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Prophylactic i.v. Igs in patients with a high risk for CMV after allo-SCT.

机译:预防性i.v.异基因SCT后具有巨细胞病毒高风险患者的Igs。

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We developed a novel algorithm to define the need for high-dose prophylactic i.v. Igs (IVIG) in periods of high risk for CMV to patients after allo-SCT. IVIG were administered only if at least one of the following, monthly-assessed, criteria was fulfilled: (1) IgG concentration <4 g/l, (2) NK (natural killer) cell count <100/microl, (3) CD4(+) cell count <100/microl, (4) acute or chronic GVHD. The primary endpoint was to determine the cumulative incidence of CMV infection in patients who received prophylactic IVIG according to the algorithm (intervention group) and compare it with that of a sequentially assessed control group, to which prophylactic IVIG were not administered. The study included 79 patients (44 in the intervention and 35 in the control group). The estimated cumulative incidence of CMV infection in the intervention and control group did not differ significantly (44 and 36%; P=0.31). Additionally, prophylactic IVIG did not reduce the frequency of CMV infection episodes. CMV disease was rare in both cohorts (5 and 9%; P=0.65). We conclude that prophylactic IVIG should not be administered after allo-SCT, even if administered selectively in a high dose to patients with delayed immune reconstitution or GVHD.
机译:我们开发了一种新颖的算法来定义对大剂量预防性静脉内注射的需求。异基因SCT后患者发生巨细胞病毒的高风险时期为Igs(IVIG)。仅在满足以下至少一项(每月评估一次)的条件时才给予IVIG:(1)IgG浓度<4 g / l,(2)NK(自然杀手)细胞计数<100 /μl,(3)CD4 (+)细胞计数<100 /微升,(4)急性或慢性GVHD。主要终点是根据算法(干预组)确定接受预防性IVIG的患者中CMV感染的累积发生率,并将其与未进行预防性IVIG的顺序评估对照组进行比较。该研究包括79例患者(干预组44例,对照组35例)。干预组和对照组中CMV感染的估计累积发生率没有显着差异(44%和36%; P = 0.31)。此外,预防性IVIG不能降低CMV感染发作的频率。在这两个队列中,CMV疾病都很罕见(5%和9%; P = 0.65)。我们得出的结论是,即使对延迟免疫重建或GVHD延迟的患者选择性地高剂量给药,也不应在allo-SCT后给予预防性IVIG。

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