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Journal of veterinary internal medicine2014; 28(4); 1318-1324; doi: 10.1111/jvim.12377

Brainstem auditory evoked responses in an equine patient population. Part II: foals.

Abstract: Reports of the use of brainstem auditory evoked response (BAER) as a diagnostic modality in foals have been limited. Objective: To describe BAER findings and associated causes of hearing loss in foals. Methods: Study group 18 foals (15 neonatal, 3 nonneonatal), control group (5 neonatal foals). Methods: Retrospective. BAER records from the Clinical Neurophysiology Laboratory were reviewed from the years of 1982 to 2013. Peak latencies, amplitudes, and interpeak intervals were measured when visible. Clinical data were extracted from the medical records. Foals were grouped under disease categories. Descriptive statistics were performed. Results: Ten neonatal foals had complete absence of BAER bilaterally and 5 had findings within reference range. Abnormalities were associated with common neonatal disorders such as sepsis, neonatal encephalopathy, neonatal isoerythrolysis, and prematurity. BAER loss also was observed in foals with specific coat color patterns such as completely or mostly white with blue irides or lavender with pale yellow irides. An American Miniature foal with marked facial deformation also lacked BAER bilaterally. One nonneonatal foal with an intracranial abscess had no detectable BAER peaks bilaterally, and 2 older foals, 1 with presumed equine protozoal myeloencephalitis and the other with progressive scoliosis and ataxia, had BAER within normal limits. Conclusions: In neonatal foals, BAER deficits commonly are complete and bilateral, and associated with common neonatal disorders and certain coat and eye color patterns. Sepsis, hypoxia, bilirubin toxicity, and prematurity should be investigated as potential causes of auditory loss in neonatal foals.
Publication Date: 2014-06-05 PubMed ID: 24903742PubMed Central: PMC4857935DOI: 10.1111/jvim.12377Google Scholar: Lookup
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  • Journal Article

Summary

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This research article explores the use of Brainstem Auditory Evoked Response (BAER) in diagnosing hearing losses in newborn and non-newborn foals, revealing its correlation to common neonatal disorders, coat and eye colors, as well as other symptoms.

Methodology

  • The researchers conducted a retrospective study, which spanned from 1982 to 2013. The study group included 18 foals (15 newborns, 3 non-newborns), while the control group consisted of 5 newborn foals.
  • They observed BAER records from the Clinical Neurophysiology Laboratory, measuring peak latencies, amplitudes, and interpeak intervals whenever they were visible.
  • Furthermore, they gathered clinical data from medical records and categorized foals into various disease groups.
  • Descriptive statistical analysis was performed on the collected data.

Findings

  • In neonatal foals, ten showed a complete absence of BAER bilaterally (on both sides), while five had results in the reference range.
  • BAER abnormalities correlated with common neonatal disorders such as sepsis, neonatal encephalopathy, neonatal isoerythrolysis, prematurity. Coating and eye color patterns also displayed a significant link with BAER loss. Foals that were completely or mostly white with blue irides or lavender with pale yellow irides frequently lacked BAER.
  • One particular American Miniature foal with significant facial deformation was found to have zero BAER bilaterally.
  • Among non-newborn foals, the BAER was undetectable in a foal diagnosed with an intracranial abscess. However, in two other older foals presumed with equine protozoal myeloencephalitis and progressing scoliosis and ataxia, BAER appeared to be within normal limits.

Conclusions

  • The study concludes that neonatal foals commonly have complete and bilateral BAER deficits. These are often linked with common neonatal disorders and specific coat and eye color patterns.
  • It also notes that sepsis, hypoxia, bilirubin toxicity, and prematurity should be further investigated as potential causes of auditory loss in neonatal foals.

Cite This Article

APA
Aleman M, Madigan JE, Williams DC, Holliday TA. (2014). Brainstem auditory evoked responses in an equine patient population. Part II: foals. J Vet Intern Med, 28(4), 1318-1324. https://doi.org/10.1111/jvim.12377

Publication

ISSN: 1939-1676
NlmUniqueID: 8708660
Country: United States
Language: English
Volume: 28
Issue: 4
Pages: 1318-1324

Researcher Affiliations

Aleman, M
  • Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, Davis, CA.
Madigan, J E
    Williams, D C
      Holliday, T A

        MeSH Terms

        • Age Factors
        • Animals
        • Animals, Newborn / physiology
        • Evoked Potentials, Auditory, Brain Stem / physiology
        • Hearing Loss / physiopathology
        • Hearing Loss / veterinary
        • Horse Diseases / physiopathology
        • Horses / physiology
        • Retrospective Studies

