTLD的患者开具了伐昔洛韦处方。 3名原发性EBV感染患者在长期EBV PCR阳性超过1年后接受了伐昔洛韦治疗。 12例患者中有4例(33%)在OLT时是EBV血清阳性的,并且在接受伐昔洛韦治疗前的初次EBV激活后显示了慢性EBV携带者状态,持续了8-10个月。每2个月检查一次外周血EBV病毒载量。主要结果是在接受伐昔洛韦治疗后,EBV病毒血症受试者的EBV拷贝数/ mL降低≥2log 10的比例。伐昔洛韦治疗的持续时间中位数为10个月(范围8-11个月)。在治疗期开始时,EBV病毒载量的中位水平为1.1 x 10(4)(范围从1 x 10(4)到1 x 10(7))。仅1例原发性急性EBV感染患者清除了EBV病毒。 EBV病毒载量在12例患者中的7例中没有变化,仅下降了1 log 10(n = 2)或2 log 10(n = 2)。结论:在这项非安慰剂对照的小型研究中,伐昔洛韦治疗不能有效降低外周血EBV病毒载量。

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