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先天性巨细胞病毒感染儿童在1岁时无神经症状的10年临床、发育及智力随访

Ten-year clinical, developmental, and intellectual follow-up of children with congenital cytomegalovirus infection without neurologic symptoms at one year of age.

作者信息

Ivarsson S A, Lernmark B, Svanberg L

机构信息

Department of Pediatrics, University of Lund, University Hospital, Malmö, Sweden.

出版信息

Pediatrics. 1997 Jun;99(6):800-3. doi: 10.1542/peds.99.6.800.

Abstract

OBJECTIVE

This study was undertaken to ascertain whether children with congenital cytomegalovirus (CMV) infection at birth, but without neurologic symptoms at 1 year of age, differed in somatic, neurologic, developmental, or intellectual status from matched control children at long-term follow-up.

MATERIAL AND METHODS

Congenital CMV infection, as demonstrated by isolation of the virus within the first week of life, was diagnosed in 44 (0.5%) of 9806 infants. From this basic CMV-infected population, children who developed neurologic disturbances including sensorineural deafness before 1 year of age were excluded (n = 7), as were those unwilling to participate (n = 2). Congenitally infected infants (n = 35) and matched control infants (n = 53) were followed up clinically and neurologically. At 21 months, development was assessed with the Griffiths' Developmental Scale and at 7 years of age neurologic status was assessed with the Stott test and intellectual development with the Wechsler Intelligence Scale for Children.

RESULTS

As reported previously, 18% (8/44) of the CMV-infected infants manifested symptoms at birth, as compared to 8% (4/53) in the control group. In the congenital CMV group 7% (2/30) children tested had abnormal Stott test results, as compared to 2% (1/43) in the control group. Thirty-two CMV-infected and 51 control group children were assessed with the Griffiths' scale at 21 months of age. The two groups did not differ significantly, either in mean scores (6.3 +/- 2.3 vs 6.1 +/- 1.9) or in the proportion of children with scores below normal (19% [6/32] vs 16% [8/51]). Twenty-five CMV-infected and 41 control group children were assessed with the Wechsler Intelligence Scale for Children at 7 years of age (median 86 months; range, 82 to 90 and 82 to 91, respectively). The two groups did not differ significantly, either in mean scores (5.8 +/- 2.0 vs 6.4 +/- 1.6) or in the proportion of children with scores below normal (12% [3/25] vs 5% [2/41]).

CONCLUSION

Children with congenital CMV infection are unlikely to be at an increased risk of subsequent neurodevelopmental or intellectual impairment if they show normal development at 12 months of age.

摘要

目的

本研究旨在确定出生时患有先天性巨细胞病毒(CMV)感染但1岁时无神经症状的儿童在长期随访中,其身体、神经、发育或智力状况与匹配的对照儿童是否存在差异。

材料与方法

在9806例婴儿中,44例(0.5%)在出生后第一周内病毒分离阳性,确诊为先天性CMV感染。在这个基本的CMV感染人群中,排除1岁前出现包括感音神经性耳聋在内的神经功能障碍的儿童(n = 7)以及不愿参与的儿童(n = 2)。对先天性感染婴儿(n = 35)和匹配的对照婴儿(n = 53)进行临床和神经学随访。在21个月时,用格里菲斯发育量表评估发育情况,在7岁时,用斯托特测试评估神经状况,用韦氏儿童智力量表评估智力发育。

结果

如先前报道,CMV感染婴儿中有18%(8/44)在出生时出现症状,而对照组为8%(4/53)。先天性CMV感染组中7%(2/30)接受测试的儿童斯托特测试结果异常,而对照组为2%(1/43)。32例CMV感染儿童和51例对照组儿童在21个月时用格里菲斯量表进行评估。两组在平均得分(6.3±2.3对6.1±1.9)或得分低于正常的儿童比例(19%[6/32]对16%[8/51])方面均无显著差异。25例CMV感染儿童和41例对照组儿童在7岁时用韦氏儿童智力量表进行评估(中位数86个月;范围分别为82至90个月和82至91个月)。两组在平均得分(5.8±2.0对6.4±1.6)或得分低于正常的儿童比例(12%[3/25]对5%[2/41])方面均无显著差异。

结论

如果先天性CMV感染儿童在12个月时发育正常,那么他们随后发生神经发育或智力损害的风险不太可能增加。

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