首页> 外文期刊>Klinische Paediatrie >Qra! VaEganciclovlr Treatment In a CIVSV Congenital Infected Enfant with Sensorineural Hearing Loss (SNHL) First Detected at 4 Months of Age
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Qra! VaEganciclovlr Treatment In a CIVSV Congenital Infected Enfant with Sensorineural Hearing Loss (SNHL) First Detected at 4 Months of Age

机译:Qra! VaEganciclovlr治疗CIVSV先天性感染婴儿并伴有感音神经性听力减退(SNHL),最早发现于4个月大

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摘要

Cytomegalovirus (CMV) is the most frequent cause of congenital viral infections with an incidence of 0.3-2.2% in developed countries of all life births. Fetal CMV-infection can develop following both primary and recurrent maternal infections and is the leading cause of nongenetic sensorineural hearing loss (SNHL) and mental retardation. Congenital infected newborns are symptomatic in 12.7% of newborns with hearing loss in 41 %, being bilateral in 67%. In infants with asymptomatic infection at birth 13.5% will eventually show developmental disorders, notably SNHL in 7.4% [Dollard S. et al. Rev Med Virol 2007; 17: 355-363; Dahle A. J. etal. J Am Acad Audiol 2000; 11: 283-290]. Antiviral treatment of congenital infected newborns and infants with CNS involvement with intravenous ganciclovir was investigated in a large randomised US-multicenter trial (phase I-III) and demonstrated both virologic and clinical benefit. Following an initial i.v. ganciclovir therapy for 2-3 weeks the orally applicable prodrug valganciclovir has been used for "off-label" long term treatment since 2005. Recently, the pharmaco-kine-tic and dynamic characteristics of valganciclovir for use in symptomatic infected neonates have been established [Kimber-lin D. W. etal. J Infect Dis 2008; 197: 836-845].
机译:巨细胞病毒(CMV)是先天性病毒感染的最常见原因,在发达国家中,所有出生婴儿的发病率均为0.3-2.2%。胎儿CMV感染可在原发性和复发性母体感染后发生,并且是非遗传性感音神经性听力丧失(SNHL)和智力低下的主要原因。先天性感染的新生儿在有症状的新生儿中占12.7%的症状,有听力损失的占41%,双侧的有67%。在出生时无症状感染的婴儿中,最终将出现13.5%的发育障碍,尤其是7.4%的SNHL [Dollard S. et al。 Rev Vi Virol 2007; 17:355-363; Dahle A.J.等人。 J Am Acad Audiol 2000; 11:283-290]。在一项大型的美国-多中心随机试验(I-III期)中研究了静脉注射更昔洛韦对先天性新生儿和中枢神经系统受累婴儿的抗病毒治疗(I-III期),并证明了病毒学和临床益处。最初的i.v.更昔洛韦疗法治疗2-3周后,口服可应用的前药缬更昔洛韦自2005年以来一直用于“标签外”长期治疗。最近,已确定用于有症状感染新生儿的缬更昔洛韦的药代动力学和动态特性[金伯林DW等。 J感染Dis 2008; 197:836-845]。

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