Sudden Sensorineural Hearing Loss: Subclinical Viral and Toxoplasmosis Infections as Aetiology and How They Alter the Clinical CourseShow others and affiliations
2011 (English)In: ORL, ISSN 0301-1569, Vol. 73, no 2, p. 110-115Article in journal (Refereed) Published
Abstract [en]
Aim: To explore in a prospective study the evidence of certain viral and toxoplasmosis infections in sudden sensorineural hearing loss (SSHL).
Methods: 84 consecutive patients with SSHL meeting certain criteria. All patients were assessed for specific IgM antibodies against cytomegalovirus, herpes simplex virus, toxoplasma and Epstein-Barr virus. All were treated with intravenous steroids and assigned to two groups: 76 IgM negative (NV group) and 8 IgM positive (no history of acute infection - V group).
Results: The mean hearing level at presentation was 86.5 dB HL (median, 100) in the V group and 60.7 dB HL (median, 61) in the NV group. The difference was statistically significant (p = 0.003). The mean hearing level following treatment was 81.8 dB HL (median, 88) in the V group and 48.7 dB HL (median, 39) in the NV group. The difference was statistically significant (p = 0.004). There was a considerable improvement in hearing after treatment only in the NV group (p < 0.000001).
Conclusions: Recent subclinical viral or toxoplasmosis infections may be involved in the pathogenesis of SSHL (in approx. 10% of cases), suggesting that SSHL is not a single disease. When certain viruses or toxoplasmoses are involved, the hearing is much worse in comparison to patients with no such indication of infection. An alteration in treatment dosage or method of steroid administration may be needed in such cases.
Place, publisher, year, edition, pages
S. Karger, 2011. Vol. 73, no 2, p. 110-115
Keywords [en]
Sensorineural hearing loss, sudden, Deafness, Virus infection, Toxoplasmosis, Cytomegalovirus, Herpes simplex virus, Epstein-Barr virus
National Category
Otorhinolaryngology
Identifiers
URN: urn:nbn:se:oru:diva-82029DOI: 10.1159/000324210ISI: 000289109400010PubMedID: 21389742Scopus ID: 2-s2.0-79952323232OAI: oai:DiVA.org:oru-82029DiVA, id: diva2:1432134
2020-05-262020-05-262020-05-26Bibliographically approved