Plosa Erin J, Esbenshade Jennifer C, Fuller M Paige, Weitkamp Jörn-Hendrik
Department of Pediatrics, Vanderbilt University School of Medicine, Monroe Carell Jr Children's Hospital at Vanderbilt, Nashville, TN, USA.
Pediatr Rev. 2012 Apr;33(4):156-63; quiz 163. doi: 10.1542/pir.33-4-156.
Although commonly asymptomatic, congenital CMV infection is the leading cause of nonhereditary SNHL. Other sequelae that may be evident only after the neonatal period can include chorioretinitis, neurodevelopmental delay with mental or motor impairment, and microcephaly. (13) • Congenital CMV infection is confirmed by detection of the virus in urine, blood, or saliva within the first 3 weeks of life by culture or polymerase chain reaction. A positive test does not necessarily confirm symptomatic CMV disease or need for treatment. (13) • Postnatal CMV infections transmitted through human milk have been reported and may be clinically relevant in extremely premature infants; however, the risk-benefit ratio of pasteurizing human milk for the prevention of postnatal CMV infection is unclear. • Ganciclovir, valganciclovir, foscarnet, cidofovir, and CMV hyperimmune globulin are effective in treating or preventing CMV infections in the immunocompromised host, but require close monitoring for associated toxicities. Treatment for congenital CMV is associated with significant toxicity and uncertain effectiveness. • Based on strong evidence, anticipatory guidance for congenital CMV infection should include hearing tests and neurodevelopmental assessments until school age. (3) In patients with symptomatic congenital CMV infection, lifelong ophthalmologic screening should be included. (4) • Based primarily on consensus, owing to lack of relevant clinical studies, it is not recommended to withhold human milk produced by CMV-seropositive mothers from healthy term infants. (5)(6) • Based on some research evidence, as well as consensus, treatment for congenital CMV is recommended only in symptomatic infants with central nervous system involvement. (9)
虽然先天性巨细胞病毒(CMV)感染通常无症状,但却是非遗传性感音神经性听力损失(SNHL)的主要原因。其他可能仅在新生儿期后才明显的后遗症包括脉络膜视网膜炎、伴有智力或运动障碍的神经发育迟缓以及小头畸形。(13)
• 在出生后3周内通过培养或聚合酶链反应在尿液、血液或唾液中检测到病毒可确诊先天性CMV感染。检测结果呈阳性不一定意味着患有症状性CMV疾病或需要治疗。(13)
• 已有报告称,通过母乳传播的产后CMV感染在极早产儿中可能具有临床相关性;然而,巴氏消毒母乳预防产后CMV感染的风险效益比尚不清楚。
• 更昔洛韦、缬更昔洛韦、膦甲酸钠、西多福韦和CMV高免疫球蛋白可有效治疗或预防免疫功能低下宿主的CMV感染,但需要密切监测相关毒性。先天性CMV的治疗存在显著毒性且疗效不确定。
• 基于有力证据,先天性CMV感染的预期指导应包括直至学龄期的听力测试和神经发育评估。(3)对于有症状性先天性CMV感染的患者,应包括终身眼科筛查。(4)
• 主要基于共识,由于缺乏相关临床研究,不建议禁止CMV血清学阳性母亲为健康足月儿提供母乳。(5)(6)
• 基于一些研究证据以及共识,仅建议对有中枢神经系统受累的有症状婴儿进行先天性CMV治疗。(9)