首页> 外文期刊>Journal of clinical virology: The official publication of the Pan American Society for Clinical Virology >Neurodevelopmental outcomes following ganciclovir therapy in symptomatic congenital cytomegalovirus infections involving the central nervous system
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Neurodevelopmental outcomes following ganciclovir therapy in symptomatic congenital cytomegalovirus infections involving the central nervous system

机译:更昔洛韦治疗涉及中枢神经系统的症状性先天性巨细胞病毒感染后的神经发育结果

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Background: Ganciclovir protects against hearing deterioration in infants with symptomatic congenital cytomegalovirus (CMV) disease involving the central nervous system (CNS). Objectives: To assess the neurodevelopmental impact of ganciclovir therapy in this population. Study design: 100 neonates were enrolled into a controlled Phase III study of symptomatic congenital CMV involving the CNS, and were randomized to either 6 weeks of intravenous ganciclovir or no treatment. Denver developmental tests were performed at 6 weeks, 6 months, and 12 months. For each age, developmental milestones that ≥90% of normal children would be expected to have achieved were identified. The numbers of milestones not met ("delays") were determined for each subject. The average number of delays per subject was compared for each treatment group. Results: At 6 months, the average number of delays was 4.46 and 7.51, respectively, for ganciclovir recipients and "no treatment" subjects (p = 0.02). At 12 months, the average number of delays was 10.06 and 17.14, respectively (p = 0.007). In a multivariate regression model, the effect of ganciclovir therapy remained statistically significant at 12 months (p = 0.007). Conclusions: Infants with symptomatic congenital CMV involving the CNS receiving intravenous ganciclovir therapy have fewer developmental delays at 6 and 12 months compared with untreated infants. Based on these data as well as the previously published data regarding ganciclovir treatment and hearing outcomes, 6 weeks of intravenous ganciclovir therapy can be considered in the management of babies with symptomatic congenital CMV disease involving the CNS. If treatment is initiated, it should be started within the first month of life and patients should be monitored closely for toxicity, especially neutropenia. Since existing data only address the treatment of symptomatic congenital CMV disease involving the CNS, these data cannot be extrapolated to neonates with other manifestations of CMV disease, including asymptomatic babies and symptomatic babies who do not have CNS involvement.
机译:背景:更昔洛韦可预防患有中枢神经系统(CNS)的有症状先天性巨细胞病毒(CMV)疾病的婴儿的听力恶化。目的:评估更昔洛韦治疗对该人群的神经发育影响。研究设计:100名新生儿参加了涉及中枢神经系统症状性先天性巨细胞病毒的对照III期研究,并随机分配给更昔洛韦静脉注射6周或不接受治疗。在第6周,6个月和12个月进行丹佛发育测试。对于每个年龄段,确定了预期将达到90%以上的正常儿童的发展里程碑。为每个主题确定未达到的里程碑数(“延迟”)。比较每个治疗组每个受试者的平均延误次数。结果:在更昔洛韦接受者和“未接受治疗”的受试者中,在6个月时的平均延误次数分别为4.46和7.51(p = 0.02)。在12个月时,平均延迟时间分别为10.06和17.14(p = 0.007)。在多变量回归模型中,更昔洛韦治疗的疗效在12个月时仍具有统计学意义(p = 0.007)。结论:与未经治疗的婴儿相比,接受静脉注射更昔洛韦治疗的中枢神经系统症状性先天性CMV婴儿在6个月和12个月时的发育延迟较少。根据这些数据以及先前发布的更昔洛韦治疗和听力结果数据,可以考虑对患有中枢神经系统症状的先天性CMV婴儿进行6周静脉更昔洛韦治疗。如果开始治疗,则应在生命的第一个月内开始治疗,并应密切监测患者的毒性,尤其是中性粒细胞减少症。由于现有数据仅涉及涉及中枢神经系统症状的先天性CMV疾病的治疗,因此这些数据不能外推至具有其他CMV疾病表现的新生儿,包括无症状婴儿和不涉及中枢神经系统疾病的有症状婴儿。

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