        References

        This article includes 39 references
        1. Spehlmann R. The Normal BAEP. 1985:204–216.
        2. Strain GM, Olcott BM, Thompson DR. Brainstem auditory‐evoked potentials in Holstein cows. J Vet Intern Med 1989;3:144–148.
          pubmed: 2778748
        3. Walsh EJ, Gorga M, McGee J. Comparisons of the development of auditory brainstem response latencies between cats and humans. Hear Res 1992;60:53–63.
          pubmed: 1500377
        4. Poncelet LC, Coppens AG, Meuris SI. Maturation of the auditory system in clinically normal puppies as reflected by the brain stem auditory‐evoked potential wave V latency‐intensity curve and rarefaction‐condensation differential potentials. Am J Vet Res 2000;61:1343–1348.
          pubmed: 11108176
        5. Poncelet LC, Coppens AG, Deltenre PF. Audiograms estimated from brainstem tone‐evoked potentials in dogs from 10 days to 1.5 months of age. J Vet Intern Med 2002;16:674–679.
          pubmed: 12465764
        6. Poncelet LC, Coppens AG, Deltenre P. Brainstem auditory evoked potential wave V latency‐intensity function in normal Dalmatian and Beagle puppies. J Vet Intern Med 2000;14:424–428.
          pubmed: 10935893
        7. Steiss JE, Bredemuehl JP, Wright JC. Nerve conduction velocities and brain stem auditory evoked responses in normal neonatal foals, compared to foals exposed to endophyte‐infected fescue in utero. Prog Vet Neurol 1991;2:252–260.
        8. Katayama A. Postnatal development of auditory function in the chicken revealed by auditory brain‐stem responses (ABRs). Electroenceph Clin Neurophysiol 1985;62:388–398.
          pubmed: 2411521
        9. Ashwal S, Staddon T, Geller M. Brainstem auditory evoked responses in the newborn lamb. Studies during postnatal development and acute hypoxia. Biol Neonate 1984;45:58–68.
          pubmed: 6696955
        10. Strain GM, Graham MC, Claxton MS. Postnatal development of brainstem auditory‐evoked potentials, electroretinograms, and visual‐evoked potentials in the calf. J Vet Intern Med 1989;3:231–237.
          pubmed: 2585370
        11. Doyle WJ, Saad MM, Fria TJ. Maturation of the auditory brain stem response in rhesus monkeys (Macaca mulatta). Electroenceph Clin Neurophysiol 1983;56:210–223.
          pubmed: 6191952
        12. Magdesian KG, Williams DC, Aleman M. Evaluation of deafness in American Paint Horses by phenotype, brainstem auditory‐evoked responses, and endothelin receptor B genotype. J Am Vet Med Assoc 2009;235:1204–1211.
          pubmed: 19912043
        13. Gray LC, Magdesian KG, Sturges BK. Suspected protozoal myeloencephalitis in a two‐month‐old colt. Vet Rec 2001;149:269–273.
          pubmed: 11558662
        14. Moreno‐Aguirre AJ, Santiago‐Rodriguez E, Harmony T. Analysis of auditory function using brainstem auditory evoked potentials and auditory steady state responses in infants with perinatal brain injury. Int J Audiol 2010;49:110–115.
          pubmed: 20151885
        15. Mwaniki MK, Atieno M, Lawn JE. Long‐term neurodevelopmental outcomes after intrauterine and neonatal insults: A systematic review. Lancet 2012;379:445–452.
          pmc: PMC3273721pubmed: 22244654
        16. Yoshikawa S, Ikeda K, Kudo T. The effects of hypoxia, premature birth, infection, ototoxic drugs, circulatory system and congenital disease on neonatal hearing loss. Auris Nasus Larynx 2004;31:361–368.
          pubmed: 15571908
        17. Aleman M, Puchalski SM, Williams DC. Brainstem auditory‐evoked responses in horses with temporohyoid osteoarthropathy. J Vet Intern Med 2008;22:1196–1202.
          pubmed: 18681921
        18. Markand ON, Farlow MR, Stevens JC. Brain‐stem auditory evoked potential abnormalities with unilateral brain‐stem lesions demonstrated by magnetic resonance imaging. Arch Neurol 1989;46:295–299.
          pubmed: 2919985
        19. Steiss JE, Cox NR, Hathcock JT. Brain stem auditory‐evoked response abnormalities in 14 dogs with confirmed central nervous system lesions. J Vet Intern Med 1994;8:293–298.
          pubmed: 7983627
        20. Brewer BD, Koterba AM. Development of a scoring system for the early diagnosis of equine neonatal sepsis. Equine Vet J 1988;20:18–22.
          pubmed: 3366100
        21. Bernard WV, Reimer JM, Cudd T. Historical factors, clinicopathologic findings, clinical features, and outcome of equine neonates presenting with or developing signs of central nervous system disease. AAEP 1995;41:222–224.
