Auditory brain stem response and otoacoustic emission results in children with end-stage renal disease

Naderpour, Masoud; Mortazavi, Forough; Jabbari-Moghaddam, Yalda; Sharifi-Movaghar, Mohammad H.

doi:10.1016/j.ijporl.2011.02.020

Cited by 15 publications

(13 citation statements)

References 15 publications

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“…In addition, uremic neuropathy may contribute to auditory dysfunction . Studies on brain‐evoked response audiometry and otoacoustic emissions tests show that cochlear or retrocochlear origins of hearing loss are common in patients with ESRD . This is particularly common in children with dialysis …”

Section: Discussionmentioning

confidence: 99%

Risk of sudden sensorineural hearing loss in patients with end‐stage renal disease undergoing dialysis

Wang

Muo

et al. 2017

Nephrology

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Section: Discussionmentioning

confidence: 99%

Risk of sudden sensorineural hearing loss in patients with end‐stage renal disease undergoing dialysis

Wang

Muo

et al. 2017

Nephrology

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“…Retrospectively, medical records of all newborns managed for EA/TEF in Tabriz Children’s Hospital and Tehran Mofid Hospital between 2007 and 2010 were reviewed. The pediatric surgery departments of these university-affiliated hospitals are tertiary referral centers for pediatric surgery in Northwestern and the capital of Iran, respectively 12,13. All infants with EA/TEF born in the indicated areas are admitted to either of the two hospitals.…”

Section: Methodsmentioning

confidence: 99%

Associated congenital anomalies between neonates with short-gap and long-gap esophageal atresia: a comparative study

Aslanabadi

Ghabili

Rouzrokh³

et al. 2011

IJGM

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Background:Predicting the presence of long-gap esophageal atresia (EA) prior to the surgery is of clinical importance. No comparison between short-gap and long-gap EA for the prevalence of VACTERL and non-VACTERL-type anomalies has yet been performed.Objective:The aim of this study was to compare VACTERL and non-VACTERL-type anomalies between patients with short-gap and long-gap EA.Methods:Retrospectively, medical records of all newborns managed for EA/tracheoesophageal fistula (TEF) in Tabriz Children’s Hospital and Tehran Mofid Hospital between 2007 and 2010 were evaluated. Demographic data and associated anomalies including both the VACTERL and non-VACTERL-type defects were listed. The VACTERL spectrum defects covered vertebral/costal, anorectal, cardiovascular, TEF, and renal- or radial-type limb anomalies. The non-VACTERL-type anomalies included hydrocephalus, orofacial defects, respiratory system anomalies, gastrointestinal anomalies, genital anomalies, and non-VACTERL limb defects. Demographic data, and the VACTERL and non-VACTERL-type anomalies were compared among children with long-gap EA and those with short-gap EA.Results:Two hundred and seventy-six children were included in the study: 230 (83.3%) in the short-gap EA group and 46 (16.7%) in the long-gap EA group. Although prevalence of the VACTERL spectrum anomalies did not differ between the two groups, the non-VACTERL anomaly was more common in the long-gap EA group (P = 0.02). Among the VACTERL-type defects, TEF was detected in 30 (65.2%) and 218 (94.7%) patients in long-gap and short-gap EA groups, respectively (P = 0.0001).Conclusion:The non-VACTERL-type anomalies, but not the VACTERL spectrum defects, are more frequent in patients with long-gap EA than those with short-gap EA.

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“…Именно ионные различия по обе стороны рейсснеровой мембраны улитки определяют микроэлектрические явления в органе Корти, которые обеспечивают высокую чувствительность слухового рецептора. Известны также схожие фармакологические влияния и патологические изменения, выявленные на ультраструктурном уровне в почке у пациентов с ХБП и улитке при сенсоневральной тугоухости [6,7].…”

Section: принятые сокращенияunclassified

Changes of the auditory function in he children with chronic kidney failure

Barilyak

Mileshina²,

Moskalets

et al. 2018

Vestn. otorinolaringol.

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The TEOAE was not registered in 17 of the 62 examined children. According to the results of the comprehensive audiological examinations, 13 children suffered from the hearing loss of different forms and severity while 5 children presented with bilateral deafness. As the duration of CRF progressed, the patients became more prone to develop hearing impairment. Hearing loss is possibly genetically determined. Among the etiological factors underlying the development of the hearing loss the high doses of immunosuppressants and aminoglycosides are considered to be the principal ones.

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Auditory brain stem response and otoacoustic emission results in children with end-stage renal disease

Cited by 15 publications

References 15 publications

Risk of sudden sensorineural hearing loss in patients with end‐stage renal disease undergoing dialysis

Risk of sudden sensorineural hearing loss in patients with end‐stage renal disease undergoing dialysis

Associated congenital anomalies between neonates with short-gap and long-gap esophageal atresia: a comparative study

Changes of the auditory function in he children with chronic kidney failure

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