Hearing assessment in transfusion dependent beta-thalassemia children on oral iron chelating agent.

IF 2 3区 医学 Q2 PEDIATRICS
Wafaa E I Mohamed, Marwa Waheed Tolba, Yara Khalid Abuelfadl, Abeer Mohamed Elgendy, Heba G A Ali
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引用次数: 0

Abstract

Background: Hearing deficit is one of the side effects of 1st generation iron chelators in β-thalassemia, however the risk of hearing deficits following 2nd generation iron chelators is not well known.

Aim: To assess hearing status of Transfusion Dependent β-thalassemia children on oral iron chelating agents and detect risk factors for hearing impairment.

Methods: This is a cross-sectional study recruited sixty children and adolescent with confirmed diagnosis of transfusion dependent β-thalassemia. Demographic and clinical characteristics collected, audiological testing were performed by the same audiologist using the same equipment for all patients including tympanometry, pure tone audiometry, speech audiometry, transient evoked otoacoustic emissions and distortion product otoacoustic emissions.

Results: Recruited children and adolescents with transfusion dependent β-thalassemia were 32 (53.3%) boys and 28 (46.7%) girls and their mean age was 11.34 ± 3.08, majority of patients 48 (80%) were on single Deferasirox. Our study revealed that among the 60 children evaluated, 16.6% exhibited some form of hearing loss. Sensorineural hearing loss (SNHL) was observed in 6.6% of the participants, while 10% had conductive hearing loss (CHL). Bilateral SNHL in 5% and bilateral CHL in 8.3% of all the cases. Hearing impairment was mild in nature, but predominantly affected high-frequency ranges, the most affected frequencies being 4000 Hz and 8000 Hz. There was no significant difference between studied thalassemia children with and without hearing impairment regarding gender, age at study entry, age at diagnosis, duration of disease and duration or dose of chelating agent (P > 0.05). Our study revealed significant difference between studied thalassemia children with and without hearing impairment regarding age of starting blood transfusion (p-value = 0.024), affected patients started blood transfusion at older age, also statistically significant difference in both groups regarding median serum ferritin was found (p-value = 0.028), lower levels were found in affected patients.

Conclusion: No significant effect of using oral iron chelation drugs was observed on frequency and type of hearing loss among the studied patients but instead the age at starting regular blood transfusion did. Screening of such group of patients for hearing impairment at diagnosis and at regular periods is recommended.

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输血依赖性-地中海贫血患儿口服铁螯合剂的听力评价。
背景:听力损失是第一代铁螯合剂治疗β-地中海贫血的副作用之一,但第二代铁螯合剂治疗后听力损失的风险尚不清楚。目的:评价输血依赖性β-地中海贫血患儿口服铁螯合剂后的听力状况,探讨其听力损害的危险因素。方法:这是一项横断面研究,招募了60名确诊为输血依赖性β-地中海贫血的儿童和青少年。收集人口学和临床特征,由同一听力学家使用相同的设备对所有患者进行听力学测试,包括鼓室测量、纯音听力学、语音听力学、瞬态诱发耳声发射和畸变产物耳声发射。结果:纳入的输血依赖性β-地中海贫血儿童和青少年中,男孩32例(53.3%),女孩28例(46.7%),平均年龄11.34±3.08岁,大多数患者48例(80%)单次使用去铁宁。我们的研究显示,在接受评估的60名儿童中,16.6%表现出某种形式的听力损失。感音神经性听力损失(SNHL)占6.6%,传导性听力损失(CHL)占10%。双侧SNHL占5%,双侧CHL占8.3%。听力损害本质上是轻微的,但主要影响高频范围,最受影响的频率是4000赫兹和8000赫兹。有听力障碍和无听力障碍的地中海贫血儿童在性别、入组年龄、诊断年龄、病程、螯合剂持续时间或剂量方面无显著差异(P < 0.05)。我们的研究显示,有听力障碍的地中海贫血儿童与无听力障碍的地中海贫血儿童在开始输血的年龄上有显著差异(p值= 0.024),患者开始输血的年龄更大,两组血清铁蛋白中位数差异也有统计学意义(p值= 0.028),患者铁蛋白水平更低。结论:口服铁螯合药物对研究患者的听力损失频率和类型无显著影响,但对开始定期输血的年龄有显著影响。建议在诊断时和定期对这类患者进行听力障碍筛查。
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来源期刊
BMC Pediatrics
BMC Pediatrics PEDIATRICS-
CiteScore
3.70
自引率
4.20%
发文量
683
审稿时长
3-8 weeks
期刊介绍: BMC Pediatrics is an open access journal publishing peer-reviewed research articles in all aspects of health care in neonates, children and adolescents, as well as related molecular genetics, pathophysiology, and epidemiology.
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