Salomè S, Malesci R, Delle Cave V, Amitrano A, Gammella R, Fanelli F, Capone E, Capasso L, Fetoni A R, Raimondi F
Division of Neonatology, Department of Translational Medical Sciences, University of Naples "Federico II", Naples, Italy.
Unit of Audiology, Department of Neurosciences, Reproductive and Odontostomatologic Sciences, University of Naples "Federico II", Naples, Italy.
Front Pediatr. 2024 Jan 4;11:1297208. doi: 10.3389/fped.2023.1297208. eCollection 2023.
Sensorineural hearing loss (SNHL) has been suggested to be possibly related to congenital toxoplasmosis (CT), although its prevalence varies from 0% to 26%. This variance appears to be dependent especially on early timing of treatment. However, the available data are based on outdated studies conducted on small groups of patients that lack homogeneity. Therefore, to establish evidence-based guidelines for audiologic monitoring in CT, we conducted a comprehensive evaluation of a large case series over a long period of time.
This is a single-center, retrospective cohort that enrolled all infants and children who were exposed to and/or congenitally infected between September 1980 and December 2022. They underwent standard serial audiological evaluations to detect possible SNHL at an early stage. The first evaluation was performed during the initial assessment to define the onset of congenital toxoplasmosis, with another evaluation conducted at least at 12 months of life.
We collected data from 1,712 patients, and 183 (10.7%) were diagnosed with CT. Among these cases, 78 children (42.6%) presented with symptomatic CT at the onset, exhibiting ocular findings (21.1%), clinical cerebral manifestations (6.1%), and/or abnormal findings on neuroimaging (35.5%). Therapy was administrated at the onset in 164 patients (89.6%) with 115 of them starting treatment prior to 2.5 months of age (0-388, median 32.00 ± 92.352 days of life). Only one patient presented with SNHL at the onset, but this was apparently unrelated to CT. The median number of audiological assessments was 2.2 ± 1.543 (2-10). No patients developed any grade of delayed hearing loss, both in treated and untreated groups. The median age at last audiological evaluation was 2.3 ± 2.18 years (1-8), although the median follow-up period was 12.4 years (±6.3), ranging from 1 to 27 years.
Based on these data, it appears that SNHL may be less frequent in CT than previously assumed. We recommend conducting an audiological assessment at the onset (within the first 2.5 months of life) to comprehensively define the type of CT onset, and then conducting another evaluation within 9 months of life.
尽管感音神经性听力损失(SNHL)在先天性弓形虫病(CT)中的患病率从0%到26%不等,但已有研究表明二者可能相关。这种差异似乎尤其取决于治疗的早期时机。然而,现有数据基于对缺乏同质性的小群体患者进行的过时研究。因此,为了制定基于证据的CT听力监测指南,我们对一个大型病例系列进行了长期的综合评估。
这是一个单中心回顾性队列研究,纳入了1980年9月至2022年12月期间所有暴露于和/或先天性感染弓形虫的婴儿和儿童。他们接受了标准的系列听力评估,以便在早期阶段检测可能的SNHL。第一次评估在初始评估时进行,以确定先天性弓形虫病的发病时间,另一次评估至少在12月龄时进行。
我们收集了1712例患者的数据,其中183例(10.7%)被诊断为CT。在这些病例中,78名儿童(42.6%)在发病时表现为有症状的CT,出现眼部表现(21.1%)、临床脑部表现(6.1%)和/或神经影像学异常表现(35.5%)。164例患者(89.6%)在发病时接受了治疗,其中115例在2.5月龄前开始治疗(0 - 388天,中位年龄32.00 ± 92.352天)。只有1例患者在发病时出现SNHL,但这显然与CT无关。听力评估的中位数为2.2 ± 1.543次(2 - 10次)。治疗组和未治疗组均无患者出现任何程度的迟发性听力损失。最后一次听力评估的中位年龄为2.3 ± 2.18岁(1 - 8岁),尽管中位随访期为12.4年(±6.3年),范围为1至27年。
基于这些数据,CT中SNHL的发生率似乎比之前假设的要低。我们建议在发病时(出生后2.5个月内)进行听力评估,以全面确定CT发病类型,然后在9个月龄内进行另一次评估。