        22. Holliday TA, Te Selle ME. Brain stem auditory‐evoked potentials of dogs: Wave forms and effects of recording electrode positions. Am J Vet Res 1985;46:845–851.
          pubmed: 4014834
        23. Holliday TA, Nelson HJ, Williams DC. Unilateral and bilateral brainstem auditory‐evoked response abnormalities in 900 Dalmatian dogs. J Vet Intern Med 1992;6:166–174.
          pubmed: 1619593
        24. Marshall AE. Brainstem auditory‐evoked response in the nonanesthetized horse and pony. Am J Vet Res 1985;46:1445–1450.
          pubmed: 4026024
        25. Rolf SL, Reed SM, Melnick W. Auditory brain stem response testing in anesthetized horses. Am J Vet Res 1987;48:910–914.
          pubmed: 3605806
        26. Toth B, Aleman M, Nogradi N. Meningitis and meningoencephalomyelitis in horses: 28 cases (1985–2010). J Am Vet Med Assoc 2012;240:580–587.
          pubmed: 22332628
        27. Rennie JM, Hagmann CF, Robertson NJ. Outcome after intrapartum hypoxic ischaemia at term. Semin Fetal Neonatal Med 2007;12:398–407.
          pubmed: 17825633
        28. Newton V. Adverse perinatal conditions and the inner ear. Semin Neonatol 2001;6:543–551.
          pubmed: 12014895
        29. Borkoski‐Barreiro SA, Falcon‐Gonzalez JC, Liminana‐Canal JM. Evaluation of very low birth weight (≤1500 g) as a rik indicator for sensorineural hearing loss. Acta Otorrinolaringol Esp 2013;64:403–408.
          pubmed: 23896490
        30. Shapiro SM. Bilirubin toxicity in the developing nervous system. Pediatr Neurol 2003;29:410–421.
          pubmed: 14684236
        31. Polkes AC, Giguere S, Lester GD. Factors associated with outcome in foals with neonatal isoerythrolysis (72 cases, 1988–2003). J Vet Intern Med 2008;22:1216–1222.
          pubmed: 18700857
        32. Shapiro SM, Popelka GR. Auditory impairment in infants at risk for bilirubin‐induced neurologic dysfunction. Semin Perinatol 2011;35:162–170.
          pubmed: 21641490
        33. de Lahunta A, Glass E. Upper motor neuron In: de Lahunta A, Glass E, eds. Veterinary Neuroanatomy and Clinical Neurology, 3rd ed. 2009:192–220.
        34. Santschi EM, Purdy AK, Valberg SJ. Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses. Mamm Genome 1998;9:306–309.
          pubmed: 9530628
        35. Metallinos DL, Bowling AT, Rine J. A missense mutation in the endothelin‐B receptor gene is associated with lethal white foal syndrome: An equine version of Hirshsprung disease. Mamm Genome 1998;9:426–431.
          pubmed: 9585428
        36. Price ER, Fisher DE. Sensorineural deafness and pigmentation genes: Melanocytes and the Mitf transcriptional network. Neuron 2001;30:15–18.
          pubmed: 11343641
        37. Page P, Parker R, Harper C. Clinical clinicopathologic, postmortem examination findings and familial history of 3 Arabians with lavender foal syndrome. J Vet Intern Med 2006;20:1491–1494.
          pubmed: 17186871
        38. Brooks SA, Gabreski N, Miller D. Whole‐Genome SNP association in the horse: Identification of a deletion in myosin Va responsible for lavender foal syndrome. PLoS Genet 2010;6:1–7.
          pmc: PMC2855325pubmed: 20419149
        39. Dacre KJP, Pirie S, Prince DP. Choke, pleuropneumonia and suspected gentamicin vestibulotoxicity in a horse. Equine Vet Educ 2003;15:27–33.

        Citations

        This article has been cited 3 times.
        1. Aleman MR, True A, Scalco R, Crowe CM, Costa LRR, Chigerwe M. Gentamicin-induced sensorineural auditory loss in healthy adult horses. J Vet Intern Med 2021 Sep;35(5):2486-2494.
          doi: 10.1111/jvim.16221pubmed: 34322916google scholar: lookup
        2. Aleman M, Davis E, Williams DC, Madigan JE, Smith F, Guedes A. Electrophysiologic Study of a Method of Euthanasia Using Intrathecal Lidocaine Hydrochloride Administered during Intravenous Anesthesia in Horses. J Vet Intern Med 2015 Nov-Dec;29(6):1676-82.
          doi: 10.1111/jvim.13607pubmed: 26332487google scholar: lookup
        3. Aleman M, Williams DC, Guedes A, Madigan JE. Cerebral and brainstem electrophysiologic activity during euthanasia with pentobarbital sodium in horses. J Vet Intern Med 2015 Mar-Apr;29(2):663-72.
          doi: 10.1111/jvim.12570pubmed: 25800436google scholar: lookup