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A Randomized Study of Quantiferon CMV-directed Versus Fixed-duration Valganciclovir Prophylaxis to Reduce Late CMV After Lung Transplantation

机译:肺部移植后Darualificeron CMV指导与固定持续时间Valganciclovir预防的随机研究

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摘要

Background. We provide the results of the first interventional study of cytomegalovirus (CMV)-specific immune monitoring to direct the length of antiviral prophylaxis in lung transplantation (LTx). Methods. Patients (n = 118) at risk of CMV infection were randomized 1:2 to either 5 months or variable length valganciclovir prophylaxis (5-11 mo post-LTx), as determined by the QuantiFERON (QFN)-CMV assay. Patients with a negative QFN-CMV assay ( 600 copies/mL) within the blood was significantly reduced in patients with a positive QFN-CMV assay compared with those without protective immunity (13% versus 67%, P = 0.0003), as was the incidence of severe viremia (> 10 000 copies/mL) (3% versus 50%, P < 0.001). Ceasing antiviral prophylaxis at 11 months in patients with a negative assay was associated with a 25% incidence of late CMV viremia. Conclusions. Cytomegalovirus immune monitoring allows an individualized approach to CMV prophylaxis and reduces late CMV infection within the lung allograft.
机译:背景。我们提供了巨细胞病毒(CMV)特异性免疫监测的第一个介入研究的结果,以指导肺移植(LTX)中的抗病毒预防长度。方法。患者(n = 118)在CMV感染的风险下被随机1:2至5个月或可变长度Valganciclovir预防(5-11mo后LTX),如Qualiferon(QFN)-CMV测定法测定。患有阴性QFN-CMV测定(600拷贝/ ml)的患者在阳性QFN-CMV测定患者中显着降低,与没有保护性免疫的患者(13%对67%,P = 0.0003),如下严重病毒血症的发病率(> 10 000份/ ml)(3%对50%,P <0.001)。在阴性测定患者中,在11个月内停止抗病毒预防与25%的晚期CMV病毒血症的发生率有关。结论。 CytomeGalovirus免疫监测允许个体化方法对CMV预防并降低肺同种异体移植物中的晚期CMV感染。

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