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(缬氨)更昔洛韦对先天性巨细胞病毒感染儿童听力的影响。

The effect of (val)ganciclovir on hearing in children with congenital cytomegalovirus infection.

作者信息

De Cuyper Elise, Acke Frederic, Keymeulen Annelies, De Leenheer Els, Van Hoecke Helen, Boudewyns An, Gilles Annick, Muylle Marie, Kuhweide Rudolf, Royackers Liesbeth, Desloovere Christian, Verstreken Margriet, Schatteman Isabelle, Dhooge Ingeborg

机构信息

Department of Head and Skin, Ghent University, Ghent, Belgium.

Department of Head and Skin, Ghent University, Ghent, Belgium; Department of Otorhinolaryngology, Ghent University Hospital, Ghent, Belgium.

出版信息

Int J Pediatr Otorhinolaryngol. 2025 Sep;196:112491. doi: 10.1016/j.ijporl.2025.112491. Epub 2025 Jul 16.

Abstract

OBJECTIVES

To assess the effect of (val)ganciclovir on long-term hearing outcome.

METHODS

This matched cohort study presents multicentric data of the Flemish CMV registry (Belgium) collected over 16 years. Treated and untreated cCMV-infected children with a minimal four-year audiological follow-up were included. Primary outcome was hearing evolution. Exact matching for risk factors of spontaneous hearing evolution was performed between the treated and untreated group. The average marginal treatment effect was calculated using a pooled regression model.

RESULTS

Of the 525 children, 98 (18.7 %) were treated. Antiviral therapy did not significantly result in more hearing improvement (RR,1.56; 95 % CI,0.48 to 4.93) or less hearing deterioration (RR,0.89; 95 % CI,0.61 to 1.25). Treatment of children with unilateral congenital hearing loss with valganciclovir for six weeks prevented contralateral late-onset hearing loss compared to untreated children (RR,2.49∗10; 95 % CI,9.19∗10 to 7.71∗10). Similarly, late-onset hearing loss could be prevented in symptomatic children with bilateral normal hearing treated with ganciclovir for six weeks (RR,3.65∗10; 95 % CI,2.16∗10 to 6.21∗10). Prolongation from six weeks to six months showed no beneficial effect on hearing improvement (RR,4.61∗10; 95 % CI,1.07∗10 to 2.32∗10), hearing deterioration (RR,1.21; 95 % CI,0.43 to 2.25), or late-onset hearing loss (RR,1.95; 95 % CI,0.63 to 5.93).

CONCLUSIONS

(Val)ganciclovir for six weeks prevented late-onset hearing loss. No additional benefit of a six-month therapy was found. These novel findings can aid in treatment decision making. Future studies with a larger sample size and investigation on the effect of valganciclovir on long-term neurological outcome are needed.

摘要

目的

评估(缬)更昔洛韦对长期听力结果的影响。

方法

这项匹配队列研究展示了比利时弗拉芒巨细胞病毒登记处16年收集的多中心数据。纳入了接受治疗和未接受治疗的先天性巨细胞病毒感染儿童,这些儿童至少有四年的听力学随访。主要结局是听力变化。在治疗组和未治疗组之间对自发听力变化的危险因素进行精确匹配。使用汇总回归模型计算平均边际治疗效果。

结果

525名儿童中,98名(18.7%)接受了治疗。抗病毒治疗并未显著带来更多的听力改善(相对危险度,1.56;95%可信区间,0.48至4.93)或更少的听力恶化(相对危险度,0.89;95%可信区间,0.61至1.25)。与未治疗的儿童相比,用缬更昔洛韦治疗单侧先天性听力损失儿童六周可预防对侧迟发性听力损失(相对危险度,2.49×10;95%可信区间,9.19×10至7.71×10)。同样,用更昔洛韦治疗六周的双侧听力正常的有症状儿童也可预防迟发性听力损失(相对危险度,3.65×10;95%可信区间,2.16×10至6.21×10)。治疗时间从六周延长至六个月对听力改善(相对危险度,4.61×10;95%可信区间,1.07×10至2.32×10)、听力恶化(相对危险度,1.21;95%可信区间,0.43至2.25)或迟发性听力损失(相对危险度,1.95;95%可信区间,0.63至5.93)均无有益影响。

结论

(缬)更昔洛韦治疗六周可预防迟发性听力损失。未发现六个月治疗有额外益处。这些新发现有助于治疗决策。未来需要进行更大样本量的研究,并调查缬更昔洛韦对长期神经学结局的影响。

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